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Journal of Familial Tumors
Volume 11, Issue 2 / 2011
English Article 
Japanese Article- Please note that metadata of J-type articlesare generated by machine-translation and the original texts are written in Japanese.
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A special feature: A cancer and heredity counseling 村上善則*, 中田光** Journal of Familial Tumors 11(2): 35-35, 2011. |
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A Current Status and a Perspective on Medical Genetics of Familial Cancer Yoshinori Murakami* Journal of Familial Tumors 11(2): 36-40, 2011. |
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Genetic Counseling for von Hippel-Lindau Disease Taro Shuin*, Ichiro Yamasaki*, Kenji Tamura* Journal of Familial Tumors 11(2): 41-44, 2011. |
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Here ditary Cancer Pro Program and Cincinnati Children's Hospital 田澤立之* Journal of Familial Tumors 11(2): 45-47, 2011. |
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Hereditary Breast and Ovarian Cancer, from the View Point of Gynecology Akira Hirasawa*,**, Tomohiko Tsuruta*, Kouji Banno*, Nobuyuki Susumu*, Kumiko Misu**, Kumiko Yazaki**, Yuko Takeda**, Koukichi Sugano**, Daisuke Aoki* Journal of Familial Tumors 11(2): 48-51, 2011. |
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Making of practice guidelines on hereditary colon cancer 岩間毅夫* Journal of Familial Tumors 11(2): 52-54, 2011. |
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Fourth pilgrimage verge gastrointestinal tract hereditary tumor society general meeting International Society for Gastrointestinal Hereditary Tumor (InSiGHT) participation report 赤木究* Journal of Familial Tumors 11(2): 55-56, 2011. |
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Collection of the 17th Japanese family-related tumor society arts and sciences meeting program, abstracts greetings 小杉眞司 Journal of Familial Tumors 11(2): A2-A3, 2011. |
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S1. Clinical application of the pharmacogenomics and the development over view 登勉, 堤正好 Journal of Familial Tumors 11(2): A20-A20, 2011. |
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Establishment of the high-precision genotype in the Japanese of the Pharmacokinetics-related gene cluster to investigate the difference that is S1-1 drug-responsive and genome sequencing method 関根章博1, 北本卓也1, 北本綾1, 水澤精穂2, 寺西啓2, 堀田紀久子1, 上嶋健治1, 小杉眞司3, 中尾一和1 Journal of Familial Tumors 11(2): A20-A21, 2011. |
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The approach present conditions and problem of PGx in the S1-2 pharmaceutical company 劉世玉 Journal of Familial Tumors 11(2): A21-A22, 2011. |
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The present conditions and problem of the PGx study in the S1-3 cancer clinical study 西尾和人 Journal of Familial Tumors 11(2): A22-A22, 2011. |
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About correspondence to PGx in the pharmaceutical administration of the S1-4 our country 三宅真二 Journal of Familial Tumors 11(2): A22-A22, 2011. |
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S2. The clinical practice of the hereditary breast cancer ovarian cancer: BRCA1/2 genetic screening and medical therapy over view 戸井雅和 Journal of Familial Tumors 11(2): A23-A23, 2011. |
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- clinical from present conditions and fine-view - basics of S2-1 BRCA1/2 study 三木義男1,2 Journal of Familial Tumors 11(2): A23-A24, 2011. |
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The internal and external situation about the application of the S2-2 BRCA genetic screening 石岡千加史 Journal of Familial Tumors 11(2): A24-A24, 2011. |
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Clinical practice of the S2-3 family-related breast cancer 野水整 Journal of Familial Tumors 11(2): A24-A25, 2011. |
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The present conditions and problem of Triple negative breast cancer treatment in the S2-4 our country 増田慎三 Journal of Familial Tumors 11(2): A25-A25, 2011. |
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The mechanism of action of the PARP inhibitor as a function of S2-5 PARP and the anticancer agent 益谷美都子 Journal of Familial Tumors 11(2): A26-A26, 2011. |
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Clinical development of the S2-6 PARP inhibitor 南博信 Journal of Familial Tumors 11(2): A26-A26, 2011. |
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S3. New aspect over view of the heredity medical care in the perinatal period 澤井英明 Journal of Familial Tumors 11(2): A27-A27, 2011. |
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A diagnosis and genetic background of the S3-1 fetuses systemic bone disease 澤井英明 Journal of Familial Tumors 11(2): A27-A27, 2011. |
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Fetal hydrocephalus by the S3-2 genetic factor 山崎麻美1, 金村米博1, 埜中正博1, 夫律子2 Journal of Familial Tumors 11(2): A28-A28, 2011. |
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Genetic problem to be found in the pregnancy by the S3-3 reproductive medicine 三浦清徳, 増崎英明 Journal of Familial Tumors 11(2): A29-A29, 2011. |
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S3-4 Beyond genetics: epigenetic code in perinatal medicine 秦健一郎 Journal of Familial Tumors 11(2): A29-A29, 2011. |
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S4. Clinical genetics over view in the primary immunodeficiency disease 沼部博直, 西小森隆太 Journal of Familial Tumors 11(2): A30-A30, 2011. |
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Base maintenance of the S4-1 primary immunodeficiency disease study 小原收1,2 Journal of Familial Tumors 11(2): A30-A30, 2011. |
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Gene practice in the S4-2 T cell line immunity abnormality symptom 森尾友宏 Journal of Familial Tumors 11(2): A31-A31, 2011. |
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Clinical genetics in the S4-3 antibody production aplasia 金兼弘和 Journal of Familial Tumors 11(2): A31-A32, 2011. |
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About the genetic screening in the self-inflammatory disease in S4-4 Japan 西小森隆太 Journal of Familial Tumors 11(2): A32-A32, 2011. |
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S5. Authorized heredity counselor over view to support next-generation heredity medical care 山内泰子, 村上裕美, 田辺記子, 大町和美, 畠山未来, 金子実基子, 佐藤友紀, 村上裕美 Journal of Familial Tumors 11(2): A33-A33, 2011. |
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S5-1 authorized counselor heredity - training, qualification, tissue, global image - 山内泰子 Journal of Familial Tumors 11(2): A33-A34, 2011. |
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For process and the future of counselor S5-2 authorized heredity ethic general plan - development - 村上裕美, 小杉眞司 Journal of Familial Tumors 11(2): A34-A35, 2011. |
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The relation of the authorized heredity counselor in the practice system establishment of familial tumor in the S5-3 Shikoku cancer center and the future prospects 大住省三, 谷水正人, 久保義郎, 青儀健二郎, 堀伸一郎, 松元隆, 白山裕子, 高橋三奈, 増田春菜, 田所かおり Journal of Familial Tumors 11(2): A35-A35, 2011. |
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Role of the heredity counselor in the S5-4 cancer center 増田春菜 Journal of Familial Tumors 11(2): A36-A36, 2011. |
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The comprehensive medicine system and heredity counseling for the S5-5 rare hereditary cardiovascular disease 森崎裕子1,2, 小野晶子1,3, 森崎隆幸1,2,4 Journal of Familial Tumors 11(2): A36-A37, 2011. |
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Activity of the authorized heredity counselor in the extensive medical research center specialized in S5-6 cardiovascular disease 小野晶子1,2, 森崎裕子1,3, 森崎隆幸1,3,4 Journal of Familial Tumors 11(2): A37-A38, 2011. |
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Stand on efforts of the - laboratory study center and the duties of the counselor authorization heredity from the situation of the authorized heredity counselor working in S5-7 laboratory study center 和泉美希子1, 金子景香1, 権藤延久1,2 Journal of Familial Tumors 11(2): A38-A38, 2011. |
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S6 The current state of prenatal screening and testing in the United States and the role of genetic counselors at Genzyme Genetics 小野塚香織1 Journal of Familial Tumors 11(2): A39-A39, 2011. |
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S7. MEN (multiple internal secretion neoplasia) over view as the heredity medical care 櫻井晃洋, 鈴木眞一 Journal of Familial Tumors 11(2): A40-A40, 2011. |
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S7-1 frequent occurrence-related internal secretion neoplasia study consortium: The conventional result and future 櫻井晃洋 Journal of Familial Tumors 11(2): A41-A41, 2011. |
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The present conditions of the genetic screening and new therapy for MEN in the S7-2 country 内野眞也 Journal of Familial Tumors 11(2): A41-A41, 2011. |
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About the making of the practice guideline in the S7-3 frequent occurrence-related internal secretion neoplasia 鈴木眞一 Journal of Familial Tumors 11(2): A42-A42, 2011. |
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S7-4 Advocacy group for patients with MEN and their family members "Mukuroji-no-Kai" むくろじの会 会長 Journal of Familial Tumors 11(2): A42-A43, 2011. |
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S7-5 Patients supporting patients with multiple endocrine neoplasia Jo Grey Journal of Familial Tumors 11(2): A43-A43, 2011. |
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Embryology - morphogenetic distortion and pathology development mechanism for T heredity medicine 塩田浩平 Journal of Familial Tumors 11(2): A44-A44, 2011. |
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S8. ELSI (ethical legal social problem) over view in genome medicine, the heredity medical care 小杉眞司 Journal of Familial Tumors 11(2): A45-A45, 2011. |
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Construction of "the study governance" in the S8-1 genomics 白井哲哉1, 三成寿作1, 加藤和人1,2,3 Journal of Familial Tumors 11(2): A46-A46, 2011. |
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S8-2 bio banking: A policy and ethic in the design of the sample collection business 増井徹 Journal of Familial Tumors 11(2): A47-A47, 2011. |
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The present conditions and problem of the issue of S8-3 rare intractable disease 小泉二郎1,2 Journal of Familial Tumors 11(2): A47-A47, 2011. |
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The heredity teaching materials to use in S8-4 Elementary School 中川奈保子1, 沼部博直2, 小杉眞司2 Journal of Familial Tumors 11(2): A48-A48, 2011. |
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S9. CNV study over view of the adulthood disease 江見充, 加藤丈夫 Journal of Familial Tumors 11(2): A49-A49, 2011. |
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S9-1 adulthood disease: Approach from CNV analysis 江見充1,2 Journal of Familial Tumors 11(2): A49-A49, 2011. |
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Copy number change of the isopentenyl diphosphate isomerase gene domain in the S9-2 isolated amyotrophic lateral sclerosis 加藤丈夫1, 江見充1,2, 佐藤秀則1,2, 豊島至3, 祖父江元4, 松原謙一2 Journal of Familial Tumors 11(2): A50-A50, 2011. |
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High-frequency genome deletion in patients with young onset type 2 diabetes by all S9-3 genome CNV analysis 工藤宏仁, 山田哲也, 片桐秀樹, 岡芳知 Journal of Familial Tumors 11(2): A50-A51, 2011. |
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CNV analysis of the S9-4 osteoporosis 浦野友彦1,2, 白木正孝3, 大内尉義2, 井上聡1,2 Journal of Familial Tumors 11(2): A51-A51, 2011. |
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High-frequency copy number deletion in the chromosome subtelomere domain in the S9-5 isolated Parkinson's disease patients 佐藤秀則, 江見充, 荒若繁樹, 和田学, 川並透, 加藤丈夫 Journal of Familial Tumors 11(2): A52-A52, 2011. |
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CNV analysis by the S9-6 MLPA method 権藤延久1,2, 高橋新1, 小林丈二1, 丸瀬英明1 Journal of Familial Tumors 11(2): A52-A52, 2011. |
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ABC of breast cancer, ovarian cancer (HBOC) hereditary for L1 権藤延久1,2, 金子景香1, 和泉美希子1 Journal of Familial Tumors 11(2): A53-A53, 2011. |
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The prospects to the introduction of the genetic analysis technology that is the latest for L2 and diagnosis application 杉本光 Journal of Familial Tumors 11(2): A53-A53, 2011. |
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The future prospects of the L3 DNA microarrays testing 田代啓, 池田陽子, 中野正和, 大見奈津江, 森和彦, 木下茂 Journal of Familial Tumors 11(2): A54-A54, 2011. |
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The present conditions of the use of microarrays in the L4 heredity medical care 小崎健次郎 Journal of Familial Tumors 11(2): A55-A55, 2011. |
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Analysis of a genetic examination of the spinocerebellar degeneration in the O-01 Chiba University Hospital and 27 cases to lack in heredity counseling - family history 澤井摂1,2, 宇津野恵美2, 金井数明3, 佐藤謙一2, 石毛崇之2, 糸賀栄2, 西村基1,2, 松下一之1,2, 桑原聡3, 野村文夫1,2 Journal of Familial Tumors 11(2): A56-A56, 2011. |
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Report of the diagnosis experience before hereditary neurodegenerative disease onset in the O-02 senior Pope 植村健吾1, 沼部博直2, 山下博史1, 近藤孝之1, 谷垣愛1, 檜川里衣1, 浦尾充子2, 富和清隆3, 高橋良輔1 Journal of Familial Tumors 11(2): A56-A56, 2011. |
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Examination of the prenatal diagnosis of the O-03 spinal muscular atrophy (SMA) 浦野真理, 相楽有規子, 斎藤加代子 Journal of Familial Tumors 11(2): A56-A56, 2011. |
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Heredity counseling of the mitochondrial illness in O-04 Kunitachi mind, the nerve medical research center 佐藤有希子, 池上弥生, 後藤雄一 Journal of Familial Tumors 11(2): A57-A57, 2011. |
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Genetic screening of Unverricht-Lundborg disease in our O-05 institution 近藤孝之, 山下博史, 植村健吾, 川又純, 谷垣愛, 檜川里衣, 小林勝哉, 人見健文, 松本理器, 池田昭夫, 高橋良輔 Journal of Familial Tumors 11(2): A57-A57, 2011. |
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Heredity counseling of O-06 autistic spectrum disorder 谷合弘子1,2, 鷲見聡1,3, 鈴森伸宏1 Journal of Familial Tumors 11(2): A57-A57, 2011. |
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Severe joint type Ehlers-Danlos syndrome to be spastic, and to follow the course progressive rapidly with the onset, pervasive developmental disorder of O-07 lower limbs 古庄知己1, 鳴海洋子1, 関島良樹1, 水内麻子1, 山下浩美1, 玉井真理子1, 櫻井晃洋1, 渡邉淳2, 福嶋義光1 Journal of Familial Tumors 11(2): A58-A58, 2011. |
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Step of O-08 Fukuoka clinical heredity meeting for the study ten years 小川昌宣1, 蓮尾泰之1, 斎藤仲道2, 當時久保正之2, 吉里俊幸3, 大久保久美子3, 結城万紀子3, 中川尚志3, 井原健二4, 石井加奈子4, 松下悠紀4, 沼田早苗5, 原田なをみ5, 岸本小百合6, 石井敦士6, 井上貴仁7, 堤信8, 金井信子9 Journal of Familial Tumors 11(2): A58-A58, 2011. |
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The present conditions of the heredity counseling in the O-09 Osaka Prefectural maternal and child care comprehensive medical care center 秋丸憲子1, 松田圭子1,2, 三島祐子1, 池川敦子1, 山本悠斗1, 岡本伸彦1 Journal of Familial Tumors 11(2): A58-A58, 2011. |
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Establishment of the pediatric heredity unit in the O-10 Tama, Tokyo area 吉橋博史1, 細川志帆2, 田中克実2, 大木寛生3 Journal of Familial Tumors 11(2): A59-A59, 2011. |
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Role of the authorized heredity counselor in the physician-led trial including O-11 pharmacogenomics (PGx) 村島京子1,2,3, 大江田知子1,4, 松井仁美1,3, 綱本郷子1,3, 小林恭子1,3, 脇恭子1, 白石一浩2, 澤田秀幸1,3,4 Journal of Familial Tumors 11(2): A59-A59, 2011. |
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Hereditary tumor practice new model system architectural attempt in the O-12 area nucleus hospital 西田千夏子1, 田村智英子1,2, 田中屋宏爾1 Journal of Familial Tumors 11(2): A59-A59, 2011. |
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Experience in the life event of patients with O-13 familial adenomatous polyposis 稲見薫1, 武田祐子1, 岩間毅夫2 Journal of Familial Tumors 11(2): A60-A60, 2011. |
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It is one patient of the familial adenomatous polyposis (FAP) who had rectal cancer after O-14 large intestine complete removal, ileoproctostomy for 20 years 龍泰彦, 赤木由人, 衣笠哲史, 石橋生哉, 田中克明, 白土一太郎, 五反田幸人, 白水和雄 Journal of Familial Tumors 11(2): A60-A60, 2011. |
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Correlative study on susceptibility to colon cancer due to the cause gene of the O-15 familial adenomatous polyposis 大石祥子1, 浦川優作1, 庵前美智子1, 吉田ひとみ1, 柴田奈美2, 竹永富妙子2, 吉澤恵2, 岡村桃花2, 山下知香2, 村上大地2, 横山幸男2, 津田聡司3, 久野隆史3, 山野智基3, 野田雅史3, 松原長秀3, 冨田尚裕3, 巽純子1,2, 藤川和男1,2, 田村和朗1,2 Journal of Familial Tumors 11(2): A60-A60, 2011. |
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Participation of base excision repair gene MYH in the O-16 colon cancer development 久野隆史1, 松原長秀1, 津田聡司1, 馬場谷彰仁1, 濱中美衣1, 山岸大介1, 塚本潔1, 山野智基1, 野田雅史1, 吉澤恵2, 田村和朗2, 冨田尚裕1 Journal of Familial Tumors 11(2): A61-A61, 2011. |
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Practice guidelines on O-17 hereditary colon cancer FAP making 岩間毅夫1, 小泉浩一2, 冨田尚裕3, 石田秀行1, 渡邉聡明4 Journal of Familial Tumors 11(2): A61-A61, 2011. |
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Present conditions report of the O-18 Lynch's syndrome practice guidelines making 冨田尚裕1, 松原長秀1, 田村和朗2, 赤木究3, 小泉浩一4, 石田秀行5, 渡邉聡明6, 岩間毅夫5 Journal of Familial Tumors 11(2): A62-A62, 2011. |
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Examination of the PMS2 genetic screening for Lynch syndrome genetic screening in the O-19 Japanese 川良毅人1, 古井陽介1, 福井崇史1, 籐森浩1, 横山士郎1, 権藤延久1, 角田美穂2, 赤木究2 Journal of Familial Tumors 11(2): A62-A62, 2011. |
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Molecular screening of the Lynch's syndrome using the O-20 colon cancer tissue 赤木究1, 角田美穂1, 高橋朱実1, 朝山雅子2, 西村洋治3, 八岡利昌3, 山口研成2, 田中洋一3 Journal of Familial Tumors 11(2): A63-A63, 2011. |
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Basic examination about the treatment strategy of O-21 MSI-positive colon cancer 田原真紀子1, 佐藤太1, 井上剛志1, 菅野康吉1, 宮倉安幸2, 安田是和2 Journal of Familial Tumors 11(2): A63-A63, 2011. |
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Association to develop from O-22 Lower uterine segment (LUS) between cancer of endometrium and Lynch syndrome 増田健太, 阪埜浩司, 矢野倉恵, 小林佑介, 植木有紗, 木須伊織, 野村弘行, 平沢晃, 進伸幸, 青木大輔 Journal of Familial Tumors 11(2): A63-A63, 2011. |
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The significance of p27 in the O-23 MEN1 mutation in the gene-negative case and the p18 gene: From the examination of the high grade MEN1 case 山田正信1, 小澤厚志1, 田口亮1, 石田恵美1, 森昌朋1, 梶博史2, 今井常夫3, 櫻井晃洋4, MENコンソーシアム1 Journal of Familial Tumors 11(2): A64-A64, 2011. |
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Advanced medical efforts in the O-24 our hospital 伊藤亜希子, 内野眞也, 渡邊陽子, 脇屋滋子, 首藤茂, 野口志郎 Journal of Familial Tumors 11(2): A64-A64, 2011. |
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About this country case of the malignant phaeochromocytoma due to the O-25 SDHB mutation 竹越一博1, 児玉ひとみ2, 緑川早苗3, 新里寿美子1, 磯部和正1, 星野雅也1, 川上康1, 田村秀樹4, 山田正信5, 渡邉淳6, 櫻井晃洋7 Journal of Familial Tumors 11(2): A64-A64, 2011. |
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1 case of the bilateral phaeochromocytoma which showed new generative cell mutation in O-26 TMEM127 gene 武市奈緒美1, 田村秀樹1,2, 加納稔子1, 石崎晃1, 杉原仁1, 渡辺淳3, 五十嵐健人4, 赤須東樹4, 島田隆3, 清水一雄4, 磯部和正5, 新里寿美子5, 竹越一博5, 及川眞一1 Journal of Familial Tumors 11(2): A65-A65, 2011. |
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Condition of a patient investigation of O-27 von Hippel Lindau (VHL) disease 山崎一郎, 田村賢司, 蘆田真吾, 執印太郎 Journal of Familial Tumors 11(2): A65-A65, 2011. |
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Efforts of the genetic information management by the electronic chart in the O-28 Osaka University Hospital 佐藤友紀1, 酒井規夫1, 金川武司1, 大友孝信1, 濱田悠介1, 國府力1, 小巻正泰1, 吉津紀久子1, 西田千夏子1, 市村沙希1, 上田郁奈代2, 松村泰志2, 野口眞三郎1 Journal of Familial Tumors 11(2): A66-A66, 2011. |
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The prospects in process and our country of O-29 Human Variome Project (HVP) 宇都宮譲二1,2, 田中誠3 Journal of Familial Tumors 11(2): A66-A66, 2011. |
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Mutation View as O-30 integration type LSDB: A function and the enlargement of data 大坪正史1, 清水信義2, 蓑島伸生1 Journal of Familial Tumors 11(2): A66-A66, 2011. |
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Calculation algorithmic design and software development of the O-31 inherited disease carriage probability 飯島弘章1, 佐藤俊哉1, 寒水孝司1, 沼部博直2 Journal of Familial Tumors 11(2): A67-A67, 2011. |
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Intractable disease conquest study business judging from the O-32 heredity medical side 福嶋義光1, 櫻井晃洋1, 涌井敬子1, 関島良樹1, 古庄知己1, 鳴海洋子1, 森崎裕子2, 森崎隆幸2 Journal of Familial Tumors 11(2): A67-A67, 2011. |
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From O-33 recognition, expectation, the attitude survey to misunderstanding - "bio bank Japan" enrolled patients 武藤香織1, 渡部麻衣子1, 洪賢秀1, 荒内貴子2, 舞原佳子3, 大森あゆみ3, 畠山未来3, 渡邉淳3,4, 島田隆3,4, 南史朗3,5 Journal of Familial Tumors 11(2): A67-A67, 2011. |
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About the second revision of the O-34 "operational guideline of the examination for pharmacogenomics" 堤正好 Journal of Familial Tumors 11(2): A68-A68, 2011. |
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Genetic polymorphism search about onset of the severe neutropenia by the O-35 docetaxel 内山智貴1, 菅野仁1,2,3, 石谷健4, 相崎潤子2, 濱田貴子2, 藤井寿一3, 松井英雄4, 斎藤加代子1,2 Journal of Familial Tumors 11(2): A68-A68, 2011. |
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Efforts to the prenatal diagnosis at the hospital attached to the O-36 Tottori University faculty of medicine 笠城典子1,2, 足立香織3, 金子周平4, 菊池義人4, 大野耕策5, 近藤章子5, 戸川雅美5, 原田省6, 原田崇6, 難波栄二2,3 Journal of Familial Tumors 11(2): A68-A68, 2011. |
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Examination about 2,000 amniotic diagnosis enforcement in the O-37 our hospital 佐藤茂1,2, 近藤朱音1,2, 後藤優美子1,2, 高橋千果1,2, 松本直1,2, 池田仁惠1,2, 森屋宏美2, 溝口満子2, 岩崎克彦1, 和泉俊一郎1,2 Journal of Familial Tumors 11(2): A69-A69, 2011. |
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The need of the authorized heredity counselor in the reporting of the amniotic fluid chromosomal analysis to O-38 pregnant woman 西山深雪1,2, 澤井英明3, 小杉眞司2 Journal of Familial Tumors 11(2): A69-A69, 2011. |
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2 cases that caused complete chorioamniotic membrane separation after O-39 amniocentesis 三宅秀彦1,2, 中西一歩1, 阿部裕子1, 林昌子1, 奥田直貴1, 川端伊久乃1, 関口敦子1, 中井章人1, 渡邉淳2, 大木由加志2, 島田隆2 Journal of Familial Tumors 11(2): A69-A69, 2011. |
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O-40 Hypermobility Syndrome in Japan 畠山未来1,2, 渡邉淳2, 古庄知己3, 川目裕1, 島田隆2 Journal of Familial Tumors 11(2): A70-A70, 2011. |
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National fact-finding of the O-41 Bardet-Biedl syndrome 平野牧人1, 山下俊英2, 生野恭司3, 岩橋博見4, 大石充5, 真野利之6, 石原立7, 田中一郎8, 柳原恵子6, 中村雄作1, 楠進9 Journal of Familial Tumors 11(2): A70-A70, 2011. |
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The need of follow-up from heredity practice - perinatal period of the O-42 perinatal period type low phosphatase symptom 渡辺淳1,2, 鈴木由美1, 菅野華子1,2, 峯克也3, 阿部崇3, Banyar Than Naing2, 竹下俊行3, 折茂英生2, 澤井英明4, 島田隆1,2 Journal of Familial Tumors 11(2): A70-A70, 2011. |
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Gene introduction - to O-43 fetal gene therapy - severe form low phosphatase symptom mouse fetuses 菅野華子1,2,3, 渡邉淳1,3, 島田隆1,3 Journal of Familial Tumors 11(2): A71-A71, 2011. |
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IL28B gene SNP analysis by O-44 GENECUBE(R) and application to an IFN treatment convalescence prediction 松尾百華1, 阿部泰典1, 杉本和史1,2, 西岡淳二1, 中谷中1,2,3, 登勉1,2 Journal of Familial Tumors 11(2): A71-A71, 2011. |
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One case of new bacterial species Mycobacterium shinjukuense which caused false-positive by an examination of O-45 tuberculosis mycol. identification 田中春華, 廣瀬春香, 竹森美紀, 木田沙緒里, 米澤広美, 宮島栄治 Journal of Familial Tumors 11(2): A71-A71, 2011. |
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Development of the Pandemic (H1N1) by the O-46 SmartAmp method 2009 virus nucleic acid test for the detection 向後泰司1,2, 石川智久2, 川井雄輝1,2, 木村恭将2, 金森基1,2, 臼井健悟2, 三谷康正1,2, 花見健志2, 相馬崇裕2, 佐賀聡美2, 石津有里2, MORLIGHEM Jean-Etienne2, LEZHAVA Alexander2, 林崎良英2 Journal of Familial Tumors 11(2): A72-A72, 2011. |
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Examination of the operational improvement of the O-47 Amplicor HPV association kit 宮原由紀子, 三浦俊昭, 林邦彦 Journal of Familial Tumors 11(2): A72-A72, 2011. |
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Quality evaluation of the RNA using the O-48 microchip electrophoresis system 竹田真由1, 斉藤邦明2, 舩渡忠男1 Journal of Familial Tumors 11(2): A72-A72, 2011. |
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Examination of plasma K-ras mutation in the gene analysis by the O-49 PNA-Clamping sequence method 丸瀬英明1, 古井陽介1, 福井崇史1, 藤森浩1, 野本忠明1, 横山士郎1, 権藤延久1, 宮野省三2, 花澤喜三郎2 Journal of Familial Tumors 11(2): A73-A73, 2011. |
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The simple and easy detection of the myotonica dystrophia (DM1) CTG amplification repeat using the O-50 Triplet repeat primed PCR (TP-PCR) method 佐藤謙一1, 糸賀栄1, 石毛崇之1,3, 宇津野恵美1,2, 澤井摂1,2,3, 西村基1,2,3, 松下一之1,2,3, 野村文夫1,2,3 Journal of Familial Tumors 11(2): A73-A73, 2011. |
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Research and development of clinical somatic gene mutation detection system (Quimple(R)) for O-51 colon cancer molecules target effect of treatment predictions 北野史朗1,2, Wanqing Liu2, Mark Ratain2, 天野雅彦1 Journal of Familial Tumors 11(2): A73-A73, 2011. |
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Analysis of the warfarin-related genetic polymorphism by device SNP Analyzer using the O-52 Invader Plus method 藤田京志1, 小笠原彩子1, 莚田泰誠2, 渡邉淳1, 島田隆1 Journal of Familial Tumors 11(2): A74-A74, 2011. |
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Search of the life-style related diseases onset risk prediction gene marker which assumed O-53 heredity epidemiology cohort a base 吉田安彦1, 辻真吾1,4, 花城薫1, 喜屋武麻美1, 森谷哲浩1, 岩本恭典1, 顔瑾1, 長嶺勝2, 崎間敦3, 大屋祐輔3, 根本靖久1 Journal of Familial Tumors 11(2): A74-A74, 2011. |
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About a genetic factor of the O-54 gout onset 谷口敦夫, 浦野和子, 関田千恵子, 井上永介, 小関由美, 市川奈緒美, 山中寿 Journal of Familial Tumors 11(2): A74-A74, 2011. |
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Association between O-55 IL-5, IL-6, seasonal polymorphism and condition of a patient convalescence of the autoimmune thyroid disease of the IL-13 gene promoter domain 渡邉幹夫1, 井上直哉1, 森田麻美1, 巽圭太2, 日高洋2, 赤水尚史3, 岩谷良則1 Journal of Familial Tumors 11(2): A75-A75, 2011. |
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CDH13 genetic polymorphism entangles it in an association between O-56 adiponectin and insulin resistance 田原康玄1, 川本龍一2, 小原克彦3, 三木哲郎3 Journal of Familial Tumors 11(2): A75-A75, 2011. |
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The combination of O-57 LDLR gene and PCSK9 mutation in the gene and examination about the LDL-C level 太田直孝1,2, 斯波真理子3,4, 藤山啓美1,2, 藤野正裕1,2, 佐野隆宏1, 岩本紀之3, 槇野久志3, 岸本一郎3, 佐野道孝1, 宮本恵宏2,5 Journal of Familial Tumors 11(2): A75-A75, 2011. |
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National fact-finding of the O-58 Costello's syndrome, CFC syndrome and study on condition of a patient 松原洋一1, 阿部裕1, 新堀哲也1, 黒澤健司2, 岡本伸彦3, 水野誠司4, 大橋博文5, 川目裕6, 緒方勤7, 呉繁夫8, 栗山進一9, 青木洋子1 Journal of Familial Tumors 11(2): A76-A76, 2011. |
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A prevalence estimate of the O-59 CHARGE syndrome and clinical examination 三島祐子1, 松田圭子1, 秋丸憲子1, 池川敦子1, 山本悠斗1, 小崎健次郎2, 岡本伸彦1 Journal of Familial Tumors 11(2): A76-A76, 2011. |
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Clinical picture and genome epigenome analysis of the O-60 this country Beckwith-Wiedemann syndrome 副島英伸, 城崎幸介, 八木ひとみ, 前田寿幸, 大塚泰史, 東元健 Journal of Familial Tumors 11(2): A76-A76, 2011. |
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One case that was complicated with the mesenchymal dysplastic placenta for O-61 Beckwith-Wiedemann syndrome, and presented estrangement for imprinting abnormality of both 三好潤也1, 坂口勲1, 大場隆1, 片渕秀隆1, 副島英伸2, 東元健2 Journal of Familial Tumors 11(2): A77-A77, 2011. |
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Making of the human fetus three dimensions stereoscopic films (Virtual Human Embryo) using O-62 "Kyoto collection" 高桑徹也1, 山田重人2, 上部千賀子2, 塩田浩平2, 巨瀬勝美3 Journal of Familial Tumors 11(2): A77-A77, 2011. |
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Morphometrical analysis of the emergence of stomach using the O-63 humans fetus MRI image 海外憲人1, 高桑徹也1, 山田重人2, 上部千賀子2, 塩田浩平2, 巨瀬勝美3 Journal of Familial Tumors 11(2): A77-A77, 2011. |
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Problem for the clinical application of the O-64 array chromosome banding 原田直樹1, 松井健1, 齋藤和正1, 霜川修1, 吉浦孝一郎2, 松本直通3, 近藤達郎4 Journal of Familial Tumors 11(2): A78-A78, 2011. |
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Genome copy number change of public adults detected by O-65 Cytogenetic Array analysis 涌井敬子1,2, 古庄知己1,2, 鳴海洋子1,2, 清水健司3, 大橋博文3, 福嶋義光1,2 Journal of Familial Tumors 11(2): A78-A78, 2011. |
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New characteristic of the disease gene cluster located in the chromosome band border which we pinpointed as O-66 human genome destabilization part 渡邊良久, 前川真人 Journal of Familial Tumors 11(2): A78-A78, 2011. |
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Report of the preimplantation diagnosis for the abortus habitualis due to translocation of chromosome in the O-67 our hospital 山本あゆみ1, 福田愛作1, 小林亮太1, 上田由美子1, 樽井幸与1, 大垣彩1, 五寶秀美1, 森本義晴2 Journal of Familial Tumors 11(2): A79-A79, 2011. |
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It is examination about the heredity counseling in the miscarriage case after O-68 infertility treatment 片桐由起子1, 福田雄介2,3, 宗晶子2,3, 松江陽一2,3, 三枝美智子2,3, 竹下直樹1, 森田峰人2 Journal of Familial Tumors 11(2): A79-A79, 2011. |
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Decision making of the pregnant woman who had a diagnosis of Trisomy18 during the O-69 pregnancy 李紅蓮1,2, 藤田秀樹1, 林聡3, 左合治彦3, 小崎里華1 Journal of Familial Tumors 11(2): A79-A79, 2011. |
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Family system case of the autosomal dominant Aicardi-Goutieres syndrome which led to a diagnosis with O-70 chillblains-like eruption 粟屋智就1, 井澤和司1, 阿部純也1, 加藤竹雄1, 平城徹2, 平城直子2, 大嶋勇成3, 西小森隆太1, 平家俊男1 Journal of Familial Tumors 11(2): A80-A80, 2011. |
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Heredity of the O-71 Tokyo Medical Univ. dermatology is foreign 三橋善比古, 堺則康, 内山真樹, 前田龍郎, 坪井良治 Journal of Familial Tumors 11(2): A80-A80, 2011. |
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One case of the Bothnia JIS trophy of the O-72 Japanese 堀田喜裕1, 細野克博1, 野嶋計寿1, 趙洋1,2, 彦谷明子1, 近藤峰生2, 蓑島伸生3 Journal of Familial Tumors 11(2): A80-A80, 2011. |
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Efforts to hereditary deafness as the O-73 advanced medical care 谷口美玲1, 北尻真一郎1, 宇佐美真一2, 伊藤壽一1, 小杉眞司3 Journal of Familial Tumors 11(2): A81-A81, 2011. |
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The detection of the mutation in the gene of 21 hydroxylase deficiency 132 families in O-74 this country 臼井健1, 革嶋幸子2, 田上哲也2, 成瀬光栄1, 島津章1 Journal of Familial Tumors 11(2): A81-A81, 2011. |
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The fact and problem of the heredity counseling of hemophilia in O-75 Japan 井上佳世1, 玉井真理子2, 関由起子3, 井上洋士4, 北村弥生5, 長濱輝代6, 丹明彦7, 久地井寿哉8, 石射いずみ8, 柿沼章子8, 大平勝美8, 山本佳世乃1, 川目裕1 Journal of Familial Tumors 11(2): A81-A81, 2011. |
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Genetic analysis of the O-76 fanconi anaemia 庵前美智子1, 内田恵美2, 吉田ひとみ1, 巽純子1,3, 南武志1,3, 藤川和男1,3, 田村和朗1,3, 矢部みはる4, 高田穣2 Journal of Familial Tumors 11(2): A82-A82, 2011. |
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Genetic screening of the O-77 erythropoietic porphyria: Analysis of this country 30 families 中野創1, 上出良一2, 川原繁3, 川田暁3 Journal of Familial Tumors 11(2): A82-A82, 2011. |
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Examination about the attitude survey of the obstetrician for O-78 family-related tumor 三浦史晴, 本田達也, 熊谷晴介, 吉崎陽, 福島明宗, 杉山徹 Journal of Familial Tumors 11(2): A82-A82, 2011. |
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Decision making "not to receive" the genetic screening in O-79 family-related tumor 仲田洋美1,2,3, 増田春菜1, 岡本陽子2, 堀伸一郎1, 久保義郎1, 白山裕子1, 松本隆1, 青義健二郎1, 大住省三1, 谷水正人1, 金子景香4, 中野芳朗7, 三好康雄5, 冨田尚裕6, 玉置知子3,7 Journal of Familial Tumors 11(2): A83-A83, 2011. |
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A relation and heredity counseling of familial tumor in O-80 cancer treatment 角田ますみ1,2, 鈴木眞一1, 中野恵一1, 福島俊彦1, 緑川早苗3, 野水整4, 竹之下誠一1 Journal of Familial Tumors 11(2): A83-A83, 2011. |
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In the case of construction - Niigata of the O-81 family-related breast cancer heredity counseling practice system 田澤立之1, 後藤清恵1, 遠山潤1,5, 栗山洋子1, 坂田英子2, 小山諭2, 佐藤信昭3, 佐野宗明4, 畠山勝義2, 中田光1 Journal of Familial Tumors 11(2): A83-A83, 2011. |
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Consensus (from multicenter questionnaire results) of O-82 hereditary, the family-related breast cancer practice 杉江知治1, 戸井雅和1, 光森道英2, 山内智佳子3, 石黒洋4, 三上芳喜5, 岡村隆仁6, 加藤大典7, 山内清明8, 稲本俊9 Journal of Familial Tumors 11(2): A84-A84, 2011. |
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Examination of the counseling example of the O-83 hereditary breast cancer, ovarian cancer syndrome 兵頭麻希1, 音部玲子1, 加瀬佳寿江1, 家護谷五月1, 大原正裕1, 松浦伸也1, 横崎恭之1, 檜山英三1, 檜山桂子1, 丸山博文1, 小林正夫1, 村上茂2 Journal of Familial Tumors 11(2): A84-A84, 2011. |
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Hope for the genetic screening of patients with O-84 ovarian cancer being performed 甲斐奈央1, 宮下美香2, 二井谷真由美2 Journal of Familial Tumors 11(2): A84-A84, 2011. |
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The present conditions of the genetic screening effective time for O-85 hereditary breast cancer, ovarian cancer (HBOC) 西村誠一郎1, 新井正美2, 細川志帆2, 岩瀬拓士1 Journal of Familial Tumors 11(2): A85-A85, 2011. |
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Risk assessment of the hereditary breast cancer ovarian cancer by the O-86 recursive fractionation 菅野康吉1,2,3,5, 牧島恵子1, 友田茉莉1,2, 三須久美子3, 平澤晃3, 武田祐子3,4, 和泉秀子5, 吉田輝彦5,6 Journal of Familial Tumors 11(2): A85-A85, 2011. |
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Efforts to the case that had difficulty in diagnosis by O-87 BRCA genetic screening 新井正美1,2, 瀧景子1, 須貝幸子2, 小松美樹2, 佐藤友理1, 西村誠一郎3, 岩瀬拓士3, 横山士郎4, 権藤延久4, 三木義男1,2 Journal of Familial Tumors 11(2): A85-A85, 2011. |
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Clinicopathologic examination of the familial breast cancer in the O-88 our hospital 前田浩幸1, 米田誠2, 中澤雅子1, 廣野靖夫1, 五井孝憲1, 飯田敦1, 片山寛次1, 伊藤浩史3, 今村好章4, 山口明夫1 Journal of Familial Tumors 11(2): A86-A86, 2011. |
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Clinicopathologic examination of the O-89 family-related breast cancer 亀嶋秀和1, 大村東生1, 鈴木やすよ1, 九冨五郎1, 平田公一1, 長谷川匡3 Journal of Familial Tumors 11(2): A86-A86, 2011. |
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Examination of the O-90 both sides breast cancer 石黒淳子, 有賀智之, 山下年成, 鈴木栄治, 堀口和美, 黒井克昌 Journal of Familial Tumors 11(2): A86-A86, 2011. |
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The situation of the inside and outside the country patients association in the P1-01 frequent occurrence-related internal secretion neoplasia (MEN) 片井みゆき1, 櫻井晃洋2 Journal of Familial Tumors 11(2): A87-A87, 2011. |
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Collaboration of patients with inherited disease in P1-02 Japan, the family group 赤間孝典1, 櫻井晃洋1, 横川吉晴2, 野見山哲夫3, 福嶋義光1 Journal of Familial Tumors 11(2): A87-A87, 2011. |
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About guidebook making of the inherited disease for the P1-03 patients and the family 飛騨美希, 山内泰子, 牧優子, 升野光雄, 黒木良和 Journal of Familial Tumors 11(2): A87-A87, 2011. |
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Experience P1-04 heredity medical care and the training about the personnel training in the U.K. 野村文夫1, 澤井摂1,2,3, 木原真紀3,5, 宇津野恵美2,3, 大町和美3,4, 葛田衣重3,6, 小黒晴美3,7, 本間裕美3,7, 羽田明3,4 Journal of Familial Tumors 11(2): A88-A88, 2011. |
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Receive heredity counseling education of P1-05 Kinki University 守井見奈, 庵前美智子, 吉田ひとみ, 巽純子, 南武志, 田村和朗, 長尾哲二, 藤川和男 Journal of Familial Tumors 11(2): A88-A88, 2011. |
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Construction of the comprehensive resource of the heredity counseling in P1-06 Japan 市川真臣, 升野光雄, 山内泰子, 黒木良和 Journal of Familial Tumors 11(2): A88-A88, 2011. |
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Evaluation as the education tool of the P1-07 heredity drama 田中敬子1, 櫻井晃洋2, 福嶋義光2 Journal of Familial Tumors 11(2): A89-A89, 2011. |
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P1-08 thinks about education of the inherited disease through the impressionistic essay of "1 liter of tear" 松本彬伸1, 巽純子1,2, 田村和朗1,2, 藤川和男1,2 Journal of Familial Tumors 11(2): A89-A89, 2011. |
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Evaluation second report as the education tool of the comics "genome card" with the P1-09 sound 河村理恵, 櫻井晃洋, 福嶋義光 Journal of Familial Tumors 11(2): A89-A89, 2011. |
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Attempt to share P1-10 heredity counseling role playing between distant places by Skype 桑原由樹1, 巽純子1, 大石祥子1, 浦川優作1, 松本彬伸1, 梅田果林2, 田村和朗1, 羽田明2, 藤川和男1 Journal of Familial Tumors 11(2): A90-A90, 2011. |
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P1-11 A Case of Li-Fraumeni syndrome: heterochronous bilateral breast cancer with heterochronous unilateral double 増村京子1, 西村誠一郎1, 新井正美2, 堀井理絵3, 秋山太3, 岩瀬拓士1 Journal of Familial Tumors 11(2): A90-A90, 2011. |
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An example of the PJS families where breast cancer developed in youth though we lacked in clinical examination of P1-12 Peutz-Jeghers Syndrome (PJS) 仲田洋美1,2,3, 増田春菜1, 田所かおり1, 堀伸一郎1, 久保義郎1, 白山裕子1, 松元隆1, 青儀健二郎1, 大住省三1, 菊内由貴1, 井上実穂1, 谷水正人1 Journal of Familial Tumors 11(2): A90-A90, 2011. |
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An example of the Lynch syndrome that developed a malignant lymphoma and sigmoid colon cancer in P1-13 heterochrony 仲田洋美1,2,3, 増田春菜1, 田所かおり1, 堀伸一郎1, 久保義郎1, 白山裕子1, 松元隆1, 青儀健二郎1, 大住省三1, 菊内由貴1, 井上実穂1, 谷水正人1 Journal of Familial Tumors 11(2): A91-A91, 2011. |
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Questionary survey about recognition and the examination promotion of the breast cancer risk of the family in patients with P1-14 breast cancer 増田春菜1, 大住省三1,2, 金子景香3, 田所かおり1, 仲田洋美1,4,5, 清藤佐知子2, 高橋三奈1,2, 原文堅2, 高嶋成輝2, 高畠大典2, 青儀健二郎1,2, 谷水正人1 Journal of Familial Tumors 11(2): A91-A91, 2011. |
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An example of the bilateral adrenal phaeochromocytoma that P1-15 new TMEM127 mutation in the gene was identified 緑川早苗1, 竹越一博2, 佐藤博亮1, 鈴木眞一3, 笹野公伸4, 渡辺毅1 Journal of Familial Tumors 11(2): A91-A91, 2011. |
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Heredity counseling of the patients of the HPPS suspicion due to the SDHB mutation that suffered from P1-16 definitive diagnosis 角田ますみ1,2, 鈴木眞一1, 中野恵一1, 福島俊彦1, 緑川早苗3, 野水整4, 竹之下誠一1 Journal of Familial Tumors 11(2): A92-A92, 2011. |
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About problems about the advanced medical operation of the P1-17 RFT genetic screening 首藤茂, 内野眞也, 渡邊陽子, 脇屋滋子, 伊藤亜希子, 野口志郎 Journal of Familial Tumors 11(2): A92-A92, 2011. |
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One case that the adrenal phaeochromocytoma of the unrepresentativeness symptom became the presenting symptoms by S891A mutation to be found in patients with P1-18 family-related medullary carcinoma of thyroid 大江瑞恵1,2, 日比八束3, 小杉眞司4,5, 倉橋浩樹1,2 Journal of Familial Tumors 11(2): A92-A92, 2011. |
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One case of MEN1 who had P1-19 TSHoma 良元紳浩1, 鈴木眞一1, 大河内千代1, 左雨元樹1, 中野恵一1, 福島俊彦1, 竹之下誠一2 Journal of Familial Tumors 11(2): A93-A93, 2011. |
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MEN1 genetic analysis in the P1-20 frequent occurrence-related internal secretion neoplasia study consortium 櫻井晃洋1,6,10, 今井常夫2,10, 梶博史3,10, 山田正信4,10, 小澤厚志4,10, 五十嵐健人5,10, 山崎雅則6,10, 内野眞也7,10, 鈴木眞一8,10, 小杉眞司9,10 Journal of Familial Tumors 11(2): A93-A93, 2011. |
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From consideration for improvement of the ethic guideline (Sansho guideline) about the P1-21 human genome, genetic analysis study and the results of the questionary survey for proposal - researcher and the overseas investigation - 位田隆一1, 高橋貴哲2, 加藤和人3 Journal of Familial Tumors 11(2): A93-A93, 2011. |
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Genetic personal information that was found without intending in P1-22 human genome, a genetic analysis study, handling of the abnormality of the genes 尾堀佐知子, 平原史樹, 山口瑞穂, 浜之上はるか, 加藤英明, 宮武聡子, 田野島美城, 奥田美加, 沢井かおり Journal of Familial Tumors 11(2): A94-A94, 2011. |
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The present conditions of the Ethical Review Board about human genome, the genetic analysis study in the P1-23 medicine system university 道和百合, 小杉眞司 Journal of Familial Tumors 11(2): A94-A94, 2011. |
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Heredity counseling of the men who have been going to know the fact that P1-24 grass widow married again 白石一浩, 村島京子 Journal of Familial Tumors 11(2): A94-A94, 2011. |
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Mainly on P1-25 registration of patient and the example of one consideration ... "tailor-made medicine realization project" about the role of the research coordinator in the chase 洪賢秀, 武藤香織, 張瓊方, 渡部麻衣子 Journal of Familial Tumors 11(2): A95-A95, 2011. |
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Is the genetic testing necessary for P1-26 public system application? It is ... from example experience of ... spinal and bulbar atrophy 葛田衣重1, 澤井摂2,3, 宇津野恵美2, 大町和美2, 金井数明2,3, 桑原聡3, 羽田明2, 野村文夫2 Journal of Familial Tumors 11(2): A95-A95, 2011. |
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Counselor authorization heredity - added to approach - consultation person in charge team of the heredity counseling for hereditary neurologic intractable diseases in the P1-27 area 山内泰子1, 千代豪昭2, 澤田甚一3,4, 野正佳余4, 狭間敬憲3,4, 升野光雄1, 黒木良和1, 戸田達史5 Journal of Familial Tumors 11(2): A96-A96, 2011. |
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Analysis of the case in genetic counselling - Tokyo children nursing hospital of the P1-28 developmental disease 赤星惠子, 椎木俊秀, 和田恵子, 牧野道子, 武智信幸, 松田光展, 武井理子, 武田さおり, 松井秀司, 奈須康子, 舟橋満寿子, 鈴木康之 Journal of Familial Tumors 11(2): A96-A96, 2011. |
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From the questionary survey to the parent of - adulthood patients looking back on childhood of the P1-29 Williams syndrome - 鬼頭由子1,2, 岡崎伸3, 富和清隆1,3,4 Journal of Familial Tumors 11(2): A97-A97, 2011. |
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Psychological effect - quantitative and qualitative study - that carrier diagnosis of the P1-30 structural chromosome aberration gives to the person and a family 金子実基子1, 大橋博文2, 篁倫子1, 川目裕1 Journal of Familial Tumors 11(2): A97-A97, 2011. |
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An example of the Gitelman syndrome where new mutation was found by P1-31 genetic testing 中山智祥1, 佐藤直之1, 常喜信彦2, 柳田靖子2, 田中友里2, 長谷弘記2 Journal of Familial Tumors 11(2): A97-A97, 2011. |
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P1-32 splice abnormal genetic screening - pit fall and approach method - 仁井見英樹, 尾川智美, 野手良剛, 林史朗, 上野智浩, 原田健右, 宇治義則, 北島勲 Journal of Familial Tumors 11(2): A98-A98, 2011. |
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Simultaneous analysis of two alcohol metabolism genetic polymorphism of P1-33 ADH1B, ALDH2 太田豊1, 有賀博文2, 佐見学1, 神田智正1, Junko Stevens2 Journal of Familial Tumors 11(2): A98-A98, 2011. |
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The measurement and significance of the P1-34 disease-related genetic screening 川口竜二1, 小久保静香1, 渡邊真紀子1, 澤谷桐子1, 李昌珪3, 櫻林郁之介4 Journal of Familial Tumors 11(2): A98-A98, 2011. |
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Genetic analysis of the odontogenic tumor which developed in P1-35 nevus basal cell carcinoma syndrome 宮下俊之1, 桐生麻衣子1, 佐々木亮2, 齋藤加代子3, 藤井克則4 Journal of Familial Tumors 11(2): A99-A99, 2011. |
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1 case of the hypotrichosis in acknowledgment of P1-36 LIPH mutation in the gene 沼田早苗1,2, 濱田尚宏1,2, 原田なをみ2,3,4, 大平智子2,3, 渡邊順子2,3, 芳野信2,3, 下村裕5, 橋本隆1,2 Journal of Familial Tumors 11(2): A99-A99, 2011. |
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Experience the heredity counseling of the P1-37 xeroderma pigmentosum 2 case 宇津野恵美1, 清水彩子2, 鎌田憲明2, 神戸直智2, 松江弘之2, 野村文夫1 Journal of Familial Tumors 11(2): A99-A99, 2011. |
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Heredity counseling of the albinism families who assume P1-38 1-week-old neonates after birth probands 浦川優作1, 庵前美智子1, 吉田ひとみ1, 巽純子1, 田村和朗1, 藤川和男1, 森脇真一2 Journal of Familial Tumors 11(2): A100-A100, 2011. |
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Analysis - of the content of information, the meeting question paper of support - parent that a parent, a family of the P1-39 "chromosome abnormal child" finds 勝元さえこ1, 荒井優気2, 鳥嶋雅子2, 浦尾充子1, 沼部博直2, 小杉眞司2 Journal of Familial Tumors 11(2): A100-A100, 2011. |
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Heredity counseling of the example that had a countryman of the P1-40 Bardet-Biedl syndrome, and had a diagnosis of retinal pigment degeneration recently 大町和美1, 萩原章2, 羽田明1,3, 野村文夫3 Journal of Familial Tumors 11(2): A100-A100, 2011. |
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Fact-finding report about the homepage in the P2-01 whole country gene medical care section 小巻正泰1,2, 佐藤友紀1, 濱田悠介1,4, 大友孝信1,4, 吉津紀久子1,3, 國府力1,6, 酒井規夫1,4, 野口眞三郎1,5 Journal of Familial Tumors 11(2): A101-A101, 2011. |
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The heredity counseling foreign present situation in the P2-02 our hospital 蓮尾泰之, 小川昌宣 Journal of Familial Tumors 11(2): A101-A101, 2011. |
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Heredity counseling for P2-03 elderly people 岡本陽子1, 管原由恵1, 三村博子1, 木村卓2, 仲田洋美1,4, 玉置知子1,3 Journal of Familial Tumors 11(2): A101-A101, 2011. |
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About the present conditions of the heredity counseling in P2-04 a variety of culture 朱肖捷, 川目裕, 山本佳世乃 Journal of Familial Tumors 11(2): A102-A102, 2011. |
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Cooperation of a psychology job and the nursing job in the P2-05 heredity outpatient department 玉井真理子, 山下浩美, 水内麻子, 福嶋義光 Journal of Familial Tumors 11(2): A102-A102, 2011. |
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Effect of the life story interview to a client concerned with P2-06 inherited disease 山本佳世乃, 川目裕 Journal of Familial Tumors 11(2): A102-A102, 2011. |
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Pay the attention to effect factor - to counselee in the P2-07 heredity counseling particularly a non-language; and - 巽純子1,2, 岡持由里2 Journal of Familial Tumors 11(2): A103-A103, 2011. |
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About lack of understanding and the misunderstanding for the genetic information of counselee and the family with the P2-08 inherited disease 深野智華, 山本佳世乃, 川目裕 Journal of Familial Tumors 11(2): A103-A103, 2011. |
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The way of the genetic screening studies education in the P2-09 medical technologist training course 神崎秀嗣 Journal of Familial Tumors 11(2): A103-A103, 2011. |
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Consideration that we maintain understanding - tutorial for the prenatal diagnosis of the P2-10 medical student 近藤朱音1,2, 大貫優子2, 佐藤茂1,2, 高橋千果1,2, 後藤優美子1,2, 溝口満子2, 和泉俊一郎1,2 Journal of Familial Tumors 11(2): A104-A104, 2011. |
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Is the VTR seeing and hearing about P2-11 Down's syndrome useful in the heredity counseling about the prenatal diagnosis? 橋本直也1, 熊耳敦子2, 堀内洋子2, 塩田恭子2, 草川功3, 草間良子2, 吉野美紀子2, 有森直子2, 山中美智子2, 佐藤孝道2, 石田也寸志3 Journal of Familial Tumors 11(2): A104-A104, 2011. |
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Questionnaire about the diagnosis notice of P2-12 Down's syndrome 鮫島希代子1, 林泰秀2 Journal of Familial Tumors 11(2): A104-A104, 2011. |
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Investigation about the health care of adults with P2-13 Down's syndrome 植田紀美子1, 岡本伸彦2, 平山哲3, 巽純子4, 松田圭子2, 秋丸憲子2, 三島祐子2, 池川敦子2, 佐川史郎5 Journal of Familial Tumors 11(2): A105-A105, 2011. |
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Activity of the P2-14 Nagano Prefectural children Hospital Down syndrome group outpatient department 荒川経子 Journal of Familial Tumors 11(2): A105-A105, 2011. |
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Enzygotic twin case of mosaicism trisomy 21 that Down's syndrome, other one child presented with a normal phenotype P2-15 one child 望月純子1,4, 狐崎雅子2,4, 天野完1, 海野信也1, 高田史男3,4 Journal of Familial Tumors 11(2): A105-A105, 2011. |
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Decision-making dilemma for the surgical treatment of congenital heart disease complicated with P2-16 Down's syndrome 清水健司1, 小島美佐子1, 大橋博文1, 小川潔2, 柿沼千秋3, 平野明美3 Journal of Familial Tumors 11(2): A106-A106, 2011. |
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Genetic screening of P2-17 tardive neurofibromatosis (NF7) 内山真樹, 堺則康, 前田龍郎, 坪井良治, 三橋善比古 Journal of Familial Tumors 11(2): A106-A106, 2011. |
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The reproductive medicine for women with P2-18 Turner syndrome and the problems 橋場剛士, 高橋香織, 佐藤卓, 末岡浩, 吉村泰典 Journal of Familial Tumors 11(2): A106-A106, 2011. |
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One case of the 4p-syndrome that presented with the fetal growth failure in the P2-19 altitude uterus, and led to intra-uterine death 山口瑞穂1, 奥田美加1, 望月昭彦1, 田野島美城1, 倉澤健太郎1, 高橋恒男1, 平原史樹2, 夫律子3 Journal of Familial Tumors 11(2): A107-A107, 2011. |
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The cooperation of a heredity clinical department and the maternity ward nurse midwife in the P2-20 our hospital: 18 Trisomy and consideration about 3 diagnosed cases 後藤優美子1,2, 近藤朱音1,2, 大貫優子2, 森屋宏美2, 辻恵子2, 横山寛子2, 溝口満子2, 和泉俊一郎1,2 Journal of Familial Tumors 11(2): A107-A107, 2011. |
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8p23.2 and consideration about the 9q13-q21 overlap which we detected by P2-21 amniotic diagnosis 佐々木由喜1, 霜川修1, 松井健1, 古郷有佳子2, 上塘正人2, 原田直樹1 Journal of Familial Tumors 11(2): A107-A107, 2011. |
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Heredity counseling of P2-22 dic (12, 22) 沼部博直1,2, 勝元さえこ1, 中山貴弘3 Journal of Familial Tumors 11(2): A108-A108, 2011. |
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The support that delivery and the gene practice part of children with P2-23 anencephaly are established 山下浩美, 玉井真理子, 古庄知己, 福嶋義光 Journal of Familial Tumors 11(2): A108-A108, 2011. |
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Ratio of neonates with congenital anomalies hospitalized in P2-24 Osaka City comprehensive medical care center NICU 藤田みどり Journal of Familial Tumors 11(2): A108-A108, 2011. |
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Hereditary multiple exostosis by the P2-25 8q24 deletion and 1, boys case who had 19 translocation type preceding B cells-related lymphocytic leukaemia 中根貴弥1,2, 合井久美子2, 杉田完爾1,2 Journal of Familial Tumors 11(2): A109-A109, 2011. |
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P2-26 fatal bone dysplasia: A present conditions report and examination about the disease name 岡要1, 澤井英明2, 沼部博直3, 浦尾充子1, 小杉眞司1, 河井昌彦4 Journal of Familial Tumors 11(2): A109-A109, 2011. |
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Heredity counseling for the P2-27 achondrogenesis merger pregnant woman 佐村修1, 水之江知哉1, 岡本啓1, 敷佐淑恵1, 中村紘子1, 川上洋介1, 竹原和宏1, 兵頭麻希2 Journal of Familial Tumors 11(2): A109-A109, 2011. |
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1 case of the ornithine transcarbamylase deficiency carrier pregnant woman who racked the brains about P2-28 counseling 谷口智子1, 竹下直樹2, 片桐由起子1, 青木千津1, 森山梓1, 田中政信1, 森田峰人1 Journal of Familial Tumors 11(2): A110-A110, 2011. |
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Literature examination about the psychosocial problem in adult patients with P2-29 Fabry disease 安田有理, 山本佳世乃, 川目裕 Journal of Familial Tumors 11(2): A110-A110, 2011. |
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Heredity counseling with the neonates with P2-30 lysosome disease mass screening enforcement 田中あけみ1, 鈴木健2, 奥山虎之3, 澤田智1, 坂口知子1, 小田絵里3, 藤川研人2, 藤直子3, 斉藤三佳1, 北川照男2 Journal of Familial Tumors 11(2): A110-A110, 2011. |
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The present conditions and problems of the amniotic fluid chromosome banding in the P2-31 Miyagi children's Hospital 宮下進1, 小澤克典1,2, 佐藤聡二郎1,2, 室月淳1,2 Journal of Familial Tumors 11(2): A111-A111, 2011. |
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Heredity counseling office visiting rate by "the pregnancy with advanced maternal age" in P2-32 high level and the community medical care organization, comparison of the amniotic diagnosis rate of use 中村博昭1,3, 本久智賀2,3, 渡邉通子3, 依藤亨3, 富和清隆3 Journal of Familial Tumors 11(2): A111-A111, 2011. |
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We examine the illness in the prenatal diagnosis of the P2-33 our hospital and cooperate 高橋千果1,2, 近藤朱音1,2, 佐藤茂1,2, 後藤優美子1,2, 森屋宏美1, 横山寛子1, 和泉俊一郎1,2 Journal of Familial Tumors 11(2): A112-A112, 2011. |
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Summary - in our prenatal diagnosis - center of the P2-34 structural chromosome aberration carrier of 10 years 渡邉通子1, 本久智賀1,2, 中村博昭1,3, 富和清隆1,4 Journal of Familial Tumors 11(2): A112-A112, 2011. |
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Pit fall case in the amniotic fluid chromosome banding that P2-35 many institutions are involved in 長田久夫1,2, 山地沙知1, 尾本暁子1, 宇津野恵美2,3, 野村文夫2,3,4 Journal of Familial Tumors 11(2): A113-A113, 2011. |
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The present conditions of the genetic counselling outpatient department in the P2-36 low risk pregnancy handling institution: Over Nuchal Traslucency (following NT) screening 都甲明子, 山口暁 Journal of Familial Tumors 11(2): A113-A113, 2011. |
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Prenatal diagnosis experience of the autosome recessive polycystic kidney which caused the recurrence in the P2-37 countryman 生野寿史, 五日市美奈, 大木泉, 芹川武大, 高桑好一, 田中憲一 Journal of Familial Tumors 11(2): A113-A113, 2011. |
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Microcephaly with the P2-38 pontcerebellum hypoplasia, mutation analysis of the CASK gene in the retardation of mental development 山本悠斗1, 林深2, 稲澤譲治2, 小野浩明3, 島川修一4, 高橋幸利5, 水野誠司6, 岡本伸彦1 Journal of Familial Tumors 11(2): A114-A114, 2011. |
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Ventricular morphometrical analysis in the P2-39 humans embryo stage 高桑徹也1, 中島崇1, 白石直樹1, 山田重人2, 上部千賀子2, 塩田浩平2, 巨瀬勝美3 Journal of Familial Tumors 11(2): A114-A114, 2011. |
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A diagnosis before onset of the Duchenne muscular dystrophy at P2-40 1 year old: The spread of genetic screening and heredity counseling of the new age when we fixed our eyes on therapeutic drug development 久保田健夫1, 中根貴弥1, 中村真理子1, 玉井眞理子1, 石黒浩毅1, 中込さと子1, 杉田完爾1, 小牧宏文2 Journal of Familial Tumors 11(2): A114-A114, 2011. |
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