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Clinical Pediatric Endocrinology 28巻 1号

発行元
日本小児内分泌学会
ISSN
0918-5739
ISSN(オンライン)
1347-7358

書籍情報から探す
開始頁
Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4) : a case report
Shinji Takeyari1, Satoshi Takakuwa1,2, Kei Miyata1, Kenichi Yamamoto1,3, Hirofumi Nakayama1,4, Yasuhisa Ohata1,5, Makoto Fujiwara1, Taichi Kitaoka1, Takuo Kubota1, Noriyuki Namba1,6, Norio Sakai1,7, Keiichi Ozono1
1Department of Pediatrics, Osaka University Graduate School of Medicine, 2Department of Pediatrics, Hyogo Prefectural Nishinomiya Hospital, 3Department of Statistical Genetics, Osaka University Graduate School of Medicine, 4The Japan Environment and Children's Study, Osaka Unit Center, 5The 1st Department of Oral and Maxillofacial Surgery, Osaka University Graduate School of Dentistry, 6Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization (JCHO), 7Child Healthcare and Genetic Science Laboratory, Division of Health Sciences, Osaka University Graduate School of Medicine
Clinical Pediatric Endocrinology 28 (1) 1-7, 2019.
  • アブストラクト: 従量制は110円(税込)、基本料金制は基本料金に含まれます。
  • 全文ダウンロード: 従量制、基本料金制の方共に770円(税込) です。
Combination therapy of propranolol, levothyroxine, and liothyronine was effective in a case of severe consumptive hypothyroidism associated with infantile hepatic hemangioma
Asami Osada1,2, Eriko Araki1, Yukio Yamashita1, Tomohiro Ishii2
1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 2Department of Pediatrics, Keio University School of Medicine
Clinical Pediatric Endocrinology 28 (1) 9-14, 2019.
  • アブストラクト: 従量制は110円(税込)、基本料金制は基本料金に含まれます。
  • 全文ダウンロード: 従量制、基本料金制の方共に770円(税込) です。
A case of pseudohypoparathyroidism type Ia with a novel frameshift mutation in the GNAS gene : early diagnosis of osteoma cutis by skin biopsy
Kazuki Kodo1, Hiroshi Maeda1, Hidechika Morimoto1, Makoto Wada2, Tetsuya Imura3, Hisakazu Nakajima1
1Department of Pediatrics, North Medical Center, Kyoto Prefectural University of Medicine, 2Department of Dermatology, North Medical Center, Kyoto Prefectural University of Medicine, 3Department of Pathology, North Medical Center, Kyoto Prefectural University of Medicine
Clinical Pediatric Endocrinology 28 (1) 15-18, 2019.
  • アブストラクト: 従量制は110円(税込)、基本料金制は基本料金に含まれます。
  • 全文ダウンロード: 従量制、基本料金制の方共に770円(税込) です。
A Japanese case of familial hypercholesterolemia with a novel mutation in the LDLR gene
Keiko Nagahara1, Rumi Hachiya2, Hayato Tada3, Hirofumi Okada3, Masakazu Yamagishi3, Kazushige Dobashi4, Katsumi Mizuno1, Yukihiro Hasegawa2
1Department of Pediatrics, Showa University School of Medicine, 2Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, 3Department of Cardiovascular and Internal Medicine, Kanazawa University Graduate School of Medicine, 4Department of Pediatrics, Showa University Koto Toyosu Hospital
Clinical Pediatric Endocrinology 28 (1) 19-22, 2019.
  • アブストラクト: 従量制は110円(税込)、基本料金制は基本料金に含まれます。
  • 全文ダウンロード: 従量制、基本料金制の方共に770円(税込) です。