後藤 正博 ごとう まさひろ 先生

来歴等

略歴

1992年　東京大学医学部卒
1992年　東京大学医学部附属病院小児科研修医
1993年　私立太田西の内病院小児科常勤医
1994年　関東労災病院小児科常勤医
1995年　国立小児病院内分泌代謝科レジデント
1998年　東京大学医学部附属病院小児科助手
2001年　英国サザンプトン大学人類遺伝学教室研究員
2004年　大宮医師会市民病院小児科常勤医
2005年　東京都立八王子小児病院小児内科医員
2010年　都立小児総合医療センター内分泌・代謝科医長
2017年　ごとう小児科・成長クリニック　院長

論文

・Goto M, Taki T, Sugie H, Miki Y, Kato H, Hayashi Y. A novel mutation in the glucose-6-phosphatase gene in Korean twins with glycogen storage disease type 1a. J Inherit Metab Dis 2000; 23: 851-852.

・Goto M, Takita J, Hashimoto N, Tateshita F, Toyoji H, Kato H, Egi S, Hayashi Y. Lack of aberrations of the BMP4, BMP2, and PTX1 genes in a patient with pituitary hypoplasia, os odontoideum, renal dysplasia, and right leg anomalies. Int J Mol Med 2002; 10: 293-297.

・Goto M, Brickwood S, Wilson DI, Wood PJ, Mason JI, Hanley NA. Steroidogenic enzyme expression within the adrenal cortex during early human gestation. Endocr Res 2002; 28: 641-645.

・Hachisu M, Oda Y, Goto M, Kobayashi K, Saheki T, Ohura T, Noma S, Kitanaka S. Citrin deficiency presenting with ketotic hypoglycaemia and hepatomegaly in childhood. Eur J Ped 2005; 164: 109-110.

・Goto M, Nishimura G, Nagai T, Yamazawa K, Ogata T. Familial Klippel-Feil anomaly and t(5;8)(q35.1;p21.1) translocation. Am J Med Genet A. 2006; 140: 1013-1015.

・Goto M, Piper Hanley K, Marcos J, Wood PJ, Wright S, Postle AD, Cameron IT, Mason JI, Wilson DI, Hanley NA. In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development. J Clin Invest. 2006; 116: 953-960.

・Goto M. Possible relationship between ring X chromosome and neonatal hypoglycaemia J Pediatr Endocrinol Metab. 2008; 11: 1103.

・Goto M, Katsumata N. X-Linked Adrenal Hypoplasia Congenita Caused by a Novel Intronic Mutation of the DAX-1 Gene. Horm Res 2009; 71: 120-124.

・Goto M, Mabe H, Nishimura G, Katsumata N. Progressive Osseous Heteroplasia Caused by a Novel Nonsense Mutation in the GNAS1 Gene. J Pediatr Endocrinol Metab. 2010; 23: 303-309.

・Daitsu T, Igaki J, Goto M, Hasegawa Y. A novel deletion mutation of the arginine vasopressin receptor 2 gene in a Japanese infant with nephrogenic diabetes insipidus. Clin Pediatr Endocrinol. 2014; 23:115-117

・Fukao T, Akiba K, Goto M, Kuwayama N, Morita M, Hori T, Aoyama Y, Venkatesan R, Wierenga R, Moriyama Y, Hashimoto T, Usuda N, Murayama K, Ohtake A, Hasegawa Y, Shigematsu Y, Hasegawa Y. The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation. J Hum Genet. 2014; 59: 609-614

・Okubo Y, Goto M, Sakakibara H, Terakawa T, Kaneko T, Miyama S. The absence of later wave components in auditory brainstem responses as an initial manifestation of type 2 Gaucher disease. Pediatr Neurol. 2014; 51: 837-839

・Goto M, Miyagawa N, Kikunaga K, Miura M, Hasegawa Y. High incidence of adrenal suppression in children with Kawasaki disease treated with intravenous immunoglobulin plus prednisolone. Endocr J. 2015; 62: 145-151

・Goto M, Miyagawa N, Kikunaga K, Miura M, Hasegawa Y. Single serum cortisol values at 09:00 h can be indices of adrenocortical function in children with Kawasaki disease treated with intravenous immunoglobulin plus prednisolone. Clin Pediatr Endocrinol. 2015; 24: 69-75

・Goto M, Shibata N, Hasegawa Y. Efficacy of single serum cortisol reading obtained between 9 AM and 10 AM as an index of adrenal function in children treated with glucocorticoids or synthetic adrenocorticotropic hormone. Clin Pediatr Endocrinol. 2016; 25: 83-9.

・Hasegawa Y, Ariyasu D, Izawa M, Igaki-Miyamoto J, Fukuma M, Hatano M, Yagi H, Goto M. Gradually increasing ethinyl estradiol for Turner syndrome may produce good final height but not ideal BMD. Endocr J. 2016 Dec 2. [Epub ahead of print]

・Nomura R, Miyai K, Kuge R, Okura T, Goto M, Hasegawa Y. Free T3 to free T4 ratio less than 2.0 suggests low T3 syndrome rather than central hypothyroidism from the age of two to eighteen years. Endocr J. 2016 Dec 22. [Epub ahead of print]

その他

• 【受賞】日本小児内分泌学会優秀演題賞

• 【受賞】Asia Pacific Paediatric Endocrine Society Kaichi Kida Award