Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Makiko Oguma"'
Autor:
Toshihiro Tajima1, Makiko Oguma1
Publikováno v:
Clinical Pediatric Endocrinology. 2022, Vol. 31 Issue 2, p98-100. 3p.
Autor:
Toshihiro Tajima, Makiko Oguma
Publikováno v:
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 31(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4f15d837fae902188798a1ae78122e0
https://pubmed.ncbi.nlm.nih.gov/35431442
https://pubmed.ncbi.nlm.nih.gov/35431442
Publikováno v:
Clinical Pediatric Endocrinology
Congenital central hypothyroidism (C-CH) is defined as hypothyroidism due to a lack of stimulation of the normal thyroid gland (1, 2). C-CH is caused by anatomical or functional impairments in neurons that secrete hypothalamic-thyrotropin releasing h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61d99cdaa4a6b881fff4e8460708e341
http://europepmc.org/articles/PMC6646241
http://europepmc.org/articles/PMC6646241
Autor:
Makiko Oguma1 r0607mi@jichi.ac.jp, Mizuki Kobayashi1, Masayo Yamazaki1, Koji Yokoyama1, Shuntaro Morikawa2, Takeshi Yamaguchi2, Takanori Yamagata1, Toshihiro Tajima1
Publikováno v:
Clinical Pediatric Endocrinology. 2018, Vol. 27 Issue 2, p95-100. 6p. 1 Diagram, 1 Graph.
Autor:
Koji Yokoyama, Masayo Yamazaki, Mizuki Kobayashi, Takanori Yamagata, Makiko Oguma, Toshihiro Tajima, Shuntaro Morikawa, Takeshi Yamaguchi
Publikováno v:
Clinical Pediatric Endocrinology. 27:95-100
Genetic defects in the immunoglobulin superfamily member 1(IGSF1) protein are the cause of congenital central hypothyroidism (C-CH). Here we report two Japanese siblings with C-CH due to a novel IGSF1 mutation. The youngest brother showed a failure t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea8fec49c5565b07e64161a38b6ebe80
https://doi.org/10.1297/cpe.27.95
https://doi.org/10.1297/cpe.27.95
Autor:
Makiko, Oguma, Mizuki, Kobayashi, Masayo, Yamazaki, Koji, Yokoyama, Shuntaro, Morikawa, Takeshi, Yamaguchi, Takanori, Yamagata, Toshihiro, Tajima
Publikováno v:
Clinical Pediatric Endocrinology
Genetic defects in the immunoglobulin superfamily member 1(IGSF1) protein are the cause of congenital central hypothyroidism (C-CH). Here we report two Japanese siblings with C-CH due to a novel IGSF1 mutation. The youngest brother showed a failure t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b8a866a8e4323490ec3f048e6bf4593
https://pubmed.ncbi.nlm.nih.gov/29662269
https://pubmed.ncbi.nlm.nih.gov/29662269
Autor:
Tohru Yorifuji, Toshihiro Tajima, Makiko Oguma, Takanori Yamagata, Masayo Yamazaki, Hideo Sugie
Publikováno v:
Clinical Pediatric Endocrinology
Neonatal diabetes mellitus (NDM) is an insulin-requiring monogenic form of diabetes that generally presents before six months of age. The following two types of NDM are known: transient NDM (TNDM) and permanent NDM (PNDM). Here we report on an infant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15073a8e22d21f222f17de9732e1f14
https://pubmed.ncbi.nlm.nih.gov/28804207
https://pubmed.ncbi.nlm.nih.gov/28804207
Publikováno v:
Clinical Pediatric Endocrinology; Jul2019, Vol. 28 Issue 3, p69-79, 11p
Autor:
Masayo Yamazaki, Hideo Sugie, Makiko Oguma, Tohru Yorifuji, Toshihiro Tajima, Takanori Yamagata
Publikováno v:
Clinical Pediatric Endocrinology; 2017, Vol. 26 Issue 3, p165-169, 5p, 1 Diagram, 1 Graph