Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Noriko Nishina-Uchida"'
Autor:
Tomohiro Ishii, Tomonobu Hasegawa, Matthew Anaka, Noriko Nishina-Uchida, Yukihiro Hasegawa, Ryuji Fukuzawa
Publikováno v:
Sexual Development. 10:185-190
Individuals with a 46,XX/46,XY karyotype are categorized as ovotesticular disorder of sexual development (ODSD) and have gonads with either an ovary on one side and a testis on the other side or a mixed ovotestis. To examine the distribution of 46,XX
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0635d6b93b52fa5b564e8c434f922b8
https://doi.org/10.1159/000448677
https://doi.org/10.1159/000448677
Autor:
Ayuko S. Suwanai, Yukihiro Hasegawa, Ryuji Fukuzawa, Chikahiko Numakura, Tomonobu Hasegawa, Noriko Nishina-Uchida
Publikováno v:
Hormone Research in Paediatrics. 80:119-128
Background: Individuals with NR5A1 mutations encoding steroidogenic factor-1 (SF1) develop a phenotypically broad range of disorders of sexual development (DSD). Based on a literature review, we noted that hypoplastic seminiferous tubules and the eme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce0680f7d5a900a304e3802c15949440
https://doi.org/10.1159/000353763
https://doi.org/10.1159/000353763
Publikováno v:
Medicine. 94:e720
Mixed gonadal dysgenesis (MGD) is a disorder of sexual development that typically has a mosaic 45,X/46,XY karyotype. A 1-year-old infant with 46,XY identified by peripheral blood karyotype demonstrated clinical manifestations and gonadal pathologic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::220d2bc8a278a123a071bd76c540e2f5
https://doi.org/10.1097/md.0000000000000720
https://doi.org/10.1097/md.0000000000000720
Identification of X Monosomy Cells From a Gonad of Mixed Gonadal Dysgenesis With a 46, XY Karyotype.
Publikováno v:
Medicine; Apr2015, Vol. 94 Issue 14, p1-5, 5p