Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Fumika Kawano-Matsuda"'
Autor:
Fumika Kawano-Matsuda1, Tomoki Maeda1, Tadashi Kaname2, Kumiko Yanagi2, Kenji Ihara1 k-ihara@oita-u.ac.jp
Publikováno v:
Clinical Pediatric Endocrinology. 2021, Vol. 30 Issue 1, p61-64. 4p.
Autor:
Tomoyo Itonaga, Makoto Fujiwara, Keiichi Ozono, Mayo Ikeuchi, Takuo Kubota, Kyoko Kiyota, Kenji Ihara, Yasuhisa Ohata, Fumika Kawano-Matsuda
Publikováno v:
CEN Case Rep
HDR syndrome is characterized by the triad of primary hypoparathyroidism, sensorineural hearing loss and renal malformation with widely variable manifestations. It is an autosomal dominant inherited disease caused by a mutation of the GATA3 (NM_00100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf978218ec54b10669b496c80fa90665
https://europepmc.org/articles/PMC8019435/
https://europepmc.org/articles/PMC8019435/
Autor:
Tomomi Yamaguchi, Yumi Shimada, Kenji Ihara, Tomona Omotobara-Yabe, Tomoyo Itonaga, Tomoki Maeda, Tomoki Kosho, Fumika Kawano-Matsuda, Miwako Maeda
Publikováno v:
Clinical dysmorphology. 29(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7938e609670690179f0870ae33210a6b
https://pubmed.ncbi.nlm.nih.gov/30946035
https://pubmed.ncbi.nlm.nih.gov/30946035
Autor:
Fumika Kawano-Matsuda, Yumi Shimada, Tomona Omotobara-Yabea, Tomoyo Itonaga, Miwako Maeda, Tomoki Maeda, Tomomi Yamaguchi, Tomoki Kosho, Kenji Ihara
Publikováno v:
Clinical Dysmorphology; Jan2020, Vol. 29 Issue 1, p49-52, 4p