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Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney-urinary tract in pediatric Turner syndrome.
Izumita Y, Nishigaki S, Satoh M, Takubo N, Numakura C, Takahashi I, Soneda S, Abe Y, Kamasaki H, Ohtsu Y, Igaki J, Hasegawa Y, Nagasaki K. Izumita Y, et al. Among authors: kamasaki h. Congenit Anom (Kyoto). 2020 Nov;60(6):175-179. doi: 10.1111/cga.12384. Epub 2020 Aug 4. Congenit Anom (Kyoto). 2020. PMID: 32638418
Language delay and developmental catch-up would be a clinical feature of pseudohypoparathyroidism type 1A during childhood.
Miyakawa Y, Takasawa K, Matsubara Y, Ihara K, Ohtsu Y, Kamasaki H, Kitsuda K, Kobayashi H, Satoh M, Sano S, Dateki S, Mochizuki H, Yokota I, Hasegawa Y, Kashimada K. Miyakawa Y, et al. Among authors: kamasaki h. Endocr J. 2019 Mar 28;66(3):215-221. doi: 10.1507/endocrj.EJ18-0326. Epub 2019 Jan 23. Endocr J. 2019. PMID: 30674755 Free article.
Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in Japan.
Ishii T, Adachi M, Takasawa K, Okada S, Kamasaki H, Kubota T, Kobayashi H, Sawada H, Nagasaki K, Numakura C, Harada S, Minamitani K, Sugihara S, Tajima T. Ishii T, et al. Among authors: kamasaki h. Horm Res Paediatr. 2018;89(3):166-171. doi: 10.1159/000486393. Epub 2018 Feb 16. Horm Res Paediatr. 2018. PMID: 29455197
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan.
Nagasaki K, Kubota T, Kobayashi H, Sawada H, Numakura C, Harada S, Takasawa K, Minamitani K, Ishii T, Okada S, Kamasaki H, Sugihara S, Adachi M, Tajima T. Nagasaki K, et al. Among authors: kamasaki h. Clin Pediatr Endocrinol. 2017;26(4):207-213. doi: 10.1297/cpe.26.207. Epub 2017 Sep 28. Clin Pediatr Endocrinol. 2017. PMID: 29026269 Free PMC article.
28 results