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Page 1
Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data.
Saitou H, Kitaoka T, Kubota T, Kanno J, Mochizuki H, Michigami T, Hasegawa K, Fujiwara I, Hamajima T, Harada D, Seki Y, Nagasaki K, Dateki S, Namba N, Tokuoka H, Pimenta JM, Cohen S, Ozono K. Saitou H, et al. Among authors: fujiwara i. Am J Med Genet A. 2024 Aug;194(8):e63612. doi: 10.1002/ajmg.a.63612. Epub 2024 Mar 30. Am J Med Genet A. 2024. PMID: 38554024
Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis.
Shima H, Tanaka T, Kamimaki T, Dateki S, Muroya K, Horikawa R, Kanno J, Adachi M, Naiki Y, Tanaka H, Mabe H, Yagasaki H, Kure S, Matsubara Y, Tajima T, Kashimada K, Ishii T, Asakura Y, Fujiwara I, Soneda S, Nagasaki K, Hamajima T, Kanzaki S, Jinno T, Ogata T, Fukami M; Japanese SHOX study group. Shima H, et al. Among authors: fujiwara i. J Hum Genet. 2016 Jul;61(7):585-91. doi: 10.1038/jhg.2016.18. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984564
Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version.
Urakami T, Hotsubo T, Ogawa Y, Kikuchi T, Usuda R, Matsui K, Hirose M, Hirai H, Abiru N, Fujiwara I, Mizuno H, Miyako K, Takahashi K, Shimada A; Committee of Pediatric Diabetes in the Japan Diabetes Society. Urakami T, et al. Among authors: fujiwara i. Diabetol Int. 2024 Aug 15;15(4):666-672. doi: 10.1007/s13340-024-00742-5. eCollection 2024 Oct. Diabetol Int. 2024. PMID: 39469563
The incidences of and risk factors for severe retinopathy requiring photocoagulation and albuminuria in Japanese patients with childhood-onset type 1 diabetes.
Takaike H, Uchigata Y, Matsuura N, Sasaki N, Amemiya S, Urakami T, Kawamura T, Kikuchi N, Sugihara S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT). Takaike H, et al. Diabetol Int. 2017 Sep 22;9(2):121-128. doi: 10.1007/s13340-017-0336-9. eCollection 2018 May. Diabetol Int. 2017. PMID: 30603359 Free PMC article.
Solitary median maxillary central incisor syndrome caused by 22q11.2 microdeletion.
Shima H, Miura A, Kawashima S, Umeki I, Sogi C, Suzuki D, Takezawa Y, Sato R, Arai-Ichinoi N, Kamimura M, Fujiwara I, Adachi M, Yamada A, Kawame H, Kikuchi A, Kanno J. Shima H, et al. Among authors: fujiwara i. Clin Pediatr Endocrinol. 2025 Jan;34(1):54-59. doi: 10.1297/cpe.2024-0024. Epub 2024 Sep 12. Clin Pediatr Endocrinol. 2025. PMID: 39777126 Free PMC article.
A case of long-term survival of SADDAN treated with growth hormone for marked short stature.
Kanno J, Katata Y, Kawashima S, Shima H, Sogi C, Umeki I, Suzuki D, Tomita H, Kamimura M, Saito-Hakoda A, Fujiwara I, Hanita T, Kikuchi A. Kanno J, et al. Among authors: fujiwara i. Clin Pediatr Endocrinol. 2024;33(3):144-150. doi: 10.1297/cpe.2023-0068. Epub 2024 Mar 10. Clin Pediatr Endocrinol. 2024. PMID: 38993719 Free PMC article.
195 results