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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. 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
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: shima h. 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.
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. 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.
935 results