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Page 1
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: arai ichinoi n. 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.
Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan.
Mikami-Saito Y, Wada Y, Arai-Ichinoi N, Nakajima Y, Suzuki-Ajihara S, Murayama K, Tanaka T, Numakura C, Hamazaki T, Igarashi N, Esaki H, Kagawa R, Kono T, Sawada T, Sawada T, Nyuzuki H, Hirai H, Fumoto S, Matsuda J, Matsunaga A, Maruyama S, Yamaguchi K, Yoshino M, Totsune E, Kikuchi A, Ohura T, Kure S. Mikami-Saito Y, et al. Among authors: arai ichinoi n. Genet Med. 2024 Aug;26(8):101165. doi: 10.1016/j.gim.2024.101165. Epub 2024 May 16. Genet Med. 2024. PMID: 38762772 Free article.
Hypoketotic hypoglycemia in citrin deficiency: a case report.
Wada Y, Arai-Ichinoi N, Kikuchi A, Sakamoto O, Kure S. Wada Y, et al. Among authors: arai ichinoi n. BMC Pediatr. 2020 Sep 22;20(1):444. doi: 10.1186/s12887-020-02349-6. BMC Pediatr. 2020. PMID: 32962675 Free PMC article.
Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia.
Wada Y, Kikuchi A, Arai-Ichinoi N, Sakamoto O, Takezawa Y, Iwasawa S, Niihori T, Nyuzuki H, Nakajima Y, Ogawa E, Ishige M, Hirai H, Sasai H, Fujiki R, Shirota M, Funayama R, Yamamoto M, Ito T, Ohara O, Nakayama K, Aoki Y, Koshiba S, Fukao T, Kure S. Wada Y, et al. Among authors: arai ichinoi n. Genet Med. 2020 Jul;22(7):1281. doi: 10.1038/s41436-020-0836-z. Genet Med. 2020. PMID: 32499603 Free article.
24 results