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Congenital Hypothyroidism Due to Truncating PAX8 Mutations: A Case Series and Molecular Function Studies.
J Clin Endocrinol Metab. 2020 Nov 1;105(11):dgaa584. doi: 10.1210/clinem/dgaa584.
J Clin Endocrinol Metab. 2020.
PMID: 32841355
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
Inoue T, Nakamura A, Iwahashi-Odano M, Tanase-Nakao K, Matsubara K, Nishioka J, Maruo Y, Hasegawa Y, Suzumura H, Sato S, Kobayashi Y, Murakami N, Nakabayashi K, Yamazawa K, Fuke T, Narumi S, Oka A, Ogata T, Fukami M, Kagami M.
Inoue T, et al. Among authors: iwahashi odano m.
Clin Epigenetics. 2020 Jun 16;12(1):86. doi: 10.1186/s13148-020-00865-x.
Clin Epigenetics. 2020.
PMID: 32546215
Free PMC article.
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Identification and functional characterization of a novel PAX8 mutation (p.His39Pro) causing familial thyroid hypoplasia.
Iwahashi-Odano M, Fujisawa Y, Ogata T, Nakashima S, Muramatsu M, Narumi S.
Iwahashi-Odano M, et al.
Clin Pediatr Endocrinol. 2020;29(4):173-178. doi: 10.1297/cpe.29.173. Epub 2020 Oct 3.
Clin Pediatr Endocrinol. 2020.
PMID: 33088016
Free PMC article.
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Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects.
Tanase-Nakao K, Iwahashi-Odano M, Sugisawa C, Abe K, Muroya K, Yamamoto Y, Kawada Y, Mushimoto Y, Ohkubo K, Kinjo S, Shimura K, Aoyama K, Mizuno H, Hotsubo T, Takahashi C, Isojima T, Kina Y, Takakuwa S, Hamada J, Sawaki M, Shigehara K, Sugimoto S, Etani Y, Narumi-Wakayama H, Mine Y, Hasegawa T, Hishinuma A, Narumi S.
Tanase-Nakao K, et al. Among authors: iwahashi odano m.
J Clin Endocrinol Metab. 2024 Feb 19:dgae098. doi: 10.1210/clinem/dgae098. Online ahead of print.
J Clin Endocrinol Metab. 2024.
PMID: 38373250
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A thyroid adenoma in a pubertal male with thyroxine-binding globulin deficiency.
Kim H, Naiki Y, Iwahashi-Odano M, Narumi S, Ito K, Ishiguro A.
Kim H, et al. Among authors: iwahashi odano m.
Clin Pediatr Endocrinol. 2024;33(1):23-26. doi: 10.1297/cpe.2023-0031. Epub 2023 Nov 12.
Clin Pediatr Endocrinol. 2024.
PMID: 38299172
Free PMC article.
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A case of syndromic congenital hypothyroidism with a 15.2 Mb interstitial deletion on 2q12.3q14.2 involving PAX8.
Iwahashi-Odano M, Kitamura M, Narumi S.
Iwahashi-Odano M, et al.
Clin Pediatr Endocrinol. 2023;32(1):65-71. doi: 10.1297/cpe.2022-0061. Epub 2022 Nov 2.
Clin Pediatr Endocrinol. 2023.
PMID: 36761496
Free PMC article.
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