Papillary thyroid carcinoma in one of identical twin patients with Pendred syndrome-Reference-Cited by-同舟云学术

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Papillary thyroid carcinoma in one of identical twin patients with Pendred syndrome

Published:2013 Issue:6 Volume:60 Page:805-811
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Sakurai Kanako¹,Hata Masahiro²,Hishinuma Akira³,Ushijima Ryo²,Okada Akiho²,Taeda Yoshinori²,Arihara Zenei¹,Fukazawa Hiroshi¹,Takahashi Kazuhiro⁴

Affiliation:

1. Department of Endocrinology and Metabolism, KKR Suifu Hospital, Mito 311-4141, Japan

2. Department of Surgery, KKR Suifu Hospital, Mito 311-4141, Japan

3. Department of Infection Control and Clinical Laboratory Medicine, Dokkyo Medical University, Tochigi 321-0293, Japan

4. Department of Endocrinology and Applied Medical Science, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.jstage.jst.go.jp/article/endocrj/60/6/60_EJ12-0396/_pdf

Reference24 articles.

1. 1. Pendred V (1896) Deaf-mutism and goitre. Lancet ii: 532.

2. 2. Kopp P, Bizhanova A (2011) Clinical and molecular characteristics of Pendred syndrome. Ann Endocrinol (Paris) 72: 88-94.

3. 3. Yoshida A, Taniguchi S, Hisatome I, Royaux IE, Green ED, et al. (2002) Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells. J Clin Endocrinol Metab 87: 3356-3361.

4. 4. Royaux IE, Suzuki K, Mori A, Katoh R, Everett LA, et al. (2000) Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 141: 839-845.

5. 5. Fraser GR (1965) Association of Congenital Deafness with Goitre (Pendred’s Syndrome) a Study of 207 Families. Ann Hum Genet 28: 201-249.

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