Severe metabolic disorders coexisting with Werner syndrome: a case report-Reference-Cited by-同舟云学术

Severe metabolic disorders coexisting with Werner syndrome: a case report

Published:2021 Issue:3 Volume:68 Page:261-267
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Li Huan¹,Yang Maoguang¹,Shen Hong¹,Wang Sisi¹,Cai Hanqing¹

Affiliation:

1. Department of Endocrinology, The Second Hospital of Jilin University, Changchun, Jilin, China

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.jstage.jst.go.jp/article/endocrj/68/3/68_EJ20-0448/_pdf

Reference39 articles.

1. 1 Epstein CJ, Martin GM, Schultz AL, Motulsky AG (1966) Werner’s syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine (Baltimore) 45: 177–221.

2. 2 Tollefsbol TO, Cohen HJ (1984) The effect of age on the accumulation of labile triosephosphate isomerase and thymidine incorporation in pokeweed mitogen stimulated human lymphocytes. J Gerontol 39: 398–405.

3. 3 (1985) On cataract in conjunction with scleroderma. Otto Werner, doctoral dissertation, 1904, Royal Ophthalmology Clinic, Royal Christian Albrecht University of Kiel. Adv Exp Med Biol 190: 1–14.

4. 4 Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, et al. (2006) The spectrum of WRN mutations in Werner syndrome patients. Hum Mutat 27: 558–567.

5. 5 Takemoto M, Mori S, Kuzuya M, Yoshimoto S, Shimamoto A, et al. (2013) Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey. Geriatr Gerontol Int 13: 475–481.

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