Seltene Formen einer Insulinresistenz: Das Köbberling-Syndrom
Author:
Funder
Medical University of Graz
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/s41969-019-00076-7.pdf
Reference8 articles.
1. Aberer F, Sourij H, Mader JK (2019) A typical clinical presentation of a woman with Kobberling syndrome. Pol Arch Intern Med 129:414–416
2. Kobberling J, Dunnigan MG (1986) Familial partial lipodystrophy: two types of an X linked dominant syndrome, lethal in the hemizygous state. J Med Genet 23:120–127
3. Jackson SN, Howlett TA, McNally PG, O’Rahilly S, Trembath RC (1997) Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophy. QJM 90:27–36
4. Herbst KL, Tannock LR, Deeb SS, Purnell JQ, Brunzell JD, Chait A (2003) Kobberling type of familial partial lipodystrophy: an underrecognized syndrome. Diabetes Care 26:1819–1824
5. Guillin-Amarelle C, Sanchez-Iglesias S, Castro-Pais A, Rodriguez-Canete L, Ordonez-Mayan L, Pazos M, Gonzalez-Mendez B, Rodriguez-Garcia S, Casanueva FF, Fernandez-Marmiesse A, Araujo-Vilar D (2016) Type 1 familial partial lipodystrophy: understanding the Kobberling syndrome. Endocrine 54:411–421
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