Phenotypic and Genetic Characteristics of Lipodystrophy: Pathophysiology, Metabolic Abnormalities, and Comorbidities
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://link.springer.com/article/10.1007/s11892-018-1099-9/fulltext.html
Reference155 articles.
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2. • Akinci B, Onay H, Demir T, Ozen S, Kayserili H, Akinci G, et al. Natural history of congenital generalized lipodystrophy: a nationwide study from Turkey. J Clin Endocrinol Metab. 2016;101(7):2759–67. https://doi.org/10.1210/jc.2016-1005 Data on natural history and disease burden of various subtypes of CGL in a metreleptin naïve cohort.
3. • Akinci B, Onay H, Demir T, Savas-Erdeve S, Gen R, Simsir IY, et al. Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy. Metabolism. 2017;72:109–19. https://doi.org/10.1016/j.metabol.2017.04.010 A multicenter prospective observational study on clinical presentations, metabolic abnormalities, and end-organ complications in patients with FPLD.
4. Ajluni N, Meral R, Neidert AH, Brady GF, Buras E, McKenna B, et al. Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort. Clin Endocrinol. 2017;86(5):698–707. https://doi.org/10.1111/cen.13311 .
5. Garg A, Misra A. Lipodystrophies: rare disorders causing metabolic syndrome. Endocrinol Metab Clin N Am. 2004;33(2):305–31. https://doi.org/10.1016/j.ecl.2004.03.003 .
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