Lipoatrophic diabetes in familial partial lipodystrophy type 2: From insulin resistance to diabetes
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference38 articles.
1. Nuclear envelope-related lipodystrophies;Guénantin;Semin Cell Dev Biol,2014
2. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy;Shackleton;Nat Genet,2000
3. Clinical and molecular prevalence of lipodystrophy in an unascertained large clinical care cohort;Gonzaga-Jauregui;Diabetes,2020
4. The diagnosis and management of lipodystrophy syndromes: a multi-society practice guideline;Brown;J Clin Endocrinol Metab,2016
5. Severe insulin resistance syndromes;Angelidi;J Clin Investig,2021
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1. Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes;International Journal of Molecular Sciences;2024-08-28
2. Diagnostic and referral pathways in patients with rare lipodystrophy and insulin-resistance syndromes: key milestones assessed from a national reference center;Orphanet Journal of Rare Diseases;2024-04-27
3. Patients' perspective on the medical pathway from first symptoms to diagnosis in genetic lipodystrophy;European Journal of Endocrinology;2023-12-21
4. Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review;The Journal of Clinical Endocrinology & Metabolism;2023-10-16
5. Familial partial lipodystrophy type 2 and obesity, two adipose tissue pathologies with different inflammatory profiles;Diabetology & Metabolic Syndrome;2023-04-21
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