Found: 7
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Clinical Characteristics of Patients With Acquired Partial Lipodystrophy: A Multicenter Retrospective Study.
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- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 3, p. e932, doi. 10.1210/clinem/dgad700
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- Article
Partial Lipodystrophy and LMNA p.R545H Variant.
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- Journal of Clinical Medicine, 2021, v. 10, n. 5, p. 1142, doi. 10.3390/jcm10051142
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- Article
Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease.
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- Frontiers in Endocrinology, 2020, v. 11, p. 1, doi. 10.3389/fendo.2020.00039
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- Article
Atypical Progeroid Syndrome and Partial Lipodystrophy Due to LMNA Gene p.R349W Mutation.
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- Journal of the Endocrine Society, 2020, v. 4, n. 10, p. 1, doi. 10.1210/jendso/bvaa108
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- Article
Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report.
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- Italian Journal of Pediatrics, 2024, v. 50, n. 1, p. 1, doi. 10.1186/s13052-024-01672-3
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- Article
Non-Classic Congenital Adrenal Hyperplasia in Childhood: A Review.
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- Sexes, 2023, v. 4, n. 4, p. 462, doi. 10.3390/sexes4040030
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- Article
411-P: Fibroblast Growth Factor 23 and Diabetic Kidney Disease Phenotypes in Type 2 Diabetes.
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- Diabetes, 2021, v. 70, p. N.PAG, doi. 10.2337/db21-411-P
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- Article