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Quoted phrase not found in phrase index: "PLIN1-related familial partial lipodystrophy"
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Clinical Spectrum of LMNA-Associated Type 2 Familial Partial Lipodystrophy: A Systematic Review.
Fernandez-Pombo A, Diaz-Lopez EJ, Castro AI, Sanchez-Iglesias S, Cobelo-Gomez S, Prado-Moraña T, Araujo-Vilar D. Fernandez-Pombo A, et al. Cells. 2023 Feb 24;12(5):725. doi: 10.3390/cells12050725. Cells. 2023. PMID: 36899861 Free PMC article. Review.
Type 2 familial partial lipodystrophy (FPLD2) is a laminopathic lipodystrophy due to pathogenic variants in the LMNA gene. ...
Type 2 familial partial lipodystrophy (FPLD2) is a laminopathic lipodystrophy due to pathogenic variants in the …
Clinical Features and Management of Non-HIV-Related Lipodystrophy in Children: A Systematic Review.
Gupta N, Asi N, Farah W, Almasri J, Barrionuevo P, Alsawas M, Wang Z, Haymond MW, Brown RJ, Murad MH. Gupta N, et al. J Clin Endocrinol Metab. 2017 Feb 1;102(2):363-374. doi: 10.1210/jc.2016-2271. J Clin Endocrinol Metab. 2017. PMID: 27967300 Free PMC article. Review.
CONTEXT: Lipodystrophy syndromes are characterized by generalized or partial absence of adipose tissue. ...Generalized fat loss involving face, neck, abdomen, thorax, and upper and lower limbs was explicitly reported in 65% to 93% of patients with congenital general …
CONTEXT: Lipodystrophy syndromes are characterized by generalized or partial absence of adipose tissue. ...Generalized fat los …
Perilipin 1: a systematic review on its functions on lipid metabolism and atherosclerosis in mice and humans.
Desgrouas C, Thalheim T, Cerino M, Badens C, Bonello-Palot N. Desgrouas C, et al. Cardiovasc Res. 2024 Mar 14;120(3):237-248. doi: 10.1093/cvr/cvae005. Cardiovasc Res. 2024. PMID: 38214891
The function of perilipin 1 in human metabolism was recently highlighted by the description of PLIN1 variants associated with various pathologies. These include severe familial partial lipodystrophy and early onset acute coronary syndrome. ...
The function of perilipin 1 in human metabolism was recently highlighted by the description of PLIN1 variants associated with various pathol …