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Congenital generalized lipodystrophies--new insights into metabolic dysfunction.
Patni N, Garg A. Patni N, et al. Among authors: garg a. Nat Rev Endocrinol. 2015 Sep;11(9):522-34. doi: 10.1038/nrendo.2015.123. Epub 2015 Aug 4. Nat Rev Endocrinol. 2015. PMID: 26239609 Review.
Congenital generalized lipodystrophy (CGL) is a heterogeneous autosomal recessive disorder characterized by a near complete lack of adipose tissue from birth and, later in life, the development of metabolic complications, such as diabetes mellitus, hypertriglycerida …
Congenital generalized lipodystrophy (CGL) is a heterogeneous autosomal recessive disorder characterized by a near complete la …
The skeleton in congenital, generalized lipodystrophy: evaluation using whole-body radiographic surveys, magnetic resonance imaging and technetium-99m bone scintigraphy.
Fleckenstein JL, Garg A, Bonte FJ, Vuitch MF, Peshock RM. Fleckenstein JL, et al. Among authors: garg a. Skeletal Radiol. 1992;21(6):381-6. doi: 10.1007/BF00241817. Skeletal Radiol. 1992. PMID: 1523434
Congenital generalized lipodystrophy (CGL) is a rare genetic disease characterized by the absence of body fat from birth. Focal bone lesions have also been reported, but their pathophysiology is poorly understood. ...
Congenital generalized lipodystrophy (CGL) is a rare genetic disease characterized by the absence of body fat from birth. Focal bone …
Peculiar distribution of adipose tissue in patients with congenital generalized lipodystrophy.
Garg A, Fleckenstein JL, Peshock RM, Grundy SM. Garg A, et al. J Clin Endocrinol Metab. 1992 Aug;75(2):358-61. doi: 10.1210/jcem.75.2.1639935. J Clin Endocrinol Metab. 1992. PMID: 1639935
Congenital generalized lipodystrophy (CGL) is a rare genetic disease with extreme paucity of fat from birth which is believed to be generalized, involving the whole body. ...Thus, patients with CGL do not have a complete absence of body fat; of interest, fat is pres …
Congenital generalized lipodystrophy (CGL) is a rare genetic disease with extreme paucity of fat from birth which is believed to be g …
Postmortem findings in congenital generalized lipodystrophy.
Chandalia M, Garg A, Vuitch F, Nizzi F. Chandalia M, et al. Among authors: garg a. J Clin Endocrinol Metab. 1995 Oct;80(10):3077-81. doi: 10.1210/jcem.80.10.7559900. J Clin Endocrinol Metab. 1995. PMID: 7559900 No abstract available.
Relationships of generalized and regional adiposity to insulin sensitivity in men.
Abate N, Garg A, Peshock RM, Stray-Gundersen J, Grundy SM. Abate N, et al. Among authors: garg a. J Clin Invest. 1995 Jul;96(1):88-98. doi: 10.1172/JCI118083. J Clin Invest. 1995. PMID: 7615840 Free PMC article.
The latter was assessed by determining subcutaneous abdominal, intraperitoneal, and retroperitoneal fat masses (using magnetic resonance imaging) and the sum of truncal and peripheral skinfold thicknesses. 39 healthy middle-aged men with a wide range of adiposity were stud …
The latter was assessed by determining subcutaneous abdominal, intraperitoneal, and retroperitoneal fat masses (using magnetic resonance ima …
Heterogeneity in adipose tissue metabolism: causes, implications and management of regional adiposity.
Abate N, Garg A. Abate N, et al. Among authors: garg a. Prog Lipid Res. 1995;34(1):53-70. doi: 10.1016/0163-7827(94)00006-8. Prog Lipid Res. 1995. PMID: 7644553 Review.
Heterogeneity in adipose tissue distribution may be determined by a combination of genetic and hormonal causes. Both factors may determine differences in metabolism of various adipose tissue compartments primarily by regulating LPL production, storage and release of triacy …
Heterogeneity in adipose tissue distribution may be determined by a combination of genetic and hormonal causes. Both factors may dete …
Severe islet amyloidosis in congenital generalized lipodystrophy.
Garg A, Chandalia M, Vuitch F. Garg A, et al. Diabetes Care. 1996 Jan;19(1):28-31. doi: 10.2337/diacare.19.1.28. Diabetes Care. 1996. PMID: 8720529
We studied pancreatic islet pathology in congenital generalized lipodystrophy, a genetic syndrome of extreme insulin resistance that may provide some clues. RESEARCH DESIGN AND METHODS: Our patient was a 24-year-old African-American woman with congenital generalized …
We studied pancreatic islet pathology in congenital generalized lipodystrophy, a genetic syndrome of extreme insulin resistance that …
Relationship of generalized and regional adiposity to insulin sensitivity in men with NIDDM.
Abate N, Garg A, Peshock RM, Stray-Gundersen J, Adams-Huet B, Grundy SM. Abate N, et al. Among authors: garg a. Diabetes. 1996 Dec;45(12):1684-93. doi: 10.2337/diab.45.12.1684. Diabetes. 1996. PMID: 8922352
Abdominal obesity, particularly excess intraperitoneal fat, is considered to play a major role in causing insulin resistance and NIDDM. ...Moreover, for each level of total and regional adiposity, NIDDM patients have a heightened state of insulin resistance....
Abdominal obesity, particularly excess intraperitoneal fat, is considered to play a major role in causing insulin resistance and NIDD …
Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22.
Peters JM, Barnes R, Bennett L, Gitomer WM, Bowcock AM, Garg A. Peters JM, et al. Among authors: garg a. Nat Genet. 1998 Mar;18(3):292-5. doi: 10.1038/ng0398-292. Nat Genet. 1998. PMID: 9500556
We carried out a genome-wide scan with a set of highly polymorphic short tandem-repeats (STR) in individuals from five well-characterized pedigrees and mapped the FPLD locus to chromosome 1q21-22. The maximum two-point lod score obtained with a highly polymor …
We carried out a genome-wide scan with a set of highly polymorphic short tandem-repeats (STR) in individuals from five well-ch …
Adipose tissue distribution pattern in patients with familial partial lipodystrophy (Dunnigan variety).
Garg A, Peshock RM, Fleckenstein JL. Garg A, et al. J Clin Endocrinol Metab. 1999 Jan;84(1):170-4. doi: 10.1210/jcem.84.1.5383. J Clin Endocrinol Metab. 1999. PMID: 9920078
Familial partial lipodystrophy, Dunnigan type (FPLD), is a rare autosomal dominant genetic disorder characterized by gradual loss of sc fat from the extremities, commencing at the time of puberty. ...We conclude that FPLD results in a characteristic absence of sc fa …
Familial partial lipodystrophy, Dunnigan type (FPLD), is a rare autosomal dominant genetic disorder characterized by gradual loss of …
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