Simha V - Search Results

1

Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.

Akinci G, Alyaarubi S, Patni N, Alhashmi N, Al-Shidhani A, Prodam F, Gagne N, Babalola F, Al Senani A, Muniraj K, Elsayed SM, Beghini M, Saydam BO, Allawati M, Vaishnav MS, Can E, Simsir IY, Sorkina E, Dursun F, Kamrath C, Cavdar U, Chakraborty PP, Dogan OA, Al Hosin A, Al Maimani A, Comunoglu N, Hamed A, Huseinbegovic T, Scherer T, Curtis J, Brown RJ, Topaloglu H, Simha V, Wabitsch M, Tuysuz B, Oral EA, Akinci B, Garg A. Akinci G, et al. Among authors: simha v. Am J Med Genet A. 2024 Jun;194(6):e63533. doi: 10.1002/ajmg.a.63533. Epub 2024 Jan 17. Am J Med Genet A. 2024. PMID: 38234231

2

Body fat distribution and metabolic derangements in patients with familial partial lipodystrophy associated with mandibuloacral dysplasia.

Simha V, Garg A. Simha V, et al. J Clin Endocrinol Metab. 2002 Feb;87(2):776-85. doi: 10.1210/jcem.87.2.8258. J Clin Endocrinol Metab. 2002. PMID: 11836320

3

Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes.

Simha V, Garg A. Simha V, et al. J Clin Endocrinol Metab. 2003 Nov;88(11):5433-7. doi: 10.1210/jc.2003-030835. J Clin Endocrinol Metab. 2003. PMID: 14602785

4

Lipodystrophy: lessons in lipid and energy metabolism.

Simha V, Garg A. Simha V, et al. Curr Opin Lipidol. 2006 Apr;17(2):162-9. doi: 10.1097/01.mol.0000217898.52197.18. Curr Opin Lipidol. 2006. PMID: 16531753 Review.

5

Body fat distribution and metabolic variables in patients with neonatal progeroid syndrome.

O'Neill B, Simha V, Kotha V, Garg A. O'Neill B, et al. Among authors: simha v. Am J Med Genet A. 2007 Jul 1;143A(13):1421-30. doi: 10.1002/ajmg.a.31840. Am J Med Genet A. 2007. PMID: 17523150

6

Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instability.

Simha V, Agarwal AK, Aronin PA, Iannaccone ST, Garg A. Simha V, et al. Am J Med Genet A. 2008 Sep 15;146A(18):2318-26. doi: 10.1002/ajmg.a.32457. Am J Med Genet A. 2008. PMID: 18698612 Free PMC article.

7

Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophy.

Simha V, Agarwal AK, Oral EA, Fryns JP, Garg A. Simha V, et al. J Clin Endocrinol Metab. 2003 Jun;88(6):2821-4. doi: 10.1210/jc.2002-021575. J Clin Endocrinol Metab. 2003. PMID: 12788894

8

Inherited lipodystrophies and hypertriglyceridemia.

Simha V, Garg A. Simha V, et al. Curr Opin Lipidol. 2009 Aug;20(4):300-8. doi: 10.1097/MOL.0b013e32832d4a33. Curr Opin Lipidol. 2009. PMID: 19494770 Review.

9

Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations.

Subramanyam L, Simha V, Garg A. Subramanyam L, et al. Among authors: simha v. Clin Genet. 2010 Jul;78(1):66-73. doi: 10.1111/j.1399-0004.2009.01350.x. Epub 2009 Dec 22. Clin Genet. 2010. PMID: 20041886 Free PMC article.

10

Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy.

Agarwal AK, Simha V, Oral EA, Moran SA, Gorden P, O'Rahilly S, Zaidi Z, Gurakan F, Arslanian SA, Klar A, Ricker A, White NH, Bindl L, Herbst K, Kennel K, Patel SB, Al-Gazali L, Garg A. Agarwal AK, et al. Among authors: simha v. J Clin Endocrinol Metab. 2003 Oct;88(10):4840-7. doi: 10.1210/jc.2003-030855. J Clin Endocrinol Metab. 2003. PMID: 14557463

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