Garg A - Search Results

1

A Novel Subtype of Acquired Generalized Lipodystrophy Associated With Subcutaneous Panniculitis-Like T-cell Lymphoma.

Hoff FW, Xing C, Garg A. Hoff FW, et al. Among authors: garg a. JCEM Case Rep. 2024 Apr 27;2(5):luae069. doi: 10.1210/jcemcr/luae069. eCollection 2024 May. JCEM Case Rep. 2024. PMID: 38681964 Free PMC article.

2

Whole-exome sequencing identifies ADRA2A mutation in atypical familial partial lipodystrophy.

Garg A, Sankella S, Xing C, Agarwal AK. Garg A, et al. JCI Insight. 2016 Jun 16;1(9):e86870. doi: 10.1172/jci.insight.86870. JCI Insight. 2016. PMID: 27376152 Free PMC article.

3

Type 1 Hyperlipoproteinemia Due to Compound Heterozygous Rare Variants in GCKR.

Shetty S, Xing C, Garg A. Shetty S, et al. Among authors: garg a. J Clin Endocrinol Metab. 2016 Nov;101(11):3884-3887. doi: 10.1210/jc.2016-2179. Epub 2016 Jul 12. J Clin Endocrinol Metab. 2016. PMID: 27403930 Free PMC article.

4

Homozygous LIPE mutation in siblings with multiple symmetric lipomatosis, partial lipodystrophy, and myopathy.

Zolotov S, Xing C, Mahamid R, Shalata A, Sheikh-Ahmad M, Garg A. Zolotov S, et al. Among authors: garg a. Am J Med Genet A. 2017 Jan;173(1):190-194. doi: 10.1002/ajmg.a.37880. Epub 2016 Nov 11. Am J Med Genet A. 2017. PMID: 27862896 Free PMC article.

5

Juvenile-onset generalized lipodystrophy due to a novel heterozygous missense LMNA mutation affecting lamin C.

Patni N, Xing C, Agarwal AK, Garg A. Patni N, et al. Among authors: garg a. Am J Med Genet A. 2017 Sep;173(9):2517-2521. doi: 10.1002/ajmg.a.38341. Epub 2017 Jul 7. Am J Med Genet A. 2017. PMID: 28686329 Free PMC article.

6

A novel autosomal recessive lipodystrophy syndrome due to homozygous LMNA variant.

Patni N, Hatab S, Xing C, Zhou Z, Quittner C, Garg A. Patni N, et al. Among authors: garg a. J Med Genet. 2020 Jun;57(6):422-426. doi: 10.1136/jmedgenet-2019-106395. Epub 2019 Dec 19. J Med Genet. 2020. PMID: 31857427 Free PMC article.

7

Face-sparing Congenital Generalized Lipodystrophy Type 1 Associated With Nonclassical Congenital Adrenal Hyperplasia.

Costa S, Sampaio L, Berta Sousa A, Xing C, Agarwal AK, Garg A. Costa S, et al. Among authors: garg a. J Clin Endocrinol Metab. 2022 Aug 18;107(9):2433-2438. doi: 10.1210/clinem/dgac406. J Clin Endocrinol Metab. 2022. PMID: 35857714 Free PMC article.

8

Early-onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family.

Hoff FW, Xing C, Simha V, Agarwal AK, Zhang X, Lekkala L, Vaishnav MS, Vuitch F, Garg A. Hoff FW, et al. Among authors: garg a. Mol Genet Genomic Med. 2024 Jan;12(1):e2299. doi: 10.1002/mgg3.2299. Epub 2023 Oct 10. Mol Genet Genomic Med. 2024. PMID: 37815015 Free PMC article.

9

Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an LMNA p.R349W Variant.

Hussain I, Jin RR, Baum HBA, Greenfield JR, Devery S, Xing C, Hegele RA, Carranza-Leon BG, Linton MF, Vuitch F, Wu KHC, Precioso DR, Oshima J, Agarwal AK, Garg A. Hussain I, et al. Among authors: garg a. J Endocr Soc. 2020 Jul 27;4(10):bvaa104. doi: 10.1210/jendso/bvaa104. eCollection 2020 Oct 1. J Endocr Soc. 2020. PMID: 32939435 Free PMC article.

10

PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.

Agarwal AK, Xing C, DeMartino GN, Mizrachi D, Hernandez MD, Sousa AB, Martínez de Villarreal L, dos Santos HG, Garg A. Agarwal AK, et al. Among authors: garg a. Am J Hum Genet. 2010 Dec 10;87(6):866-72. doi: 10.1016/j.ajhg.2010.10.031. Am J Hum Genet. 2010. PMID: 21129723 Free PMC article.

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