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Year Number of Results
2008 1
2015 3
2016 8
2017 2
2018 4
2019 4
2020 1
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Page 1
Lipodystrophy Syndromes.
Hussain I, Garg A. Hussain I, et al. Endocrinol Metab Clin North Am. 2016 Dec;45(4):783-797. doi: 10.1016/j.ecl.2016.06.012. Epub 2016 Oct 6. Endocrinol Metab Clin North Am. 2016. PMID: 27823605 Review.
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline.
Brown RJ, Araujo-Vilar D, Cheung PT, Dunger D, Garg A, Jack M, Mungai L, Oral EA, Patni N, Rother KI, von Schnurbein J, Sorkina E, Stanley T, Vigouroux C, Wabitsch M, Williams R, Yorifuji T. Brown RJ, et al. J Clin Endocrinol Metab. 2016 Dec;101(12):4500-4511. doi: 10.1210/jc.2016-2466. Epub 2016 Oct 6. J Clin Endocrinol Metab. 2016. PMID: 27710244 Free PMC article. Review.
Lipodystrophies, dyslipidaemias and atherosclerotic cardiovascular disease.
Hussain I, Patni N, Garg A. Hussain I, et al. Pathology. 2019 Feb;51(2):202-212. doi: 10.1016/j.pathol.2018.11.004. Epub 2018 Dec 27. Pathology. 2019. PMID: 30595509 Free PMC article. Review.
Congenital generalized lipodystrophies--new insights into metabolic dysfunction.
Patni N, Garg A. Patni N, et al. 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.
Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.
Wambach JA, Wegner DJ, Patni N, Kircher M, Willing MC, Baldridge D, Xing C, Agarwal AK, Vergano SAS, Patel C, Grange DK, Kenney A, Najaf T, Nickerson DA, Bamshad MJ, Cole FS, Garg A. Wambach JA, et al. Am J Hum Genet. 2018 Dec 6;103(6):968-975. doi: 10.1016/j.ajhg.2018.10.010. Epub 2018 Nov 7. Am J Hum Genet. 2018. PMID: 30414627 Free PMC article.
Efficacy of Metreleptin Treatment in Familial Partial Lipodystrophy Due to PPARG vs LMNA Pathogenic Variants.
Sekizkardes H, Cochran E, Malandrino N, Garg A, Brown RJ. Sekizkardes H, et al. J Clin Endocrinol Metab. 2019 Aug 1;104(8):3068-3076. doi: 10.1210/jc.2018-02787. J Clin Endocrinol Metab. 2019. PMID: 31194872 Free PMC article.
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. 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.
Lipodystrophy syndromes.
Herranz P, de Lucas R, Pérez-España L, Mayor M. Herranz P, et al. Dermatol Clin. 2008 Oct;26(4):569-78, ix. doi: 10.1016/j.det.2008.05.004. Dermatol Clin. 2008. PMID: 18793991 Free PMC article. Review.
JCL roundtable: Diagnosis and clinical management of lipodystrophy.
Brown WV, Garg A, Gorden P, Shamburek R. Brown WV, et al. J Clin Lipidol. 2016 Jul-Aug;10(4):728-736. doi: 10.1016/j.jacl.2016.06.005. Epub 2016 Jul 5. J Clin Lipidol. 2016. PMID: 27578101 Review.
How to explain the AKT phosphorylation of downstream targets in the wake of recent findings.
Agarwal AK. Agarwal AK. Proc Natl Acad Sci U S A. 2018 Jul 3;115(27):E6099-E6100. doi: 10.1073/pnas.1808461115. Epub 2018 Jun 15. Proc Natl Acad Sci U S A. 2018. PMID: 29907611 Free PMC article. No abstract available.
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