PubMed (Bookshelf cited) for id: 318592

Year	Number of Results
1999	1
2001	1
2002	2
2003	3
2004	4
2005	1
2006	2
2007	2
2008	5
2009	4
2010	3
2011	2
2012	3
2013	3
2014	2
2015	1
2024	0

1

Leptin in congenital and HIV-associated lipodystrophy.

Tsoukas MA, Farr OM, Mantzoros CS. Tsoukas MA, et al. Metabolism. 2015 Jan;64(1):47-59. doi: 10.1016/j.metabol.2014.07.017. Epub 2014 Aug 12. Metabolism. 2015. PMID: 25267014 Review.

2

Towards a mechanistic understanding of lipodystrophy and seipin functions.

Wee K, Yang W, Sugii S, Han W. Wee K, et al. Biosci Rep. 2014 Oct 2;34(5):e00141. doi: 10.1042/BSR20140114. Biosci Rep. 2014. PMID: 25195639 Free PMC article. Review.

3

Early infantile cardiomyopathy and liver disease: a multisystemic disorder caused by congenital lipodystrophy.

Debray FG, Baguette C, Colinet S, Van Maldergem L, Verellen-Dumouin C. Debray FG, et al. Mol Genet Metab. 2013 Jun;109(2):227-9. doi: 10.1016/j.ymgme.2013.04.011. Epub 2013 Apr 23. Mol Genet Metab. 2013. PMID: 23647707

4

A new seipin-associated neurodegenerative syndrome.

Guillén-Navarro E, Sánchez-Iglesias S, Domingo-Jiménez R, Victoria B, Ruiz-Riquelme A, Rábano A, Loidi L, Beiras A, González-Méndez B, Ramos A, López-González V, Ballesta-Martínez MJ, Garrido-Pumar M, Aguiar P, Ruibal A, Requena JR, Araújo-Vilar D. Guillén-Navarro E, et al. J Med Genet. 2013 Jun;50(6):401-9. doi: 10.1136/jmedgenet-2013-101525. Epub 2013 Apr 6. J Med Genet. 2013. PMID: 23564749

5

A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction.

Jeninga EH, de Vroede M, Hamers N, Breur JM, Verhoeven-Duif NM, Berger R, Kalkhoven E. Jeninga EH, et al. JIMD Rep. 2012;4:47-54. doi: 10.1007/8904_2011_86. Epub 2011 Nov 4. JIMD Rep. 2012. PMID: 23430896 Free PMC article.

6

Seipin regulates excitatory synaptic transmission in cortical neurons.

Wei S, Soh SL, Qiu W, Yang W, Seah CJ, Guo J, Ong WY, Pang ZP, Han W. Wei S, et al. J Neurochem. 2013 Feb;124(4):478-89. doi: 10.1111/jnc.12099. Epub 2012 Dec 27. J Neurochem. 2013. PMID: 23173741 Free article.

7

Seipin: from human disease to molecular mechanism.

Cartwright BR, Goodman JM. Cartwright BR, et al. J Lipid Res. 2012 Jun;53(6):1042-55. doi: 10.1194/jlr.R023754. Epub 2012 Apr 2. J Lipid Res. 2012. PMID: 22474068 Free PMC article. Review.

8

Clinical review#: Lipodystrophies: genetic and acquired body fat disorders.

Garg A. Garg A. J Clin Endocrinol Metab. 2011 Nov;96(11):3313-25. doi: 10.1210/jc.2011-1159. Epub 2011 Aug 24. J Clin Endocrinol Metab. 2011. PMID: 21865368 Free PMC article. Review.

9

Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.

Graul-Neumann LM, Kienitz T, Robinson PN, Baasanjav S, Karow B, Gillessen-Kaesbach G, Fahsold R, Schmidt H, Hoffmann K, Passarge E. Graul-Neumann LM, et al. Am J Med Genet A. 2010 Nov;152A(11):2749-55. doi: 10.1002/ajmg.a.33690. Am J Med Genet A. 2010. PMID: 20979188

10

Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutations.

Shastry S, Delgado MR, Dirik E, Turkmen M, Agarwal AK, Garg A. Shastry S, et al. Am J Med Genet A. 2010 Sep;152A(9):2245-53. doi: 10.1002/ajmg.a.33578. Am J Med Genet A. 2010. PMID: 20684003 Free PMC article.

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