My NCBI | Sign In
RSS Settings
  • Search:

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

    Results: 1 to 20 of 194

    1.

    Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety.

    Haque WA, Oral EA, Dietz K, Bowcock AM, Agarwal AK, Garg A.

    Diabetes Care. 2003 May;26(5):1350-5.PMID: 12716787 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Gender differences in the prevalence of metabolic complications in familial partial lipodystrophy (Dunnigan variety).

    Garg A.

    J Clin Endocrinol Metab. 2000 May;85(5):1776-82.PMID: 10843151 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene.

    Garg A, Vinaitheerthan M, Weatherall PT, Bowcock AM.

    J Clin Endocrinol Metab. 2001 Jan;86(1):59-65.PMID: 11231979 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Elevated serum C-reactive protein and free fatty acids among nondiabetic carriers of missense mutations in the gene encoding lamin A/C (LMNA) with partial lipodystrophy.

    Hegele RA, Kraw ME, Ban MR, Miskie BA, Huff MW, Cao H.

    Arterioscler Thromb Vasc Biol. 2003 Jan 1;23(1):111-6.PMID: 12524233 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.

    Speckman RA, Garg A, Du F, Bennett L, Veile R, Arioglu E, Taylor SI, Lovett M, Bowcock AM.

    Am J Hum Genet. 2000 Apr;66(4):1192-8. Erratum in: Am J Hum Genet 2000 Sep;67(3):775. PMID: 10739751 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities.

    Vantyghem MC, Pigny P, Maurage CA, Rouaix-Emery N, Stojkovic T, Cuisset JM, Millaire A, Lascols O, Vermersch P, Wemeau JL, Capeau J, Vigouroux C.

    J Clin Endocrinol Metab. 2004 Nov;89(11):5337-46.PMID: 15531479 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophy.

    Vantyghem MC, Vincent-Desplanques D, Defrance-Faivre F, Capeau J, Fermon C, Valat AS, Lascols O, Hecart AC, Pigny P, Delemer B, Vigouroux C, Wemeau JL.

    J Clin Endocrinol Metab. 2008 Jun;93(6):2223-9. Epub 2008 Mar 25.PMID: 18364375 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.

    Vigouroux C, Magré J, Vantyghem MC, Bourut C, Lascols O, Shackleton S, Lloyd DJ, Guerci B, Padova G, Valensi P, Grimaldi A, Piquemal R, Touraine P, Trembath RC, Capeau J.

    Diabetes. 2000 Nov;49(11):1958-62.PMID: 11078466 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    LMNA R482Q mutation in partial lipodystrophy associated with reduced plasma leptin concentration.

    Hegele RA, Cao H, Huff MW, Anderson CM.

    J Clin Endocrinol Metab. 2000 Sep;85(9):3089-93.PMID: 10999791 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Phenotypic gender differences in subjects with familial partial lipodystrophy (Dunnigan variety) due to a nuclear lamin A/C R482W mutation.

    Araújo-Vilar D, Loidi L, Domínguez F, Cabezas-Cerrato J.

    Horm Metab Res. 2003 Jan;35(1):29-35.PMID: 12669268 [PubMed - indexed for MEDLINE]Related articles

    11.

    Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.

    Cao H, Hegele RA.

    Hum Mol Genet. 2000 Jan 1;9(1):109-12.PMID: 10587585 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Hepatic steatosis in Dunnigan-type familial partial lipodystrophy.

    Lüdtke A, Genschel J, Brabant G, Bauditz J, Taupitz M, Koch M, Wermke W, Worman HJ, Schmidt HH.

    Am J Gastroenterol. 2005 Oct;100(10):2218-24.PMID: 16181372 [PubMed - indexed for MEDLINE]Related articles

    13.

    Heterogeneity of nuclear lamin A mutations in Dunnigan-type familial partial lipodystrophy.

    Hegele RA, Cao H, Anderson CM, Hramiak IM.

    J Clin Endocrinol Metab. 2000 Sep;85(9):3431-5.PMID: 10999845 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    A case of Dunnigan-type familial partial lipodystrophy (FPLD) due to lamin A/C (LMNA) mutations complicated by end-stage renal disease.

    Imachi H, Murao K, Ohtsuka S, Fujiwara M, Muraoka T, Hosokawa H, Ishida T.

    Endocrine. 2009 Feb;35(1):18-21. Epub 2008 Nov 15.PMID: 19011997 [PubMed - indexed for MEDLINE]Related articles

    15.

    Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA gene.

    Owen KR, Donohoe M, Ellard S, Hattersley AT.

    Diabet Med. 2003 Oct;20(10):823-7.PMID: 14510863 [PubMed - indexed for MEDLINE]Related articles

    16.

    Post-mortem findings in familial partial lipodystrophy, Dunnigan variety.

    Haque WA, Vuitch F, Garg A.

    Diabet Med. 2002 Dec;19(12):1022-5.PMID: 12647844 [PubMed - indexed for MEDLINE]Related articles

    17.

    Long-term efficacy of leptin replacement in patients with Dunnigan-type familial partial lipodystrophy.

    Park JY, Javor ED, Cochran EK, DePaoli AM, Gorden P.

    Metabolism. 2007 Apr;56(4):508-16.PMID: 17379009 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Adipose tissue distribution pattern in patients with familial partial lipodystrophy (Dunnigan variety).

    Garg A, Peshock RM, Fleckenstein JL.

    J Clin Endocrinol Metab. 1999 Jan;84(1):170-4.PMID: 9920078 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Serum adiponectin and leptin levels in patients with lipodystrophies.

    Haque WA, Shimomura I, Matsuzawa Y, Garg A.

    J Clin Endocrinol Metab. 2002 May;87(5):2395.PMID: 11994394 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Familial partial lipodystrophy: a monogenic form of the insulin resistance syndrome.

    Hegele RA.

    Mol Genet Metab. 2000 Dec;71(4):539-44. Review.PMID: 11136544 [PubMed - indexed for MEDLINE]Related articles

    Supplemental Content

    Filter your results:

    Find related data

    Recent activity