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    Results: 1 to 20 of 177

    1.

    Köbberling type of familial partial lipodystrophy: an underrecognized syndrome.

    Herbst KL, Tannock LR, Deeb SS, Purnell JQ, Brunzell JD, Chait A.

    Diabetes Care. 2003 Jun;26(6):1819-24.PMID: 12766116 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    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

    3.

    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

    4.

    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

    5.

    New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.

    Decaudain A, Vantyghem MC, Guerci B, Hécart AC, Auclair M, Reznik Y, Narbonne H, Ducluzeau PH, Donadille B, Lebbé C, Béréziat V, Capeau J, Lascols O, Vigouroux C.

    J Clin Endocrinol Metab. 2007 Dec;92(12):4835-44. Epub 2007 Aug 21.PMID: 17711925 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    A novel heterozygous mutation in peroxisome proliferator-activated receptor-gamma gene in a patient with familial partial lipodystrophy.

    Agarwal AK, Garg A.

    J Clin Endocrinol Metab. 2002 Jan;87(1):408-11.PMID: 11788685 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Phenomics, lipodystrophy, and the metabolic syndrome.

    Hegele RA.

    Trends Cardiovasc Med. 2004 May;14(4):133-7. Review.PMID: 15177263 [PubMed - indexed for MEDLINE]Related articles

    8.

    [Primary lipodystrophies]

    Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C.

    Ann Endocrinol (Paris). 2007 Feb;68(1):10-20. Epub 2007 Feb 21. French. PMID: 17320032 [PubMed - indexed for MEDLINE]Related articles

    9.

    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

    10.

    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

    11.

    Insulin resistance in human partial lipodystrophy.

    Hegele RA.

    Curr Atheroscler Rep. 2000 Sep;2(5):397-404. Review.PMID: 11122771 [PubMed - indexed for MEDLINE]Related articles

    12.

    Premature atherosclerosis associated with monogenic insulin resistance.

    Hegele RA.

    Circulation. 2001 May 8;103(18):2225-9.PMID: 11342468 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    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

    14.

    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

    15.

    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

    16.

    Mesangiocapillary glomerulonephritis type 2 associated with familial partial lipodystrophy (Dunnigan-Kobberling syndrome).

    Owen KR, Donohoe M, Ellard S, Clarke TJ, Nicholls AJ, Hattersley AT, Bingham C.

    Nephron Clin Pract. 2004;96(2):c35-8.PMID: 14988595 [PubMed - indexed for MEDLINE]Related articles

    17.

    Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-gamma.

    Savage DB, Tan GD, Acerini CL, Jebb SA, Agostini M, Gurnell M, Williams RL, Umpleby AM, Thomas EL, Bell JD, Dixon AK, Dunne F, Boiani R, Cinti S, Vidal-Puig A, Karpe F, Chatterjee VK, O'Rahilly S.

    Diabetes. 2003 Apr;52(4):910-7.PMID: 12663460 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    PPARG F388L, a transactivation-deficient mutant, in familial partial lipodystrophy.

    Hegele RA, Cao H, Frankowski C, Mathews ST, Leff T.

    Diabetes. 2002 Dec;51(12):3586-90.PMID: 12453919 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    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

    20.

    Monogenic forms of insulin resistance: apertures that expose the common metabolic syndrome.

    Hegele RA.

    Trends Endocrinol Metab. 2003 Oct;14(8):371-7. Review.PMID: 14516935 [PubMed - indexed for MEDLINE]Related articles

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