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Journal Abstract Search

183 related items for PubMed ID: 17325275

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  • 4. 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. PubMed ID: 15531479
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  • 5. Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism.
    Vantyghem MC, Faivre-Defrance F, Marcelli-Tourvieille S, Fermon C, Evrard A, Bourdelle-Hego MF, Vigouroux C, Defebvre L, Delemer B, Wemeau JL.
    Clin Endocrinol (Oxf); 2007 Aug; 67(2):247-9. PubMed ID: 17524034
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  • 7. Increased skeletal muscle volume in women with familial partial lipodystrophy, Dunnigan variety.
    Ji H, Weatherall P, Adams-Huet B, Garg A.
    J Clin Endocrinol Metab; 2013 Aug; 98(8):E1410-3. PubMed ID: 23783098
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  • 8. Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy.
    Wójcik S, Nogalska A, Engel WK, Askanas V.
    Folia Morphol (Warsz); 2008 Feb; 67(1):6-12. PubMed ID: 18335407
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  • 12. [Histopathological features of biopsied peroneus brevis muscle in patients with peripheral neuropathies].
    Yamashita M, Yamamoto T, Nakamura M.
    No To Shinkei; 2003 Dec; 55(12):1033-9. PubMed ID: 14870573
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  • 15. Myostatin expression in muscular dystrophies and mitochondrial encephalomyopathies.
    Castro-Gago M, Blanco-Barca MO, Eiris-Puñal J, Carneiro I, Arce VM, Devesa J.
    Pediatr Neurol; 2006 Apr; 34(4):281-4. PubMed ID: 16638502
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  • 17. Powerful genes--myostatin regulation of human muscle mass.
    McNally EM.
    N Engl J Med; 2004 Jun 24; 350(26):2642-4. PubMed ID: 15215479
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  • 18. Myostatin promotes a fibrotic phenotypic switch in multipotent C3H 10T1/2 cells without affecting their differentiation into myofibroblasts.
    Artaza JN, Singh R, Ferrini MG, Braga M, Tsao J, Gonzalez-Cadavid NF.
    J Endocrinol; 2008 Feb 24; 196(2):235-49. PubMed ID: 18252947
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  • 19. 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 24; 49(11):1958-62. PubMed ID: 11078466
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  • 20. Serum retinol binding protein 4 in patients with familial partial lipodystrophy.
    Godoy-Matos AF, Moreira RO, MacDowell R, Bendet I, Mory PB, Moises RS.
    Clin Biochem; 2009 Jul 24; 42(10-11):1183-6. PubMed ID: 19303000
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