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Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin.
Piñol-Ripoll G, Shatunov A, Cabello A, Larrodé P, de la Puerta I, Pelegrín J, Ramos FJ, Olivé M, Goldfarb LG. Piñol-Ripoll G, et al. Among authors: goldfarb lg. Neuromuscul Disord. 2009 Jun;19(6):418-22. doi: 10.1016/j.nmd.2009.04.004. Epub 2009 May 9. Neuromuscul Disord. 2009. PMID: 19433360 Free PMC article.
Dominant-negative effects of a novel mutation in the filamin myopathy.
van der Ven PF, Odgerel Z, Fürst DO, Goldfarb LG, Kono S, Miyajima H. van der Ven PF, et al. Among authors: goldfarb lg. Neurology. 2010 Dec 7;75(23):2137-8. doi: 10.1212/WNL.0b013e3182031bb3. Neurology. 2010. PMID: 21135393 No abstract available.
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy.
Olivé M, Odgerel Z, Martínez A, Poza JJ, Bragado FG, Zabalza RJ, Jericó I, Gonzalez-Mera L, Shatunov A, Lee HS, Armstrong J, Maraví E, Arroyo MR, Pascual-Calvet J, Navarro C, Paradas C, Huerta M, Marquez F, Rivas EG, Pou A, Ferrer I, Goldfarb LG. Olivé M, et al. Among authors: goldfarb lg. Neuromuscul Disord. 2011 Aug;21(8):533-42. doi: 10.1016/j.nmd.2011.05.002. Epub 2011 Jun 14. Neuromuscul Disord. 2011. PMID: 21676617 Free PMC article.
Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.
Kley RA, Serdaroglu-Oflazer P, Leber Y, Odgerel Z, van der Ven PF, Olivé M, Ferrer I, Onipe A, Mihaylov M, Bilbao JM, Lee HS, Höhfeld J, Djinović-Carugo K, Kong K, Tegenthoff M, Peters SA, Stenzel W, Vorgerd M, Goldfarb LG, Fürst DO. Kley RA, et al. Among authors: goldfarb lg. Brain. 2012 Sep;135(Pt 9):2642-60. doi: 10.1093/brain/aws200. Brain. 2012. PMID: 22961544 Free PMC article.
176 results