Olivé M - Search Results

1

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. 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.

2

Myotilinopathy: refining the clinical and myopathological phenotype.

Olivé M, Goldfarb LG, Shatunov A, Fischer D, Ferrer I. Olivé M, et al. Brain. 2005 Oct;128(Pt 10):2315-26. doi: 10.1093/brain/awh576. Epub 2005 Jun 9. Brain. 2005. PMID: 15947064 Free article.

3

Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.

Olivé M, Armstrong J, Miralles F, Pou A, Fardeau M, Gonzalez L, Martínez F, Fischer D, Martínez Matos JA, Shatunov A, Goldfarb L, Ferrer I. Olivé M, et al. Neuromuscul Disord. 2007 Jun;17(6):443-50. doi: 10.1016/j.nmd.2007.02.009. Epub 2007 Apr 5. Neuromuscul Disord. 2007. PMID: 17418574 Free PMC article.

4

Molecular pathology of myofibrillar myopathies.

Ferrer I, Olivé M. Ferrer I, et al. Among authors: olive m. Expert Rev Mol Med. 2008 Sep 3;10:e25. doi: 10.1017/S1462399408000793. Expert Rev Mol Med. 2008. PMID: 18764962 Review.

5

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient.

Olivé M, Shatunov A, Gonzalez L, Carmona O, Moreno D, Quereda LG, Martinez-Matos JA, Goldfarb LG, Ferrer I. Olivé M, et al. Neuromuscul Disord. 2008 Dec;18(12):929-33. doi: 10.1016/j.nmd.2008.07.009. Epub 2008 Oct 22. Neuromuscul Disord. 2008. PMID: 18948002 Free PMC article.

6

Nemaline myopathy type 6: clinical and myopathological features.

Olivé M, Goldfarb LG, Lee HS, Odgerel Z, Blokhin A, Gonzalez-Mera L, Moreno D, Laing NG, Sambuughin N. Olivé M, et al. Muscle Nerve. 2010 Dec;42(6):901-7. doi: 10.1002/mus.21788. Muscle Nerve. 2010. PMID: 21104864 Free PMC article.

7

Myofibrillar myopathies: new developments.

Olivé M, Kley RA, Goldfarb LG. Olivé M, et al. Curr Opin Neurol. 2013 Oct;26(5):527-35. doi: 10.1097/WCO.0b013e328364d6b1. Curr Opin Neurol. 2013. PMID: 23995273 Free PMC article. Review.

8

A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failure.

Pfeffer G, Sambuughin N, Olivé M, Tyndel F, Toro C, Goldfarb LG, Chinnery PF. Pfeffer G, et al. Among authors: olive m. Neuromuscul Disord. 2014 Mar;24(3):241-4. doi: 10.1016/j.nmd.2013.12.001. Epub 2013 Dec 11. Neuromuscul Disord. 2014. PMID: 24444549 Free PMC article.

9

Oxidative stress in desminopathies and myotilinopathies: a link between oxidative damage and abnormal protein aggregation.

Janué A, Olivé M, Ferrer I. Janué A, et al. Among authors: olive m. Brain Pathol. 2007 Oct;17(4):377-88. doi: 10.1111/j.1750-3639.2007.00087.x. Epub 2007 Sep 4. Brain Pathol. 2007. PMID: 17784878 Free PMC article.

10

Generalized muscle pseudo-hypertrophy and stiffness associated with the myotilin Ser55Phe mutation: a novel myotilinopathy phenotype?

Gamez J, Armstrong J, Shatunov A, Selva-O'Callaghan A, Dominguez-Oronoz R, Ortega A, Goldfarb L, Ferrer I, Olivé M. Gamez J, et al. Among authors: olive m. J Neurol Sci. 2009 Feb 15;277(1-2):167-71. doi: 10.1016/j.jns.2008.10.019. Epub 2008 Nov 22. J Neurol Sci. 2009. PMID: 19027924 Free PMC article.

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