Pou A - Search Results

1

Distinct muscle imaging patterns in myofibrillar myopathies.

Fischer D, Kley RA, Strach K, Meyer C, Sommer T, Eger K, Rolfs A, Meyer W, Pou A, Pradas J, Heyer CM, Grossmann A, Huebner A, Kress W, Reimann J, Schröder R, Eymard B, Fardeau M, Udd B, Goldfarb L, Vorgerd M, Olivé M. Fischer D, et al. Among authors: pou a. Neurology. 2008 Sep 2;71(10):758-65. doi: 10.1212/01.wnl.0000324927.28817.9b. Neurology. 2008. PMID: 18765652 Free PMC article.

2

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. Among authors: pou a. 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.

3

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: pou a. 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.

4

Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients.

Gallardo E, Rojas-García R, de Luna N, Pou A, Brown RH Jr, Illa I. Gallardo E, et al. Among authors: pou a. Neurology. 2001 Dec 11;57(11):2136-8. doi: 10.1212/wnl.57.11.2136. Neurology. 2001. PMID: 11739845

5

Primary cerebral abscess due to nocardia presenting as 'ghost tumor'. Clinical and pathological study.

Roquer J, Pou A, Herraiz J, Campodarve I, Sequeira T, Vilató J, Alameda F, Serrano R. Roquer J, et al. Among authors: pou a. Eur Neurol. 1990;30(5):254-7. doi: 10.1159/000117357. Eur Neurol. 1990. PMID: 2269313

6

SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings.

Cuscó I, Barceló MJ, Rojas-García R, Illa I, Gámez J, Cervera C, Pou A, Izquierdo G, Baiget M, Tizzano EF. Cuscó I, et al. Among authors: pou a. J Neurol. 2006 Jan;253(1):21-5. doi: 10.1007/s00415-005-0912-y. Epub 2005 Jun 28. J Neurol. 2006. PMID: 15981080

7

Sensory neuronopathy and Sjögren's syndrome: clinical and immunologic study of two patients.

Graus F, Pou A, Kanterewicz E, Anderson NE. Graus F, et al. Among authors: pou a. Neurology. 1988 Oct;38(10):1637-9. doi: 10.1212/wnl.38.10.1637. Neurology. 1988. PMID: 3419610

8

New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations.

Olivé M, Abdul-Hussein S, Oldfors A, González-Costello J, van der Ven PF, Fürst DO, González L, Moreno D, Torrejón-Escribano B, Alió J, Pou A, Ferrer I, Tajsharghi H. Olivé M, et al. Among authors: pou a. Hum Mol Genet. 2015 Jul 1;24(13):3638-50. doi: 10.1093/hmg/ddv108. Epub 2015 Mar 23. Hum Mol Genet. 2015. PMID: 25801283

9

Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study.

Ferrer I, Olivé M, Rivera R, Pou A, Narberhaus B, Ugarte A. Ferrer I, et al. Among authors: pou a. Neuropathol Appl Neurobiol. 1995 Jun;21(3):255-61. doi: 10.1111/j.1365-2990.1995.tb01057.x. Neuropathol Appl Neurobiol. 1995. PMID: 7477734

10

Normal proprioceptive trigeminal afferents in patients with Sjögren's syndrome and sensory neuronopathy.

Valls-Sole J, Graus F, Font J, Pou A, Tolosa ES. Valls-Sole J, et al. Among authors: pou a. Ann Neurol. 1990 Dec;28(6):786-90. doi: 10.1002/ana.410280609. Ann Neurol. 1990. PMID: 2285265

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