Milà M - Search Results

1

REM sleep behavior disorder and vocal cord paralysis in Machado-Joseph disease.

Iranzo A, Muñoz E, Santamaria J, Vilaseca I, Milà M, Tolosa E. Iranzo A, et al. Among authors: mila m. Mov Disord. 2003 Oct;18(10):1179-83. doi: 10.1002/mds.10509. Mov Disord. 2003. PMID: 14534924

2

Intranuclear inclusions, neuronal loss and CAG mosaicism in two patients with Machado-Joseph disease.

Muñoz E, Rey MJ, Milà M, Cardozo A, Ribalta T, Tolosa E, Ferrer I. Muñoz E, et al. Among authors: mila m. J Neurol Sci. 2002 Aug 15;200(1-2):19-25. doi: 10.1016/s0022-510x(02)00110-7. J Neurol Sci. 2002. PMID: 12127671

3

Dentatorubropallidoluysian atrophy in a spanish family: a clinical, radiological, pathological, and genetic study.

Muñoz E, Milà M, Sánchez A, Latorre P, Ariza A, Codina M, Ballesta F, Tolosa E. Muñoz E, et al. Among authors: mila m. J Neurol Neurosurg Psychiatry. 1999 Dec;67(6):811-4. doi: 10.1136/jnnp.67.6.811. J Neurol Neurosurg Psychiatry. 1999. PMID: 10567506 Free PMC article.

4

FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening.

Rodriguez-Revenga L, Gómez-Anson B, Muñoz E, Jiménez D, Santos M, Tintoré M, Martín G, Brieva L, Milà M. Rodriguez-Revenga L, et al. Among authors: mila m. Mol Neurobiol. 2007 Jun;35(3):324-8. doi: 10.1007/s12035-007-0020-3. Mol Neurobiol. 2007. PMID: 17917121

5

SCA8 in the Spanish population including one homozygous patient.

Tazón B, Badenas C, Jiménez L, Muñoz E, Milà M. Tazón B, et al. Among authors: mila m. Clin Genet. 2002 Nov;62(5):404-9. doi: 10.1034/j.1399-0004.2002.620509.x. Clin Genet. 2002. PMID: 12431257

6

Association between BDNF Val66Met polymorphism and age at onset in Huntington disease.

Alberch J, López M, Badenas C, Carrasco JL, Milà M, Muñoz E, Canals JM. Alberch J, et al. Among authors: mila m. Neurology. 2005 Sep 27;65(6):964-5. doi: 10.1212/01.wnl.0000175977.57661.b1. Neurology. 2005. PMID: 16186551 No abstract available.

7

Chorea-ballism associated with familial amyotrophic lateral sclerosis. A clinical, genetic, and neuropathological study.

Gamez J, Corbera-Bellalta M, Mila M, López-Lisbona R, Boluda S, Ferrer I. Gamez J, et al. Among authors: mila m. Mov Disord. 2008 Feb 15;23(3):434-8. doi: 10.1002/mds.21856. Mov Disord. 2008. PMID: 18072201

8

Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma.

Gelpi E, Botta-Orfila T, Bodi L, Marti S, Kovacs G, Grau-Rivera O, Lozano M, Sánchez-Valle R, Muñoz E, Valldeoriola F, Pagonabarraga J, Tartaglia GG, Milà M. Gelpi E, et al. Among authors: mila m. Brain. 2017 Aug 1;140(8):e51. doi: 10.1093/brain/awx156. Brain. 2017. PMID: 28899011 No abstract available.

9

Role of the CDKN2A locus in patients with multiple primary melanomas.

Puig S, Malvehy J, Badenas C, Ruiz A, Jimenez D, Cuellar F, Azon A, Gonzàlez U, Castel T, Campoy A, Herrero J, Martí R, Brunet-Vidal J, Milà M. Puig S, et al. Among authors: mila m. J Clin Oncol. 2005 May 1;23(13):3043-51. doi: 10.1200/JCO.2005.08.034. J Clin Oncol. 2005. PMID: 15860862

10

Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injection.

Oliva R, Margarit E, Ballescá JL, Carrió A, Sánchez A, Milà M, Jiménez L, Alvarez-Vijande JR, Ballesta F. Oliva R, et al. Among authors: mila m. Fertil Steril. 1998 Sep;70(3):506-10. doi: 10.1016/s0015-0282(98)00195-2. Fertil Steril. 1998. PMID: 9757880 Free article. Clinical Trial.

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