Bataller L - Search Results

1

Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain.

Baviera-Muñoz R, Carretero-Vilarroig L, Vázquez-Costa JF, Morata-Martínez C, Campins-Romeu M, Muelas N, Sastre-Bataller I, Martínez-Torres I, Pérez-García J, Sivera R, Sevilla T, Vilchez JJ, Jaijo T, Espinós C, Millán JM, Bataller L, Aller E. Baviera-Muñoz R, et al. Among authors: bataller l. Neurol Genet. 2022 Nov 14;8(6):e200038. doi: 10.1212/NXG.0000000000200038. eCollection 2022 Dec. Neurol Genet. 2022. PMID: 36530930 Free PMC article.

2

[Limbic encephalitis: the new cell membrane antigens and a proposal of clinical-immunological classification with therapeutic implications].

Dalmau J, Bataller L. Dalmau J, et al. Among authors: bataller l. Neurologia. 2007 Oct;22(8):526-37. Neurologia. 2007. PMID: 18000762 Review. Spanish.

3

Clinical outcome in adult onset idiopathic or paraneoplastic opsoclonus-myoclonus.

Bataller L, Graus F, Saiz A, Vilchez JJ; Spanish Opsoclonus-Myoclonus Study Group. Bataller L, et al. Brain. 2001 Feb;124(Pt 2):437-43. doi: 10.1093/brain/124.2.437. Brain. 2001. PMID: 11157570

4

[Neuroimaging study with morphometric analysis of hereditary and idiopathic ataxia].

Villanueva-Haba V, Garcés-Sánchez M, Bataller L, Palau F, Vílchez J. Villanueva-Haba V, et al. Among authors: bataller l. Neurologia. 2001 Mar;16(3):105-11. Neurologia. 2001. PMID: 11333779 Spanish.

5

Autoantigen diversity in the opsoclonus-myoclonus syndrome.

Bataller L, Rosenfeld MR, Graus F, Vilchez JJ, Cheung NK, Dalmau J. Bataller L, et al. Ann Neurol. 2003 Mar;53(3):347-53. doi: 10.1002/ana.10462. Ann Neurol. 2003. PMID: 12601702

6

Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy.

Sevilla T, Jaijo T, Nauffal D, Collado D, Chumillas MJ, Vilchez JJ, Muelas N, Bataller L, Domenech R, Espinós C, Palau F. Sevilla T, et al. Among authors: bataller l. Brain. 2008 Nov;131(Pt 11):3051-61. doi: 10.1093/brain/awn228. Epub 2008 Sep 23. Brain. 2008. PMID: 18812441

7

Mesial temporal sclerosis as a complication of hematologic cancer.

Sivera R, Bataller L, Martínez J, Villanueva V. Sivera R, et al. Among authors: bataller l. J Neurol. 2009 Oct;256(10):1759-61. doi: 10.1007/s00415-009-5168-5. Epub 2009 May 12. J Neurol. 2009. PMID: 19434437 No abstract available.

8

Reversible paraneoplastic limbic encephalitis associated with antibodies to the AMPA receptor.

Bataller L, Galiano R, García-Escrig M, Martínez B, Sevilla T, Blasco R, Vílchez JJ, Dalmau J. Bataller L, et al. Neurology. 2010 Jan 19;74(3):265-7. doi: 10.1212/WNL.0b013e3181cb3e52. Neurology. 2010. PMID: 20083804 Free PMC article. No abstract available.

9

Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease.

Sivera R, Espinós C, Vílchez JJ, Mas F, Martínez-Rubio D, Chumillas MJ, Mayordomo F, Muelas N, Bataller L, Palau F, Sevilla T. Sivera R, et al. Among authors: bataller l. J Peripher Nerv Syst. 2010 Dec;15(4):334-44. doi: 10.1111/j.1529-8027.2010.00286.x. J Peripher Nerv Syst. 2010. PMID: 21199105

10

Peripheral nerve hyperexcitability: a clinical and immunologic study of 38 patients.

Rubio-Agusti I, Perez-Miralles F, Sevilla T, Muelas N, Chumillas MJ, Mayordomo F, Azorin I, Carmona E, Moscardo F, Palau J, Jacobson L, Vincent A, Vilchez JJ, Bataller L. Rubio-Agusti I, et al. Among authors: bataller l. Neurology. 2011 Jan 11;76(2):172-8. doi: 10.1212/WNL.0b013e3182061b1e. Neurology. 2011. PMID: 21220721

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