Detalhe da pesquisa
1.
Blood miRNA expression pattern is a possible risk marker for natalizumab-associated progressive multifocal leukoencephalopathy in multiple sclerosis patients.
Mult Scler
; 20(14): 1851-9, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24852919
2.
ANKRD55 and DHCR7 are novel multiple sclerosis risk loci.
Genes Immun
; 13(3): 253-7, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22130326
3.
Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis.
Mult Scler
; 18(7): 983-90, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22183936
4.
Validation of IRF5 as multiple sclerosis risk gene: putative role in interferon beta therapy and human herpes virus-6 infection.
Genes Immun
; 12(1): 40-5, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20861862
5.
Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.
Genes Immun
; 12(2): 110-5, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20944657
6.
The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis.
Genes Immun
; 11(5): 439-45, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20508602
7.
Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1.
Psychol Med
; 40(3): 487-95, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19627641
8.
Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene.
Am J Med Genet B Neuropsychiatr Genet
; 153B(7): 1283-91, 2010 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20872767
9.
MiR-219a-5p Enriched Extracellular Vesicles Induce OPC Differentiation and EAE Improvement More Efficiently Than Liposomes and Polymeric Nanoparticles.
Pharmaceutics
; 12(2)2020 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32098213
10.
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis.
Neurogenetics
; 9(3): 173-82, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18563459
11.
Molecular characterization of putative modulatory factors in two Spanish families with A1555G deafness.
Audiol Neurootol
; 13(5): 320-7, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18391568
12.
Minimizing creatine kinase variability in rats for neuromuscular research purposes.
Lab Anim
; 42(1): 19-25, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18348763
13.
Models for Studying Myelination, Demyelination and Remyelination.
Neuromolecular Med
; 19(2-3): 181-192, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28536996
14.
Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease.
Neurosci Lett
; 406(3): 235-9, 2006 Oct 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-16904828
15.
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.
Brain
; 128(Pt 4): 732-42, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15689361
16.
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.
Neurology
; 59(8): 1197-202, 2002 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-12391347
17.
Mitochondrial polymporphisms in Parkinson's Disease.
Neurosci Lett
; 370(2-3): 171-4, 2004 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-15488317
18.
Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defect.
Genes Brain Behav
; 8(1): 53-9, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18823405
19.
Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients.
Mult Scler
; 15(1): 124-8, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18755822
20.
Identification of (1H)-pyrroles as histone deacetylase inhibitors with antitumoral activity.
Oncogene
; 28(11): 1477-84, 2009 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19169274