José Felix
Martí Massó
José Felix Martí Massó-rekin lankidetzan egindako argitalpenak (10)
2006
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Apolipoprotein E ε4 allele in familial and sporadic Parkinson's disease
Neuroscience Letters, Vol. 406, Núm. 3, pp. 235-239
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Parkinson's disease due to the R1441G mutation in Dardarin: A founder effect in the Basques
Movement Disorders, Vol. 21, Núm. 11, pp. 1954-1959
2005
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Familial Parkinson's disease: Clinical and genetic analysis of four Basque families
Annals of Neurology, Vol. 57, Núm. 3, pp. 365-372
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LGMD2A: Genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene
Brain, Vol. 128, Núm. 4, pp. 732-742
2004
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Mitochondrial polymporphisms in Parkinson's Disease
Neuroscience Letters, Vol. 370, Núm. 2-3, pp. 171-174
2002
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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
Human Molecular Genetics, Vol. 11, Núm. 9, pp. 1119-1128
1999
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Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large Basque pedigree linked to chromosome 10q
Annals of Neurology, Vol. 45, Núm. 2, pp. 182-188
1998
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Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain)
Brain, Vol. 121, Núm. 9, pp. 1735-1747
1996
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Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy
Genetic Epidemiology, Vol. 13, Núm. 5, pp. 483-487
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Frequency of myotonic dystrophy gene carriers in cataract patients
Journal of Medical Genetics, Vol. 33, Núm. 3, pp. 221-223