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Acta Neurologica Scandinavica|January 30, 1999
Clinical features and genetic analysis of a Spanish family with spinocerebellar ataxia 6J Arpa, A Cuesta, A Cruz-Martínez, et al.
Journal of Medical Genetics|March 2, 1999
Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxiaJ García-Planells, A Cuesta, J J Vilchez, et al.
Neurologia (Barcelona, Spain)|November 1, 1995
[Huntington disease: clinical and genetic study in a Spanish population]M P Solís Pérez, F Palau Martínez, J A Burguera Hernández, et al.
Neurologia (Barcelona, Spain)|December 12, 2001
[Results of a program of presymptomatic diagnosis of Huntington's disease: evaluation of a 6 year period]M P Solís-Pérez, J A Burguera, F Palau, et al.
Gene|October 31, 2000
dfh is a Drosophila homolog of the Friedreich's ataxia disease geneJ Cañizares, J M Blanca, J A Navarro, et al.
Cancer Genetics and Cytogenetics|March 1, 1990
11q23 abnormalities in children with acute nonlymphocytic leukemia (M4-M5). Association with previous chemotherapyF Prieto, F Palau, L Badia, et al.
Journal of the Peripheral Nervous System : JPNS|April 10, 1999
Early onset cerebellar ataxia and preservation of tendon reflexes: clinical phenotypes associated with GAA trinucleotide repeat expanded and non-expanded genotypesM De Castro, A Cruz-Martínez, J J Vílchez, et al.
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