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M Frontali

Showing results (21-30 of 47) with videos related to

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Neurology|March 10, 2010
Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trialG Ristori, S Romano, A Visconti, et al.
American Journal of Human Genetics|March 20, 2001
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36E M Valente, A R Bentivoglio, P H Dixon, et al.
Annals of Human Genetics|January 1, 1991
Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA clusterM Frontali, C Iodice, P Lulli, et al.
Nature Genetics|August 1, 1993
Trinucleotide repeat length instability and age of onset in Huntington's diseaseM Duyao, C Ambrose, R Myers, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
Brain : a Journal of Neurology|February 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian familyG Sabbadini, A Francia, L Calandriello, et al.
Gene|December 23, 1999
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosomeF Trettel, E Mantuano, V Calabresi, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Predictive testing for Huntington's disease: ten years' experience in two Italian centresP Mandich, G Jacopini, E Di Maria, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Neurology|March 10, 2010
Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trialG Ristori, S Romano, A Visconti, et al.
American Journal of Human Genetics|March 20, 2001
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36E M Valente, A R Bentivoglio, P H Dixon, et al.
Annals of Human Genetics|January 1, 1991
Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA clusterM Frontali, C Iodice, P Lulli, et al.
Nature Genetics|August 1, 1993
Trinucleotide repeat length instability and age of onset in Huntington's diseaseM Duyao, C Ambrose, R Myers, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
Brain : a Journal of Neurology|February 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian familyG Sabbadini, A Francia, L Calandriello, et al.
Gene|December 23, 1999
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosomeF Trettel, E Mantuano, V Calabresi, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Predictive testing for Huntington's disease: ten years' experience in two Italian centresP Mandich, G Jacopini, E Di Maria, et al.
Pageof 5