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P Giunti

Showing results (21-30 of 52) with videos related to

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Electroencephalography and Clinical Neurophysiology|September 1, 1991
P300 variations in parkinsonian patients before and during dopaminergic monotherapy: a suggested dopamine component in P300P Stanzione, F Fattapposta, P Giunti, et al.
Human Molecular Genetics|September 16, 1998
De novo expansion of intermediate alleles in spinocerebellar ataxia 7G Stevanin, P Giunti, G D Belal, et al.
Minerva Cardioangiologica|July 1, 1981
[Regional hemorheological effects induced by muscular exertion in peripheral obstructive arteriopathy. II]M A Perego, G Sergio, M Espureo, et al.
American Journal of Human Genetics|July 27, 1999
Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3P F Worth, P Giunti, C Gardner-Thorpe, et al.
Acta Neurologica Belgica|August 1, 1987
Electrophysiological (EEG, BAEP, VEP) study in patients with beta-thalassemia majorG Amabile, E Stefano, I Bianco, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Journal of Submicroscopic Cytology and Pathology|July 1, 1993
Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadismA Malandrini, M Villanova, P Piomboni, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG)G Stevanin, G David, A Dürr, 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.
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.
Pageof 6

Showing results (21-30 of 52) with videos related to

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Pageof 6
Electroencephalography and Clinical Neurophysiology|September 1, 1991
P300 variations in parkinsonian patients before and during dopaminergic monotherapy: a suggested dopamine component in P300P Stanzione, F Fattapposta, P Giunti, et al.
Human Molecular Genetics|September 16, 1998
De novo expansion of intermediate alleles in spinocerebellar ataxia 7G Stevanin, P Giunti, G D Belal, et al.
Minerva Cardioangiologica|July 1, 1981
[Regional hemorheological effects induced by muscular exertion in peripheral obstructive arteriopathy. II]M A Perego, G Sergio, M Espureo, et al.
American Journal of Human Genetics|July 27, 1999
Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3P F Worth, P Giunti, C Gardner-Thorpe, et al.
Acta Neurologica Belgica|August 1, 1987
Electrophysiological (EEG, BAEP, VEP) study in patients with beta-thalassemia majorG Amabile, E Stefano, I Bianco, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Journal of Submicroscopic Cytology and Pathology|July 1, 1993
Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadismA Malandrini, M Villanova, P Piomboni, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG)G Stevanin, G David, A Dürr, 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.
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.
Pageof 6