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M Frontali

Showing results (31-40 of 47) with videos related to

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Annals of Neurology|March 4, 1998
Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1M Mascalchi, M Tosetti, R Plasmati, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Brain : a Journal of Neurology|May 1, 1997
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13L Calandriello, L Veneziano, A Francia, et al.
European Urology|January 1, 1992
DNA markers in diagnosis of adult dominant polycystic kidney diseaseL Veneziano, A R D'Angelo, L Burrai, et al.
American Journal of Medical Genetics|February 24, 2001
Family and molecular data for a fine analysis of age at onset in Huntington diseaseF Squitieri, G Sabbadini, P Mandich, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
American Journal of Human Genetics|September 1, 1992
Neurofibromatosis type 2 appears to be a genetically homogeneous diseaseS A Narod, D M Parry, J Parboosingh, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onsetE M Valente, A R Bentivoglio, E Cassetta, et al.
Annals of Neurology|March 23, 2001
DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onsetE M Valente, A R Bentivoglio, E Cassetta, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Annals of Neurology|March 4, 1998
Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1M Mascalchi, M Tosetti, R Plasmati, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Brain : a Journal of Neurology|May 1, 1997
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13L Calandriello, L Veneziano, A Francia, et al.
European Urology|January 1, 1992
DNA markers in diagnosis of adult dominant polycystic kidney diseaseL Veneziano, A R D'Angelo, L Burrai, et al.
American Journal of Medical Genetics|February 24, 2001
Family and molecular data for a fine analysis of age at onset in Huntington diseaseF Squitieri, G Sabbadini, P Mandich, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
American Journal of Human Genetics|September 1, 1992
Neurofibromatosis type 2 appears to be a genetically homogeneous diseaseS A Narod, D M Parry, J Parboosingh, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onsetE M Valente, A R Bentivoglio, E Cassetta, et al.
Annals of Neurology|March 23, 2001
DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onsetE M Valente, A R Bentivoglio, E Cassetta, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Pageof 5