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F Squitieri

Showing results (41-50 of 53) with videos related to

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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.
Behavioural Neurology|September 16, 2017
Cognitive Impairment in Relapsing-Remitting Multiple Sclerosis Patients with Very Mild Clinical DisabilityS Migliore, A Ghazaryan, I Simonelli, et al.
American Journal of Human Genetics|October 1, 1994
Proceed with care: direct predictive testing for Huntington diseaseC M Benjamin, S Adam, S Wiggins, et al.
Clinical Genetics|May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotypeB N Smith, S Bevan, C Vance, et al.
Cerebral Cortex (New York, N.Y. : 1991)|January 7, 2012
Multimodal MRI analysis of the corpus callosum reveals white matter differences in presymptomatic and early Huntington's diseaseM Di Paola, E Luders, A Cherubini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismV Bonifati, P Rizzu, F Squitieri, et al.
Multiple Sclerosis and Related Disorders|November 26, 2018
Emotional processing in RRMS patients: Dissociation between behavioural and neurophysiological responseS Migliore, G Curcio, C Porcaro, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 10, 2004
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian familiesC Mariotti, C Gellera, M Rimoldi, et al.
Neuroscience Letters|March 17, 2011
Whole body cholesterol metabolism is impaired in Huntington's diseaseV Leoni, C Mariotti, L Nanetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 15, 2000
Cavernous angiomas of the nervous system in Italy: clinical and genetic studyF Squitieri, V Maglione, M G Buzzi, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
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.
Behavioural Neurology|September 16, 2017
Cognitive Impairment in Relapsing-Remitting Multiple Sclerosis Patients with Very Mild Clinical DisabilityS Migliore, A Ghazaryan, I Simonelli, et al.
American Journal of Human Genetics|October 1, 1994
Proceed with care: direct predictive testing for Huntington diseaseC M Benjamin, S Adam, S Wiggins, et al.
Clinical Genetics|May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotypeB N Smith, S Bevan, C Vance, et al.
Cerebral Cortex (New York, N.Y. : 1991)|January 7, 2012
Multimodal MRI analysis of the corpus callosum reveals white matter differences in presymptomatic and early Huntington's diseaseM Di Paola, E Luders, A Cherubini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismV Bonifati, P Rizzu, F Squitieri, et al.
Multiple Sclerosis and Related Disorders|November 26, 2018
Emotional processing in RRMS patients: Dissociation between behavioural and neurophysiological responseS Migliore, G Curcio, C Porcaro, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 10, 2004
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian familiesC Mariotti, C Gellera, M Rimoldi, et al.
Neuroscience Letters|March 17, 2011
Whole body cholesterol metabolism is impaired in Huntington's diseaseV Leoni, C Mariotti, L Nanetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 15, 2000
Cavernous angiomas of the nervous system in Italy: clinical and genetic studyF Squitieri, V Maglione, M G Buzzi, et al.
Pageof 6