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F Squitieri

Showing results (21-30 of 53) with videos related to

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Acta Neurologica|August 1, 1989
Benign essential tremor. A clinical survey of 82 patients from Campania, a region of southern ItalyA Mengano, L Di Maio, M A Maggio, et al.
Human Mutation|January 1, 1997
Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriersB Giovannone, G Sabbadini, L Di Maio, et al.
Cell Death and Differentiation|May 27, 2006
Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjectsA Ciammola, J Sassone, L Alberti, et al.
Journal of Medical Genetics|December 1, 1993
Molecular analysis of late onset Huntington's diseaseB Kremer, F Squitieri, H Telenius, et al.
American Journal of Medical Genetics|September 25, 2001
Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob diseaseA Ladogana, S Almonti, R Petraroli, et al.
Cerebral Cortex (New York, N.Y. : 1991)|April 8, 2014
The Corticospinal Tract in Huntington's DiseaseO Phillips, F Squitieri, C Sanchez-Castaneda, et al.
Human Molecular Genetics|February 1, 1995
Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington diseaseH Telenius, E Almqvist, B Kremer, et al.
Journal of Medical Genetics|December 1, 1993
Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic casesY P Goldberg, S E Andrew, J Theilmann, et al.
Human Brain Mapping|June 5, 2014
MRI measures of corpus callosum iron and myelin in early Huntington's diseaseM Di Paola, O R Phillips, C Sanchez-Castaneda, et al.
Human Molecular Genetics|July 1, 1994
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Acta Neurologica|August 1, 1989
Benign essential tremor. A clinical survey of 82 patients from Campania, a region of southern ItalyA Mengano, L Di Maio, M A Maggio, et al.
Human Mutation|January 1, 1997
Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriersB Giovannone, G Sabbadini, L Di Maio, et al.
Cell Death and Differentiation|May 27, 2006
Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjectsA Ciammola, J Sassone, L Alberti, et al.
Journal of Medical Genetics|December 1, 1993
Molecular analysis of late onset Huntington's diseaseB Kremer, F Squitieri, H Telenius, et al.
American Journal of Medical Genetics|September 25, 2001
Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob diseaseA Ladogana, S Almonti, R Petraroli, et al.
Cerebral Cortex (New York, N.Y. : 1991)|April 8, 2014
The Corticospinal Tract in Huntington's DiseaseO Phillips, F Squitieri, C Sanchez-Castaneda, et al.
Human Molecular Genetics|February 1, 1995
Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington diseaseH Telenius, E Almqvist, B Kremer, et al.
Journal of Medical Genetics|December 1, 1993
Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic casesY P Goldberg, S E Andrew, J Theilmann, et al.
Human Brain Mapping|June 5, 2014
MRI measures of corpus callosum iron and myelin in early Huntington's diseaseM Di Paola, O R Phillips, C Sanchez-Castaneda, et al.
Human Molecular Genetics|July 1, 1994
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.
Pageof 6