Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

I Castaldo

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 5, 2005
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) familyM Ragno, A C Perretti, I Castaldo, et al.
European Journal of Paediatric Dentistry|December 22, 2011
Evaluation of long-term effects in patients treated with Fränkel-2 applianceL Perillo, M I Castaldo, R Cannavale, et al.
European Journal of Paediatric Dentistry|April 20, 2013
Treatment effects of R-appliance and Fränkel-2 in Class II division 1 malocclusionsR Showkatbakhsh, M I Castaldo, A Jamilian, 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.
Journal of the Neurological Sciences|June 10, 1998
Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1L Trojano, L Chiacchio, D Grossi, 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|February 1, 1994
Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian populationL Pianese, S Cocozza, G Campanella, et al.
Neurology|May 29, 2001
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathyF Barbieri, M T Pellecchia, E Esposito, et al.
Neurology|April 1, 1995
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian familyA Filla, G De Michele, S Banfi, et al.
Journal of the Neurological Sciences|August 30, 2008
Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: a cardiovascular neurophysiologic studyG De Joanna, A De Rosa, E Salvatore, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 5, 2005
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) familyM Ragno, A C Perretti, I Castaldo, et al.
European Journal of Paediatric Dentistry|December 22, 2011
Evaluation of long-term effects in patients treated with Fränkel-2 applianceL Perillo, M I Castaldo, R Cannavale, et al.
European Journal of Paediatric Dentistry|April 20, 2013
Treatment effects of R-appliance and Fränkel-2 in Class II division 1 malocclusionsR Showkatbakhsh, M I Castaldo, A Jamilian, 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.
Journal of the Neurological Sciences|June 10, 1998
Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1L Trojano, L Chiacchio, D Grossi, 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|February 1, 1994
Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian populationL Pianese, S Cocozza, G Campanella, et al.
Neurology|May 29, 2001
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathyF Barbieri, M T Pellecchia, E Esposito, et al.
Neurology|April 1, 1995
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian familyA Filla, G De Michele, S Banfi, et al.
Journal of the Neurological Sciences|August 30, 2008
Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: a cardiovascular neurophysiologic studyG De Joanna, A De Rosa, E Salvatore, et al.
Pageof 2