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

S Cocozza

Showing results (21-30 of 81) with videos related to

Pageof 9
Sort By:
American Journal of Human Genetics|September 1, 1996
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxiaA Filla, G De Michele, F Cavalcanti, et al.
Acta Neurologica|August 1, 1992
Genetic linkage analysis and presymptomatic testing in Huntington's disease. First report in ItalyL Di Maio, S Boiano, F Squitieri, et al.
Human Molecular Genetics|November 13, 1998
Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxiaG De Michele, F Cavalcanti, C Criscuolo, et al.
Arquivos De Neuro-Psiquiatria|May 29, 1999
Clinical and molecular studies in five Brazilian cases of Friedreich ataxiaI V Schwartz, L B Jardim, A C Puga, et al.
Neural Networks : the Official Journal of the International Neural Network Society|February 8, 2008
Interactive data analysis and clustering of genomic dataA Ciaramella, S Cocozza, F Iorio, et al.
Journal of Neurology|April 29, 1998
Determinants of onset age in Friedreich's ataxiaG De Michele, A Filla, C Criscuolo, et al.
Neuropediatrics|February 1, 1996
Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 casesG De Michele, L Di Maio, A Filla, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Journal of Medical Genetics|April 3, 2004
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotypeM Giacchetti, A Monticelli, I De Biase, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|September 30, 1987
[Strategy for the identification of new DNA polymorphisms: diagnostic application as genetic markers]S Cocozza, A Monticelli, S Garofalo, et al.
Pageof 9

Showing results (21-30 of 81) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|September 1, 1996
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxiaA Filla, G De Michele, F Cavalcanti, et al.
Acta Neurologica|August 1, 1992
Genetic linkage analysis and presymptomatic testing in Huntington's disease. First report in ItalyL Di Maio, S Boiano, F Squitieri, et al.
Human Molecular Genetics|November 13, 1998
Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxiaG De Michele, F Cavalcanti, C Criscuolo, et al.
Arquivos De Neuro-Psiquiatria|May 29, 1999
Clinical and molecular studies in five Brazilian cases of Friedreich ataxiaI V Schwartz, L B Jardim, A C Puga, et al.
Neural Networks : the Official Journal of the International Neural Network Society|February 8, 2008
Interactive data analysis and clustering of genomic dataA Ciaramella, S Cocozza, F Iorio, et al.
Journal of Neurology|April 29, 1998
Determinants of onset age in Friedreich's ataxiaG De Michele, A Filla, C Criscuolo, et al.
Neuropediatrics|February 1, 1996
Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 casesG De Michele, L Di Maio, A Filla, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Journal of Medical Genetics|April 3, 2004
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotypeM Giacchetti, A Monticelli, I De Biase, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|September 30, 1987
[Strategy for the identification of new DNA polymorphisms: diagnostic application as genetic markers]S Cocozza, A Monticelli, S Garofalo, et al.
Pageof 9