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S Cocozza

Showing results (71-80 of 81) with videos related to

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AJNR. American Journal of Neuroradiology|March 2, 2023
MR Imaging Signs of Gadolinium Retention Are Not Associated with Long-Term Motor and Cognitive Outcomes in Multiple SclerosisA Scaravilli, M Tranfa, G Pontillo, et al.
AJNR. American Journal of Neuroradiology|December 22, 2018
Determinants of Deep Gray Matter Atrophy in Multiple Sclerosis: A Multimodal MRI StudyG Pontillo, S Cocozza, R Lanzillo, et al.
AJNR. American Journal of Neuroradiology|September 17, 2021
A Combined Radiomics and Machine Learning Approach to Overcome the Clinicoradiologic Paradox in Multiple SclerosisG Pontillo, S Tommasin, R Cuocolo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Accuracy of clinical diagnostic criteria for Friedreich's ataxiaA Filla, G De Michele, G Coppola, et al.
AJNR. American Journal of Neuroradiology|October 21, 2017
Redefining the Pulvinar Sign in Fabry DiseaseS Cocozza, C Russo, A Pisani, et al.
European Journal of Neurology|October 2, 2019
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian familiesM Lieto, V Riso, D Galatolo, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
Clinical Genetics|June 18, 2016
Identification of C12orf4 as a gene for autosomal recessive intellectual disabilityA K Philips, M Pinelli, C I de Bie, et al.
Annals of Neurology|February 16, 1999
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
AJNR. American Journal of Neuroradiology|March 2, 2023
MR Imaging Signs of Gadolinium Retention Are Not Associated with Long-Term Motor and Cognitive Outcomes in Multiple SclerosisA Scaravilli, M Tranfa, G Pontillo, et al.
AJNR. American Journal of Neuroradiology|December 22, 2018
Determinants of Deep Gray Matter Atrophy in Multiple Sclerosis: A Multimodal MRI StudyG Pontillo, S Cocozza, R Lanzillo, et al.
AJNR. American Journal of Neuroradiology|September 17, 2021
A Combined Radiomics and Machine Learning Approach to Overcome the Clinicoradiologic Paradox in Multiple SclerosisG Pontillo, S Tommasin, R Cuocolo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Accuracy of clinical diagnostic criteria for Friedreich's ataxiaA Filla, G De Michele, G Coppola, et al.
AJNR. American Journal of Neuroradiology|October 21, 2017
Redefining the Pulvinar Sign in Fabry DiseaseS Cocozza, C Russo, A Pisani, et al.
European Journal of Neurology|October 2, 2019
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian familiesM Lieto, V Riso, D Galatolo, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
Clinical Genetics|June 18, 2016
Identification of C12orf4 as a gene for autosomal recessive intellectual disabilityA K Philips, M Pinelli, C I de Bie, et al.
Annals of Neurology|February 16, 1999
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
Pageof 9