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G De Joanna

Showing results (1-10 of 7) with videos related to

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Lupus|August 1, 1995
Benign intracranial hypertension: a non-thrombotic complication of the primary antiphospholipid syndrome?G Orefice, G De Joanna, M Coppola, et al.
Journal of Human Genetics|March 18, 2000
Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndromeG De Joanna, F M Santorelli, C Casali, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2002
Is Ross syndrome a dysautonomic disorder only? An electrophysiologic and histologic studyA Perretti, M Nolano, G De Joanna, et al.
Journal of Inherited Metabolic Disease|May 9, 2000
Multiple mtDNA deletions: clinical and molecular correlationsF M Santorelli, G De Joanna, C Casali, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 29, 2000
Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the diseaseL Santoro, A Perretti, B Lanzillo, 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.
Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Lupus|August 1, 1995
Benign intracranial hypertension: a non-thrombotic complication of the primary antiphospholipid syndrome?G Orefice, G De Joanna, M Coppola, et al.
Journal of Human Genetics|March 18, 2000
Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndromeG De Joanna, F M Santorelli, C Casali, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2002
Is Ross syndrome a dysautonomic disorder only? An electrophysiologic and histologic studyA Perretti, M Nolano, G De Joanna, et al.
Journal of Inherited Metabolic Disease|May 9, 2000
Multiple mtDNA deletions: clinical and molecular correlationsF M Santorelli, G De Joanna, C Casali, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 29, 2000
Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the diseaseL Santoro, A Perretti, B Lanzillo, 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.
Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.
Pageof 1