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Ferdinanda Annesi

Showing results (11-20 of 25) with videos related to

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Epilepsy Research|February 28, 2007
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsyElvira V De Marco, Antonio Gambardella, Ferdinanda Annesi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's diseasePatrizia Tarantino, Elvira Valeria De Marco, Grazia Annesi, et al.
Journal of Personalized Medicine|April 30, 2021
Thermal Liquid Biopsy (TLB) of Blood Plasma as a Potential Tool to Help in the Early Diagnosis of Multiple SclerosisFerdinanda Annesi, Sonia Hermoso-Durán, Bruno Rizzuti, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2005
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizuresMassimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 9, 2005
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger patternPaola Valentino, Grazia Annesi, Innocenza C Cirò Candiano, et al.
Epilepsia|June 15, 2007
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutationEleonora Colosimo, Antonio Gambardella, Massimo Mantegazza, et al.
Archives of Neurology|April 13, 2005
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory studyMario Zappia, Grazia Annesi, Giuseppe Nicoletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 9, 2011
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in southern ItalyValentina Greco, Elvira Valeria De Marco, Francesca Emanuela Rocca, et al.
Annals of Neurology|October 22, 2005
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complexGrazia Annesi, Giovanni Savettieri, Pierfrancesco Pugliese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2007
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern ItalyElvira V De Marco, Grazia Annesi, Patrizia Tarantino, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Epilepsy Research|February 28, 2007
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsyElvira V De Marco, Antonio Gambardella, Ferdinanda Annesi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's diseasePatrizia Tarantino, Elvira Valeria De Marco, Grazia Annesi, et al.
Journal of Personalized Medicine|April 30, 2021
Thermal Liquid Biopsy (TLB) of Blood Plasma as a Potential Tool to Help in the Early Diagnosis of Multiple SclerosisFerdinanda Annesi, Sonia Hermoso-Durán, Bruno Rizzuti, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2005
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizuresMassimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 9, 2005
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger patternPaola Valentino, Grazia Annesi, Innocenza C Cirò Candiano, et al.
Epilepsia|June 15, 2007
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutationEleonora Colosimo, Antonio Gambardella, Massimo Mantegazza, et al.
Archives of Neurology|April 13, 2005
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory studyMario Zappia, Grazia Annesi, Giuseppe Nicoletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 9, 2011
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in southern ItalyValentina Greco, Elvira Valeria De Marco, Francesca Emanuela Rocca, et al.
Annals of Neurology|October 22, 2005
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complexGrazia Annesi, Giovanni Savettieri, Pierfrancesco Pugliese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2007
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern ItalyElvira V De Marco, Grazia Annesi, Patrizia Tarantino, et al.
Pageof 3