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Alessandro Ferraris

Showing results (11-20 of 52) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
GIGYF2 variants are not associated with Parkinson's disease in ItalyMonica Bonetti, Alessandro Ferraris, Martina Petracca, et al.
Materials (Basel, Switzerland)|January 26, 2019
From Design to Manufacture of a Carbon Fiber Monocoque for a Three-Wheeler Vehicle PrototypeAlessandro Messana, Lorenzo Sisca, Alessandro Ferraris, et al.
Brain Sciences|July 29, 2023
The Language of Pain in the Hypermobile Ehlers-Danlos Syndrome: Metaphors as a Key to Understanding the Experience of Pain and as a Rehabilitation ToolFilippo Camerota, Rachele Mariani, Giulia Cordiano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional studyVania Gelmetti, Alessandro Ferraris, Livia Brusa, et al.
BMC Genomics|July 2, 2008
Microarray analysis identifies a common set of cellular genes modulated by different HCV replicon clonesAnna Rita Ciccaglione, Cinzia Marcantonio, Elena Tritarelli, et al.
Clinical Chemistry|September 23, 2003
CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencingOrazio Palmieri, Stephen Toth, Alessandro Ferraris, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2014
Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian familiesLucia Ricciardi, Simona Petrucci, Arianna Guidubaldi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2013
Alpha-synuclein gene duplication: marked intrafamilial variability in two novel pedigreesAntonio E Elia, Simona Petrucci, Alfonso Fasano, et al.
Human Mutation|September 27, 2002
Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing lossAlessandro Ferraris, Eric Rappaport, Rosa Santacroce, et al.
Genes|December 23, 2022
Congenital Defects in a Patient Carrying a Novel Homozygous <i>AEBP1</i> Variant: Further Expansion of the Phenotypic Spectrum of Ehlers-Danlos Syndrome Classical-like Type 2?Niccolò Di Giosaffatte, Alessandro Ferraris, Federica Gaudioso, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
GIGYF2 variants are not associated with Parkinson's disease in ItalyMonica Bonetti, Alessandro Ferraris, Martina Petracca, et al.
Materials (Basel, Switzerland)|January 26, 2019
From Design to Manufacture of a Carbon Fiber Monocoque for a Three-Wheeler Vehicle PrototypeAlessandro Messana, Lorenzo Sisca, Alessandro Ferraris, et al.
Brain Sciences|July 29, 2023
The Language of Pain in the Hypermobile Ehlers-Danlos Syndrome: Metaphors as a Key to Understanding the Experience of Pain and as a Rehabilitation ToolFilippo Camerota, Rachele Mariani, Giulia Cordiano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional studyVania Gelmetti, Alessandro Ferraris, Livia Brusa, et al.
BMC Genomics|July 2, 2008
Microarray analysis identifies a common set of cellular genes modulated by different HCV replicon clonesAnna Rita Ciccaglione, Cinzia Marcantonio, Elena Tritarelli, et al.
Clinical Chemistry|September 23, 2003
CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencingOrazio Palmieri, Stephen Toth, Alessandro Ferraris, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2014
Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian familiesLucia Ricciardi, Simona Petrucci, Arianna Guidubaldi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2013
Alpha-synuclein gene duplication: marked intrafamilial variability in two novel pedigreesAntonio E Elia, Simona Petrucci, Alfonso Fasano, et al.
Human Mutation|September 27, 2002
Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing lossAlessandro Ferraris, Eric Rappaport, Rosa Santacroce, et al.
Genes|December 23, 2022
Congenital Defects in a Patient Carrying a Novel Homozygous <i>AEBP1</i> Variant: Further Expansion of the Phenotypic Spectrum of Ehlers-Danlos Syndrome Classical-like Type 2?Niccolò Di Giosaffatte, Alessandro Ferraris, Federica Gaudioso, et al.
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