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Nereo Bresolin

Showing results (221-230 of 346) with videos related to

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BMC Neurology|August 28, 2020
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENGDavide Villa, Claudia Cinnante, Gloria Valcamonica, et al.
Cellular and Molecular Life Sciences : CMLS|December 24, 2011
Variants in SNAP25 are targets of natural selection and influence verbal performances in womenRachele Cagliani, Stefania Riva, Cecilia Marino, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
Metabolic Brain Disease|August 6, 2021
Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous MalformationsSilvia Lanfranconi, Lorenzo Piergallini, Dario Ronchi, et al.
Immunity|May 28, 2013
A 175 million year history of T cell regulatory molecules reveals widespread selection, with adaptive evolution of disease allelesDiego Forni, Rachele Cagliani, Uberto Pozzoli, et al.
Neurology|November 2, 2012
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutationLaura Ghezzi, Elio Scarpini, Mario Rango, et al.
Parkinsonism & Related Disorders|January 4, 2018
A de novo C19orf12 heterozygous mutation in a patient with MPANEdoardo Monfrini, Valentina Melzi, Gabriele Buongarzone, et al.
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Journal of the Neurological Sciences|September 20, 2005
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsyMonica Sciacco, Alessandro Prelle, Gigliola Fagiolari, et al.
Annals of Neurology|May 16, 2007
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis miceFederica Locatelli, Stefania Corti, Dimitra Papadimitriou, et al.
Pageof 35

Showing results (221-230 of 346) with videos related to

Sort By:
Pageof 35
BMC Neurology|August 28, 2020
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENGDavide Villa, Claudia Cinnante, Gloria Valcamonica, et al.
Cellular and Molecular Life Sciences : CMLS|December 24, 2011
Variants in SNAP25 are targets of natural selection and influence verbal performances in womenRachele Cagliani, Stefania Riva, Cecilia Marino, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
Metabolic Brain Disease|August 6, 2021
Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous MalformationsSilvia Lanfranconi, Lorenzo Piergallini, Dario Ronchi, et al.
Immunity|May 28, 2013
A 175 million year history of T cell regulatory molecules reveals widespread selection, with adaptive evolution of disease allelesDiego Forni, Rachele Cagliani, Uberto Pozzoli, et al.
Neurology|November 2, 2012
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutationLaura Ghezzi, Elio Scarpini, Mario Rango, et al.
Parkinsonism & Related Disorders|January 4, 2018
A de novo C19orf12 heterozygous mutation in a patient with MPANEdoardo Monfrini, Valentina Melzi, Gabriele Buongarzone, et al.
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Journal of the Neurological Sciences|September 20, 2005
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsyMonica Sciacco, Alessandro Prelle, Gigliola Fagiolari, et al.
Annals of Neurology|May 16, 2007
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis miceFederica Locatelli, Stefania Corti, Dimitra Papadimitriou, et al.
Pageof 35