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V Silani

Showing results (81-90 of 96) with videos related to

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Annals of Neurology|December 1, 1996
Clinical and pathological features in hydrocarbon-induced parkinsonismG Pezzoli, O Strada, V Silani, et al.
Human Mutation|February 19, 2009
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosisLucia Corrado, A Ratti, C Gellera, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.
Rejuvenation Research|October 8, 2011
Intracerebroventricular administration of human umbilical cord blood cells delays disease progression in two murine models of motor neuron degenerationP Bigini, P Veglianese, G Andriolo, et al.
Human Molecular Genetics|July 1, 1996
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity geneA Pizzuti, F Amati, G Calabrese, et al.
Science (New York, N.Y.)|June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's diseaseC Zuccato, A Ciammola, D Rigamonti, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 20, 2019
CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrumC Morelli, C Tiloca, C Colombrita, et al.
Neurology|September 11, 2009
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortN Ticozzi, V Silani, A L LeClerc, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosisN Ticozzi, C Vance, A L Leclerc, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 27, 2011
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosisR Del Bo, C Tiloca, V Pensato, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Annals of Neurology|December 1, 1996
Clinical and pathological features in hydrocarbon-induced parkinsonismG Pezzoli, O Strada, V Silani, et al.
Human Mutation|February 19, 2009
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosisLucia Corrado, A Ratti, C Gellera, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.
Rejuvenation Research|October 8, 2011
Intracerebroventricular administration of human umbilical cord blood cells delays disease progression in two murine models of motor neuron degenerationP Bigini, P Veglianese, G Andriolo, et al.
Human Molecular Genetics|July 1, 1996
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity geneA Pizzuti, F Amati, G Calabrese, et al.
Science (New York, N.Y.)|June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's diseaseC Zuccato, A Ciammola, D Rigamonti, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 20, 2019
CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrumC Morelli, C Tiloca, C Colombrita, et al.
Neurology|September 11, 2009
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortN Ticozzi, V Silani, A L LeClerc, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosisN Ticozzi, C Vance, A L Leclerc, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 27, 2011
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosisR Del Bo, C Tiloca, V Pensato, et al.
Pageof 10