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A Quattrone

Showing results (251-260 of 273) with videos related to

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Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.
Genomics|February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22A Bolino, E R Levy, M Muglia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 6, 2003
Association of tau gene polymorphism with Parkinson's diseaseM Zappia, G Annesi, G Nicoletti, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 8, 2006
Cognitive dysfunction in patients with relapsing-remitting multiple sclerosisU Nocentini, P Pasqualetti, S Bonavita, et al.
Neurology|January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern ItalyM Muglia, M Zappia, V Timmerman, et al.
Clinical Genetics|May 2, 2007
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's diseaseD Civitelli, P Tarantino, G Nicoletti, et al.
Neurology|August 12, 2004
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASILR Mazzei, F L Conforti, P L Lanza, et al.
Neurology|July 27, 2001
The parkin gene is not involved in late-onset Parkinson's diseaseR L Oliveri, M Zappia, G Annesi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 6, 2007
Alpha-synuclein promoter haplotypes and dementia in Parkinson's diseaseE V De Marco, P Tarantino, F E Rocca, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 25, 2014
Is overwork weakness relevant in Charcot-Marie-Tooth disease?G Piscosquito, M M Reilly, A Schenone, et al.
Pageof 28

Showing results (251-260 of 273) with videos related to

Sort By:
Pageof 28
Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.
Genomics|February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22A Bolino, E R Levy, M Muglia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 6, 2003
Association of tau gene polymorphism with Parkinson's diseaseM Zappia, G Annesi, G Nicoletti, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 8, 2006
Cognitive dysfunction in patients with relapsing-remitting multiple sclerosisU Nocentini, P Pasqualetti, S Bonavita, et al.
Neurology|January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern ItalyM Muglia, M Zappia, V Timmerman, et al.
Clinical Genetics|May 2, 2007
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's diseaseD Civitelli, P Tarantino, G Nicoletti, et al.
Neurology|August 12, 2004
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASILR Mazzei, F L Conforti, P L Lanza, et al.
Neurology|July 27, 2001
The parkin gene is not involved in late-onset Parkinson's diseaseR L Oliveri, M Zappia, G Annesi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 6, 2007
Alpha-synuclein promoter haplotypes and dementia in Parkinson's diseaseE V De Marco, P Tarantino, F E Rocca, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 25, 2014
Is overwork weakness relevant in Charcot-Marie-Tooth disease?G Piscosquito, M M Reilly, A Schenone, et al.
Pageof 28