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Nereo Bresolin

Showing results (181-190 of 346) with videos related to

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Neuroscience Letters|November 8, 2006
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar DegenerationChiara Fenoglio, Daniela Galimberti, Laura Piccio, et al.
Molecular Biology of the Cell|June 26, 2009
The low-affinity receptor for neurotrophins p75NTR plays a key role for satellite cell function in muscle repair acting via RhoADaniela Deponti, Roberta Buono, Giuseppina Catanzaro, et al.
Journal of Neurology|November 12, 2010
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's diseaseFrancesca Cortini, Chiara Fenoglio, Eliana Venturelli, et al.
Neurobiology of Aging|April 10, 2007
Association of a NOS1 promoter repeat with Alzheimer's diseaseDaniela Galimberti, Elio Scarpini, Eliana Venturelli, et al.
Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Journal of Child Neurology|July 28, 2009
Muscular dystrophy: central nervous system alpha-dystroglycan glycosylation defects and brain malformationGigliola Fagiolari, Anna Cappellini, Rachele Cagliani, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Brain : a Journal of Neurology|May 4, 2006
The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological functionChris Panzeri, Clara De Palma, Andrea Martinuzzi, et al.
Plos One|May 22, 2008
Correlation of circulating CD133+ progenitor subclasses with a mild phenotype in Duchenne muscular dystrophy patientsChiara Marchesi, Marzia Belicchi, Mirella Meregalli, et al.
Pediatric Neurology|October 18, 2011
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation siteMaria Grazia D'Angelo, Maria Luisa Lorusso, Federica Civati, et al.
Pageof 35

Showing results (181-190 of 346) with videos related to

Sort By:
Pageof 35
Neuroscience Letters|November 8, 2006
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar DegenerationChiara Fenoglio, Daniela Galimberti, Laura Piccio, et al.
Molecular Biology of the Cell|June 26, 2009
The low-affinity receptor for neurotrophins p75NTR plays a key role for satellite cell function in muscle repair acting via RhoADaniela Deponti, Roberta Buono, Giuseppina Catanzaro, et al.
Journal of Neurology|November 12, 2010
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's diseaseFrancesca Cortini, Chiara Fenoglio, Eliana Venturelli, et al.
Neurobiology of Aging|April 10, 2007
Association of a NOS1 promoter repeat with Alzheimer's diseaseDaniela Galimberti, Elio Scarpini, Eliana Venturelli, et al.
Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Journal of Child Neurology|July 28, 2009
Muscular dystrophy: central nervous system alpha-dystroglycan glycosylation defects and brain malformationGigliola Fagiolari, Anna Cappellini, Rachele Cagliani, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Brain : a Journal of Neurology|May 4, 2006
The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological functionChris Panzeri, Clara De Palma, Andrea Martinuzzi, et al.
Plos One|May 22, 2008
Correlation of circulating CD133+ progenitor subclasses with a mild phenotype in Duchenne muscular dystrophy patientsChiara Marchesi, Marzia Belicchi, Mirella Meregalli, et al.
Pediatric Neurology|October 18, 2011
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation siteMaria Grazia D'Angelo, Maria Luisa Lorusso, Federica Civati, et al.
Pageof 35