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Nereo Bresolin

Showing results (261-270 of 346) with videos related to

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Frontiers in Neurology|July 15, 2021
Early Findings in Neonatal Cases of <i>RYR1</i>-Related Congenital MyopathiesEleonora Mauri, Daniela Piga, Alessandra Govoni, et al.
Annals of Neurology|February 26, 2005
Vascular endothelial growth factor gene variability is associated with increased risk for ADRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Human Mutation|August 16, 2005
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophiesRachele Cagliani, Francesca Magri, Antonio Toscano, et al.
BMC Neurology|November 8, 2020
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutationArianna Manini, Tommaso Bocci, Alice Migazzi, et al.
Journal of Alzheimer'S Disease : JAD|January 25, 2011
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindredAnna M Pietroboni, Giorgio G Fumagalli, Laura Ghezzi, et al.
European Journal of Human Genetics : EJHG|December 23, 2011
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairmentDario Ronchi, Monica Sciacco, Andreina Bordoni, et al.
Pharmacological Research|February 7, 2012
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patientsMaria Grazia D'Angelo, Sandra Gandossini, Filippo Martinelli Boneschi, et al.
Journal of Alzheimer'S Disease : JAD|April 24, 2010
VEGF haplotypes are associated with increased risk to progressive supranuclear palsy and corticobasal syndromeBarbara Borroni, Roberto Del Bo, Stefano Goldwurm, et al.
Neuroscience Letters|November 1, 2005
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosisChiara Fenoglio, Daniela Galimberti, Maria Ban, et al.
Journal of Alzheimer'S Disease : JAD|June 5, 2009
MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levelsDaniela Galimberti, Eliana Venturelli, Chiara Villa, et al.
Pageof 35

Showing results (261-270 of 346) with videos related to

Sort By:
Pageof 35
Frontiers in Neurology|July 15, 2021
Early Findings in Neonatal Cases of <i>RYR1</i>-Related Congenital MyopathiesEleonora Mauri, Daniela Piga, Alessandra Govoni, et al.
Annals of Neurology|February 26, 2005
Vascular endothelial growth factor gene variability is associated with increased risk for ADRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Human Mutation|August 16, 2005
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophiesRachele Cagliani, Francesca Magri, Antonio Toscano, et al.
BMC Neurology|November 8, 2020
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutationArianna Manini, Tommaso Bocci, Alice Migazzi, et al.
Journal of Alzheimer'S Disease : JAD|January 25, 2011
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindredAnna M Pietroboni, Giorgio G Fumagalli, Laura Ghezzi, et al.
European Journal of Human Genetics : EJHG|December 23, 2011
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairmentDario Ronchi, Monica Sciacco, Andreina Bordoni, et al.
Pharmacological Research|February 7, 2012
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patientsMaria Grazia D'Angelo, Sandra Gandossini, Filippo Martinelli Boneschi, et al.
Journal of Alzheimer'S Disease : JAD|April 24, 2010
VEGF haplotypes are associated with increased risk to progressive supranuclear palsy and corticobasal syndromeBarbara Borroni, Roberto Del Bo, Stefano Goldwurm, et al.
Neuroscience Letters|November 1, 2005
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosisChiara Fenoglio, Daniela Galimberti, Maria Ban, et al.
Journal of Alzheimer'S Disease : JAD|June 5, 2009
MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levelsDaniela Galimberti, Eliana Venturelli, Chiara Villa, et al.
Pageof 35