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M Pandolfo

Showing results (101-110 of 116) with videos related to

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Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
European Journal of Neurology|February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutationsR Del Bo, S Ghezzi, S Corti, et al.
Human Molecular Genetics|September 25, 1997
Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranesV Campuzano, L Montermini, Y Lutz, et al.
American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.
Cerebellum (London, England)|December 6, 2013
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxiasA Matilla-Dueñas, T Ashizawa, A Brice, et al.
Trials|October 8, 2021
INHALE: the impact of using FilmArray Pneumonia Panel molecular diagnostics for hospital-acquired and ventilator-associated pneumonia on antimicrobial stewardship and patient outcomes in UK Critical Care-study protocol for a multicentre randomised controlled trialJuliet High, Virve I Enne, Julie A Barber, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
European Neurology|November 14, 2012
Prospective analysis of falls in dominant ataxiasE M R Fonteyn, T Schmitz-Hübsch, C C P Verstappen, et al.
Neurology|May 23, 2007
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.
Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.
Pageof 12

Showing results (101-110 of 116) with videos related to

Sort By:
Pageof 12
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
European Journal of Neurology|February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutationsR Del Bo, S Ghezzi, S Corti, et al.
Human Molecular Genetics|September 25, 1997
Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranesV Campuzano, L Montermini, Y Lutz, et al.
American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.
Cerebellum (London, England)|December 6, 2013
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxiasA Matilla-Dueñas, T Ashizawa, A Brice, et al.
Trials|October 8, 2021
INHALE: the impact of using FilmArray Pneumonia Panel molecular diagnostics for hospital-acquired and ventilator-associated pneumonia on antimicrobial stewardship and patient outcomes in UK Critical Care-study protocol for a multicentre randomised controlled trialJuliet High, Virve I Enne, Julie A Barber, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
European Neurology|November 14, 2012
Prospective analysis of falls in dominant ataxiasE M R Fonteyn, T Schmitz-Hübsch, C C P Verstappen, et al.
Neurology|May 23, 2007
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.
Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.
Pageof 12