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Maria Liguori

Showing results (61-70 of 66) with videos related to

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Genes|October 23, 2021
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis PatientsNadia Barizzone, Rachele Cagliani, Chiara Basagni, et al.
Journal of Neuroimmunology|October 25, 2003
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian populationMaria Liguori, Stephen Sawcer, Efrosini Setakis, et al.
Brain : a Journal of Neurology|December 26, 2007
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesPatrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 31, 2013
Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?Katja Lohmann, Alexander Schmidt, Arne Schillert, et al.
Journal of Neuroimmunology|August 29, 2006
Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans, Maria Ban, David Booth, et al.
Arquivos Brasileiros De Cardiologia|September 17, 2015
[V Guideline of the Brazilian Society of Cardiology on Acute Myocardial Infarction Treatment with ST Segment Elevation]Álvaro Avezum Junior, André Feldman, Antônio Carlos de Camargo Carvalho, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Genes|October 23, 2021
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis PatientsNadia Barizzone, Rachele Cagliani, Chiara Basagni, et al.
Journal of Neuroimmunology|October 25, 2003
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian populationMaria Liguori, Stephen Sawcer, Efrosini Setakis, et al.
Brain : a Journal of Neurology|December 26, 2007
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesPatrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 31, 2013
Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?Katja Lohmann, Alexander Schmidt, Arne Schillert, et al.
Journal of Neuroimmunology|August 29, 2006
Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans, Maria Ban, David Booth, et al.
Arquivos Brasileiros De Cardiologia|September 17, 2015
[V Guideline of the Brazilian Society of Cardiology on Acute Myocardial Infarction Treatment with ST Segment Elevation]Álvaro Avezum Junior, André Feldman, Antônio Carlos de Camargo Carvalho, et al.
Pageof 7