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Rim Amouri

Showing results (31-40 of 42) with videos related to

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American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
The Lancet. Neurology|June 10, 2008
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic studyMary M Hulihan, Lianna Ishihara-Paul, Jennifer Kachergus, et al.
Human Mutation|December 17, 2008
ATP13A2 variability in Parkinson diseaseCarles Vilariño-Güell, Alexandra I Soto, Sarah J Lincoln, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2006
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countriesHiroyuki Tomiyama, Yuanzhe Li, Manabu Funayama, et al.
The Lancet. Neurology|October 4, 2016
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association studyJoanne Trinh, Emil K Gustavsson, Carles Vilariño-Güell, et al.
Brain : a Journal of Neurology|January 14, 2012
A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2CSerge Herson, Faycal Hentati, Aude Rigolet, et al.
Nature Communications|October 23, 2019
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegiaMatias Wagner, Daniel P S Osborn, Ina Gehweiler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2006
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease familiesLianna Ishihara, Rachel A Gibson, Liling Warren, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
The Lancet. Neurology|June 10, 2008
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic studyMary M Hulihan, Lianna Ishihara-Paul, Jennifer Kachergus, et al.
Human Mutation|December 17, 2008
ATP13A2 variability in Parkinson diseaseCarles Vilariño-Güell, Alexandra I Soto, Sarah J Lincoln, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2006
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countriesHiroyuki Tomiyama, Yuanzhe Li, Manabu Funayama, et al.
The Lancet. Neurology|October 4, 2016
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association studyJoanne Trinh, Emil K Gustavsson, Carles Vilariño-Güell, et al.
Brain : a Journal of Neurology|January 14, 2012
A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2CSerge Herson, Faycal Hentati, Aude Rigolet, et al.
Nature Communications|October 23, 2019
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegiaMatias Wagner, Daniel P S Osborn, Ina Gehweiler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2006
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease familiesLianna Ishihara, Rachel A Gibson, Liling Warren, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
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