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Alexandra Dürr

Showing results (11-20 of 106) with videos related to

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Human Genetics|April 4, 2008
Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessiveSuzanne Lesage, Ebba Lohmann, François Tison, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 9, 2003
State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosisThomas Gasser, Susan Bressman, Alexandra Dürr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2008
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonismAgnès Camuzat, Marc Romana, Alexandra Dürr, et al.
Neuro-Degenerative Diseases|June 29, 2007
Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's diseaseSuzanne Lesage, Laurence Leclere, Ebba Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2009
Restless legs syndrome, rapid eye movement sleep behavior disorder, and hypersomnia in patients with two parkin mutationsNadège Limousin, Eric Konofal, Elias Karroum, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 7, 2018
Rapid exhaustion of auditory neural conduction in a prototypical mitochondrial disease, Friedreich ataxiaFabrice Giraudet, Perrine Charles, Thierry Mom, et al.
American Journal of Human Genetics|September 9, 2005
LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th centurySuzanne Lesage, Anne-Louise Leutenegger, Pablo Ibanez, et al.
Archives of Neurology|January 13, 2006
Atypical Gilles de la Tourette Syndrome with beta-mannosidase deficiencyFrédéric Sedel, Karen Friderici, Katherine Nummy, et al.
Neurogenetics|April 14, 2006
A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A geneMichito Namekawa, Isabelle Nelson, Pascale Ribai, et al.
Parkinsonism & Related Disorders|August 23, 2008
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutationsEbba Lohmann, Laurence Leclere, Francesca De Anna, et al.
Pageof 11

Showing results (11-20 of 106) with videos related to

Sort By:
Pageof 11
Human Genetics|April 4, 2008
Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessiveSuzanne Lesage, Ebba Lohmann, François Tison, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 9, 2003
State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosisThomas Gasser, Susan Bressman, Alexandra Dürr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2008
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonismAgnès Camuzat, Marc Romana, Alexandra Dürr, et al.
Neuro-Degenerative Diseases|June 29, 2007
Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's diseaseSuzanne Lesage, Laurence Leclere, Ebba Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2009
Restless legs syndrome, rapid eye movement sleep behavior disorder, and hypersomnia in patients with two parkin mutationsNadège Limousin, Eric Konofal, Elias Karroum, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 7, 2018
Rapid exhaustion of auditory neural conduction in a prototypical mitochondrial disease, Friedreich ataxiaFabrice Giraudet, Perrine Charles, Thierry Mom, et al.
American Journal of Human Genetics|September 9, 2005
LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th centurySuzanne Lesage, Anne-Louise Leutenegger, Pablo Ibanez, et al.
Archives of Neurology|January 13, 2006
Atypical Gilles de la Tourette Syndrome with beta-mannosidase deficiencyFrédéric Sedel, Karen Friderici, Katherine Nummy, et al.
Neurogenetics|April 14, 2006
A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A geneMichito Namekawa, Isabelle Nelson, Pascale Ribai, et al.
Parkinsonism & Related Disorders|August 23, 2008
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutationsEbba Lohmann, Laurence Leclere, Francesca De Anna, et al.
Pageof 11