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Ebba Lohmann

Showing results (21-30 of 77) with videos related to

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Archives of Neurology|September 17, 2003
Coding polymorphisms in the parkin gene and susceptibility to Parkinson diseaseChristoph-Burkhard Lücking, Véronique Chesneau, Ebba Lohmann, et al.
Neuro-Degenerative Diseases|April 30, 2020
Patients with Lately Diagnosed Cerebrotendinous XanthomatosisGulshan Yunisova, Zeynep Tufekcioglu, Okan Dogu, et al.
Neurobiology of Aging|April 17, 2012
Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patientsEbba Lohmann, Rita J Guerreiro, Nihan Erginel-Unaltuna, et al.
Archives of Neurology|April 17, 2008
Rapid eye movement sleep disturbances in Huntington diseaseIsabelle Arnulf, Jørgen Nielsen, Ebba Lohmann, et al.
Human Genomics|July 29, 2021
A comprehensive analysis of copy number variation in a Turkish dementia cohortNadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 30, 2016
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset ParkinsonismAnamika Giri, Gamze Guven, Hasmet Hanagasi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
Parkinsonism & Related Disorders|December 18, 2017
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in TurkeyChristoph Kessler, Burcu Atasu, Hasmet Hanagasi, et al.
Archives of Neurology|September 13, 2006
Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1Anne-Louise Leutenegger, Mustafa A M Salih, Pablo Ibáñez, et al.
Archives of Neurology|August 18, 2004
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, et al.
Pageof 8

Showing results (21-30 of 77) with videos related to

Sort By:
Pageof 8
Archives of Neurology|September 17, 2003
Coding polymorphisms in the parkin gene and susceptibility to Parkinson diseaseChristoph-Burkhard Lücking, Véronique Chesneau, Ebba Lohmann, et al.
Neuro-Degenerative Diseases|April 30, 2020
Patients with Lately Diagnosed Cerebrotendinous XanthomatosisGulshan Yunisova, Zeynep Tufekcioglu, Okan Dogu, et al.
Neurobiology of Aging|April 17, 2012
Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patientsEbba Lohmann, Rita J Guerreiro, Nihan Erginel-Unaltuna, et al.
Archives of Neurology|April 17, 2008
Rapid eye movement sleep disturbances in Huntington diseaseIsabelle Arnulf, Jørgen Nielsen, Ebba Lohmann, et al.
Human Genomics|July 29, 2021
A comprehensive analysis of copy number variation in a Turkish dementia cohortNadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 30, 2016
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset ParkinsonismAnamika Giri, Gamze Guven, Hasmet Hanagasi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
Parkinsonism & Related Disorders|December 18, 2017
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in TurkeyChristoph Kessler, Burcu Atasu, Hasmet Hanagasi, et al.
Archives of Neurology|September 13, 2006
Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1Anne-Louise Leutenegger, Mustafa A M Salih, Pablo Ibáñez, et al.
Archives of Neurology|August 18, 2004
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, et al.
Pageof 8