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Ebba Lohmann

Showing results (1-10 of 77) with videos related to

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Frontiers in Neurology|February 15, 2017
Needs and Requirements of Modern Biobanks on the Example of Dystonia SyndromesEbba Lohmann, Thomas Gasser, Kathrin Grundmann
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 11, 2020
Event-related potential changes due to early-onset Parkinson's disease in parkin (PARK2) gene mutation carriers and non-carriersAtilla Uslu, Mehmet Ergen, Hasan Demirci, et al.
Parkinsonism & Related Disorders|October 25, 2011
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhoodEbba Lohmann, Çiğdem Köroğlu, Hasmet A Hanagasi, 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.
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.
The International Journal of Neuroscience|October 15, 2011
The impact of familial structure on Parkinson's disease in Istanbul Medical School, TurkeyEbba Lohmann, Haşmet A Hanağası, Hakan Gürvit, et al.
Sleep & Breathing = Schlaf & Atmung|August 3, 2012
Clinical and polysomnographic features of a large Turkish pedigree with restless leg syndrome and periodic limb movementsGülsen Babacan-Yildiz, Esra Gürsoy, Mehmet Kolukisa, et al.
Molecular Biology Reports|January 27, 2019
Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohortGamze Guven, Eren Vurgun, Basar Bilgic, et al.
Parkinsonism & Related Disorders|March 27, 2012
Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging methodBasar Bilgic, Ali Bayram, Ali Bilgin Arslan, 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 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
Frontiers in Neurology|February 15, 2017
Needs and Requirements of Modern Biobanks on the Example of Dystonia SyndromesEbba Lohmann, Thomas Gasser, Kathrin Grundmann
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 11, 2020
Event-related potential changes due to early-onset Parkinson's disease in parkin (PARK2) gene mutation carriers and non-carriersAtilla Uslu, Mehmet Ergen, Hasan Demirci, et al.
Parkinsonism & Related Disorders|October 25, 2011
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhoodEbba Lohmann, Çiğdem Köroğlu, Hasmet A Hanagasi, 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.
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.
The International Journal of Neuroscience|October 15, 2011
The impact of familial structure on Parkinson's disease in Istanbul Medical School, TurkeyEbba Lohmann, Haşmet A Hanağası, Hakan Gürvit, et al.
Sleep & Breathing = Schlaf & Atmung|August 3, 2012
Clinical and polysomnographic features of a large Turkish pedigree with restless leg syndrome and periodic limb movementsGülsen Babacan-Yildiz, Esra Gürsoy, Mehmet Kolukisa, et al.
Molecular Biology Reports|January 27, 2019
Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohortGamze Guven, Eren Vurgun, Basar Bilgic, et al.
Parkinsonism & Related Disorders|March 27, 2012
Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging methodBasar Bilgic, Ali Bayram, Ali Bilgin Arslan, 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.
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