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Ebba Lohmann

Showing results (31-40 of 77) with videos related to

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Annals of Neurology|October 22, 2005
G2019S LRRK2 mutation in French and North African families with Parkinson's diseaseSuzanne Lesage, Pablo Ibanez, Ebba Lohmann, et al.
Parkinsonism & Related Disorders|March 15, 2016
A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish familyHasmet A Hanagasi, Anamika Giri, Ece Kartal, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2006
Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutationsMichael Schüpbach, Ebba Lohmann, Mathieu Anheim, et al.
Movement Disorders Clinical Practice|July 31, 2025
FBXO7 Pathogenic Variants in Early-Onset Parkinsonism: Insights from a Neuroimaging Perspective and Review of the LiteratureErdi Şahin, Bedia Samanci, Gül Yalçın Çakmaklı, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 1, 2016
Vitamin D deficiency might pose a greater risk for ApoEɛ4 non-carrier Alzheimer's disease patientsErdinç Dursun, Merve Alaylıoğlu, Başar Bilgiç, et al.
Journal of Alzheimer'S Disease : JAD|November 27, 2018
Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal DementiaGamze Guven, Başar Bilgic, Zeynep Tufekcioglu, et al.
Archives of Neurology|May 21, 2003
Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography studyStéphane Thobois, Maria-Joao Ribeiro, Ebba Lohmann, et al.
Archives of Neurology|January 14, 2009
Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanismsPablo Ibáñez, Suzanne Lesage, Sabine Janin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2008
Are parkin patients particularly suited for deep-brain stimulation?Ebba Lohmann, Marie-Laure Welter, Valérie Fraix, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 21, 2009
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutationsMaria-João Ribeiro, Stéphane Thobois, Ebba Lohmann, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Annals of Neurology|October 22, 2005
G2019S LRRK2 mutation in French and North African families with Parkinson's diseaseSuzanne Lesage, Pablo Ibanez, Ebba Lohmann, et al.
Parkinsonism & Related Disorders|March 15, 2016
A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish familyHasmet A Hanagasi, Anamika Giri, Ece Kartal, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2006
Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutationsMichael Schüpbach, Ebba Lohmann, Mathieu Anheim, et al.
Movement Disorders Clinical Practice|July 31, 2025
FBXO7 Pathogenic Variants in Early-Onset Parkinsonism: Insights from a Neuroimaging Perspective and Review of the LiteratureErdi Şahin, Bedia Samanci, Gül Yalçın Çakmaklı, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 1, 2016
Vitamin D deficiency might pose a greater risk for ApoEɛ4 non-carrier Alzheimer's disease patientsErdinç Dursun, Merve Alaylıoğlu, Başar Bilgiç, et al.
Journal of Alzheimer'S Disease : JAD|November 27, 2018
Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal DementiaGamze Guven, Başar Bilgic, Zeynep Tufekcioglu, et al.
Archives of Neurology|May 21, 2003
Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography studyStéphane Thobois, Maria-Joao Ribeiro, Ebba Lohmann, et al.
Archives of Neurology|January 14, 2009
Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanismsPablo Ibáñez, Suzanne Lesage, Sabine Janin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2008
Are parkin patients particularly suited for deep-brain stimulation?Ebba Lohmann, Marie-Laure Welter, Valérie Fraix, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 21, 2009
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutationsMaria-João Ribeiro, Stéphane Thobois, Ebba Lohmann, et al.
Pageof 8