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Ebba Lohmann

Showing results (41-50 of 77) with videos related to

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Human Molecular Genetics|October 16, 2010
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's diseaseSuzanne Lesage, Mathieu Anheim, Christel Condroyer, et al.
Neurobiology of Aging|July 19, 2017
Mutations in TYROBP are not a common cause of dementia in a Turkish cohortLee Darwent, Susana Carmona, Ebba Lohmann, et al.
JAMA Neurology|January 16, 2013
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementRita João Guerreiro, Ebba Lohmann, José Miguel Brás, et al.
BMC Neurology|March 29, 2022
Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature reviewBurcu Atasu, Ayse Nur Ozdag Acarlı, Basar Bilgic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2012
Exome sequencing in a family with restless legs syndromeAnne Weissbach, Katharina Siegesmund, Norbert Brüggemann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
A new F-box protein 7 gene mutation causing typical Parkinson's diseaseEbba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, et al.
Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.
Neurobiology of Aging|June 5, 2012
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Suzanne Lesage, Christel Condroyer, Stephan Klebe, et al.
Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|October 16, 2010
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's diseaseSuzanne Lesage, Mathieu Anheim, Christel Condroyer, et al.
Neurobiology of Aging|July 19, 2017
Mutations in TYROBP are not a common cause of dementia in a Turkish cohortLee Darwent, Susana Carmona, Ebba Lohmann, et al.
JAMA Neurology|January 16, 2013
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementRita João Guerreiro, Ebba Lohmann, José Miguel Brás, et al.
BMC Neurology|March 29, 2022
Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature reviewBurcu Atasu, Ayse Nur Ozdag Acarlı, Basar Bilgic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2012
Exome sequencing in a family with restless legs syndromeAnne Weissbach, Katharina Siegesmund, Norbert Brüggemann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
A new F-box protein 7 gene mutation causing typical Parkinson's diseaseEbba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, et al.
Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.
Neurobiology of Aging|June 5, 2012
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Suzanne Lesage, Christel Condroyer, Stephan Klebe, et al.
Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
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