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Christos Proukakis

Showing results (1-10 of 64) with videos related to

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Neurobiology of Disease|July 27, 2020
Somatic mutations in neurodegeneration: An updateChristos Proukakis
Brain Communications|July 22, 2022
Somatic mutations may contribute to asymmetry in neurodegenerative disordersChristos Proukakis
American Journal of Human Genetics|October 2, 2002
Is the transportation highway the right road for hereditary spastic paraplegia?Andrew H Crosby, Christos Proukakis
Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2013
Somatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary dataChristos Proukakis, Henry Houlden, Anthony H Schapira
Movement Disorders : Official Journal of the Movement Disorder Society|September 22, 2023
Sex Distribution of GBA1 Variants Carriers with Dementia with Lewy Bodies and Parkinson's DiseaseMarco Toffoli, Anthony H V Schapira, Christos Proukakis
The Lancet. Neurology|November 15, 2008
Hereditary spastic paraplegia: clinical features and pathogenetic mechanismsSara Salinas, Christos Proukakis, Andrew Crosby, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 18, 2022
Somatic CNV Detection by Single-Cell Whole-Genome Sequencing in Postmortem Human BrainDiego Perez-Rodriguez, Maria Kalyva, Catherine Santucci, et al.
Journal of the Neurological Sciences|May 7, 2011
Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in malesChristos Proukakis, David Moore, Robyn Labrum, et al.
Frontiers in Neurology|June 14, 2019
The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement DisorderMatthew Benger, Kshitij Mankad, Christos Proukakis, et al.
Communications Biology|May 9, 2025
Reply to: Is Gauchian genotyping of GBA1 variants reliable?Marco Toffoli, Anthony H V Schapira, Fritz J Sedlazeck, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Neurobiology of Disease|July 27, 2020
Somatic mutations in neurodegeneration: An updateChristos Proukakis
Brain Communications|July 22, 2022
Somatic mutations may contribute to asymmetry in neurodegenerative disordersChristos Proukakis
American Journal of Human Genetics|October 2, 2002
Is the transportation highway the right road for hereditary spastic paraplegia?Andrew H Crosby, Christos Proukakis
Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2013
Somatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary dataChristos Proukakis, Henry Houlden, Anthony H Schapira
Movement Disorders : Official Journal of the Movement Disorder Society|September 22, 2023
Sex Distribution of GBA1 Variants Carriers with Dementia with Lewy Bodies and Parkinson's DiseaseMarco Toffoli, Anthony H V Schapira, Christos Proukakis
The Lancet. Neurology|November 15, 2008
Hereditary spastic paraplegia: clinical features and pathogenetic mechanismsSara Salinas, Christos Proukakis, Andrew Crosby, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 18, 2022
Somatic CNV Detection by Single-Cell Whole-Genome Sequencing in Postmortem Human BrainDiego Perez-Rodriguez, Maria Kalyva, Catherine Santucci, et al.
Journal of the Neurological Sciences|May 7, 2011
Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in malesChristos Proukakis, David Moore, Robyn Labrum, et al.
Frontiers in Neurology|June 14, 2019
The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement DisorderMatthew Benger, Kshitij Mankad, Christos Proukakis, et al.
Communications Biology|May 9, 2025
Reply to: Is Gauchian genotyping of GBA1 variants reliable?Marco Toffoli, Anthony H V Schapira, Fritz J Sedlazeck, et al.
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