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Christos Proukakis

Showing results (21-30 of 64) with videos related to

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Genomics|April 5, 2003
The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegiaFrancesca D Ciccarelli, Christos Proukakis, Heema Patel, et al.
Journal of Neurochemistry|October 13, 2005
Human spastin has multiple microtubule-related functionsSara Salinas, Rafael E Carazo-Salas, Christos Proukakis, et al.
Journal of Neurology|September 17, 2004
A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegiaThomas T Warner, Heema Patel, Christos Proukakis, et al.
Acta Neuropathologica|April 22, 2019
Selective vulnerability in α-synucleinopathiesJavier Alegre-Abarrategui, Katherine R Brimblecombe, Rosalind F Roberts, et al.
Nature Communications|January 6, 2026
VACmap: an accurate long-read aligner for unraveling complex genomic rearrangementsHongyu Ding, Fritz J Sedlazeck, Christos Proukakis, et al.
Neurology|February 22, 2013
A novel α-synuclein missense mutation in Parkinson diseaseChristos Proukakis, Christopher G Dudzik, Timothy Brier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 21, 2012
Hyposmia and cognitive impairment in Gaucher disease patients and carriersAlisdair McNeill, Raquel Duran, Christos Proukakis, et al.
Nature Genetics|July 23, 2002
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaHeema Patel, Harold Cross, Christos Proukakis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2019
Evolution and clustering of prodromal parkinsonian features in GBA1 carriersStephen Mullin, Michelle Beavan, Jonathan Bestwick, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2021
Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's DiseaseMarco Toffoli, Abigail Higgins, Chiao Lee, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
Genomics|April 5, 2003
The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegiaFrancesca D Ciccarelli, Christos Proukakis, Heema Patel, et al.
Journal of Neurochemistry|October 13, 2005
Human spastin has multiple microtubule-related functionsSara Salinas, Rafael E Carazo-Salas, Christos Proukakis, et al.
Journal of Neurology|September 17, 2004
A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegiaThomas T Warner, Heema Patel, Christos Proukakis, et al.
Acta Neuropathologica|April 22, 2019
Selective vulnerability in α-synucleinopathiesJavier Alegre-Abarrategui, Katherine R Brimblecombe, Rosalind F Roberts, et al.
Nature Communications|January 6, 2026
VACmap: an accurate long-read aligner for unraveling complex genomic rearrangementsHongyu Ding, Fritz J Sedlazeck, Christos Proukakis, et al.
Neurology|February 22, 2013
A novel α-synuclein missense mutation in Parkinson diseaseChristos Proukakis, Christopher G Dudzik, Timothy Brier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 21, 2012
Hyposmia and cognitive impairment in Gaucher disease patients and carriersAlisdair McNeill, Raquel Duran, Christos Proukakis, et al.
Nature Genetics|July 23, 2002
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaHeema Patel, Harold Cross, Christos Proukakis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2019
Evolution and clustering of prodromal parkinsonian features in GBA1 carriersStephen Mullin, Michelle Beavan, Jonathan Bestwick, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2021
Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's DiseaseMarco Toffoli, Abigail Higgins, Chiao Lee, et al.
Pageof 7