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Christos Proukakis

Showing results (11-20 of 64) with videos related to

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Lancet (London, England)|July 22, 2008
Exit, pursued by a bearChristos Proukakis, Anastasios Bonakis, Ali M Salman, et al.
Neuroscience Letters|May 15, 2013
α-Synuclein mutations cluster around a putative protein loopEleanna Kara, Patrick A Lewis, Helen Ling, et al.
Journal of the Neurological Sciences|August 7, 2002
Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegiaChristos Proukakis, Paul E Hart, Amy Cornish, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2022
Somatic SNCA Copy Number Variants in Multiple System Atrophy are Related to Pathology and InclusionsMonica Emili Garcia-Segura, Diego Perez-Rodriguez, Darren Chambers, et al.
Journal of Neuroscience Research|March 10, 2007
Spastin and microtubules: Functions in health and diseaseSara Salinas, Rafael E Carazo-Salas, Christos Proukakis, et al.
Journal of Neurology|September 17, 2004
Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegiaChristos Proukakis, Harold Cross, Heema Patel, et al.
Frontiers in Neurology|November 16, 2020
Investigation of Somatic Mutations in Human Brains Targeting Genes Associated With Parkinson's DiseaseMelissa Leija-Salazar, Alan Pittman, Katya Mokretar, et al.
JAMA Neurology|December 16, 2014
Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohortMichelle Beavan, Alisdair McNeill, Christos Proukakis, et al.
The Journal of Biological Chemistry|February 25, 2017
α-Synuclein structural features inhibit harmful polyunsaturated fatty acid oxidation, suggesting roles in neuroprotectionGiorgia De Franceschi, Chiara Fecchio, Ronit Sharon, et al.
American Journal of Human Genetics|October 18, 2003
Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementiaMichael A Simpson, Harold Cross, Christos Proukakis, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Lancet (London, England)|July 22, 2008
Exit, pursued by a bearChristos Proukakis, Anastasios Bonakis, Ali M Salman, et al.
Neuroscience Letters|May 15, 2013
α-Synuclein mutations cluster around a putative protein loopEleanna Kara, Patrick A Lewis, Helen Ling, et al.
Journal of the Neurological Sciences|August 7, 2002
Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegiaChristos Proukakis, Paul E Hart, Amy Cornish, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2022
Somatic SNCA Copy Number Variants in Multiple System Atrophy are Related to Pathology and InclusionsMonica Emili Garcia-Segura, Diego Perez-Rodriguez, Darren Chambers, et al.
Journal of Neuroscience Research|March 10, 2007
Spastin and microtubules: Functions in health and diseaseSara Salinas, Rafael E Carazo-Salas, Christos Proukakis, et al.
Journal of Neurology|September 17, 2004
Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegiaChristos Proukakis, Harold Cross, Heema Patel, et al.
Frontiers in Neurology|November 16, 2020
Investigation of Somatic Mutations in Human Brains Targeting Genes Associated With Parkinson's DiseaseMelissa Leija-Salazar, Alan Pittman, Katya Mokretar, et al.
JAMA Neurology|December 16, 2014
Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohortMichelle Beavan, Alisdair McNeill, Christos Proukakis, et al.
The Journal of Biological Chemistry|February 25, 2017
α-Synuclein structural features inhibit harmful polyunsaturated fatty acid oxidation, suggesting roles in neuroprotectionGiorgia De Franceschi, Chiara Fecchio, Ronit Sharon, et al.
American Journal of Human Genetics|October 18, 2003
Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementiaMichael A Simpson, Harold Cross, Christos Proukakis, et al.
Pageof 7