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Patrick Cras

Showing results (111-120 of 179) with videos related to

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Acta Neurologica Belgica|July 28, 2020
Practices and opinions about disclosure of the diagnosis of Alzheimer's disease to patients with MCI or dementia: a survey among Belgian medical experts in the field of dementiaEric Mormont, Jean-Christophe Bier, Rose Bruffaerts, et al.
Acta Neurologica Belgica|October 6, 2022
Effectiveness and safety of safinamide in routine clinical practice in a Belgian Parkinson's disease population: an open-label, levodopa add-on study, Bruno Bergmans, Philip Bourgeois, et al.
Neurobiology of Aging|March 27, 2009
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian populationBram Meeus, Karen Nuytemans, David Crosiers, et al.
Annals of Neurology|September 30, 2004
alpha-Synuclein promoter confers susceptibility to Parkinson's diseasePhilippe Pals, Sarah Lincoln, Jonathan Manning, et al.
Experimental Gerontology|June 27, 2007
Neuroinflammation in Parkinson's patients and MPTP-treated mice is not restricted to the nigrostriatal system: microgliosis and differential expression of interleukin-1 receptors in the olfactory bulbAnne Vroon, Benjamin Drukarch, John G J M Bol, et al.
BMC Research Notes|May 25, 2016
Automated PGP9.5 immunofluorescence staining: a valuable tool in the assessment of small fiber neuropathy?Nathalie Van Acker, Michael Ragé, Ellen Sluydts, et al.
Acta Neuropathologica|March 29, 2018
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's diseaseArne De Roeck, Lena Duchateau, Jasper Van Dongen, et al.
Clinical Interventions in Aging|October 28, 2016
European Society for Swallowing Disorders - European Union Geriatric Medicine Society white paper: oropharyngeal dysphagia as a geriatric syndromeLaura Wj Baijens, Pere Clavé, Patrick Cras, et al.
Human Mutation|April 11, 2008
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson diseaseVeerle Bogaerts, Karen Nuytemans, Joke Reumers, et al.
Archives of Neurology|May 12, 2010
Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosisIlse Gijselinck, Sebastiaan Engelborghs, Githa Maes, et al.
Pageof 18

Showing results (111-120 of 179) with videos related to

Sort By:
Pageof 18
Acta Neurologica Belgica|July 28, 2020
Practices and opinions about disclosure of the diagnosis of Alzheimer's disease to patients with MCI or dementia: a survey among Belgian medical experts in the field of dementiaEric Mormont, Jean-Christophe Bier, Rose Bruffaerts, et al.
Acta Neurologica Belgica|October 6, 2022
Effectiveness and safety of safinamide in routine clinical practice in a Belgian Parkinson's disease population: an open-label, levodopa add-on study, Bruno Bergmans, Philip Bourgeois, et al.
Neurobiology of Aging|March 27, 2009
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian populationBram Meeus, Karen Nuytemans, David Crosiers, et al.
Annals of Neurology|September 30, 2004
alpha-Synuclein promoter confers susceptibility to Parkinson's diseasePhilippe Pals, Sarah Lincoln, Jonathan Manning, et al.
Experimental Gerontology|June 27, 2007
Neuroinflammation in Parkinson's patients and MPTP-treated mice is not restricted to the nigrostriatal system: microgliosis and differential expression of interleukin-1 receptors in the olfactory bulbAnne Vroon, Benjamin Drukarch, John G J M Bol, et al.
BMC Research Notes|May 25, 2016
Automated PGP9.5 immunofluorescence staining: a valuable tool in the assessment of small fiber neuropathy?Nathalie Van Acker, Michael Ragé, Ellen Sluydts, et al.
Acta Neuropathologica|March 29, 2018
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's diseaseArne De Roeck, Lena Duchateau, Jasper Van Dongen, et al.
Clinical Interventions in Aging|October 28, 2016
European Society for Swallowing Disorders - European Union Geriatric Medicine Society white paper: oropharyngeal dysphagia as a geriatric syndromeLaura Wj Baijens, Pere Clavé, Patrick Cras, et al.
Human Mutation|April 11, 2008
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson diseaseVeerle Bogaerts, Karen Nuytemans, Joke Reumers, et al.
Archives of Neurology|May 12, 2010
Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosisIlse Gijselinck, Sebastiaan Engelborghs, Githa Maes, et al.
Pageof 18