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Patrick Cras

Showing results (141-150 of 179) with videos related to

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Annals of Neurology|May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Acta Neuropathologica|August 13, 2005
Redox metals and oxidative abnormalities in human prion diseasesRobert B Petersen, Sandra L Siedlak, Hyoung-gon Lee, et al.
Alzheimer'S Research & Therapy|July 16, 2017
No added diagnostic value of non-phosphorylated tau fraction (p-tau<sub>rel</sub>) in CSF as a biomarker for differential dementia diagnosisJoery Goossens, Maria Bjerke, Hanne Struyfs, et al.
Acta Neuropathologica Communications|February 13, 2021
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's diseaseStefanie Smolders, Stéphanie Philtjens, David Crosiers, et al.
Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.
Neurobiology of Aging|October 15, 2013
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementiaElise Cuyvers, Karolien Bettens, Stéphanie Philtjens, et al.
Neurology|April 3, 2016
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutationTobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, et al.
Neurobiology of Aging|January 11, 2017
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patientsFederica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, et al.
Acta Neuropathologica|March 16, 2020
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide exportShaun Martin, Stefanie Smolders, Chris Van den Haute, et al.
Annals of Neurology|May 1, 2016
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international studyLynne I McGuire, Anna Poleggi, Ilaria Poggiolini, et al.
Pageof 18

Showing results (141-150 of 179) with videos related to

Sort By:
Pageof 18
Annals of Neurology|May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Acta Neuropathologica|August 13, 2005
Redox metals and oxidative abnormalities in human prion diseasesRobert B Petersen, Sandra L Siedlak, Hyoung-gon Lee, et al.
Alzheimer'S Research & Therapy|July 16, 2017
No added diagnostic value of non-phosphorylated tau fraction (p-tau<sub>rel</sub>) in CSF as a biomarker for differential dementia diagnosisJoery Goossens, Maria Bjerke, Hanne Struyfs, et al.
Acta Neuropathologica Communications|February 13, 2021
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's diseaseStefanie Smolders, Stéphanie Philtjens, David Crosiers, et al.
Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.
Neurobiology of Aging|October 15, 2013
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementiaElise Cuyvers, Karolien Bettens, Stéphanie Philtjens, et al.
Neurology|April 3, 2016
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutationTobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, et al.
Neurobiology of Aging|January 11, 2017
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patientsFederica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, et al.
Acta Neuropathologica|March 16, 2020
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide exportShaun Martin, Stefanie Smolders, Chris Van den Haute, et al.
Annals of Neurology|May 1, 2016
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international studyLynne I McGuire, Anna Poleggi, Ilaria Poggiolini, et al.
Pageof 18