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P De Deyn

Showing results (441-450 of 493) with videos related to

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Brain : a Journal of Neurology|September 29, 2022
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrumHelena Gossye, Sara Van Mossevelde, Anne Sieben, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 3, 2014
Sperm-associated antigen 16 is a novel target of the humoral autoimmune response in multiple sclerosisLaura de Bock, Klaartje Somers, Judith Fraussen, et al.
Acta Neurologica Belgica|August 4, 2005
Long-term follow up of glatiramer acetate compassionate use in BelgiumC J M Sindic, P Seeldrayers, L Vande Gaer, et al.
Clinical Neurology and Neurosurgery|December 11, 2012
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the youngIsabel De Brabander, Laetitia Yperzeele, Chantal Ceuterick-De Groote, et al.
Toxicology Letters|December 18, 2021
iPSC-derived cortical neurons to study sporadic Alzheimer disease: A transcriptome comparison with post-mortem brain samplesM C T Verheijen, J Krauskopf, F Caiment, et al.
Progress in Neurobiology|December 8, 2022
Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism: Possible implication for Alzheimer's diseaseMarine Denechaud, Sarah Geurs, Thomas Comptdaer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 27, 2019
Pre-analytical stability of novel cerebrospinal fluid biomarkersEline A J Willemse, Yannick Vermeiren, Maria-Salud Garcia-Ayllon, et al.
Molecular Psychiatry|October 21, 2015
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoterI Gijselinck, S Van Mossevelde, J van der Zee, et al.
Nature|July 25, 2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Marc Cruts, Ilse Gijselinck, Julie van der Zee, et al.
Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Pageof 50

Showing results (441-450 of 493) with videos related to

Sort By:
Pageof 50
Brain : a Journal of Neurology|September 29, 2022
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrumHelena Gossye, Sara Van Mossevelde, Anne Sieben, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 3, 2014
Sperm-associated antigen 16 is a novel target of the humoral autoimmune response in multiple sclerosisLaura de Bock, Klaartje Somers, Judith Fraussen, et al.
Acta Neurologica Belgica|August 4, 2005
Long-term follow up of glatiramer acetate compassionate use in BelgiumC J M Sindic, P Seeldrayers, L Vande Gaer, et al.
Clinical Neurology and Neurosurgery|December 11, 2012
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the youngIsabel De Brabander, Laetitia Yperzeele, Chantal Ceuterick-De Groote, et al.
Toxicology Letters|December 18, 2021
iPSC-derived cortical neurons to study sporadic Alzheimer disease: A transcriptome comparison with post-mortem brain samplesM C T Verheijen, J Krauskopf, F Caiment, et al.
Progress in Neurobiology|December 8, 2022
Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism: Possible implication for Alzheimer's diseaseMarine Denechaud, Sarah Geurs, Thomas Comptdaer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 27, 2019
Pre-analytical stability of novel cerebrospinal fluid biomarkersEline A J Willemse, Yannick Vermeiren, Maria-Salud Garcia-Ayllon, et al.
Molecular Psychiatry|October 21, 2015
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoterI Gijselinck, S Van Mossevelde, J van der Zee, et al.
Nature|July 25, 2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Marc Cruts, Ilse Gijselinck, Julie van der Zee, et al.
Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Pageof 50