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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 spectrum
Helena 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 sclerosis
Laura de Bock, Klaartje Somers, Judith Fraussen, et al.
Acta Neurologica Belgica
|
August 4, 2005
Long-term follow up of glatiramer acetate compassionate use in Belgium
C 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 young
Isabel 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 samples
M 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 disease
Marine 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 biomarkers
Eline 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 promoter
I 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 17q21
Marc 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 cohort
Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
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of 50
Search research articles
Search
Showing results (441-450 of 493) with videos related to
Sort By:
Page
of 50
Brain : a Journal of Neurology
|
September 29, 2022
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum
Helena 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 sclerosis
Laura de Bock, Klaartje Somers, Judith Fraussen, et al.
Acta Neurologica Belgica
|
August 4, 2005
Long-term follow up of glatiramer acetate compassionate use in Belgium
C 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 young
Isabel 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 samples
M 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 disease
Marine 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 biomarkers
Eline 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 promoter
I 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 17q21
Marc 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 cohort
Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Page
of 50