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of 2
pro vyhledávání: '"Bas Nijmeijer"'
Autor:
Annemiek Dols, Philip Scheltens, Fred van Ruissen, Bas Nijmeijer, Yolande A.L. Pijnenburg, Flora Gossink, Anke A. Dijkstra, Cora Aalfs, Petra Cohn Hokke, Max L. Stek
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry. BMJ Publishing Group
Gossink, F, Dols, A, Stek, M L, Scheltens, P, Nijmeijer, B, Cohn Hokke, P, Dijkstra, A, van Ruisssen, F, Aalfs, C & Pijnenburg, Y A L 2021, ' Early life involvement in C9orf72 repeat expansion carriers ', Journal of Neurology, Neurosurgery and Psychiatry . https://doi.org/10.1136/jnnp-2020-325994
Gossink, F, Dols, A, Stek, M L, Scheltens, P, Nijmeijer, B, Cohn Hokke, P, Dijkstra, A, van Ruisssen, F, Aalfs, C & Pijnenburg, Y A L 2021, ' Early life involvement in C9orf72 repeat expansion carriers ', Journal of Neurology, Neurosurgery and Psychiatry . https://doi.org/10.1136/jnnp-2020-325994
ObjectivesThe chromosome 9 open reading frame 72 gene (C9orf72) hexanucleotide repeat expansion (C9orf72RE) is the most common genetic cause of behavioural variant frontotemporal dementia (bvFTD). Since the onset of the C9orf72RE-associated disease i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5577727aacaee74d3475787cebbaf461
https://research.vumc.nl/en/publications/62703bb9-0320-42a1-8d3f-ea24e902f7bc
https://research.vumc.nl/en/publications/62703bb9-0320-42a1-8d3f-ea24e902f7bc
Autor:
Annemieke J.M. Rozemuller, Hulya Ulugut Erkoyun, Anke A. Dijkstra, Philip Scheltens, Marta Scarioni, Sven J. van der Lee, Fatih Tepgec, Bas Nijmeijer, Zerrin Yıldırım, Frederik Barkhof, Başar Bilgiç, Petra E. Cohn-Hokke, Hakan Gurvit, Wiesje M. van der Flier, Yolande A.L. Pijnenburg, Anne Nelissen, Bedia Samanci, Rosalina M. L. van Spaendonk
Publikováno v:
Journal of Alzheimer s disease, 79(3), 1195-1201. IOS Press
Erkoyun, H U, van der Lee, S J, Nijmeijer, B, van Spaendonk, R, Nelissen, A, Scarioni, M, Dijkstra, A, Samancı, B, Gürvit, H, Yıldırım, Z, Tepgeç, F, Bilgic, B, Barkhof, F, Rozemuller, A, van der Flier, W M, Scheltens, P, Cohn-Hokke, P & Pijnenburg, Y 2021, ' The right temporal variant of frontotemporal dementia is not genetically sporadic: A case series ', Journal of Alzheimer's Disease, vol. 79, no. 3, pp. 1195-1201 . https://doi.org/10.3233/JAD-201191
Journal of Alzheimer's Disease, 79(3), 1195-1201. IOS Press
Journal of Alzheimer's Disease
Erkoyun, H U, van der Lee, S J, Nijmeijer, B, van Spaendonk, R, Nelissen, A, Scarioni, M, Dijkstra, A, Samancı, B, Gürvit, H, Yıldırım, Z, Tepgeç, F, Bilgic, B, Barkhof, F, Rozemuller, A, van der Flier, W M, Scheltens, P, Cohn-Hokke, P & Pijnenburg, Y 2021, ' The right temporal variant of frontotemporal dementia is not genetically sporadic: A case series ', Journal of Alzheimer's Disease, vol. 79, no. 3, pp. 1195-1201 . https://doi.org/10.3233/JAD-201191
Journal of Alzheimer's Disease, 79(3), 1195-1201. IOS Press
Journal of Alzheimer's Disease
Background: Right temporal variant frontotemporal dementia (rtvFTD) has been generally considered as a right sided variant of semantic variant primary progressive aphasia (svPPA), which is a genetically sporadic disorder. Recently, we have shown that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff4a26e4512286ee103f3530be297034
https://pure.amc.nl/en/publications/the-right-temporal-variant-of-frontotemporal-dementia-is-not-genetically-sporadic(b65b6072-2f5e-4fbe-a638-9ce1717e90d3).html
https://pure.amc.nl/en/publications/the-right-temporal-variant-of-frontotemporal-dementia-is-not-genetically-sporadic(b65b6072-2f5e-4fbe-a638-9ce1717e90d3).html