Search research articles
Contact Us
Filters
Showing results (71-80 of 107) with videos related to
Page
of 11
Sort By:
Journal of Neuropathology and Experimental Neurology
|
February 27, 2021
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets Neurodegeneration
Anne Sieben, Tim Van Langenhove, Yannick Vermeiren, et al.
Annals of Neurology
|
May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques
Bart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurology
|
November 24, 2012
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13
Dominique Hervé, Hugues Chabriat, Mélanie Rigal, et al.
American Journal of Medical Genetics. Part A
|
May 20, 2004
Möbius sequence, Robin complex, and hypotonia: severe expression of brainstem disruption spectrum versus Carey-Fineman-Ziter syndrome
Alain Verloes, Pierre Bitoun, Anne Heuskin, et al.
Acta Neuropathologica
|
March 13, 2014
Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis
Julia K Götzl, Kohji Mori, Markus Damme, 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 disease
Stefanie Smolders, Stéphanie Philtjens, David Crosiers, 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 diagnosis
Joery Goossens, Maria Bjerke, Hanne Struyfs, et al.
Brain : a Journal of Neurology
|
August 8, 2007
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder
Veerle Bogaerts, Sebastiaan Engelborghs, Samir Kumar-Singh, et al.
Neurobiology of Aging
|
December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology
|
February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
Julie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 107) with videos related to
Sort By:
Page
of 11
Journal of Neuropathology and Experimental Neurology
|
February 27, 2021
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets Neurodegeneration
Anne Sieben, Tim Van Langenhove, Yannick Vermeiren, et al.
Annals of Neurology
|
May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques
Bart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurology
|
November 24, 2012
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13
Dominique Hervé, Hugues Chabriat, Mélanie Rigal, et al.
American Journal of Medical Genetics. Part A
|
May 20, 2004
Möbius sequence, Robin complex, and hypotonia: severe expression of brainstem disruption spectrum versus Carey-Fineman-Ziter syndrome
Alain Verloes, Pierre Bitoun, Anne Heuskin, et al.
Acta Neuropathologica
|
March 13, 2014
Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis
Julia K Götzl, Kohji Mori, Markus Damme, 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 disease
Stefanie Smolders, Stéphanie Philtjens, David Crosiers, 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 diagnosis
Joery Goossens, Maria Bjerke, Hanne Struyfs, et al.
Brain : a Journal of Neurology
|
August 8, 2007
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder
Veerle Bogaerts, Sebastiaan Engelborghs, Samir Kumar-Singh, et al.
Neurobiology of Aging
|
December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology
|
February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
Julie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Page
of 11