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Jean-Jacques Martin

Showing results (71-80 of 107) with videos related to

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Journal of Neuropathology and Experimental Neurology|February 27, 2021
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets NeurodegenerationAnne 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 plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurology|November 24, 2012
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13Dominique 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 syndromeAlain Verloes, Pierre Bitoun, Anne Heuskin, et al.
Acta Neuropathologica|March 13, 2014
Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosisJulia 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 diseaseStefanie 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 diagnosisJoery 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 disorderVeerle 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 ALSIlse 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 FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Journal of Neuropathology and Experimental Neurology|February 27, 2021
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets NeurodegenerationAnne 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 plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurology|November 24, 2012
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13Dominique 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 syndromeAlain Verloes, Pierre Bitoun, Anne Heuskin, et al.
Acta Neuropathologica|March 13, 2014
Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosisJulia 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 diseaseStefanie 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 diagnosisJoery 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 disorderVeerle 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 ALSIlse 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 FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Pageof 11