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Matt Baker

Showing results (41-50 of 88) with videos related to

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Annals of Neurology|September 20, 2006
Characteristics of frontotemporal dementia patients with a Progranulin mutationEdward D Huey, Jordan Grafman, Eric M Wassermann, et al.
Brain : a Journal of Neurology|February 21, 2012
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9pGing-Yuek R Hsiung, Mariely DeJesus-Hernandez, Howard H Feldman, et al.
Acta Neuropathologica|November 16, 2011
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72Melissa E Murray, Mariely DeJesus-Hernandez, Nicola J Rutherford, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 22, 2018
Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case reportCyril Pottier, Evadnie Rampersaud, Matt Baker, et al.
Neurobiology of Disease|March 16, 2002
A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notchZareen Amtul, Patrick A Lewis, Sian Piper, et al.
Journal of Neurology|April 7, 2024
Progression to corticobasal syndrome: a longitudinal study of patients with nonfluent primary progressive aphasia and primary progressive apraxia of speechDanna P Garcia-Guaqueta, Hugo Botha, Rene L Utianski, et al.
Parkinsonism & Related Disorders|September 2, 2014
A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal studyShinsuke Fujioka, Bradley F Boeve, Joseph E Parisi, et al.
Archives of Neurology|February 10, 2010
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Brain : a Journal of Neurology|January 23, 2009
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersNiCole Finch, Matt Baker, Richard Crook, et al.
Acta Neuropathologica|August 8, 2013
Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72Melissa E Murray, Kevin F Bieniek, M Banks Greenberg, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Annals of Neurology|September 20, 2006
Characteristics of frontotemporal dementia patients with a Progranulin mutationEdward D Huey, Jordan Grafman, Eric M Wassermann, et al.
Brain : a Journal of Neurology|February 21, 2012
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9pGing-Yuek R Hsiung, Mariely DeJesus-Hernandez, Howard H Feldman, et al.
Acta Neuropathologica|November 16, 2011
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72Melissa E Murray, Mariely DeJesus-Hernandez, Nicola J Rutherford, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 22, 2018
Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case reportCyril Pottier, Evadnie Rampersaud, Matt Baker, et al.
Neurobiology of Disease|March 16, 2002
A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notchZareen Amtul, Patrick A Lewis, Sian Piper, et al.
Journal of Neurology|April 7, 2024
Progression to corticobasal syndrome: a longitudinal study of patients with nonfluent primary progressive aphasia and primary progressive apraxia of speechDanna P Garcia-Guaqueta, Hugo Botha, Rene L Utianski, et al.
Parkinsonism & Related Disorders|September 2, 2014
A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal studyShinsuke Fujioka, Bradley F Boeve, Joseph E Parisi, et al.
Archives of Neurology|February 10, 2010
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Brain : a Journal of Neurology|January 23, 2009
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersNiCole Finch, Matt Baker, Richard Crook, et al.
Acta Neuropathologica|August 8, 2013
Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72Melissa E Murray, Kevin F Bieniek, M Banks Greenberg, et al.
Pageof 9