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Matt Baker

Showing results (51-60 of 88) with videos related to

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Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
Neurocase|November 6, 2012
Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?Emilia J Sitek, Ewa Narozanska, Anna Barczak, et al.
American Journal of Neurodegenerative Disease|April 14, 2016
The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in FloridaThomas A Ravenscroft, Cyril Pottier, Melissa E Murray, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Annals of Neurology|February 22, 2008
TDP-43 A315T mutation in familial motor neuron diseaseMichael A Gitcho, Robert H Baloh, Sumi Chakraverty, et al.
Brain : a Journal of Neurology|October 13, 2006
Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic studyBradley F Boeve, Matt Baker, Dennis W Dickson, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
American Journal of Human Genetics|November 20, 2010
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasmaMinerva M Carrasquillo, Alexandra M Nicholson, NiCole Finch, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
Neurocase|November 6, 2012
Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?Emilia J Sitek, Ewa Narozanska, Anna Barczak, et al.
American Journal of Neurodegenerative Disease|April 14, 2016
The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in FloridaThomas A Ravenscroft, Cyril Pottier, Melissa E Murray, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Annals of Neurology|February 22, 2008
TDP-43 A315T mutation in familial motor neuron diseaseMichael A Gitcho, Robert H Baloh, Sumi Chakraverty, et al.
Brain : a Journal of Neurology|October 13, 2006
Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic studyBradley F Boeve, Matt Baker, Dennis W Dickson, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
American Journal of Human Genetics|November 20, 2010
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasmaMinerva M Carrasquillo, Alexandra M Nicholson, NiCole Finch, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Pageof 9