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Thomas D Bird

Showing results (51-60 of 190) with videos related to

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Neuroreport|February 28, 2017
Assessment of mutations in KCNN2 and ZNF135 to patient neurological symptomsVijeta Raghuram, Sydney Weber, Jacob Raber, et al.
Brain : a Journal of Neurology|April 9, 2010
Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2Suman Jayadev, James B Leverenz, Ellen Steinbart, et al.
American Journal of Human Genetics|November 20, 2001
Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathiesValerie A Street, Jeff D Goldy, Alana S Golden, et al.
Annals of Neurology|February 21, 2013
CDC7 inhibition blocks pathological TDP-43 phosphorylation and neurodegenerationNicole F Liachko, Pamela J McMillan, Chris R Guthrie, et al.
Archives of Neurology|January 13, 2006
Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypesJulie A Hodapp, Gregory T Carter, Hillary P Lipe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Archives of Neurology|May 12, 2010
The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer diseaseChang-En Yu, Elizabeth Marchani, Georg Nikisch, et al.
Muscle & Nerve|March 21, 2012
The magnetic resonance imaging spectrum of facioscapulohumeral muscular dystrophySeth D Friedman, Sandra L Poliachik, Gregory T Carter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutationEllen M Wijsman, E Warwick Daw, Xuesong Yu, et al.
Archives of Neurology|August 8, 2002
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qterZoran Brkanac, Laura Bylenok, Magali Fernandez, et al.
Pageof 19

Showing results (51-60 of 190) with videos related to

Sort By:
Pageof 19
Neuroreport|February 28, 2017
Assessment of mutations in KCNN2 and ZNF135 to patient neurological symptomsVijeta Raghuram, Sydney Weber, Jacob Raber, et al.
Brain : a Journal of Neurology|April 9, 2010
Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2Suman Jayadev, James B Leverenz, Ellen Steinbart, et al.
American Journal of Human Genetics|November 20, 2001
Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathiesValerie A Street, Jeff D Goldy, Alana S Golden, et al.
Annals of Neurology|February 21, 2013
CDC7 inhibition blocks pathological TDP-43 phosphorylation and neurodegenerationNicole F Liachko, Pamela J McMillan, Chris R Guthrie, et al.
Archives of Neurology|January 13, 2006
Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypesJulie A Hodapp, Gregory T Carter, Hillary P Lipe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Archives of Neurology|May 12, 2010
The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer diseaseChang-En Yu, Elizabeth Marchani, Georg Nikisch, et al.
Muscle & Nerve|March 21, 2012
The magnetic resonance imaging spectrum of facioscapulohumeral muscular dystrophySeth D Friedman, Sandra L Poliachik, Gregory T Carter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutationEllen M Wijsman, E Warwick Daw, Xuesong Yu, et al.
Archives of Neurology|August 8, 2002
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qterZoran Brkanac, Laura Bylenok, Magali Fernandez, et al.
Pageof 19