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D Bird

Showing results (521-530 of 780) with videos related to

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JAMA|May 4, 1994
Alzheimer's disease, apolipoprotein E4, and genderH Payami, K R Montee, J A Kaye, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
Peptide Research|July 1, 1992
Somatostatin-gene expression in the postmortem adult and fetal human brainE G Stopa, G R Uhl, B F O'Hara, et al.
American Journal of Human Genetics|February 1, 1991
X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13W H Raskind, E Wijsman, R A Pagon, et al.
Neurology|June 15, 2007
Neural transplantation in Huntington disease: long-term grafts in two patientsC D Keene, J A Sonnen, P D Swanson, et al.
The Journal of Physiology|August 1, 1979
Dopamine and homovanillic acid concentrations in the post-mortem brain in schizophrenia [proceedings]E D Bird, T J Crow, L L Iversen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 familiesElizabeth E Marchani, Thomas D Bird, Ellen J Steinbart, et al.
Archives of Neurology|September 13, 2006
Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer diseaseKiri L Brickell, Ellen J Steinbart, Malia Rumbaugh, et al.
Archives of Neurology|December 17, 2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gammaIchiro Yabe, Hidenao Sasaki, Dong-Hui Chen, et al.
The American Journal of Psychiatry|December 1, 2000
Familial aggregation of psychotic symptoms in Huntington's diseaseD Tsuang, E W Almqvist, H Lipe, et al.
Pageof 78

Showing results (521-530 of 780) with videos related to

Sort By:
Pageof 78
JAMA|May 4, 1994
Alzheimer's disease, apolipoprotein E4, and genderH Payami, K R Montee, J A Kaye, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
Peptide Research|July 1, 1992
Somatostatin-gene expression in the postmortem adult and fetal human brainE G Stopa, G R Uhl, B F O'Hara, et al.
American Journal of Human Genetics|February 1, 1991
X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13W H Raskind, E Wijsman, R A Pagon, et al.
Neurology|June 15, 2007
Neural transplantation in Huntington disease: long-term grafts in two patientsC D Keene, J A Sonnen, P D Swanson, et al.
The Journal of Physiology|August 1, 1979
Dopamine and homovanillic acid concentrations in the post-mortem brain in schizophrenia [proceedings]E D Bird, T J Crow, L L Iversen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 familiesElizabeth E Marchani, Thomas D Bird, Ellen J Steinbart, et al.
Archives of Neurology|September 13, 2006
Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer diseaseKiri L Brickell, Ellen J Steinbart, Malia Rumbaugh, et al.
Archives of Neurology|December 17, 2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gammaIchiro Yabe, Hidenao Sasaki, Dong-Hui Chen, et al.
The American Journal of Psychiatry|December 1, 2000
Familial aggregation of psychotic symptoms in Huntington's diseaseD Tsuang, E W Almqvist, H Lipe, et al.
Pageof 78