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T D Bird

Showing results (141-150 of 194) with videos related to

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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.
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, 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.
Neurology|August 23, 2000
Late-onset SCA2: 33 CAG repeats are sufficient to cause diseaseM Fernandez, M E McClain, R A Martinez, et al.
Nature Genetics|April 7, 1999
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)M D Koob, M L Moseley, L J Schut, et al.
Science (New York, N.Y.)|August 18, 1995
A familial Alzheimer's disease locus on chromosome 1E Levy-Lahad, E M Wijsman, E Nemens, et al.
Human Molecular Genetics|September 16, 1998
CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patientsK F Benson, M Horwitz, J Wolff, et al.
The American Journal of Psychiatry|February 1, 1990
Neuropathological findings in patients with clinical diagnoses of probable Alzheimer's diseaseS C Risse, M A Raskind, D Nochlin, et al.
Alzheimer Disease and Associated Disorders|January 1, 1990
Myoclonus, seizures, and paratonia in Alzheimer diseaseS C Risse, T H Lampe, T D Bird, et al.
Pageof 20

Showing results (141-150 of 194) with videos related to

Sort By:
Pageof 20
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.
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, 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.
Neurology|August 23, 2000
Late-onset SCA2: 33 CAG repeats are sufficient to cause diseaseM Fernandez, M E McClain, R A Martinez, et al.
Nature Genetics|April 7, 1999
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)M D Koob, M L Moseley, L J Schut, et al.
Science (New York, N.Y.)|August 18, 1995
A familial Alzheimer's disease locus on chromosome 1E Levy-Lahad, E M Wijsman, E Nemens, et al.
Human Molecular Genetics|September 16, 1998
CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patientsK F Benson, M Horwitz, J Wolff, et al.
The American Journal of Psychiatry|February 1, 1990
Neuropathological findings in patients with clinical diagnoses of probable Alzheimer's diseaseS C Risse, M A Raskind, D Nochlin, et al.
Alzheimer Disease and Associated Disorders|January 1, 1990
Myoclonus, seizures, and paratonia in Alzheimer diseaseS C Risse, T H Lampe, T D Bird, et al.
Pageof 20