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D E Bulman

Showing results (1-10 of 52) with videos related to

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Human Molecular Genetics|January 1, 1997
Phenotype variation and newcomers in ion channel disordersD E Bulman
Parkinsonism & Related Disorders|September 10, 2002
Parkinson's genetics--creating exciting new insightsD A Grimes, D E Bulman
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1991
Allele frequencies of the third component of complement (C3) in MS patientsD E Bulman, H Armstrong, G C Ebers
Brain : a Journal of Neurology|April 1, 1995
The skeletal muscle sodium and chloride channel diseasesA J Hudson, G C Ebers, D E Bulman
Journal of Medical Genetics|April 4, 2000
Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profilesC M Armour, D E Bulman, A G Hunter
Brain : a Journal of Neurology|April 1, 1991
Age of onset in siblings concordant for multiple sclerosisD E Bulman, A D Sadovnick, G C Ebers
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 14, 2005
Neurofilament M gene in a French-Canadian population with Parkinson's diseaseF Han, D E Bulman, M Panisset, et al.
Human Mutation|January 1, 1992
Frameshift duplication resulting in truncated dystrophin in a patient with Duchenne muscular dystrophyX Hu, D E Bulman, P N Ray, et al.
Atherosclerosis|July 17, 1999
An approach to ascertain probands with a non-traditional risk factor for carotid atherosclerosisJ D Spence, P A Barnett, D E Bulman, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 7, 2007
LRRK2 screening in a Canadian Parkinson's disease cohortD A Grimes, L Racacho, F Han, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|January 1, 1997
Phenotype variation and newcomers in ion channel disordersD E Bulman
Parkinsonism & Related Disorders|September 10, 2002
Parkinson's genetics--creating exciting new insightsD A Grimes, D E Bulman
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1991
Allele frequencies of the third component of complement (C3) in MS patientsD E Bulman, H Armstrong, G C Ebers
Brain : a Journal of Neurology|April 1, 1995
The skeletal muscle sodium and chloride channel diseasesA J Hudson, G C Ebers, D E Bulman
Journal of Medical Genetics|April 4, 2000
Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profilesC M Armour, D E Bulman, A G Hunter
Brain : a Journal of Neurology|April 1, 1991
Age of onset in siblings concordant for multiple sclerosisD E Bulman, A D Sadovnick, G C Ebers
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 14, 2005
Neurofilament M gene in a French-Canadian population with Parkinson's diseaseF Han, D E Bulman, M Panisset, et al.
Human Mutation|January 1, 1992
Frameshift duplication resulting in truncated dystrophin in a patient with Duchenne muscular dystrophyX Hu, D E Bulman, P N Ray, et al.
Atherosclerosis|July 17, 1999
An approach to ascertain probands with a non-traditional risk factor for carotid atherosclerosisJ D Spence, P A Barnett, D E Bulman, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 7, 2007
LRRK2 screening in a Canadian Parkinson's disease cohortD A Grimes, L Racacho, F Han, et al.
Pageof 6