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Annals of Neurology
|
October 23, 1997
Apolipoprotein E genotypes in a neuropathological series from the Consortium to Establish a Registry for Alzheimer's Disease
K A Welsh-Bohmer, M Gearing, A M Saunders, et al.
Journal of Neuroimmunology
|
November 1, 1993
Binding of IgG to amyloid beta A4 peptide via the heavy-chain hinge region with preservation of antigen binding
D Huang, M Martin, D Hu, et al.
Transactions of the American Neurological Association
|
January 1, 1981
On the mechanism of pathogenesis of human myasthenia gravis
A D Roses, P Hudgson, M W McAdams, et al.
Annals of the New York Academy of Sciences
|
January 1, 1987
Thymectomy as primary therapy in myasthenia gravis
C W Olanow, A S Wechsler, M Sirotkin-Roses, et al.
Human Mutation
|
January 1, 1994
Detecting prion protein gene mutations by denaturing gradient gel electrophoresis
J K Fink, M L Peacock, J T Warren, et al.
Neuroreport
|
April 20, 1999
Increased neuronal damage in apolipoprotein E-deficient mice following global ischaemia
K Horsburgh, S Kelly, J McCulloch, et al.
Transactions of the American Neurological Association
|
January 1, 1975
Specificity of biochemical and biophysical tests in Duchenne and myotonic muscular dystrophy, carrier states, and congenital myotonia
A D Roses, S H Appel, D A Butterfield, et al.
Annals of Neurology
|
February 1, 1987
Training clinical neuroscientists
R C Griggs, J B Martin, A S Penn, et al.
The New England Journal of Medicine
|
February 1, 1976
Carrier detection in Duchenne muscular dystrophy
A D Roses, M J Roses, S E Miller, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1990
Molecular markers for myoblast transplantation in GRMD
R J Bartlett, N J Sharp, W Y Hung, et al.
Page
of 35
Search research articles
Search
Showing results (141-150 of 347) with videos related to
Sort By:
Page
of 35
Annals of Neurology
|
October 23, 1997
Apolipoprotein E genotypes in a neuropathological series from the Consortium to Establish a Registry for Alzheimer's Disease
K A Welsh-Bohmer, M Gearing, A M Saunders, et al.
Journal of Neuroimmunology
|
November 1, 1993
Binding of IgG to amyloid beta A4 peptide via the heavy-chain hinge region with preservation of antigen binding
D Huang, M Martin, D Hu, et al.
Transactions of the American Neurological Association
|
January 1, 1981
On the mechanism of pathogenesis of human myasthenia gravis
A D Roses, P Hudgson, M W McAdams, et al.
Annals of the New York Academy of Sciences
|
January 1, 1987
Thymectomy as primary therapy in myasthenia gravis
C W Olanow, A S Wechsler, M Sirotkin-Roses, et al.
Human Mutation
|
January 1, 1994
Detecting prion protein gene mutations by denaturing gradient gel electrophoresis
J K Fink, M L Peacock, J T Warren, et al.
Neuroreport
|
April 20, 1999
Increased neuronal damage in apolipoprotein E-deficient mice following global ischaemia
K Horsburgh, S Kelly, J McCulloch, et al.
Transactions of the American Neurological Association
|
January 1, 1975
Specificity of biochemical and biophysical tests in Duchenne and myotonic muscular dystrophy, carrier states, and congenital myotonia
A D Roses, S H Appel, D A Butterfield, et al.
Annals of Neurology
|
February 1, 1987
Training clinical neuroscientists
R C Griggs, J B Martin, A S Penn, et al.
The New England Journal of Medicine
|
February 1, 1976
Carrier detection in Duchenne muscular dystrophy
A D Roses, M J Roses, S E Miller, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1990
Molecular markers for myoblast transplantation in GRMD
R J Bartlett, N J Sharp, W Y Hung, et al.
Page
of 35