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Neurology
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May 1, 1977
Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophy
A D Roses, M J Roses, G A Nicholson, et al.
Neurology
|
January 1, 1977
Evaluation and detection of Duchenne's and Becker's muscular dystrophy carriers by manual muscle testing
M S Roses, M T Nicholson, C S Kircher, et al.
Human Molecular Genetics
|
August 1, 1993
A triplet repeat polymorphism in a gene expressed in human hypothalamus
K L Phillips, D M Gartrell, A D Roses, et al.
Science (New York, N.Y.)
|
November 20, 1973
Phosphorylation of muscle membranes: identification of a membrane-bound protein kinase
C G Andrew, A D Roses, R R Almon, et al.
Nature
|
September 9, 1976
Spin label study of erythrocyte membrane fluidity in myotonic and Duchenne muscular dystrophy and congenital myotonia
D A Butterfield, D B Chesnut, S H Appel, et al.
Neurology
|
June 1, 1993
Novel polymorphism in the A4 region of the amyloid precursor protein gene in a patient without Alzheimer's disease
M L Peacock, J T Warren, A D Roses, et al.
The European Journal of Neuroscience
|
December 21, 2000
Increased neuronal damage and apoE immunoreactivity in human apolipoprotein E, E4 isoform-specific, transgenic mice after global cerebral ischaemia
K Horsburgh, J McCulloch, M Nilsen, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
May 1, 1995
Risk of intracranial aneurysms in families with subarachnoid hemorrhage
M J Alberts, A Quinones, C Graffagnino, et al.
Neurology
|
February 1, 1981
No direct correlation between serum antiacetylcholine receptor antibody levels and clinical state of individual patients with myasthenia gravis
A D Roses, C W Olanow, M W McAdams, et al.
Nucleic Acids Research
|
October 25, 1991
A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17
A M Lucas, J M Vance, J M Stajich, et al.
Page
of 35
Search research articles
Search
Showing results (121-130 of 347) with videos related to
Sort By:
Page
of 35
Neurology
|
May 1, 1977
Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophy
A D Roses, M J Roses, G A Nicholson, et al.
Neurology
|
January 1, 1977
Evaluation and detection of Duchenne's and Becker's muscular dystrophy carriers by manual muscle testing
M S Roses, M T Nicholson, C S Kircher, et al.
Human Molecular Genetics
|
August 1, 1993
A triplet repeat polymorphism in a gene expressed in human hypothalamus
K L Phillips, D M Gartrell, A D Roses, et al.
Science (New York, N.Y.)
|
November 20, 1973
Phosphorylation of muscle membranes: identification of a membrane-bound protein kinase
C G Andrew, A D Roses, R R Almon, et al.
Nature
|
September 9, 1976
Spin label study of erythrocyte membrane fluidity in myotonic and Duchenne muscular dystrophy and congenital myotonia
D A Butterfield, D B Chesnut, S H Appel, et al.
Neurology
|
June 1, 1993
Novel polymorphism in the A4 region of the amyloid precursor protein gene in a patient without Alzheimer's disease
M L Peacock, J T Warren, A D Roses, et al.
The European Journal of Neuroscience
|
December 21, 2000
Increased neuronal damage and apoE immunoreactivity in human apolipoprotein E, E4 isoform-specific, transgenic mice after global cerebral ischaemia
K Horsburgh, J McCulloch, M Nilsen, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
May 1, 1995
Risk of intracranial aneurysms in families with subarachnoid hemorrhage
M J Alberts, A Quinones, C Graffagnino, et al.
Neurology
|
February 1, 1981
No direct correlation between serum antiacetylcholine receptor antibody levels and clinical state of individual patients with myasthenia gravis
A D Roses, C W Olanow, M W McAdams, et al.
Nucleic Acids Research
|
October 25, 1991
A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17
A M Lucas, J M Vance, J M Stajich, et al.
Page
of 35