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Results of search for 'au:"Roses, A D"', page 6 of 18
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Authors
Alberts, M J
Appel, S H
Bartlett, R J
Conneally, P M
Gaskell, P C
Gilbert, J R
Haines, J L
Hung, W Y
Pericak-Vance, M A
Roses, A D
Saunders, A M
Schmechel, D E
Scott, W K
Small, G W
Speer, M C
Stajich, J M
Strittmatter, W J
Vance, J M
Yamaoka, L
Yamaoka, L H
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Topics
Adult
Age of Onset
Aged
Alleles
Alzheimer Disease
Animals
Apolipoproteins E
Female
Genetic Linkage
Genotype
Humans
Male
Middle Aged
Muscular Dystrophies
Pedigree
Polymorphism, Genetic
analysis
blood
genetics
metabolism
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101.
Thymectomy in late-onset myasthenia gravis.
[electronic resource]
by
Olanow, C W
Lane, R J
Roses, A D
Producer:
19820420
In:
Archives of neurology
vol. 39
Online resources:
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102.
Electrocardiographic abnormalities in carriers of Duchenne muscular dystrophy.
[electronic resource]
by
Lane, R J
Gardner-Medwin, D
Roses, A D
Producer:
19800627
In:
Neurology
vol. 30
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103.
Dinucleotide repeat polymorphism at the human gene for the brain-derived neurotrophic factor (BDNF).
[electronic resource]
by
Pröschel, M
Saunders, A
Roses, A D
Müller, C R
Producer:
19930623
In:
Human molecular genetics
vol. 1
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104.
Impaired neuronal plasticity in transgenic mice expressing human apolipoprotein E4 compared to E3 in a model of entorhinal cortex lesion.
[electronic resource]
by
White, F
Nicoll, J A
Roses, A D
Horsburgh, K
Producer:
20010927
In:
Neurobiology of disease
vol. 8
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105.
Increased phosphorylated components of erythrocyte membrane spectrin band II with reference to Duchenne muscular dystrophy.
[electronic resource]
by
Roses, A D
Herbstreith, M
Metcalf, B
Appel, S H
Producer:
19770103
In:
Journal of the neurological sciences
vol. 30
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106.
Reversal of presynaptic deficits of apolipoprotein E-deficient mice in human apolipoprotein E transgenic mice.
[electronic resource]
by
Chapman, S
Sabo, T
Roses, A D
Michaelson, D M
Producer:
20000914
In:
Neuroscience
vol. 97
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107.
Phenytoin and membrane fluidity in myotonic dystrophy.
[electronic resource]
by
Roses, A D
Butterfield, A
Appel, S H
Chestnut, D B
Producer:
19751107
In:
Archives of neurology
vol. 32
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108.
Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy.
[electronic resource]
by
Gilchrist, J M
Pericak-Vance, M
Silverman, L
Roses, A D
Producer:
19880216
In:
Neurology
vol. 38
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109.
The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic studies.
[electronic resource]
by
Prystowsky, E N
Pritchett, E L
Roses, A D
Gallagher, J
Producer:
19800119
In:
Circulation
vol. 60
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110.
A molecular genetic study of intracerebral hemorrhage.
[electronic resource]
by
Graffagnino, C
Herbstreith, M H
Roses, A D
Alberts, M J
Producer:
19941104
In:
Archives of neurology
vol. 51
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111.
Nicotinic neuronal acetylcholine receptor alpha-3 subunit transcription in normal and myasthenic thymus.
[electronic resource]
by
Mihovilovic, M
Hulette, C
Mittelstaedt, J
Austin, C
Roses, A D
Producer:
19930923
In:
Annals of the New York Academy of Sciences
vol. 681
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112.
A chromosome 19 CA-dinucleotide repeat polymorphism.
[electronic resource]
by
Phillips, K L
Garbutt, J H
Roses, A D
Lee, J E
Producer:
19930831
In:
Human molecular genetics
vol. 1
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113.
Biochemical relationships between muscle and erythrocyte membrane. Interpretations with respect to Duchenne muscular dystrophy.
[electronic resource]
by
Roses, A D
Herbstreith, M H
Metcalf, B S
Hartwig, G B
Producer:
19790716
In:
Electroencephalography and clinical neurophysiology. Supplement
no. 34
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114.
The natural history of cardiac conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiology studies.
[electronic resource]
by
Prystowsky, E N
Pritchett, E L
Gallagher, J J
Roses, A D
Producer:
19810219
In:
Transactions of the American Neurological Association
vol. 104
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115.
Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophy.
[electronic resource]
by
Roses, A D
Roses, M J
Nicholson, G A
Roe, C R
Producer:
19770622
In:
Neurology
vol. 27
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116.
Identification of abnormally [32P]-phosphorylated cyanogen bromide cleavage product of erythrocyte membrane spectrin in Duchenne muscular dystrophy.
[electronic resource]
by
Roses, A D
Shile, P E
Herbstreith, M H
Balakrishnan, C V
Producer:
19811025
In:
Neurology
vol. 31
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117.
Neonatal myasthenia gravis in the infant of an asymptomatic thymectomized mother.
[electronic resource]
by
Olanow, C W
Lane, R J
Hull, K L
Roses, A D
Producer:
19821012
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
vol. 9
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118.
Myotonic muscular dystrophy: morphology, histochemistry, and growth characteristics of cultured skin fibroblasts.
[electronic resource]
by
Hartwig, G B
Miller, S E
Frost, A P
Roses, A D
Producer:
19820614
In:
Muscle & nerve
vol. 5
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119.
Risk of intracranial aneurysms in families with subarachnoid hemorrhage.
[electronic resource]
by
Alberts, M J
Quinones, A
Graffagnino, C
Friedman, A
Roses, A D
Producer:
19950907
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
vol. 22
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120.
Novel polymorphism in the A4 region of the amyloid precursor protein gene in a patient without Alzheimer's disease.
[electronic resource]
by
Peacock, M L
Warren, J T
Roses, A D
Fink, J K
Producer:
19940602
In:
Neurology
vol. 43
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