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| ARTICLES
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Ocular myopathy
A. Magora; H. Zauberman
Arch Neurol. 1969;20:1-8.
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Scapuloperoneal amytrophy
J. C. Meadows; C. D. Marsden
Arch Neurol. 1969;20:9-12.
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Hyperkalemic periodic paralysis. Intracellular electromyographic studies
J. E. Brooks
Arch Neurol. 1969;20:13-18.
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Electron microscopic observations in infantile neuroaxonal dystrophy. Report of a cortical biopsy and review of the recent literature
M. M. Herman; P. R. Huttenlocher; K. G. Bensch
Arch Neurol. 1969;20:19-34.
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Cerebral hypoxic damage in fetus and newborn. Basic patterns and their clinical significance
A. Towbin
Arch Neurol. 1969;20:35-43.
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Congenital hyperuricemia. An inborn error of purine metabolism associated with psychomotor retardation, athetosis, and self-mutilation
P. H. Berman; M. E. Balis; J. Dancis
Arch Neurol. 1969;20:44-53.
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Serum and cerebrospinal fluid enzymes in cerebrovascular disease. Creatine phosphokinase, aldolase, and lactic dehydrogenase
A. H. Wolintz; L. D. Jacobs; N. Christoff; M. Solomon; N. Chernik
Arch Neurol. 1969;20:54-61.
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Giant neuronal mitochondria in a infant with microcephaly and seizure disorder
K. Suzuki; I. Rapin
Arch Neurol. 1969;20:62-72.
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Neurological and intellectual sequelae of hydrocephalus
K. M. Laurence
Arch Neurol. 1969;20:73-81.
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Visual form agnosia. A specific defect in visual discrimination
D. F. Benson; J. P. Greenberg
Arch Neurol. 1969;20:82-89.
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The frontal lobes revisited. The case for a second look
K. E. Livingston
Arch Neurol. 1969;20:90-95.
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Long-term follow-up of a callosal-sectioned patient. Report of a case
M. N. Goldstein; R. J. Joynt
Arch Neurol. 1969;20:96-102.
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Tay-Sachs' disease
R. H. Wilkins; I. A. Brody
Arch Neurol. 1969;20:103-111.
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