Annals of Neurology: Vol 35, No 5

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The American Neurological Association is a professional society of academic neurologists and neuroscientists devoted to advancing the goals of academic neurology; to training and educating neurologists and other physicians in the neurologic sciences; and to expanding both our understanding of diseases of the nervous system and our ability to treat them.

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Annals of Neurology: Volume 35, Issue 5

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Editorials

Stopping antiepileptic drugs in children: When and why

Glucose transport and phosphorylation: Which is rate limiting for brain glucose utilization?

Neurological Progress

Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease

Brief Review

Zoster sine herpete, A clinical variant

Original Articles

Discontinuing antiepileptic drugs in children with epilepsy: A prospective study

Decreased concentrations of GLUT1 and GLUT3 glucose transporters in the brains of patients with Alzheimer's disease

Hereditary motor and sensory neuropathy with calf hypertrophy is associated with 17p 11.2 duplication

Nerve biopsy findings in different patterns of proximal diabetic neuropathy

N-acetylgalactosaminyl GD1a is a target molecule for serum antibody in Guillain-Barré syndrome

Correlation of clinical features and findings on cranial magnetic resonance imaging with urinary myelin basic protein-like material in patients with multiple sclerosis

Neurophysiological properties of pallidal neurons in Parkinson's disease

Elevated central nervous system prostaglandins in human immunodeficiency virus—associated dementia

Transgenic mouse brain histopathology resembles early Alzheimer's disease

Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis

Brief Communications

Parkinsonism induced by solvent abuse

Astasia and gait failure with damage of the pontomesencephalic locomotor region

Elevated serum levels of endothelial leukocyte adhesion molecules in Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy

Cerebellar α-Ketoglutarate dehydrogenase activity is reduced in spinocerebellar ataxia type 1

Absence of postoperative hyponatremia syndrome in young, healthy females

Neurological complications from fat emulsion therapy

Diagnosis of Epstein-Barr virus–induced central nervous system infections by DNA amplification from cerebrospinal fluid

Letters

Mitochondrial DNA mutations in Leber's optic neuropathy

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