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Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy
- Pages: 353-354
- First Published: September 1995
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Kindreds of dominantly inherited Parkinson's disease: Keys to the riddle
- Pages: 355-356
- First Published: September 1995
Neurological Progress
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Aging, energy, and oxidative stress in neurodegenerative diseases
- Pages: 357-366
- First Published: September 1995
Original Articles
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Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin
- Pages: 367-372
- First Published: September 1995
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A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation
- Pages: 373-378
- First Published: September 1995
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Bilateral fetal nigral transplantation into the postcommissural putamen in Parkinson's disease
- Pages: 379-388
- First Published: September 1995
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The subacute levodopa test for evaluating long-duration response in parkinson's disease
- Pages: 389-395
- First Published: September 1995
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Proton nuclear magnetic resonance spectroscopic imaging of human temporal lobe epilepsy at 4.1 T
- Pages: 396-404
- First Published: September 1995
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Enhanced endothelial cell adhesion of human cerebrospinal fluid lymphocytes
- Pages: 405-413
- First Published: September 1995
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Cellular activity underlying altered brain metabolism during focal epileptic activity
- Pages: 414-420
- First Published: September 1995
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Amyloid β-proteins 1—40 and 1—42(43) in the soluble fraction of extra- and intracranial blood vessels
- Pages: 421-428
- First Published: September 1995
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An adenoviral vector can transfer lacZ expression into schwann cells in culture and in sciatic nerve
- Pages: 429-436
- First Published: September 1995
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Recovery of hypermetria after a cerebellar stroke occurs as a multistage process
- Pages: 437-445
- First Published: September 1995
Expedited Publication
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Deficiency of brain synaptic dystrophin in human duchenne muscular dystrophy
- Pages: 446-449
- First Published: September 1995
Brief Communications
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Genotype-phenotype correlation in adult-onset acid maltase deficiency
- Pages: 450-454
- First Published: September 1995
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A search for human T-cell leukemia virus type I in the lesions of patients with tropical spastic paraparesis and polymyositis
- Pages: 454-460
- First Published: September 1995
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Apolipoprotein E ϵ4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis
- Pages: 460-463
- First Published: September 1995
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Lack of an association between apolipoprotein E ϵ4 and Alzheimer's disease in elderly nigerians
- Pages: 463-465
- First Published: September 1995
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Influx of nonactivated T lymphocytes into the cerebrospinal fluid during relapse of multiple sclerosis
- Pages: 465-468
- First Published: September 1995
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A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis
- Pages: 468-472
- First Published: September 1995
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Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies
- Pages: 472-477
- First Published: September 1995
Special Report
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Diabetic polyneuropathy in controlled clinical trials: Consensus report of the peripheral nerve society
- Pages: 478-482
- First Published: September 1995
Letter
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Pentoxifylline: Clinical application in human immunodeficiency virus—associated optic neuropathy
- Page: 483
- First Published: September 1995
Books
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Evaluation and treatment of myopathies. By R. C. Griggs, MD. J. R. Mendell. MD, and R. G. Miller, MD Philadelphia, PA, F. A. Davis Co., 1995 $135.00
- Page: 484
- First Published: September 1995
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Companion to clinical neurology. By William Pryse-Phillips Boston, Little, Brown. 1995 1024 pp, illustrated, $99.95
- Page: 484
- First Published: September 1995
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Handbook of dystonia. Neurological disease and therapy series, No 39. Edited by J. K. C. Tsui and D. B. Calne New York, Marcel Dekker, 1995 469 pp, illustrated. $165.00
- Page: 484
- First Published: September 1995
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Ethical issues in neurology. By James L. Bernat Stoneham, MA, Butterworth-Heinemann, 1995 364 pp
- Pages: 484-485
- First Published: September 1995