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Editorials
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Mitochondrial encephalomyopathies: Back to mendelian genetics
- Pages: 693-694
- First Published: 01 June 2001
Original Articles
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Decreased interleukin-10 and increased interleukin-12p40 mRNA are associated with disease activity and characterize different disease stages in multiple sclerosis
- Pages: 695-703
- First Published: 01 June 2001
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From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation
- Pages: 704-715
- First Published: 01 June 2001
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Brainstem mechanisms of autonomic dysfunction in encephalopathy-associated Shiga toxin 2 intoxication
- Pages: 716-723
- First Published: 01 June 2001
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Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain
- Pages: 724-735
- First Published: 01 June 2001
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ABT-431, a D1 receptor agonist prodrug, has efficacy in Parkinson's disease
- Pages: 736-741
- First Published: 01 June 2001
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Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan gypsies: Clinical and electrophysiological observations
- Pages: 742-750
- First Published: 01 June 2001
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Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype
- Pages: 751-757
- First Published: 01 June 2001
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Anti-GalNAc-GD1a antibody–associated Guillain-Barré syndrome with a predominantly distal weakness without cranial nerve impairment and sensory disturbance
- Pages: 758-768
- First Published: 01 June 2001
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Decreased striatal monoaminergic terminals in multiple system atrophy detected with positron emission tomography
- Pages: 769-777
- First Published: 01 June 2001
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Corticostriatal plasticity is restricted by myelin-associated neurite growth inhibitors in the adult rat
- Pages: 778-786
- First Published: 01 June 2001
Brief Communications
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Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I
- Pages: 787-790
- First Published: 01 June 2001
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Chromatic sensitive epilepsy: A variant of photosensitive epilepsy
- Pages: 790-793
- First Published: 01 June 2001
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Diffusion-weighted magnetic resonance imaging: Detection of ischemic injury 39 minutes after onset in a stroke patient
- Pages: 794-797
- First Published: 01 June 2001
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The postmigrational development of polymicrogyria documented by magnetic resonance imaging from 31 weeks' postconceptional age
- Pages: 798-801
- First Published: 01 June 2001
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Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?
- Pages: 801-805
- First Published: 01 June 2001
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Association of anti-Yo (type I) antibody with paraneoplastic cerebellar degeneration in the setting of transitional cell carcinoma of the bladder: Detection of Yo antigen in tumor tissue and fall in antibody titers following tumor removal
- Pages: 805-809
- First Published: 01 June 2001
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Ataxia with isolated vitamin E deficiency: A Japanese family carrying a novel mutation in the α-tocopherol transfer protein gene
- Pages: 809-812
- First Published: 01 June 2001
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A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
- Pages: 812-816
- First Published: 01 June 2001
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Relation of JC virus DNA in the cerebrospinal fluid to survival in acquired immunodeficiency syndrome patients with biopsy-proven progressive multifocal leukoencephalopathy
- Pages: 816-820
- First Published: 01 June 2001
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Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
- Pages: 820-823
- First Published: 01 June 2001
Letters
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Malignant glioma: Who benefits from adjuvant chemotherapy?
- Page: 824
- First Published: 01 June 2001
Book Reviews
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Goldensohn's EEG interpretation: Problems of overreading and underreading, 2nd ed
- Page: 826
- First Published: 01 June 2001