Found: 28
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Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Decreased striatal monoaminergic terminals in multiple system atrophy detected with positron emission tomography.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Mitochondrial encephalomyopathies: back to Mendelian genetics.
- Published in:
- 1999
- By:
- Publication type:
- commentary
ABT-431, a D1 receptor agonist prodrug, has efficacy in Parkinson's disease.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan gypsies: Clinical and electrophysiological observations.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 742, doi. 10.1002/1531-8249(199906)45:6<742::AID-ANA8>3.0.CO;2-N
- By:
- Publication type:
- Article
Ataxia with isolated vitamin E deficiency: a Japanese family carrying a novel mutation in the alpha-tocopherol transfer protein gene.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Diffusion-weighted magnetic resonance imaging: detection of ischemic injury 39 minutes after onset in a stroke patient.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Decreased interleukin-10 and increased interleukin-12p40 mRNA are associated with disease activity and characterize different disease stages in multiple sclerosis.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Atlas of clinical neurology.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 825, doi. 10.1002/1531-8249(199906)45:6<825::AID-ANA26>3.0.CO;2-F
- By:
- Publication type:
- Article
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.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 812, doi. 10.1002/1531-8249(199906)45:6<812::AID-ANA20>3.0.CO;2-2
- By:
- Publication type:
- Article
Epilepsy: A comprehensive textbook.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 825, doi. 10.1002/1531-8249(199906)45:6<825::AID-ANA25>3.0.CO;2-I
- By:
- Publication type:
- Article
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.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Anti-GalNAc-GD1a antibody-associated Guillain-Barré syndrome with a predominantly distal weakness without cranial nerve impairment and sensory disturbance.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 758, doi. 10.1002/1531-8249(199906)45:6<758::AID-ANA10>3.0.CO;2-N
- By:
- Publication type:
- Article
Relation of JC virus DNA in the cerebrospinal fluid to survival in acquired immunodeficiency syndrome patients with biopsy-proven progressive multifocal leukoencephalopathy.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Chromatic sensitive epilepsy: a variant of photosensitive epilepsy.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Reply.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 824, doi. 10.1002/1531-8249(199906)45:6<824::AID-ANA24>3.0.CO;2-M
- By:
- Publication type:
- Article
Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 801, doi. 10.1002/1531-8249(199906)45:6<801::AID-ANA17>3.0.CO;2-N
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- Publication type:
- Article
News and comment.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. xii, doi. 10.1002/1531-8249(199906)45:6<::AID-ANA28>3.0.CO;2-9
- Publication type:
- Article
Interleukin-12: amiss in MS.
- Published in:
- 1999
- By:
- Publication type:
- commentary
Goldensohn's EEG interpretation: Problems of overreading and underreading, 2nd ed.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 826, doi. 10.1002/1531-8249(199906)45:6<826::AID-ANA27>3.0.CO;2-B
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- Publication type:
- Article
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Corticostriatal plasticity is restricted by myelin-associated neurite growth inhibitors in the adult rat.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Malignant glioma: Who benefits from adjuvant chemotherapy?
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 824, doi. 10.1002/1531-8249(199906)45:6<824::AID-ANA23>3.0.CO;2-P
- By:
- Publication type:
- Article
The postmigrational development of polymicrogyria documented by magnetic resonance imaging from 31 weeks' postconceptional age.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Brainstem mechanisms of autonomic dysfunction in encephalopathy-associated Shiga toxin 2 intoxication.
- Published in:
- Annals of Neurology, 1999, v. 45, n. 6, p. 716, doi. 10.1002/1531-8249(199906)45:6<716::AID-ANA5>3.0.CO;2-N
- By:
- Publication type:
- Article
From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.
- Published in:
- 1999
- By:
- Publication type:
- journal article