Journal list menu
Export Citations
Download PDFs
Masthead
Original Articles
Full Access
full
Consequences of neonatal seizures in the rat: Morphological and behavioral effects
- Pages: 845-857
- First Published: 08 October 2004
Full Access
full
Imaging epileptogenic tubers in children with tuberous sclerosis complex usingα-[11C]Methyl-L-tryptophan positron emission tomography
- Pages: 858-866
- First Published: 08 October 2004
Full Access
full
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329 Ser mutation in the glycogen-branching enzyme gene
- Pages: 867-872
- First Published: 08 October 2004
Full Access
full
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family
- Pages: 873-881
- First Published: 08 October 2004
Full Access
full
β-Trace protein in cerebrospinal fluid: A blood–CSF barrier–related evaluation in neurological diseases
- Pages: 882-889
- First Published: 08 October 2004
Full Access
full
Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2
- Pages: 890-899
- First Published: 08 October 2004
Full Access
full
Aicardi-Goutières syndrome: An update and results of interferon-α studies
- Pages: 900-907
- First Published: 08 October 2004
Full Access
full
Risk of unprovoked seizure after acute symptomatic seizure: Effect of status epilepticus
- Pages: 908-912
- First Published: 08 October 2004
Full Access
full
Neuromuscular blockade by IgG antibodies from patients with Guillain-Barré syndrome: A macro-patch-clamp study
- Pages: 913-922
- First Published: 08 October 2004
Full Access
full
Remodeling of neuronal circuitries in human temporal lobe epilepsy: Increased expression of highly polysialylated neural cell adhesion molecule in the hippocampus and the entorhinal cortex
- Pages: 923-934
- First Published: 08 October 2004
Full Access
full
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals
- Pages: 935-941
- First Published: 08 October 2004
Full Access
full
Reduction in HTLV-I proviral load and spontaneous lymphoproliferation in HTLV-I–associated myelopathy/tropical spastic paraparesis patients treated with humanized anti-tac
- Pages: 942-947
- First Published: 08 October 2004
Full Access
full
Vigabatrin increases human brain homocarnosine and improves seizure control
- Pages: 948-952
- First Published: 08 October 2004
Full Access
full
Bilateral high-frequency stimulation of the internal globus pallidus in advanced Parkinson's disease
- Pages: 953-961
- First Published: 08 October 2004
Brief Communications
Full Access
full
The mitochondrial DNA A8344G mutation in leigh syndrome revealed by analysis in paraffin-embedded sections: Revisiting the past
- Pages: 962-964
- First Published: 08 October 2004
Full Access
full
The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease
- Pages: 965-967
- First Published: 08 October 2004
Full Access
full
Muscle fiber immaturity and inactivity reduce myonecrosis in duchenne muscular dystrophy
- Pages: 967-971
- First Published: 08 October 2004
Full Access
full
A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype
- Pages: 971-976
- First Published: 08 October 2004
Full Access
full
Utility of anti-Hu antibodies in the diagnosis of paraneoplastic sensory neuropathy
- Pages: 976-980
- First Published: 08 October 2004
Full Access
full
Increased circulating antiganglioside antibodies in primary and secondary progressive multiple sclerosis
- Pages: 980-983
- First Published: 08 October 2004
Letters
Full Access
full
Susceptibility to multiple sclerosis and the immunoglobulin heavy chain gene cluster
- Page: 984
- First Published: 08 October 2004
Full Access
full
Questionable role of adult-onset focal dystonia among sporadic dystonia patients
- Pages: 984-985
- First Published: 08 October 2004
Full Access
full
Missense mutation E318G of the presenilin-1 gene appears to be a nonpathogenic polymorphism
- Pages: 985-986
- First Published: 08 October 2004
Book Reviews
Full Access
full
Diagnosis and management of neonatal seizures. By Eli M. Mizrahi and Peter Kellaway Philadelphia, Lippincott-Raven, 1998 192 pp, illustrated, $79.00
- Page: 988
- First Published: 08 October 2004