| 61 |
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A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome/
|
Crimi, M
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Advanstar Communications [etc.]
|
2003
|
|
|
|
| 62 |
|
A model of atypical absence seizures: EEG, pharmacology, and developmental characterization/
|
Cortez, M A
|
Advanstar Communications [etc.]
|
2001
|
|
|
|
| 63 |
|
A mutated CCR5 gene may have favorable prognostic implications in MS/
|
Kantor, R
|
Advanstar Communications [etc.]
|
2003
|
|
|
|
| 64 |
|
Amyloid beta 1-42 and tau in cerebrospinal fluid after severe traumatic brain injury/
|
Franz, G
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Advanstar Communications [etc.]
|
2003
|
|
|
|
| 65 |
|
Amyloidoma of a spinal root/
|
McKechnie, S
|
Advanstar Communications [etc.]
|
2003
|
|
|
|
| 66 |
|
Analgesic use: A predictor of chronic pain and medication overuse headache: The Head-HUNT Study/
|
Zwart, J.-A
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Advanstar Communications [etc.]
|
2003
|
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| 67 |
|
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease/
|
Zerr, I
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Advanstar Communications [etc.]
|
2000
|
|
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| 68 |
|
Anatomic dissociation of auditory and visual naming in the lateral temporal cortex/
|
Hamberger, M J
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Advanstar Communications [etc.]
|
2001
|
|
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| 69 |
|
An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia/
|
Higgins, J J
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Advanstar Communications [etc.]
|
2001
|
|
|
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| 70 |
|
A neuropathological, stereo-EEG, and MRI study of subcortical band heterotopia/
|
Mai, R
|
Advanstar Communications [etc.]
|
2003
|
|
|
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| 71 |
|
A new mutation in a family with cold-aggravated myotonia disrupts Na+ channel inactivation/
|
Wu, F-F
|
Advanstar Communications [etc.]
|
2001
|
|
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| 72 |
|
An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy/
|
Higgins, J J
|
Advanstar Communications [etc.]
|
2000
|
|
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| 73 |
|
An improved ELISA for screening for neutralizing anti-IFN-beta antibodies in MS patients/
|
Pachner, A. R
|
Advanstar Communications [etc.]
|
2003
|
|
|
|
| 74 |
|
Anosognosia and asomatognosia during intracarotid amobarbital inactivation/
|
Meador, K J
|
Advanstar Communications [etc.]
|
2000
|
|
|
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| 75 |
|
A novel de novo mutation in the desmin gene causes desmin myopathy with toxic aggregates/
|
Sugawara, M
|
Advanstar Communications [etc.]
|
2000
|
|
|
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| 76 |
|
A novel form of autophagic vacuolar myopathy with late-onset and multiorgan involvement/
|
Kaneda, D
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Advanstar Communications [etc.]
|
2003
|
|
|
|
| 77 |
|
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21/
|
Rajab, A
|
Advanstar Communications [etc.]
|
2003
|
|
|
|
| 78 |
|
A novel KCNQ2 K^+ channel mutation in benign neonatal convulsions and centrotemporal spikes/
|
Coppola, G
|
Advanstar Communications [etc.]
|
2003
|
|
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| 79 |
|
A novel laminin a2 isoform in severe laminin a2 deficient congenital muscular dystrophy/
|
Pegoraro, E
|
Advanstar Communications [etc.]
|
2000
|
|
|
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| 80 |
|
A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome/
|
Hjermind, L. E
|
Advanstar Communications [etc.]
|
2003
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