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All Genetics
Citations 351-360 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Temporal bone histopathology in dominantly inherited audiovestibular syndrome
- A. Ishiyama, G. Ishiyama, I. Lopez, J. Jen, G. Kim, and R. W. Baloh
Neurology 2004; 63: 1859-1862.
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- ARTICLES
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease
- H. Hochstrasser, P. Bauer, U. Walter, S. Behnke, J. Spiegel, I. Csoti, B. Zeiler, A. Bornemann, J. Pahnke, G. Becker, O. Riess, and D. Berg
Neurology 2004; 63: 1912-1917.
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- ARTICLES
A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation
- Joseph J. Higgins, Joanna Pucilowska, Roni Q. Lombardi, and John P. Rooney
Neurology 2004; 63: 1927-1931.
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- BRIEF COMMUNICATIONS
A novel candidate region for ALS on chromosome 14q11.2
- M. J. Greenway, M. D. Alexander, S. Ennis, B. J. Traynor, B. Corr, E. Frost, A. Green, and O. Hardiman
Neurology 2004; 63: 1936-1938.
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- BRIEF COMMUNICATIONS
Single-fiber EMG in familial hemiplegic migraine
- G. M. Terwindt, E. E. Kors, A. A. Vein, M. D. Ferrari, and J. G. van Dijk
Neurology 2004; 63: 1942-1943.
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- CLINICAL/SCIENTIFIC NOTES
No CCM2 mutations in a cohort of 31 sporadic cases
- D. J. Verlaan, S. B. Laurent, G. A. Rouleau, and A. M. Siegel
Neurology 2004; 63: 1979.
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- CLINICAL/SCIENTIFIC NOTES
Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation
- S. T. Pendlebury, P. M. Rothwell, A. Dalton, and E. A. Burton
Neurology 2004; 63: 1982-1983.
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- ARTICLES
Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation
- W. S. Brooks, J. B.J. Kwok, G. M. Halliday, A. K. Godbolt, M. N. Rossor, H. Creasey, A. O. Jones, and P. R. Schofield
Neurology 2004; 63: 1613-1617.
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- BRIEF COMMUNICATIONS
A presenilin 1 R278I mutation presenting with language impairment
- A. K. Godbolt, J. A. Beck, J. Collinge, P. Garrard, J. D. Warren, N. C. Fox, and M. N. Rossor
Neurology 2004; 63: 1702-1704.
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- BRIEF COMMUNICATIONS
The occurrence of Guillain-Barré syndrome within families
- K. Geleijns, B. A. Brouwer, B. C. Jacobs, J. J. Houwing-Duistermaat, C. M. van Duijn, and P. A. van Doorn
Neurology 2004; 63: 1747-1750.
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