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All Genetics
Citations 401-410 of 676 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Clonal evolution as pathogenetic mechanism in relapse of primary CNS lymphoma
- H. Pels, M. Montesinos-Rongen, C. Schaller, D. Van Roost, U. Schlegel, O. D. Wiestler, and M. Deckert
Neurology 2004; 63: 167-169.
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- CLINICAL/SCIENTIFIC NOTES
Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A
- S. Pereira, J. P. Vieira, F. Barroca, P. Roll, R. Carvalhas, P. Cau, S. Sequeira, P. Genton, and P. Szepetowski
Neurology 2004; 63: 191-192.
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- ARTICLES
APOE- 2 allele associated with higher prevalence of sporadic Parkinson disease
- Xuemei Huang, Peter C. Chen, and Charles Poole
Neurology 2004; 62: 2198-2202.
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- ARTICLES
Autosomal dominant striatal degeneration (ADSD): Clinical description and mapping to 5q13–5q14
- G. Kuhlenbäumer, P. Lüdemann, A. Schirmacher, E. De Vriendt, G. Hünermund, P. Young, M. Hund-Georgiadis, G. Schuierer, H. Möller, E. B. Ringelstein, C. Van Broeckhoven, V. Timmerman, and F. Stögbauer
Neurology 2004; 62: 2203-2208.
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- BRIEF COMMUNICATIONS
Molecular genetic and proteomic analysis of synchronous malignant gliomas
- Z. Zhuang, Y. -S. Lee, W. Zeng, M. Furuta, T. Valyi-Nagy, M. D. Johnson, C. L. Vnencak-Jones, R. L. Woltjer, and R. J. Weil
Neurology 2004; 62: 2316-2319.
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- ARTICLES
Impact of APOE genotype on neuropathologic and neurochemical markers of Alzheimer disease
- P. Tiraboschi, L. A. Hansen, E. Masliah, M. Alford, L. J. Thal, and J. Corey-Bloom
Neurology 2004; 62: 1977-1983.
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- ARTICLES
Longitudinal changes in cognition and behavior in asymptomatic carriers of the APOE e4 allele
- R. J. Caselli, E. M. Reiman, D. Osborne, J. G. Hentz, L. C. Baxter, J. L. Hernandez, and G. G. Alexander
Neurology 2004; 62: 1990-1995.
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- ARTICLES
The relative influence of environment and genes in episodic tension-type headache
- Vibeke Ulrich, Morten Gervil, and Jes Olesen
Neurology 2004; 62: 2065-2069.
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- BRIEF COMMUNICATIONS
APOE 4 allele is associated with reduced cerebrospinal fluid levels of Aß42
- J. A. Prince, H. Zetterberg, N. Andreasen, J. Marcusson, and K. Blennow
Neurology 2004; 62: 2116-2118.
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- BRIEF COMMUNICATIONS
A novel MPZ gene mutation in congenital neuropathy with hypomyelination
- A. Kochanski, H. Drac, D. Kabzinska, B. Ryniewicz, K. Rowinska-Marcinska, A. Nowakowski, and I. Hausmanowa-Petrusewicz
Neurology 2004; 62: 2122-2123.
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