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Neurology
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All Genetics

Citations 411-420 of 679 total displayed.

Past content (since Jan 2001):

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. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
APOE {epsilon}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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
P. Ibáñez, E. Lohmann, P. Pollak, F. Durif, C. Tranchant, Y. Agid, A. Dürr, and A. Brice
Neurology 2004; 62: 2133-2134. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
A monozygotic twin pair discordant for narcolepsy and CSF hypocretin-1
Y. Dauvilliers, S. Maret, C. Bassetti, B. Carlander, M. Billiard, J. Touchon, and M. Tafti
Neurology 2004; 62: 2137-2138. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene
A. D’Amico, A. Tessa, A. Sabino, E. Bertini, F. M. Santorelli, and S. Servidei
Neurology 2004; 62: 2138-2139. [Full text] [PDF]  

EXPEDITED BRIEF COMMUNICATION
{alpha}-Synuclein in blood and brain from familial Parkinson disease with SNCA locus triplication
D. W. Miller, S. M. Hague, J. Clarimon, M. Baptista, K. Gwinn-Hardy, M. R. Cookson, and A. B. Singleton
Neurology 2004; 62: 1835-1838. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
K. Jurkat-Rott, T. Freilinger, J. P. Dreier, J. Herzog, H. Göbel, G. C. Petzold, P. Montagna, T. Gasser, F. Lehmann-Horn, and M. Dichgans
Neurology 2004; 62: 1857-1861. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesis
P. Moretti, A. P. Lieberman, E. A. Wilde, B. I. Giordani, K. J. Kluin, R. A. Koeppe, S. Minoshima, D. E. Kuhl, W. K. Seltzer, and N. L. Foster
Neurology 2004; 62: 1865-1868. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Autosomal dominant occipital cephalocele
Alexander G. Bassuk, David McLone, Robin Bowman, and John A. Kessler
Neurology 2004; 62: 1888-1890. [Abstract] [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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