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Neurology
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All Genetics

Citations 351-360 of 676 total displayed.

Past content (since Jan 2001):

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Full text] [PDF]  

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. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

EDITORIALS
What does PINK1 mean for Parkinson diseases?
Andrew Singleton
Neurology 2004; 63: 1350-1351. [Full text] [PDF]  

BRIEF COMMUNICATIONS
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations
Y. Hatano, K. Sato, B. Elibol, H. Yoshino, Y. Yamamura, V. Bonifati, H. Shinotoh, M. Asahina, S. Kobayashi, A. R. Ng, R. L. Rosales, S. Hassin-Baer, Y. Shinar, C. S. Lu, H. C. Chang, Y. H. Wu-Chou, F. B. Ataç, T. Kobayashi, T. Toda, Y. Mizuno, and N. Hattori
Neurology 2004; 63: 1482-1485. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
PINK1 (PARK6) associated Parkinson disease in Ireland
D. G. Healy, P. M. Abou-Sleiman, J. M. Gibson, O. A. Ross, S. Jain, S. Gandhi, D. Gosal, M. M.K. Muqit, N. W. Wood, and T. Lynch
Neurology 2004; 63: 1486-1488. [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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