All Genetics

Citations 431-440 of 676 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly

U. Aguglia, A. Gambardella, G. J. Breedveld, R. L. Oliveri, E. Le Piane, D. Messina, A. Quattrone, and P. Heutink
Neurology 2004; 62: 1613-1615. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci

N. Pankratz, S. K. Uniacke, C. A. Halter, A. Rudolph, C. W. Shults, P. M. Conneally, T. Foroud, W. C. Nichols, and the Parkinson Study Group
Neurology 2004; 62: 1616-1618. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

Z. K. Wszolek, R. F. Pfeiffer, Y. Tsuboi, R. J. Uitti, R. D. McComb, A. J. Stoessl, A. J. Strongosky, A. Zimprich, B. Müller-Myhsok, M. J. Farrer, T. Gasser, D. B. Calne, and D. W. Dickson
Neurology 2004; 62: 1619-1622. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism

D. Seripa, M. G. Matera, R. P. D’Andrea, C. Gravina, C. Masullo, A. Daniele, A. Bizzarro, M. Rinaldi, P. Antuono, D. R. Wekstein, G. Dal Forno, and V. M. Fazio
Neurology 2004; 62: 1631-1633. [Abstract] [Full text] [PDF]  

EDITORIALS
A clever road from myopathology to genes: The myotilin story

George Karpati and Michael Sinnreich
Neurology 2004; 62: 1248-1249. [Full text] [PDF]  

VIEWS & REVIEWS
Gene therapy of the brain: The trans-vascular approach

Felix Schlachetzki, Yun Zhang, Ruben J. Boado, and William M. Pardridge
Neurology 2004; 62: 1275-1281. [Abstract] [Full text] [PDF]  

ARTICLES
Mutations in myotilin cause myofibrillar myopathy

Duygu Selcen and Andrew G. Engel
Neurology 2004; 62: 1363-1371. [Abstract] [Full text] [PDF]  

ARTICLES
Regional metabolism in primary torsion dystonia: Effects of penetrance and genotype

M. Carbon, S. Su, V. Dhawan, D. Raymond, S. Bressman, and D. Eidelberg
Neurology 2004; 62: 1384-1390. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA^His gene

R. W. Taylor, A. M. Schaefer, M. T. McDonnell, R. K.H. Petty, A. M. Thomas, E. L. Blakely, C. M. Hayes, R. McFarland, and D. M. Turnbull
Neurology 2004; 62: 1420-1423. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Giant axon and neurofilament accumulation in Charcot–Marie–Tooth disease type 2E

G. M. Fabrizi, T. Cavallaro, C. Angiari, L. Bertolasi, I. Cabrini, M. Ferrarini, and N. Rizzuto
Neurology 2004; 62: 1429-1431. [Abstract] [Full text] [PDF]  

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