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Neurology
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All Genetics

Citations 361-370 of 679 total displayed.

Past content (since Jan 2001):

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]  

BRIEF COMMUNICATIONS
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy
D. D’Agostino, M. Bertelli, S. Gallo, S. Cecchin, E. Albiero, P. G. Garofalo, A. Gambardella, J.-M. St. Hilaire, H. Kwiecinski, E. Andermann, and M. Pandolfo
Neurology 2004; 63: 1500-1502. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Clinical phenotype of Brazilian families with spinocerebellar ataxia 10
H. A.G. Teive, B. B. Roa, S. Raskin, P. Fang, W. O. Arruda, Y. Correa Neto, R. Gao, L. C. Werneck, and T. Ashizawa
Neurology 2004; 63: 1509-1512. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency
A. Schiller, R. A. Wevers, G. C.H. Steenbergen, N. Blau, and H. H. Jung
Neurology 2004; 63: 1524-1526. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Coincidence of two genetic forms of Charcot–Marie–Tooth disease in a single family
C. Verny, N. Ravisé, A-L. Leutenegger, F. Pouplard, O. Dubourg, S. Tardieu, F. Dubas, A. Brice, E. Genin, and E. LeGuern
Neurology 2004; 63: 1527-1529. [Abstract] [Full text] [PDF]  

EDITORIALS
Posterior cortical dementia: Lost but not forgetting
Charles J. Duffy
Neurology 2004; 63: 1148-1149. [Full text] [PDF]  

EDITORIALS
Resident and Fellow Page Update
Karen C. Johnston
Neurology 2004; 63: 1154. [Full text] [PDF]  

ARTICLES
Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy
D. F. Tang-Wai, N. R. Graff-Radford, B. F. Boeve, D. W. Dickson, J. E. Parisi, R. Crook, R. J. Caselli, D. S. Knopman, and R. C. Petersen
Neurology 2004; 63: 1168-1174. [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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