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Neurology
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All Genetics

Citations 31-40 of 676 total displayed.

Past content (since Jan 2001):

CLINICAL/SCIENTIFIC NOTES
DYSTONIC TREMOR PRESENTING AS PARKINSONISM: LONG-TERM FOLLOW-UP OF SWEDDs
Peter G. Bain
Neurology 2009; 72: 1443-1445. [Full text] [PDF]  

NEUROIMAGES
The small, spastic, and furrowed tongue of Allgrove syndrome
Henry Houlden
Neurology 2009; 72: 1366. [Full text] [PDF]  

ARTICLES
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
B. Ben Zeev, A. Bebbington, G. Ho, H. Leonard, N. de Klerk, E. Gak, M. Vecksler, and J. Christodoulou
Neurology 2009; 72: 1242-1247. [Abstract] [Full text] [PDF]  

ARTICLES
Etiology of musician’s dystonia: Familial or environmental?
A. Schmidt, H. -C. Jabusch, E. Altenmüller, J. Hagenah, N. Brüggemann, K. Lohmann, L. Enders, P. L. Kramer, R. Saunders-Pullman, S. B. Bressman, A. Münchau, and C. Klein
Neurology 2009; 72: 1248-1254. [Abstract] [Full text] [PDF]  

ARTICLES
A mechanism for low penetrance in an ALS family with a novel SOD1 deletion
L. Zinman, H. N. Liu, C. Sato, Y. Wakutani, A. F. Marvelle, D. Moreno, K. E. Morrison, K. L. Mohlke, J. Bilbao, J. Robertson, and E. Rogaeva
Neurology 2009; 72: 1153-1159. [Abstract] [Full text] [PDF]  

ARTICLES
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H
G. M. Fabrizi, F. Taioli, T. Cavallaro, S. Ferrari, L. Bertolasi, M. Casarotto, N. Rizzuto, T. Deconinck, V. Timmerman, and P. De Jonghe
Neurology 2009; 72: 1160-1164. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY
B. Segarane, A. Li, R. Paudel, S. Scholz, J. Neumann, A. Lees, T. Revesz, J. Hardy, C. J. Mathias, N. W. Wood, J. Holton, and H. Houlden
Neurology 2009; 72: 1185-1186. [Full text] [PDF]  

ARTICLES
APOE {varepsilon}2 is associated with intact cognition but increased Alzheimer pathology in the oldest old
Daniel J. Berlau, María M. Corrada, Elizabeth Head, and Claudia H. Kawas
Neurology 2009; 72: 829-834. [Abstract] [Full text] [PDF]  

ARTICLES
Age at intracranial aneurysm rupture among generations: Familial Intracranial Aneurysm Study
D. Woo, R. Hornung, L. Sauerbeck, R. Brown, I. Meissner, J. Huston, T. Foroud, J. Broderick For the FIA Investigators
Neurology 2009; 72: 695-698. [Abstract] [Full text] [PDF]  

ARTICLES
Fat metabolism during exercise in patients with McArdle disease
M. C. Ørngreen, T. D. Jeppesen, S. Tvede Andersen, T. Taivassalo, S. Hauerslev, N. Preisler, R. G. Haller, G. van Hall, and J. Vissing
Neurology 2009; 72: 718-724. [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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