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Neurology
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Association studies in genetics

Citations 1-10 of 147 total displayed.

Most recent content (27 Oct 2009):

EDITORIALS
Predicting treatment responses to IV immunoglobulins: Can we already ask the genes?
Helmar C. Lehmann and Bernd C. Kieseier
Neurology 2009; 73: 1344-1345. [Full text] [PDF]  

ARTICLES
Single nucleotide polymorphism of TAG-1 influences IVIg responsiveness of Japanese patients with CIDP
M. Iijima, M. Tomita, S. Morozumi, Y. Kawagashira, T. Nakamura, H. Koike, M. Katsuno, N. Hattori, F. Tanaka, M. Yamamoto, and G. Sobue
Neurology 2009; 73: 1348-1352. [Abstract] [Full text] [PDF]  

Past content (since Jan 2001):

EDITORIALS
Predicting treatment responses to IV immunoglobulins. Can we already ask the genes?
Helmar C. Lehmann and Bernd C. Kieseier
Neurology first published on September 23, 2009 as doi: WNL.0b013e3181beed49. Rapid PDF  

ARTICLES
Single nucleotide polymorphism of TAG-1 influences IVIg responsiveness of Japanese patients with CIDP
M. Iijima, M. Tomita, S. Morozumi, Y. Kawagashira, T. Nakamura, H. Koike, M. Katsuno, N. Hattori, F. Tanaka, M. Yamamoto, and G. Sobue
Neurology first published on September 23, 2009 as doi: WNL.0b013e3181bd1139. [Abstract] Rapid PDF  

ARTICLES
Common genetic markers and prediction of recurrent events after ischemic stroke in young adults
A. Pezzini, M. Grassi, E. Del Zotto, C. Lodigiani, P. Ferrazzi, A. Spalloni, R. Patella, A. Giossi, I. Volonghi, L. Iacoviello, M. Magoni, L. L. Rota, M. Rasura, and A. Padovani
Neurology 2009; 73: 717-723. [Abstract] [Full text] [PDF]  

ARTICLES
Risk alleles for multiple sclerosis in multiplex families
M. J. D’Netto, H. Ward, K. M. Morrison, S. V. Ramagopalan, D. A. Dyment, G. C. DeLuca, L. Handunnetthi, A. D. Sadovnick, and G. C. Ebers
Neurology 2009; 72: 1984-1988. [Abstract] [Full text] [PDF]  

EDITORIALS
Variation on a theme: Identifying sequence variation in disease genes and defining pathogenicity
Lorraine N. Clark
Neurology 2009; 72: 1882-1883. [Full text] [PDF]  

ARTICLES
Variation in GIGYF2 is not associated with Parkinson disease
W. C. Nichols, D. K. Kissell, N. Pankratz, M. W. Pauciulo, V. E. Elsaesser, K. A. Clark, C. A. Halter, A. Rudolph, J. Wojcieszek, R. F. Pfeiffer, T. Foroud For the Parkinson Study Group–PROGENI Investigators
Neurology 2009; 72: 1886-1892. [Abstract] [Full text] [PDF]  

ARTICLES
Age and founder effect of SOD1 A4V mutation causing ALS
M. Saeed, Y. Yang, H-X Deng, W-Y Hung, N. Siddique, L. Dellefave, C. Gellera, P. M. Andersen, and T. Siddique
Neurology 2009; 72: 1634-1639. [Abstract] [Full text] [PDF]  

ARTICLES
Effect of APOE genotype on amyloid plaque load and gray matter volume in Alzheimer disease
A. Drzezga, T. Grimmer, G. Henriksen, M. Mühlau, R. Perneczky, I. Miederer, C. Praus, C. Sorg, A. Wohlschläger, M. Riemenschneider, H. J. Wester, H. Foerstl, M. Schwaiger, and A. Kurz
Neurology 2009; 72: 1487-1494. [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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