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Neurology
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Association studies in genetics

Citations 71-80 of 147 total displayed.

Past content (since Jan 2001):

ARTICLES
Genetic association between the APOE*4 allele and Lewy bodies in Alzheimer disease
D. W. Tsuang, R. K. Wilson, O. L. Lopez, E. K. Luedecking-Zimmer, J. B. Leverenz, S. T. DeKosky, M. I. Kamboh, and R. L. Hamilton
Neurology 2005; 64: 509-513. [Abstract] [Full text] [PDF]  

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HLA-DR,DQ and APOE genotypes and gender influence in Sardinian primary progressive MS
E. Cocco, A. Sotgiu, G. Costa, M. R. Murru, C. Mancosu, R. Murru, M. Lai, P. Contu, and M. G. Marrosu
Neurology 2005; 64: 564-566. [Abstract] [Full text] [PDF]  

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The HLA locus and multiple sclerosis in Sicily
D. Brassat, G. Salemi, L. F. Barcellos, G. McNeill, P. Proia, S. L. Hauser, J. R. Oksenberg, and G. Savettieri
Neurology 2005; 64: 361-363. [Abstract] [Full text] [PDF]  

ARTICLES
HLA class II alleles are not a general susceptibility factor in Guillain–Barré syndrome
K. Geleijns, G. M.Th. Schreuder, B. C. Jacobs, K. Sintnicolaas, R. van Koningsveld, J. Meulstee, J. D. Laman, and P. A. van Doorn
Neurology 2005; 64: 44-49. [Abstract] [Full text] [PDF]  

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A functional serotonin transporter gene polymorphism is associated with migraine with aura
M. Marziniak, R. Mössner, A. Schmitt, K. P. Lesch, and C. Sommer
Neurology 2005; 64: 157-159. [Abstract] [Full text] [PDF]  

ARTICLES
Polymorphisms in glutathione S-transferase omega-1 and AD, vascular dementia, and stroke
H. Kölsch, M. Linnebank, D. Lütjohann, F. Jessen, U. Wüllner, U. Harbrecht, K. M. Thelen, M. Kreis, F. Hentschel, A. Schulz, K. von Bergmann, W. Maier, and R. Heun
Neurology 2004; 63: 2255-2260. [Abstract] [Full text] [PDF]  

ARTICLES
Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
T. E. Dudding, K. Friend, P. W. Schofield, S. Lee, I. A. Wilkinson, and R. I. Richards
Neurology 2004; 63: 2288-2292. [Abstract] [Full text] [PDF]  

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Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis
U. A. Badrising, G. M.Th. Schreuder, M. J. Giphart, K. Geleijns, J. J.G.M. Verschuuren, A. R. Wintzen, and the Dutch IBM Study Group
Neurology 2004; 63: 2396-2398. [Abstract] [Full text] [PDF]  

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No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS
W. J. Broom, M. J. Parton, C. A. Vance, C. Russ, P. M. Andersen, V. Hansen, P. N. Leigh, J. F. Powell, A. Al-Chalabi, and C. E. Shaw
Neurology 2004; 63: 2419-2422. [Abstract] [Full text] [PDF]  

ARTICLES
Correlating phenotype and genotype in the periodic paralyses
T. M. Miller, M. R. Dias da Silva, H. A. Miller, H. Kwiecinski, J. R. Mendell, R. Tawil, P. McManis, R. C. Griggs, C. Angelini, S. Servidei, J. Petajan, M. C. Dalakas, L. P.W. Ranum, Y. H. Fu, and L. J. Ptácek
Neurology 2004; 63: 1647-1655. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* 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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