Genetics

Citations 1-10 of 216 total displayed.

Most recent content (1 Jun 2006):

Editorial commentaries
Anti-myelin antibodies in multiple sclerosis: clinically useful?

C H Polman and J Killestein
J Neurol Neurosurg Psychiatry 2006; 77: 712. [Extract] [Full text]  

Past content (since Jul 1999):

Short reports
Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson’s disease cohort

C H Williams-Gray, A Goris, T Foltynie, J Brown, M Maranian, A Walton, D A S Compston, S J Sawcer, and R A Barker
J Neurol Neurosurg Psychiatry 2006; 77: 665-667. [Abstract] [Full text]  

Papers
The -synuclein gene in multiple system atrophy

T Ozawa, D G Healy, P M Abou-Sleiman, K R Ahmadi, N Quinn, A J Lees, K Shaw, U Wullner, J Berciano, J C Moller, C Kamm, K Burk, K A Josephs, P Barone, E Tolosa, D B Goldstein, G Wenning, F Geser, J L Holton, T Gasser, T Revesz, N W Wood the European MSA study group
J Neurol Neurosurg Psychiatry 2006; 77: 464-467. [Abstract] [Full text]  

Short reports
Genetic associations between cathepsin D exon 2 CT polymorphism and Alzheimer’s disease, and pathological correlations with genotype

Y Davidson, L Gibbons, A Pritchard, J Hardicre, J Wren, J Tian, J Shi, C Stopford, C Julien, J Thompson, A Payton, U Thaker, A J Hayes, T Iwatsubo, S M Pickering-Brown, N Pendleton, M A Horan, A Burns, N Purandare, C L Lendon, D Neary, J S Snowden, and D M A Mann
J Neurol Neurosurg Psychiatry 2006; 77: 515-517. [Abstract] [Full text]  

Short reports
Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort

G Kuhlenbäumer, K Berger, A Huge, E Lange, C Kessler, U John, H Funke, D G Nabavi, F Stögbauer, E B Ringelstein, and M Stoll
J Neurol Neurosurg Psychiatry 2006; 77: 521-524. [Abstract] [Full text]  

Short reports
Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutation

H M E Bienfait, C G Faber, F Baas, A A W M Gabreëls-Festen, J H T M Koelman, J E Hoogendijk, J J Verschuuren, J H J Wokke, and M de Visser
J Neurol Neurosurg Psychiatry 2006; 77: 534-537. [Abstract] [Full text]  

Short reports
An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPP

E Bellone, P Balestra, G Ribizzi, A Schenone, G Zocchi, E Di Maria, F Ajmar, and P Mandich
J Neurol Neurosurg Psychiatry 2006 77: 538 -540; published online before print as 10.1136/jnnp.2005.075242 [Abstract] [Full text]  

Letters
Association of CYP46 intron 2 polymorphism in Finnish Alzheimer’s disease samples and a global scale summary

S Helisalmi, S Vepsäläinen, A M Koivisto, A Mannermaa, S Iivonen, M Hiltunen, V Kiviniemi, and H Soininen
J Neurol Neurosurg Psychiatry 2006; 77: 421-422. [Extract] [Full text]  

Papers
The apolipoprotein E 4 allele selectively increases the risk of frontotemporal lobar degeneration in males

R Srinivasan, Y Davidson, L Gibbons, A Payton, A M T Richardson, A Varma, C Julien, C Stopford, J Thompson, M A Horan, N Pendleton, S M Pickering-Brown, D Neary, J S Snowden, and D M A Mann
J Neurol Neurosurg Psychiatry 2006; 77: 154-158. [Abstract] [Full text]  

Papers
Facial emotion recognition in myotonic dystrophy type 1 correlates with CTG repeat expansion

S Winblad, P Hellström, C Lindberg, and S Hansen
J Neurol Neurosurg Psychiatry 2006; 77: 219-223. [Abstract] [Full text]  

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