Dementia

Apolipoprotein E4 is only a weak predictor of dementia and cognitive decline in the general population
A G Yip, C Brayne, D Easton, D C Rubinsztein

Journal of Medical Genetics Sep 2002, 39 (9) 639-643; DOI: 10.1136/jmg.39.9.639
Association of an interleukin 1B gene polymorphism (−511) with Parkinson's disease in Finnish patients
K M Mattila, J O Rinne, T Lehtimäki, M Röyttä, J-P Ahonen, M Hurme

Journal of Medical Genetics Jun 2002, 39 (6) 400-402; DOI: 10.1136/jmg.39.6.400
An investigation of ACE as a risk factor for dementia and cognitive decline in the general population
A G Yip, C Brayne, D Easton, D C Rubinsztein

Journal of Medical Genetics Jun 2002, 39 (6) 403-406; DOI: 10.1136/jmg.39.6.403
Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation
S Kudo, Y Nomura, M Segawa, N Fujita, M Nakao, S Hammer, C Schanen, I Terai, M Tamura

Journal of Medical Genetics Feb 2002, 39 (2) 132-136; DOI: 10.1136/jmg.39.2.132
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease
M-L Jacquemont, D Campion, V Hahn, C Tallaksen, T Frebourg, A Brice, A Durr

Journal of Medical Genetics Feb 2002, 39 (2) e2; DOI: 10.1136/jmg.39.2.e2
Identification and characterisation of mutations underlying Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)
G-J Lee-Chen, S-P Lin, S-Z Lin, C-K Chuang, K-T Hsiao, C-F Huang, W-C Lien

Journal of Medical Genetics Feb 2002, 39 (2) e3; DOI: 10.1136/jmg.39.2.e3
Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36
Daniel J Hampshire, Emma Roberts, Yanick Crow, Jacquelyn Bond, Ammar Mubaidin, Abdul-Latif Wriekat, Amir Al-Din, C Geoffrey Woods

Journal of Medical Genetics Oct 2001, 38 (10) 680-682; DOI: 10.1136/jmg.38.10.680
Peutz-Jeghers families unlinked toSTK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma
Sylviane Olschwang, Cécile Boisson, Gilles Thomas

Journal of Medical Genetics Jun 2001, 38 (6) 356-360; DOI: 10.1136/jmg.38.6.356
Genetic association of anLBP-1c/CP2/LSFgene polymorphism with late onset Alzheimer's disease
Alison E Taylor, Agustin Yip, Carol Brayne, Douglas Easton, John Grimley Evans, John Xuereb, Nigel Cairns, Margaret M Esiri, David C Rubinsztein

Journal of Medical Genetics Apr 2001, 38 (4) 232-233; DOI: 10.1136/jmg.38.4.232
New problems in testing for Huntington's disease: the issue of intermediate and reduced penetrance alleles
ANNEKE MAAT-KIEVIT, MONIQUE LOSEKOOT, HANNEKE VAN DEN BOER-VAN DEN BERG, GERT-JAN VAN OMMEN, MARTINUS NIERMEIJER, MARTIJN BREUNING, AAD TIBBEN

Journal of Medical Genetics Apr 2001, 38 (4) e12; DOI: 10.1136/jmg.38.4.e12

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