Parkinson's disease

Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families
W C Nichols, N Pankratz, S K Uniacke, M W Pauciulo, C Halter, A Rudolph, P M Conneally, T Foroud

Journal of Medical Genetics Jul 2002, 39 (7) 489-492; DOI: 10.1136/jmg.39.7.489
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism
C Piccoli, M Ripoli, G Quarato, R Scrima, A D’Aprile, D Boffoli, M Margaglione, C Criscuolo, G De Michele, A Sardanelli, S Papa, N Capitanio

Journal of Medical Genetics Sep 2008, 45 (9) 596-602; DOI: 10.1136/jmg.2008.058628
Dipeptidyl carboxypeptidase 1 (DCP1) and butyrylcholinesterase (BCHE) gene interactions with the apolipoprotein E ε4 allele as risk factors in Alzheimer's disease and in Parkinson's disease with coexisting Alzheimer pathology
Kari M Mattila, Juha O Rinne, Matias Röyttä, Pekka Laippala, Timo Pietilä, Hannu Kalimo, Timo Koivula, Harry Frey, Terho Lehtimäki

Journal of Medical Genetics Oct 2000, 37 (10) 766-770; DOI: 10.1136/jmg.37.10.766
Size bias of fragile X premutation alleles in late-onset movement disorders
Sebastien Jacquemont, Maureen A Leehey, Randi J Hagerman, Laurel A Beckett, Paul J Hagerman

Journal of Medical Genetics Oct 2006, 43 (10) 804-809; DOI: 10.1136/jmg.2006.042374
Parkinsonism among Gaucher disease carriers
O Goker-Alpan, R Schiffmann, M E LaMarca, R L Nussbaum, A McInerney-Leo, E Sidransky

Journal of Medical Genetics Dec 2004, 41 (12) 937-940; DOI: 10.1136/jmg.2004.024455
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function
P J Lockhart, S Lincoln, M Hulihan, J Kachergus, K Wilkes, G Bisceglio, D C Mash, M J Farrer

Journal of Medical Genetics Mar 2004, 41 (3) e22; DOI: 10.1136/jmg.2003.011106
Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome
F Tassone, R J Hagerman, D Garcia-Arocena, E W Khandjian, C M Greco, P J Hagerman

Journal of Medical Genetics Apr 2004, 41 (4) e43; DOI: 10.1136/jmg.2003.012518
Neuroferritinopathy in a French family with late onset dominant dystonia
P F Chinnery, A R J Curtis, C Fey, A Coulthard, D Crompton, A Curtis, A Lombés, J Burn

Journal of Medical Genetics May 2003, 40 (5) e69; DOI: 10.1136/jmg.40.5.e69
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

Main menu

Parkinson's disease

Pages

Log in using your username and password

Main menu

Log in using your username and password

You are here

Parkinson's disease

Pages