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A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, Zimprich A, Gasser T, Hanson M, Waseem S, Singleton A, McMahon FJ, Anvret M, Sydow O, Olson L. Buervenich S, et al. Among authors: olson l. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
Human fetal dopamine neurons grafted into the striatum in two patients with severe Parkinson's disease. A detailed account of methodology and a 6-month follow-up.
Lindvall O, Rehncrona S, Brundin P, Gustavii B, Astedt B, Widner H, Lindholm T, Björklund A, Leenders KL, Rothwell JC, Frackowiak R, Marsden D, Johnels B, Steg G, Freedman R, Hoffer BJ, Seiger A, Bygdeman M, Strömberg I, Olson L. Lindvall O, et al. Among authors: olson l. Arch Neurol. 1989 Jun;46(6):615-31. doi: 10.1001/archneur.1989.00520420033021. Arch Neurol. 1989. PMID: 2786405
Alcohol dehydrogenase alleles in Parkinson's disease.
Buervenich S, Sydow O, Carmine A, Zhang Z, Anvret M, Olson L. Buervenich S, et al. Among authors: olson l. Mov Disord. 2000 Sep;15(5):813-8. doi: 10.1002/1531-8257(200009)15:5<813::aid-mds1008>3.0.co;2-y. Mov Disord. 2000. PMID: 11009184
NURR1 mutations in cases of schizophrenia and manic-depressive disorder.
Buervenich S, Carmine A, Arvidsson M, Xiang F, Zhang Z, Sydow O, Jönsson EG, Sedvall GC, Leonard S, Ross RG, Freedman R, Chowdari KV, Nimgaonkar VL, Perlmann T, Anvret M, Olson L. Buervenich S, et al. Among authors: olson l. Am J Med Genet. 2000 Dec 4;96(6):808-13. doi: 10.1002/1096-8628(20001204)96:6<808::aid-ajmg23>3.0.co;2-e. Am J Med Genet. 2000. PMID: 11121187
2,005 results