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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Hague S, Rogaeva E, Hernandez D, Gulick C, Singleton A, Hanson M, Johnson J, Weiser R, Gallardo M, Ravina B, Gwinn-Hardy K, Crawley A, St George-Hyslop PH, Lang AE, Heutink P, Bonifati V, Hardy J, Singleton A. Hague S, et al. Among authors: rogaeva e. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685
Homozygous inheritance of the Machado-Joseph disease gene.
Lang AE, Rogaeva EA, Tsuda T, Hutterer J, St George-Hyslop P. Lang AE, et al. Among authors: rogaeva ea. Ann Neurol. 1994 Sep;36(3):443-7. doi: 10.1002/ana.410360318. Ann Neurol. 1994. PMID: 8080254
Association between bleomycin hydrolase and Alzheimer's disease in caucasians.
Farrer LA, Abraham CR, Haines JL, Rogaeva EA, Song Y, McGraw WT, Brindle N, Premkumar S, Scott WK, Yamaoka LH, Saunders AM, Roses AD, Auerbach SA, Sorbi S, Duara R, Pericak-Vance MA, St George-Hyslop PH. Farrer LA, et al. Among authors: rogaeva ea. Ann Neurol. 1998 Nov;44(5):808-11. doi: 10.1002/ana.410440515. Ann Neurol. 1998. PMID: 9818937
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion.
De Jonghe C, Cruts M, Rogaeva EA, Tysoe C, Singleton A, Vanderstichele H, Meschino W, Dermaut B, Vanderhoeven I, Backhovens H, Vanmechelen E, Morris CM, Hardy J, Rubinsztein DC, St George-Hyslop PH, Van Broeckhoven C. De Jonghe C, et al. Among authors: rogaeva ea. Hum Mol Genet. 1999 Aug;8(8):1529-40. doi: 10.1093/hmg/8.8.1529. Hum Mol Genet. 1999. PMID: 10401002
Association between angiotensin-converting enzyme and Alzheimer disease.
Farrer LA, Sherbatich T, Keryanov SA, Korovaitseva GI, Rogaeva EA, Petruk S, Premkumar S, Moliaka Y, Song YQ, Pei Y, Sato C, Selezneva ND, Voskresenskaya S, Golimbet V, Sorbi S, Duara R, Gavrilova S, St George-Hyslop PH, Rogaev EI. Farrer LA, et al. Among authors: rogaeva ea. Arch Neurol. 2000 Feb;57(2):210-4. doi: 10.1001/archneur.57.2.210. Arch Neurol. 2000. PMID: 10681079 Clinical Trial.
Comparison of clinical and pathological phenotypes in two ethnically and geographically unrelated pedigrees segregating an equivalent presenilin 1 mutation.
Jorge R, Mangone C, Castano E, Perandones C, Rogaeva E, St George-Hyslop P, El Hachimi KH, Foncin JF, Robinson RG, Bruni AC. Jorge R, et al. Among authors: rogaeva e. J Neuropsychiatry Clin Neurosci. 2000 Summer;12(3):359-63. doi: 10.1176/jnp.12.3.359. J Neuropsychiatry Clin Neurosci. 2000. PMID: 10956569
429 results