Rogaeva E - Search Results

1

Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

Gabryelewicz T, Masellis M, Berdynski M, Bilbao JM, Rogaeva E, St George-Hyslop P, Barczak A, Czyzewski K, Barcikowska M, Wszolek Z, Black SE, Zekanowski C. Gabryelewicz T, et al. Among authors: rogaeva e. J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413. J Alzheimers Dis. 2010. PMID: 20930269 Free PMC article.

2

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

3

The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.

Ikeda M, Sharma V, Sumi SM, Rogaeva EA, Poorkaj P, Sherrington R, Nee L, Tsuda T, Oda N, Watanabe M, Aoki M, Shoji M, Abe K, Itoyama Y, Hirai S, Schellenberg GD, Bird TD, St George-Hyslop PH. Ikeda M, et al. Among authors: rogaeva ea. Ann Neurol. 1996 Dec;40(6):912-7. doi: 10.1002/ana.410400614. Ann Neurol. 1996. PMID: 9007097

4

Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease.

Brindle N, Song Y, Rogaeva E, Premkumar S, Levesque G, Yu G, Ikeda M, Nishimura M, Paterson A, Sorbi S, Duara R, Farrer L, St George-Hyslop P. Brindle N, et al. Among authors: rogaeva e. Hum Mol Genet. 1998 May;7(5):933-5. doi: 10.1093/hmg/7.5.933. Hum Mol Genet. 1998. PMID: 9536099

5

Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.

Rogaeva E, Premkumar S, Song Y, Sorbi S, Brindle N, Paterson A, Duara R, Levesque G, Yu G, Nishimura M, Ikeda M, O'Toole C, Kawarai T, Jorge R, Vilarino D, Bruni AC, Farrer LA, St George-Hyslop PH. Rogaeva E, et al. JAMA. 1998 Aug 19;280(7):614-8. doi: 10.1001/jama.280.7.614. JAMA. 1998. PMID: 9718052

6

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions.

Kertesz A, Kawarai T, Rogaeva E, St George-Hyslop P, Poorkaj P, Bird TD, Munoz DG. Kertesz A, et al. Among authors: rogaeva e. Neurology. 2000 Feb 22;54(4):818-27. doi: 10.1212/wnl.54.4.818. Neurology. 2000. PMID: 10690970

7

Molecular genetics of Alzheimer's disease: the role of beta-amyloid and the presenilins.

Tandon A, Rogaeva E, Mullan M, St George-Hyslop PH. Tandon A, et al. Among authors: rogaeva e. Curr Opin Neurol. 2000 Aug;13(4):377-84. doi: 10.1097/00019052-200008000-00003. Curr Opin Neurol. 2000. PMID: 10970053 Review.

8

Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations.

Rogaeva EA, Fafel KC, Song YQ, Medeiros H, Sato C, Liang Y, Richard E, Rogaev EI, Frommelt P, Sadovnick AD, Meschino W, Rockwood K, Boss MA, Mayeux R, St George-Hyslop P. Rogaeva EA, et al. Neurology. 2001 Aug 28;57(4):621-5. doi: 10.1212/wnl.57.4.621. Neurology. 2001. PMID: 11524469

9

Genetic markers in the diagnosis of Alzheimer's disease.

Rogaeva E, Tandon A, St George-Hyslop PH. Rogaeva E, et al. J Alzheimers Dis. 2001 Jun;3(3):293-304. doi: 10.3233/jad-2001-3304. J Alzheimers Dis. 2001. PMID: 12214050

10

PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier.

Rogaeva E, Bergeron C, Sato C, Moliaka I, Kawarai T, Toulina A, Song YQ, Kolesnikova T, Orlacchio A, Bernardi G, St George-Hyslop PH. Rogaeva E, et al. Neurology. 2003 Oct 14;61(7):1005-7. doi: 10.1212/wnl.61.7.1005. Neurology. 2003. PMID: 14557582

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