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Journal Abstract Search

66 related items for PubMed ID: 7485229

  • 21. Clinical features of a neuropathologically verified familial Alzheimer's cohort with onset in the fourth decade: comparison with senile onset Alzheimer's disease and etiopathogenic implications.
    Reisberg B, Ferris SH, Franssen E, Jenkins EC, Wisniewski KE.
    Prog Clin Biol Res; 1989; 317():43-54. PubMed ID: 2690108
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  • 22. Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.
    Alberts MJ, Pericak-Vance MA, Royal V, Bebout J, Gaskell P, Thomas J, Hung WY, Clark C, Earl N, Roses AD.
    Ann Neurol; 1991 Aug; 30(2):216-9. PubMed ID: 1680304
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  • 23. [The relationship between prion protein gene codon 129 polymorphism and Alzheimer's disease].
    Qian HR, Wang LN, Zhu MW.
    Zhonghua Nei Ke Za Zhi; 2006 Nov; 45(11):922-5. PubMed ID: 17313881
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  • 24. Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease.
    Poleggi A, Bizzarro A, Acciarri A, Antuono P, Bagnoli S, Cellini E, Forno GD, Giannattasio C, Lauria A, Matera MG, Nacmias B, Puopolo M, Seripa D, Sorbi S, Wekstein DR, Pocchiari M, Masullo C.
    Eur J Neurol; 2008 Feb; 15(2):173-8. PubMed ID: 18217885
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  • 25. Octapeptide repeat alteration mutations of the prion protein gene in clinically diagnosed Alzheimer's disease and frontotemporal dementia.
    Nan H, Liu L, Chen Z, Chu M, Li J, Jing D, Wang Y, Wu L.
    Clin Genet; 2023 Sep; 104(3):350-355. PubMed ID: 37148197
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  • 27. Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil.
    Pimentel LF, Gomes da Cunha JE, Morelato RL, de Paula F, de Oliveira JR.
    Neurol Res; 2014 Sep; 36(9):775-8. PubMed ID: 24620982
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  • 28. Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region.
    Kamino K, Orr HT, Payami H, Wijsman EM, Alonso ME, Pulst SM, Anderson L, O'dahl S, Nemens E, White JA.
    Am J Hum Genet; 1992 Nov; 51(5):998-1014. PubMed ID: 1415269
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  • 29. Childhood onset in familial prion disease with a novel mutation in the PRNP gene.
    Rogaeva E, Zadikoff C, Ponesse J, Schmitt-Ulms G, Kawarai T, Sato C, Salehi-Rad S, St George-Hyslop P, Lang AE.
    Arch Neurol; 2006 Jul; 63(7):1016-21. PubMed ID: 16831973
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  • 30. Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in AD.
    Golanska E, Hulas-Bigoszewska K, Rutkiewicz E, Styczynska M, Peplonska B, Barcikowska M, Bratosiewicz-Wasik J, Liberski PP.
    Neurology; 2004 Jan 27; 62(2):313-5. PubMed ID: 14745079
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  • 31. Amyloid precursor protein mutation at codon 713 (Ala-->Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent).
    Forsell C, Lannfelt L.
    Neurosci Lett; 1995 Jan 23; 184(2):90-3. PubMed ID: 7724053
    [Abstract] [Full Text] [Related]

  • 32. Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series.
    McNaughton D, Knight W, Guerreiro R, Ryan N, Lowe J, Poulter M, Nicholl DJ, Hardy J, Revesz T, Lowe J, Rossor M, Collinge J, Mead S.
    Neurobiol Aging; 2012 Feb 23; 33(2):426.e13-21. PubMed ID: 21193246
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  • 39. Prion protein gene in Alzheimer's disease.
    Caramelli P.
    Arq Neuropsiquiatr; 2013 Jul 23; 71(7):419-20. PubMed ID: 23857620
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