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116 related items for PubMed ID: 2964224
21. Genotype-phenotype analysis in early-onset Alzheimer's disease due to presenilin-1 mutations at codon 139. Hanisch F, Kölmel HW. Eur J Med Res; 2004 Jul 30; 9(7):361-4. PubMed ID: 15337637 [Abstract] [Full Text] [Related]
22. SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family. Perry RT, Go RC, Harrell LE, Acton RT. Am J Med Genet; 1995 Feb 27; 60(1):12-8. PubMed ID: 7485229 [Abstract] [Full Text] [Related]
23. [Genetics and Alzheimer's disease]. Manzano S, González JL, Marcos A, Matías-Guiu J. Neurologia; 2009 Mar 27; 24(2):83-9. PubMed ID: 19322684 [Abstract] [Full Text] [Related]
35. Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families. Van Broeckhoven C, Genthe AM, Vandenberghe A, Horsthemke B, Backhovens H, Raeymaekers P, Van Hul W, Wehnert A, Gheuens J, Cras P. Nature; 1988 Jan 27; 329(6135):153-5. PubMed ID: 3306405 [Abstract] [Full Text] [Related]
37. [Familial Alzheimer's disease: a study of HLA markers]. Delasnerie-Lauprêtre N, Calot M, Ohayon E, Foucault C, Cambon-de-Mouzon A, Clanet M, Cathala F. Biomed Pharmacother; 1983 Mar 27; 37(4):186-8. PubMed ID: 6581838 [Abstract] [Full Text] [Related]
39. Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology. Mullan M, Houlden H, Crawford F, Kennedy A, Rogues P, Rossor M. Am J Med Genet; 1993 Oct 15; 48(3):129-30. PubMed ID: 8291565 [Abstract] [Full Text] [Related]