Goldgaber D - Search Results

1

Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases.

Saunders AM, Schmader K, Breitner JC, Benson MD, Brown WT, Goldfarb L, Goldgaber D, Manwaring MG, Szymanski MH, McCown N, et al. Saunders AM, et al. Among authors: goldgaber d. Lancet. 1993 Sep 18;342(8873):710-1. doi: 10.1016/0140-6736(93)91709-u. Lancet. 1993. PMID: 8103823

2

Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease.

Strittmatter WJ, Weisgraber KH, Huang DY, Dong LM, Salvesen GS, Pericak-Vance M, Schmechel D, Saunders AM, Goldgaber D, Roses AD. Strittmatter WJ, et al. Among authors: goldgaber d. Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8098-102. doi: 10.1073/pnas.90.17.8098. Proc Natl Acad Sci U S A. 1993. PMID: 8367470 Free PMC article.

3

Complex genetic disease: can genetic strategies in Alzheimer's disease and new genetic mechanisms be applied to epilepsy?

Roses AD, Pericak-Vance MA, Saunders AM, Schmechel D, Goldgaber D, Strittmatter W. Roses AD, et al. Among authors: goldgaber d. Epilepsia. 1994;35 Suppl 1:S20-8. doi: 10.1111/j.1528-1157.1994.tb05925.x. Epilepsia. 1994. PMID: 8293721 Review.

4

Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease.

Schmechel DE, Saunders AM, Strittmatter WJ, Crain BJ, Hulette CM, Joo SH, Pericak-Vance MA, Goldgaber D, Roses AD. Schmechel DE, et al. Among authors: goldgaber d. Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9649-53. doi: 10.1073/pnas.90.20.9649. Proc Natl Acad Sci U S A. 1993. PMID: 8415756 Free PMC article.

5

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

Goldfarb LG, Brown P, Goldgaber D, Garruto RM, Yanagihara R, Asher DM, Gajdusek DC. Goldfarb LG, et al. Among authors: goldgaber d. Lancet. 1990 Jul 21;336(8708):174-5. doi: 10.1016/0140-6736(90)91693-5. Lancet. 1990. PMID: 1973487 No abstract available.

6

Sequestration of amyloid beta-peptide.

Goldgaber D, Schwarzman AI, Bhasin R, Gregori L, Schmechel D, Saunders AM, Roses AD, Strittmatter WJ. Goldgaber D, et al. Ann N Y Acad Sci. 1993 Sep 24;695:139-43. doi: 10.1111/j.1749-6632.1993.tb23042.x. Ann N Y Acad Sci. 1993. PMID: 8239272 Review.

7

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome.

Goldfarb LG, Brown P, Goldgaber D, Asher DM, Rubenstein R, Brown WT, Piccardo P, Kascsak RJ, Boellaard JW, Gajdusek DC. Goldfarb LG, et al. Among authors: goldgaber d. Exp Neurol. 1990 Jun;108(3):247-50. doi: 10.1016/0014-4886(90)90130-k. Exp Neurol. 1990. PMID: 2190844

8

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome.

Goldgaber D, Goldfarb LG, Brown P, Asher DM, Brown WT, Lin S, Teener JW, Feinstone SM, Rubenstein R, Kascsak RJ, et al. Goldgaber D, et al. Exp Neurol. 1989 Nov;106(2):204-6. doi: 10.1016/0014-4886(89)90095-2. Exp Neurol. 1989. PMID: 2572450

9

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.

Speer MC, Goldgaber D, Goldfarb LG, Roses AD, Pericak-Vance MA. Speer MC, et al. Among authors: goldgaber d. Genomics. 1991 Feb;9(2):366-8. doi: 10.1016/0888-7543(91)90266-h. Genomics. 1991. PMID: 1672296

10

African-American TOMM40'523-APOE haplotypes are admixture of West African and Caucasian alleles.

Roses AD, Lutz MW, Saunders AM, Goldgaber D, Saul R, Sundseth SS, Akkari PA, Roses SM, Gottschalk WK, Whitfield KE, Vostrov AA, Hauser MA, Allingham RR, Burns DK, Chiba-Falek O, Welsh-Bohmer KA. Roses AD, et al. Among authors: goldgaber d. Alzheimers Dement. 2014 Nov;10(6):592-601.e2. doi: 10.1016/j.jalz.2014.06.009. Epub 2014 Sep 26. Alzheimers Dement. 2014. PMID: 25260913 Free article.

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