AAAAAA
Results:
1-21
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Results: 21
Authors:
Bertram, L
Hayward, B
Lake, SL
Falls, K
Van Eerdewegh, P
Blacker, D
Citation: L. Bertram et al., Family-based tests of association in the presence and absence of known linkage, GENET EPID, 21, 2001, pp. S292-S297
Authors:
Bertram, L
Guenette, S
Jones, J
Keeney, D
Mullin, K
Crystal, A
Basu, S
Yhu, S
Deng, A
Rebeck, GW
Hyman, BT
Go, R
McInnis, M
Blacker, D
Tanzi, R
Citation: L. Bertram et al., No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer disease, ANN NEUROL, 49(1), 2001, pp. 114-116
Authors:
Bertram, L
Blacker, D
Crystal, AS
Jones, J
Keeney, D
MacKenzie-Ingano, L
Mullin, K
Basu, S
Yhu, S
McInnis, M
Go, RCP
Saunders, AJ
Tanzi, RE
Citation: L. Bertram et al., Candidate genes showing no evidence of association with Alzheimer's disease: Results of the NIMH-AD genetics initiative, ALZHEIMER'S DISEASE, 2001, pp. 45-51
Authors:
Tanzi, RE
Blacker, D
Citation: Re. Tanzi et D. Blacker, Genetic screening in Alzheimer's disease, GENERATIONS, 24(1), 2000, pp. 58-63
Authors:
Bertram, L
Blacker, D
Crystal, A
Mullin, K
Keeney, D
Jones, J
Basu, S
Yhu, S
Guenette, S
McInnis, M
Go, R
Tanzi, R
Citation: L. Bertram et al., Candidate genes showing no evidence for association or linkage with Alzheimer's disease using family-based methodologies, EXP GERONT, 35(9-10), 2000, pp. 1353-1361
Authors:
Blacker, D
Citation: D. Blacker, The institutional autonomy of education, J PHIL EDUC, 34(2), 2000, pp. 229-246
Evidence against association of the FE65 gene (APBB1) intron 13 polymorphism in Alzheimer's patients
Authors:
Guenette, SY
Bertram, L
Crystal, A
Bakondi, B
Hyman, BT
Rebeck, GW
Tanzi, RE
Blacker, D
Citation: Sy. Guenette et al., Evidence against association of the FE65 gene (APBB1) intron 13 polymorphism in Alzheimer's patients, NEUROSCI L, 296(1), 2000, pp. 17-20
Authors:
Buxbaum, JD
Lilliehook, C
Chan, JY
Go, RCP
Bassett, SS
Tanzi, RE
Wasco, W
Blacker, D
Citation: Jd. Buxbaum et al., Genomic structure, expression pattern, and chromosomal localization of thehuman calsenilin gene: no association between an exonic polymorphism and Alzheimer's disease, NEUROSCI L, 294(3), 2000, pp. 135-138
Authors:
Blacker, D
Citation: D. Blacker, Proceduralism and the orthodox backlash against students' rights, AM J EDUC, 108(4), 2000, pp. 318-355
Authors:
Collins, JS
Perry, RT
Watson, B
Harrell, LE
Acton, RT
Blacker, D
Albert, MS
Tanzi, RE
Bassett, SS
McInnis, MG
Campbell, RD
Go, RCP
Citation: Js. Collins et al., Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative, AM J MED G, 96(6), 2000, pp. 823-830
Authors:
Blacker, D
Citation: D. Blacker, High rate of complete recanalization and dramatic clinical recovery duringtPA infusion when continuously monitored with 2-MHz transcranial Doppler monitoring, STROKE, 31(12), 2000, pp. 3080-3080
Authors:
Bertram, L
Blacker, D
Mullin, K
Keeney, D
Jones, J
Basu, S
Yhu, S
McInnis, MG
Go, RCP
Vekrellis, K
Selkoe, DJ
Saunders, AJ
Tanzi, RE
Citation: L. Bertram et al., Evidence for genetic linkage of Alzheimer's disease to chromosome 10q, SCIENCE, 290(5500), 2000, pp. 2302
Authors:
Blacker, D
Citation: D. Blacker, New insights into genetic aspects of Alzheimer's disease - Does genetic information make a difference in clinical practice?, POSTGR MED, 108(5), 2000, pp. 119
Authors:
Blacker, D
Carroll, W
Citation: D. Blacker et W. Carroll, Acute ataxic sensory neuropathy, Sjogren's syndrome and C-4 deficiency, AUST NZ J M, 30(4), 2000, pp. 516-517
Authors:
Lake, SL
Blacker, D
Laird, NM
Citation: Sl. Lake et al., Family-based tests of association in the presence of linkage, AM J HU GEN, 67(6), 2000, pp. 1515-1525
Authors:
Mokliatchouk, O
Blacker, D
Rabinowitz, D
Citation: O. Mokliatchouk et al., Association tests for traits with variable age at onset, HUMAN HERED, 51(1-2), 2000, pp. 46-53
Authors:
Blacker, D
Tanzi, RE
Citation: D. Blacker et Re. Tanzi, Genetic testing in the early diagnosis of Alzheimer's disease, CUR CLIN N, 2000, pp. 105-125
Authors:
Blacker, D
Crystal, AS
Wilcox, MA
Laird, NM
Tanzi, RE
Citation: D. Blacker et al., An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease - Reply, NAT GENET, 22(1), 1999, pp. 21-22
Authors:
Van Eerdewegh, P
Dupuis, J
Santangelo, SL
Hayward, LB
Blacker, D
Citation: P. Van Eerdewegh et al., The importance of watching our weights: How the choice of weights for non-independent sib pairs can dramatically alter results, GENET EPID, 17, 1999, pp. S373-S378
Authors:
Blacker, D
Citation: D. Blacker, Education as immortality: Toward the rehabilitation of an ideal (Acknowledging classical wisdom as mentor in the western teaching tradition), RELIG EDUC, 93(1), 1998, pp. 8-28
Authors:
Laird, NM
Blacker, D
Wilcox, M
Citation: Nm. Laird et al., The sib transmission/disequilibrium test is a Mantel-Haenszel test, AM J HU GEN, 63(6), 1998, pp. 1915-1915
Risultati:
1-21
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