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Results:
1-9
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Results: 9
Authors:
Arango, D
Cruts, M
Torres, O
Backhovens, H
Serrano, ML
Villareal, E
Montanes, P
Matallana, D
Cano, C
Van Broeckhoven, C
Jacquier, M
Citation: D. Arango et al., Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia, AM J MED G, 103(2), 2001, pp. 138-143
Authors:
Theuns, J
Del-Favero, J
Dermaut, B
van Duijn, CM
Backhovens, H
Van den Broeck, M
Serneels, S
Corsmit, E
Van Broeckhoven, C
Cruts, M
Citation: J. Theuns et al., Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression, HUM MOL GEN, 9(3), 2000, pp. 325-331
Authors:
Kumar-Singh, S
De Jonghe, C
Cruts, M
Kleinert, R
Wang, R
Mercken, M
De Strooper, B
Vanderstichele, H
Lofgren, A
Vanderhoeven, I
Backhovens, H
Vanmechelen, E
Kroisel, PM
Van Broeckhoven, C
Citation: S. Kumar-singh et al., Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease, HUM MOL GEN, 9(18), 2000, pp. 2589-2598
Authors:
Dermaut, B
Cruts, M
Backhovens, H
Lubke, U
Van Everbroeck, B
Sciot, R
Dom, R
Martin, JJ
Van Broeckhoven, C
Cras, P
Citation: B. Dermaut et al., Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin1 missense substitution and a prion protein gene insertion, J NEUROL, 247(5), 2000, pp. 364-368
Authors:
van Duijn, CM
Cruts, M
Theuns, J
Van Gassen, G
Backhovens, H
van den Broeck, M
Wehnert, A
Serneels, S
Hofman, A
Van Broeckhoven, C
Citation: Cm. Van Duijn et al., Genetic association of the presenilin-1 regulatory region with early-onsetAlzheimer's disease in a population-based sample, EUR J HUM G, 7(7), 1999, pp. 801-806
Authors:
De Jonghe, C
Cruts, M
Rogaeva, EA
Tysoe, C
Singleton, A
Vanderstichele, H
Meschino, W
Dermaut, D
Vanderhoeven, I
Backhovens, H
Vanmechelen, E
Morris, CM
Hardy, J
Rubinsztein, DC
St George-Hyslop, PH
Van Broeckhoven, C
Citation: C. De Jonghe et al., Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A beta 42 secretion, HUM MOL GEN, 8(8), 1999, pp. 1529-1540
Authors:
Roks, G
Dermaut, B
Heutink, P
Julliams, A
Backhovens, H
Van de Broeck, M
Serneels, S
Hofman, A
Van Broeckhoven, C
van Duijn, CM
Cruts, M
Citation: G. Roks et al., Mutation screening of the tau gene in patients with early-onset Alzheimer's disease, NEUROSCI L, 277(2), 1999, pp. 137-139
Authors:
Dermaut, B
Cruts, M
Slooter, AJC
Van Gestel, S
De Jonghe, C
Backhovens, H
Vanderstichele, H
Vanmechelen, E
Breteler, MMB
Hofman, A
Hendriks, L
Van Duijn, CM
Van Broeckhoven, C
Citation: B. Dermaut et al., Glu318Gly in presenilin-1 is a neutral mutation in relation to dementia: The Rotterdam study, ALZHEIMER'S DISEASE AND RELATED DISORDERS, 1999, pp. 87-92
Authors:
Roks, G
Cruts, M
Bullido, MJ
Backhovens, H
Artiga, MJ
Hofman, A
Valdivieso, F
Van Broeckhoven, C
Van Duijn, CM
Citation: G. Roks et al., The -491 A/T polymorphism in the regulatory region of the Apolipoprotein Egene and early-onset Alzheimer's disease, NEUROSCI L, 258(2), 1998, pp. 65-68
Risultati:
1-9
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