-
1
-
-
0034968974
-
Incidence of dementia: Does gender make a difference?
-
DOI 10.1016/S0197-4580(01)00231-7, PII S0197458001002317
-
Ruitenberg A, Ott A, van Swieten JC, Hofman A, Breteler MM. Incidence of dementia: does gender make a difference? Neurobiol Aging. 2001;22: 575-580. (Pubitemid 32607742)
-
(2001)
Neurobiology of Aging
, vol.22
, Issue.4
, pp. 575-580
-
-
Ruitenberg, A.1
Ott, A.2
Van Swieten, J.C.3
Hofman, A.4
Breteler, M.M.B.5
-
2
-
-
0036327146
-
Vascular dementia revisited: Diagnosis, pathogenesis, treatment, and prevention
-
DOI 10.1016/S0025-7125(02)00008-1, PII S0025712502000081
-
Román GC. Vascular dementia revisited: diagnosis, pathogenesis, treatment, and prevention. Med Clin North Am. 2002;86:477-499. (Pubitemid 34810644)
-
(2002)
Medical Clinics of North America
, vol.86
, Issue.3
, pp. 477-499
-
-
Roman, G.C.1
-
3
-
-
77950303632
-
Association between APOE epsilon4 allele and vascular dementia: The Cache County study
-
Chuang YF, Hayden KM, Norton MC, Tschanz J, Breitner JC, Welsh-Bohmer KA, et al. Association between APOE epsilon4 allele and vascular dementia: The Cache County study. Dement Geriatr Cogn Disord. 2010;29:248-253.
-
(2010)
Dement Geriatr Cogn Disord
, vol.29
, pp. 248-253
-
-
Chuang, Y.F.1
Hayden, K.M.2
Norton, M.C.3
Tschanz, J.4
Breitner, J.C.5
Welsh-Bohmer, K.A.6
-
4
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
DOI 10.1038/383707a0
-
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 1996;383:707-710. (Pubitemid 26360644)
-
(1996)
Nature
, vol.383
, Issue.6602
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
Vahedi, K.4
Chabriat, H.5
Mouton, P.6
Alamowitch, S.7
Domenga, V.8
Cecillion, M.9
Marechal, E.10
Maciazek, J.11
Vayssiere, C.12
Cruaud, C.13
Cabanis, E.-A.14
Ruchoux, M.M.15
Weissanbach, J.16
Bach, J.F.17
Bousser, M.G.18
Tournier-Lasserve, E.19
-
5
-
-
79955484414
-
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
-
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet. 2011;43:429-435.
-
(2011)
Nat Genet
, vol.43
, pp. 429-435
-
-
Hollingworth, P.1
Harold, D.2
Sims, R.3
Gerrish, A.4
Lambert, J.C.5
Carrasquillo, M.M.6
-
6
-
-
77952307991
-
Genome-wide analysis of genetic loci associated with Alzheimer disease
-
Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA. 2010;303:1832-1840.
-
(2010)
JAMA.
, vol.303
, pp. 1832-1840
-
-
Seshadri, S.1
Fitzpatrick, A.L.2
Ikram, M.A.3
Destefano, A.L.4
Gudnason, V.5
Boada, M.6
-
7
-
-
80054717387
-
The Rotterdam Study: 2012 objectives and design update
-
Hofman A, van Duijn CM, Franco OH, Ikram MA, Janssen HL, Klaver CC, et al. The Rotterdam Study: 2012 objectives and design update. Eur J Epidemiol. 2011;26:657-686.
-
(2011)
Eur J Epidemiol
, vol.26
, pp. 657-686
-
-
Hofman, A.1
Van Duijn, C.M.2
Franco, O.H.3
Ikram, M.A.4
Janssen, H.L.5
Klaver, C.C.6
-
8
-
-
0032521394
-
Incidence and risk of dementia: The Rotterdam Study
-
Ott A, Breteler MM, van Harskamp F, Stijnen T, Hofman A. Incidence and risk of dementia. The Rotterdam Study. Am J Epidemiol. 1998;147: 574-580. (Pubitemid 28134244)
-
(1998)
American Journal of Epidemiology
, vol.147
, Issue.6
, pp. 574-580
-
-
Ott, A.1
Breteler, M.M.B.2
Van Harskamp, F.3
Stijnen, T.4
Hofman, A.5
-
9
-
-
0027534657
-
Vascular dementia: Diagnostic criteria for research studies: Report of the NINDS-AIREN International Workshop
-
Román GC, Tatemichi TK, Erkinjuntti T, Cummings JL, Masdeu JC, Garcia JH, et al. Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop. Neurology. 1993;43: 250-260. (Pubitemid 23060253)
-
(1993)
Neurology
, vol.43
, Issue.2
, pp. 250-260
-
-
Roman, G.C.1
Tatemichi, T.K.2
Erkinjuntti, T.3
Cummings, J.L.4
Masdeu, J.C.5
Garcia, J.H.6
Amaducci, L.7
Orgogozo, J.-M.8
Brun, A.9
Hofman, A.10
Moody, D.M.11
O'Brien, M.D.12
Yamaguchi, T.13
Grafman, J.14
Drayer, B.P.15
Bennett, D.A.16
Fisher, M.17
Ogata, J.18
Kokmen, E.19
-
10
-
-
65949090748
-
Genomewide association studies of stroke
-
Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, et al. Genomewide association studies of stroke. N Engl J Med. 2009;360:1718-1728.
-
(2009)
N Engl J Med
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
Seshadri, S.2
Bis, J.C.3
Fornage, M.4
Destefano, A.L.5
Aulchenko, Y.S.6
-
11
-
-
0024600723
-
Structural organization of the human androgen receptor gene
-
Kuiper GG, Faber PW, van Rooij HC, van der Korput JA, Ris-Stalpers C, Klaassen P, et al. Structural organization of the human androgen receptor gene. J Mol Endocrinol. 1989;2:R1-R4. (Pubitemid 19117460)
-
(1989)
Journal of Molecular Endocrinology
, vol.2
, Issue.3
-
-
Kuiper, G.G.J.M.1
Faber, P.W.2
Van Rooij, H.C.J.3
Van Der Korput, J.A.G.M.4
Ris-Stalpers, C.5
Klaassen, P.6
Trapman, J.7
Brinkmann, A.O.8
-
12
-
-
0029111987
-
Human androgen insensitivity syndrome
-
Brown TR. Human androgen insensitivity syndrome. J Androl. 1995;16: 299-303.
-
(1995)
J Androl
, vol.16
, pp. 299-303
-
-
Brown, T.R.1
-
13
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature. 1991;352:77-79. (Pubitemid 21896702)
-
(1991)
Nature
, vol.352
, Issue.6330
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
14
-
-
64149099061
-
Bulbar and spinal muscular atrophy (Kennedy's disease): A review
-
Finsterer J. Bulbar and spinal muscular atrophy (Kennedy's disease): A review. Eur J Neurol. 2009;16:556-561.
-
(2009)
Eur J Neurol
, vol.16
, pp. 556-561
-
-
Finsterer, J.1
-
15
-
-
74749106336
-
Are cognitive and behavioural deficits a part of the clinical picture in Kennedy's disease? A case study
-
Mirowska-Guzel D, Seniow J, Sułek A, Leśniak M, Członkowska A. Are cognitive and behavioural deficits a part of the clinical picture in Kennedy's disease? A case study. Neurocase. 2009;15:332-337.
-
(2009)
Neurocase
, vol.15
, pp. 332-337
-
-
Mirowska-Guzel, D.1
Seniow, J.2
Sułek, A.3
Leśniak, M.4
Członkowska, A.5
-
16
-
-
0142157544
-
Androgen receptor CAG repeat polymorphism is associated with cognitive function in older men
-
DOI 10.1016/S0006-3223(03)00115-X
-
Yaffe K, Edwards ER, Lui LY, Zmuda JM, Ferrell RE, Cauley JA. Androgen receptor CAG repeat polymorphism is associated with cognitive function in older men. Biol Psychiatry. 2003;54:943-946. (Pubitemid 37311358)
-
(2003)
Biological Psychiatry
, vol.54
, Issue.9
, pp. 943-946
-
-
Yaffe, K.1
Edwards, E.R.2
Lui, L.-Y.3
Zmuda, J.M.4
Ferrell, R.E.5
Cauley, J.A.6
-
17
-
-
0345268657
-
Association of the androgen receptor CAG repeat polymorphism with Alzheimer's disease in men
-
DOI 10.1016/S0304-3940(03)00069-7
-
Lehmann DJ, Butler HT, Warden DR, Combrinck M, King E, Nicoll JA, et al. Association of the androgen receptor CAG repeat polymorphism with Alzheimer's disease in men. Neurosci Lett. 2003;340:87-90. (Pubitemid 36369281)
-
(2003)
Neuroscience Letters
, vol.340
, Issue.2
, pp. 87-90
-
-
Lehmann, D.J.1
Butler, H.T.2
Warden, D.R.3
Combrinck, M.4
King, E.5
Nicoll, J.A.R.6
Budge, M.M.7
De Jager, C.A.8
Hogervorst, E.9
Esiri, M.M.10
Ragoussis, J.11
Smith, A.D.12
-
18
-
-
68949205721
-
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
-
Hillmer AM, Freudenberg J, Myles S, Herms S, Tang K, Hughes DA, et al. Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness. Hum Genet. 2009;126:255-264.
-
(2009)
Hum Genet
, vol.126
, pp. 255-264
-
-
Hillmer, A.M.1
Freudenberg, J.2
Myles, S.3
Herms, S.4
Tang, K.5
Hughes, D.A.6
-
19
-
-
79960123455
-
Cathepsin D gene and the risk of Alzheimer's disease: A population-based study and meta-analysis
-
Schuur M, Ikram MA, van Swieten JC, Isaacs A, Vergeer-Drop JM, Hofman A, et al. Cathepsin D gene and the risk of Alzheimer's disease: A population-based study and meta-analysis. Neurobiol Aging. 2011;32: 1607-1614.
-
(2011)
Neurobiol Aging
, vol.32
, pp. 1607-1614
-
-
Schuur, M.1
Ikram, M.A.2
Van Swieten, J.C.3
Isaacs, A.4
Vergeer-Drop, J.M.5
Hofman, A.6
-
20
-
-
12244264435
-
Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits
-
DOI 10.1093/bioinformatics/19.1.149
-
Purcell S, Cherny SS, Sham PC. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics. 2003;19:149-150. (Pubitemid 36150192)
-
(2003)
Bioinformatics
, vol.19
, Issue.1
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
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