-
1
-
-
0000293742
-
Uber eine eigenartige Erkrankurg der Hirnrinde
-
Translated by: Wilkins RH & Brody IA. Archives of Neurology, 1969; 21:109-110
-
Alzheimer A. (1970) Uber eine eigenartige Erkrankurg der Hirnrinde (Translated by: Wilkins RH & Brody IA. Archives of Neurology, 1969; 21:109-110). Allgemeine Zeitschrift für Psychiatrie und Psychisch-Gerichtlich Medicin, 64:146-148
-
(1970)
Allgemeine Zeitschrift für Psychiatrie und Psychisch-Gerichtlich Medicin
, vol.64
, pp. 146-148
-
-
Alzheimer, A.1
-
3
-
-
0027961102
-
Reliability and validity of NINCDS-ADRDA criteria for Alzheimer's disease
-
Blacker D, Albert MS, Bassett SS, Go RCP, Harrell LE, Folstein MF (1994) Reliability and validity of NINCDS-ADRDA criteria for Alzheimer's disease. Archives of Neurology 51:1198-1204
-
(1994)
Archives of Neurology
, vol.51
, pp. 1198-1204
-
-
Blacker, D.1
Albert, M.S.2
Bassett, S.S.3
Go, R.C.P.4
Harrell, L.E.5
Folstein, M.F.6
-
4
-
-
0014313861
-
The association between quantitative measures of dementia and of senile change in the cerebral grey matter of elderly subjects
-
Blessed G, Tomlinson B, Roth M (1968) The association between quantitative measures of dementia and of senile change in the cerebral grey matter of elderly subjects. British Journal of Psychiatry 114:797-811
-
(1968)
British Journal of Psychiatry
, vol.114
, pp. 797-811
-
-
Blessed, G.1
Tomlinson, B.2
Roth, M.3
-
5
-
-
0017133142
-
Neurotransmitter-related enzymes and indices of hypoxia in senile dementia and other abiotrophies
-
Bowen DM, Smith CB, White P, Davison AN (1976) Neurotransmitter-related enzymes and indices of hypoxia in senile dementia and other abiotrophies. Brain 99:459-496
-
(1976)
Brain
, vol.99
, pp. 459-496
-
-
Bowen, D.M.1
Smith, C.B.2
White, P.3
Davison, A.N.4
-
6
-
-
0026075602
-
Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene
-
Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J (1991) Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene. Nature 353:844-846
-
(1991)
Nature
, vol.353
, pp. 844-846
-
-
Chartier-Harlin, M.C.1
Crawford, F.2
Houlden, H.3
Warren, A.4
Hughes, D.5
Fidani, L.6
Goate, A.7
Rossor, M.8
Roques, P.9
Hardy, J.10
-
7
-
-
0029813255
-
The presenilin genes: A new gene family involved in Alzheimer disease pathology
-
in press
-
Cruts M, Hendriks L, Van Broeckhoven C (1996) The presenilin genes: a new gene family involved in Alzheimer disease pathology. Human Molecular Genetics, in press
-
(1996)
Human Molecular Genetics
-
-
Cruts, M.1
Hendriks, L.2
Van Broeckhoven, C.3
-
8
-
-
0030582181
-
Visualisation and quantification of rates of atrophy in Alzheimer's disease
-
Fox NC, Freeborough PA, Rossor MN (1996a) Visualisation and quantification of rates of atrophy in Alzheimer's disease. Lancet 348:94-97
-
(1996)
Lancet
, vol.348
, pp. 94-97
-
-
Fox, N.C.1
Freeborough, P.A.2
Rossor, M.N.3
-
9
-
-
0011434164
-
Clinicopathological features of early onset Familial Alzheimer's Disease associated with the M139V mutation in the Presenilin I gene
-
in press
-
Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques P, Collinge J, Hardy J, Hutton M, Stevens JM, Warrington EK, Rossor MN (1996b) Clinicopathological features of early onset Familial Alzheimer's Disease associated with the M139V mutation in the Presenilin I gene. Brain: in press
-
(1996)
Brain
-
-
Fox, N.C.1
Kennedy, A.M.2
Harvey, R.J.3
Lantos, P.L.4
Roques, P.5
Collinge, J.6
Hardy, J.7
Hutton, M.8
Stevens, J.M.9
Warrington, E.K.10
Rossor, M.N.11
-
10
-
-
0011429934
-
Presymptomatic Hippocampal Atrophy in Familial Alzheimer's Disease: A Longitidinal MRI Study of a family with an amyloid precursor protein 717 val->gly mutation
-
in press
-
Fox NC, Warrington EK, Hartikainen P, Kennedy AM, Stevens J, Freeborough P, Rossor MN (1996c) Presymptomatic Hippocampal Atrophy in Familial Alzheimer's Disease: A Longitidinal MRI Study of a family with an amyloid precursor protein 717 val->gly mutation. Brain: in press
-
(1996)
Brain
-
-
Fox, N.C.1
Warrington, E.K.2
Hartikainen, P.3
Kennedy, A.M.4
Stevens, J.5
Freeborough, P.6
Rossor, M.N.7
-
11
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A, Chartier Harlin M, Mullan M, Brown J, Crawford F, Fidani L, Guiffra L, Haynes A, Irving N, James L, Mant R, Newton P, Rooke K, Roques P, Talbot C, Pericak Vance M, Roses A, Williamson R, Rossor M, Owen M, Hardy J (1991) Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349:704-706
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.1
Chartier Harlin, M.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fidani, L.6
Guiffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak Vance, M.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.21
more..
-
12
-
-
0029960873
-
Identification of famous faces and famous names in early Alzheimer's disease. Relationship to anterograde episodic and general semantic memory
-
Greene JD, Hodges JR (1996) Identification of famous faces and famous names in early Alzheimer's disease. Relationship to anterograde episodic and general semantic memory. Brain 119:111-128
-
(1996)
Brain
, vol.119
, pp. 111-128
-
-
Greene, J.D.1
Hodges, J.R.2
-
13
-
-
0029591413
-
Autobiographical memory and executive function in early dementia of Alzheimer type
-
Greene JDW, Hodges JR, Baddeley AD (1995) Autobiographical memory and executive function in early dementia of Alzheimer type. Neuropsychologia 33:1647-1670
-
(1995)
Neuropsychologia
, vol.33
, pp. 1647-1670
-
-
Greene, J.D.W.1
Hodges, J.R.2
Baddeley, A.D.3
-
14
-
-
0028067657
-
Chromosome 14-encoded Alzheimer's disease: Genetic and Clinicopathological description
-
Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Poyhonen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R (1994) Chromosome 14-encoded Alzheimer's disease: genetic and Clinicopathological description. Annals of Neurology 36:362-367
-
(1994)
Annals of Neurology
, vol.36
, pp. 362-367
-
-
Haltia, M.1
Viitanen, M.2
Sulkava, R.3
Ala-Hurula, V.4
Poyhonen, M.5
Goldfarb, L.6
Brown, P.7
Levy, E.8
Houlden, H.9
Crook, R.10
-
15
-
-
0025061059
-
The Lewy body variant of Alzheimer's disease - A clinical and pathological entity
-
Hansen L, Salmon D, Galasko D, Masliah E, Katzman R, DeTeresa R, Thal L, Pay MM, Hofstetter R, Klauber M, Rice V, Butters N, Alford M (1990) The Lewy body variant of Alzheimer's disease - a clinical and pathological entity. Neurology 40:1-8
-
(1990)
Neurology
, vol.40
, pp. 1-8
-
-
Hansen, L.1
Salmon, D.2
Galasko, D.3
Masliah, E.4
Katzman, R.5
DeTeresa, R.6
Thal, L.7
Pay, M.M.8
Hofstetter, R.9
Klauber, M.10
Rice, V.11
Butters, N.12
Alford, M.13
-
16
-
-
0029044162
-
Does early onset Alzheimer disease constitute a distinct subtype? The contribution of molecular genetics
-
Harvey RJ, Rossor MN. Does early onset Alzheimer disease constitute a distinct subtype? The contribution of molecular genetics. Alzheimer disease & Associated Disorders 9 (Suppl 1):7-13
-
Alzheimer Disease & Associated Disorders
, vol.9
, Issue.SUPPL. 1
, pp. 7-13
-
-
Harvey, R.J.1
Rossor, M.N.2
-
17
-
-
0026597219
-
MR-based hippocampal volumetry in the diagnosis of Alzheimer's disease
-
Jack CR, Petersen RC, O'Brien PC, Tangalos EG (1992) MR-based hippocampal volumetry in the diagnosis of Alzheimer's disease. Neurology, 42:183-188
-
(1992)
Neurology
, vol.42
, pp. 183-188
-
-
Jack, C.R.1
Petersen, R.C.2
O'Brien, P.C.3
Tangalos, E.G.4
-
19
-
-
0025299234
-
Alzheimer's disease. Age at onset and Single Photon Emission Computed Tomographic patterns of regional cerebral blood flow
-
Jagust WJ, Reed B, Seab P, Budinger T (1990b) Alzheimer's disease. Age at onset and Single Photon Emission Computed Tomographic patterns of regional cerebral blood flow. Archives of Neurology 47:628-633
-
(1990)
Archives of Neurology
, vol.47
, pp. 628-633
-
-
Jagust, W.J.1
Reed, B.2
Seab, P.3
Budinger, T.4
-
20
-
-
0028921599
-
Increased cerebrospinal fluid tau in patients with Alzheimer's disease
-
Jensen M, Basun H, Lannfelt L (1995) Increased cerebrospinal fluid tau in patients with Alzheimer's disease. Neurosci Lett 186:189-191
-
(1995)
Neurosci Lett
, vol.186
, pp. 189-191
-
-
Jensen, M.1
Basun, H.2
Lannfelt, L.3
-
21
-
-
0026469523
-
Detection in life of confirmed Alzheimer's disease using a simple measurement of medial temporal lobe atrophy by computed tomography
-
Jobst KA, Smith AD, Szatmari M, Molyneux A, Esiri ME, King E, Smith A, Jaskowski A, McDonald B, Wald N (1992) Detection in life of confirmed Alzheimer's disease using a simple measurement of medial temporal lobe atrophy by computed tomography. Lancet 340:1179-1183
-
(1992)
Lancet
, vol.340
, pp. 1179-1183
-
-
Jobst, K.A.1
Smith, A.D.2
Szatmari, M.3
Molyneux, A.4
Esiri, M.E.5
King, E.6
Smith, A.7
Jaskowski, A.8
McDonald, B.9
Wald, N.10
-
22
-
-
0028796841
-
Deficits in cerebral glucose metabolism demonstrated by positron emission tomography in individuals at risk of familial Alzheimer's disease
-
Kennedy AM, Frackowiak RSJ, Newman SK, Bloomfield PM, Seaward J, Roques P, Lewington G, Cunningham VJ, Rossor MN (1995a) Deficits in cerebral glucose metabolism demonstrated by positron emission tomography in individuals at risk of familial Alzheimer's disease. Neurosci Lett 186:17-20
-
(1995)
Neurosci Lett
, vol.186
, pp. 17-20
-
-
Kennedy, A.M.1
Frackowiak, R.S.J.2
Newman, S.K.3
Bloomfield, P.M.4
Seaward, J.5
Roques, P.6
Lewington, G.7
Cunningham, V.J.8
Rossor, M.N.9
-
23
-
-
0028910851
-
Chromosome 14 linked familial Alzheimer's disease: A clinico-pathological study of a single pedigree
-
Kennedy AM, Newman SK, Frackowiak RSJ, Cunningham VJ, Roques P, Stevens J, Neary D, Bruton CJ, Warrington EK, Rossor MN (1995b) Chromosome 14 linked familial Alzheimer's disease: A clinico-pathological study of a single pedigree. Brain 118:185-205
-
(1995)
Brain
, vol.118
, pp. 185-205
-
-
Kennedy, A.M.1
Newman, S.K.2
Frackowiak, R.S.J.3
Cunningham, V.J.4
Roques, P.5
Stevens, J.6
Neary, D.7
Bruton, C.J.8
Warrington, E.K.9
Rossor, M.N.10
-
24
-
-
0028971443
-
Amyloid beta-peptide in cerebrospinal fluid in individuals with the Swedish Alzheimer amyloid precursor protein mutation
-
Lannfelt L, Basun H, Vigo Pelfrey C, Wahlund LO, Winblad B, Lieberburg I, Schenk D (1995) Amyloid beta-peptide in cerebrospinal fluid in individuals with the Swedish Alzheimer amyloid precursor protein mutation. Neurosci Lett 199:203-206
-
(1995)
Neurosci Lett
, vol.199
, pp. 203-206
-
-
Lannfelt, L.1
Basun, H.2
Vigo Pelfrey, C.3
Wahlund, L.O.4
Winblad, B.5
Lieberburg, I.6
Schenk, D.7
-
25
-
-
0029087026
-
Candidate gene for the chromosome I familial Alzheimer's disease locus
-
Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WIJ, Yu C, Jondro PD, Schmidt SD, Wang K, Crowley AC, Fu Y, Guenette SY, Galas D, Nemens E, Wijsman EM, Bird TD, Schellenberg GD, Tanzi RE (1995) Candidate gene for the chromosome I familial Alzheimer's disease locus. Science 269:973-977
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
Pettingell, W.I.J.6
Yu, C.7
Jondro, P.D.8
Schmidt, S.D.9
Wang, K.10
Crowley, A.C.11
Fu, Y.12
Guenette, S.Y.13
Galas, D.14
Nemens, E.15
Wijsman, E.M.16
Bird, T.D.17
Schellenberg, G.D.18
Tanzi, R.E.19
-
27
-
-
0021882237
-
Heterogeneity in dementia of the Alzheimer type. Evidence of subgroups
-
Mayeux R, Stern Y, Spanton S (1985) Heterogeneity in dementia of the Alzheimer type. Evidence of subgroups. Neurology 35:453-460
-
(1985)
Neurology
, vol.35
, pp. 453-460
-
-
Mayeux, R.1
Stern, Y.2
Spanton, S.3
-
28
-
-
0021271971
-
Clinical diagnosis of Alzheimer's Disease: Report of the NINCDS-ADRDA work group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
-
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM (1984) Clinical diagnosis of Alzheimer's Disease: Report of the NINCDS-ADRDA work group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 34:939-944
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
29
-
-
0024411917
-
Clinical and pathological aspects of Parkinsonism in Alzheimer's Disease. A role for extranigral factors?
-
Morris JC, Drazner M, Fulling K, Grant EA, Goldring J (1989) Clinical and pathological aspects of Parkinsonism in Alzheimer's Disease. A role for extranigral factors? Archives of Neurology 46:651-657
-
(1989)
Archives of Neurology
, vol.46
, pp. 651-657
-
-
Morris, J.C.1
Drazner, M.2
Fulling, K.3
Grant, E.A.4
Goldring, J.5
-
30
-
-
0026907151
-
A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid
-
Mullan M, Crawford F, Axelman K, Houlden H, Lilius L, Winblad B, Lannfelt L (1992) A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. Nature Genetics 1:345-347
-
(1992)
Nature Genetics
, vol.1
, pp. 345-347
-
-
Mullan, M.1
Crawford, F.2
Axelman, K.3
Houlden, H.4
Lilius, L.5
Winblad, B.6
Lannfelt, L.7
-
31
-
-
0027426406
-
Age-of-onset in familial early-onset Alzheimer's disease correlates with genetic etiology
-
Mullan M, Houlden H, Crawford F, Kennedy A, Roques P, Rossor M (1993) Age-of-onset in familial early-onset Alzheimer's disease correlates with genetic etiology. American Journal of Medical Genetics 48:129-130
-
(1993)
American Journal of Medical Genetics
, vol.48
, pp. 129-130
-
-
Mullan, M.1
Houlden, H.2
Crawford, F.3
Kennedy, A.4
Roques, P.5
Rossor, M.6
-
33
-
-
0021267015
-
Neurochemical characteristics of early and late onset types of Alzheimer's disease
-
Rossor MN, Iversen LL, Reynolds GP, Mountjoy CQ, Roth M (1984) Neurochemical characteristics of early and late onset types of Alzheimer's disease. British Medical Journal 288:961-964
-
(1984)
British Medical Journal
, vol.288
, pp. 961-964
-
-
Rossor, M.N.1
Iversen, L.L.2
Reynolds, G.P.3
Mountjoy, C.Q.4
Roth, M.5
-
34
-
-
0029899593
-
Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation [16]
-
Rossor MN, Fox NC, Beck J, Campbell TC, Collinge J (1966) Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation [16]. Lancet 347:1560
-
(1966)
Lancet
, vol.347
, pp. 1560
-
-
Rossor, M.N.1
Fox, N.C.2
Beck, J.3
Campbell, T.C.4
Collinge, J.5
-
35
-
-
0026471656
-
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14
-
Schellenberg GD, Bird TD, Wijsman EM, Orr HT, Anderson L, Nemens E, White JA, Bonnycastle L, Weber JL, Alonso MF, Potter H, Heston LL, Martin GM (1992) Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14. Science 258:668-671
-
(1992)
Science
, vol.258
, pp. 668-671
-
-
Schellenberg, G.D.1
Bird, T.D.2
Wijsman, E.M.3
Orr, H.T.4
Anderson, L.5
Nemens, E.6
White, J.A.7
Bonnycastle, L.8
Weber, J.L.9
Alonso, M.F.10
Potter, H.11
Heston, L.L.12
Martin, G.M.13
-
36
-
-
0029004341
-
Cloning of a gene bearing mis-sense mutations in early-onset familial Alzheimer's disease
-
Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, Chi H, Lin C, Li G, Holman K, Tsuda T, Mar L, Foncin J-F, Bruni AC, Montesi MP, Sorbi S, Rainero I, Pinessi L, Nee L, Chumakov I, Pollen D, Borrkes A, Sanseau P, Polinsky RJ, Wasco W, Da Silva HAR, Haines JL, Pericak-Vance MA, Tanzi RE, Roses AD, Fraser PE, Rommens JM, St George-Hyslop PH (1995) Cloning of a gene bearing mis-sense mutations in early-onset familial Alzheimer's disease. Nature 375:754-760
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Li, G.9
Holman, K.10
Tsuda, T.11
Mar, L.12
Foncin, J.-F.13
Bruni, A.C.14
Montesi, M.P.15
Sorbi, S.16
Rainero, I.17
Pinessi, L.18
Nee, L.19
Chumakov, I.20
Pollen, D.21
Borrkes, A.22
Sanseau, P.23
Polinsky, R.J.24
Wasco, W.25
Da Silva, H.A.R.26
Haines, J.L.27
Pericak-Vance, M.A.28
Tanzi, R.E.29
Roses, A.D.30
Fraser, P.E.31
Rommens, J.M.32
St George-Hyslop, P.H.33
more..
-
37
-
-
8944241774
-
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant
-
Sherrington R, Froelich S, Sorbi S, Campion D, Chi JI, Rogaeva EA, Levesque G, Rogaev EI, Lin C, Liang Y, Ikeda M, Mar L, Brice A, Agid Y, Percy ML, ClergetDarpoux F, Piacentini S, Marcon G, Nacmius B, Amaducci L, Frèbourg T, Lannfelt L, Rommons JM, St George Hyslop PH (1996) Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. Human Molecular Genetics 5:985-988
-
(1996)
Human Molecular Genetics
, vol.5
, pp. 985-988
-
-
Sherrington, R.1
Froelich, S.2
Sorbi, S.3
Campion, D.4
Chi, J.I.5
Rogaeva, E.A.6
Levesque, G.7
Rogaev, E.I.8
Lin, C.9
Liang, Y.10
Ikeda, M.11
Mar, L.12
Brice, A.13
Agid, Y.14
Percy, M.L.15
ClergetDarpoux, F.16
Piacentini, S.17
Marcon, G.18
Nacmius, B.19
Amaducci, L.20
Frèbourg, T.21
Lannfelt, L.22
Rommons, J.M.23
St George Hyslop, P.H.24
more..
-
38
-
-
0028950856
-
Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer disease
-
Small GW, Mazziotta JC, Collins MT, Baxter LR, Phelps ME, Mandelkern MA, Kaplan A, La Rue A, Adamson CF, Chang L, Guze BH, Corder EH, Saunders AM, Haines JL, Pericak-Vance MA, Roses AD (1995) Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer disease. JAMA 273:942-947
-
(1995)
JAMA
, vol.273
, pp. 942-947
-
-
Small, G.W.1
Mazziotta, J.C.2
Collins, M.T.3
Baxter, L.R.4
Phelps, M.E.5
Mandelkern, M.A.6
Kaplan, A.7
La Rue, A.8
Adamson, C.F.9
Chang, L.10
Guze, B.H.11
Corder, E.H.12
Saunders, A.M.13
Haines, J.L.14
Pericak-Vance, M.A.15
Roses, A.D.16
-
39
-
-
0028821049
-
Decreased hippocampal volume asymmetry on MRIs in nondemented elderly subjects carrying the apolipoprotein E epsilon 4 allele
-
Soininen H, Partanen K, Pitkanen A, Hallikainen M, Hanninen T, Helisalmi S, Mannermaa A, Ryynanen M, Koivisto K, Riekkinen PS (1995) Decreased hippocampal volume asymmetry on MRIs in nondemented elderly subjects carrying the apolipoprotein E epsilon 4 allele. Neurology 45:391-392
-
(1995)
Neurology
, vol.45
, pp. 391-392
-
-
Soininen, H.1
Partanen, K.2
Pitkanen, A.3
Hallikainen, M.4
Hanninen, T.5
Helisalmi, S.6
Mannermaa, A.7
Ryynanen, M.8
Koivisto, K.9
Riekkinen, P.S.10
-
41
-
-
0025605245
-
Clinical and Positron Emission Tomographic studies in the 'Extrapyramidal Syndrome' of Dementia of the Alzheimer type
-
Tyrrell PJ, Sawle GV, Ibanez V, Bloomfield P, Leenders K, Frackowiak RSJ, Rossor MN (1990) Clinical and Positron Emission Tomographic studies in the 'Extrapyramidal Syndrome' of Dementia of the Alzheimer type. Archives of Neurology 47:1318-1323
-
(1990)
Archives of Neurology
, vol.47
, pp. 1318-1323
-
-
Tyrrell, P.J.1
Sawle, G.V.2
Ibanez, V.3
Bloomfield, P.4
Leenders, K.5
Frackowiak, R.S.J.6
Rossor, M.N.7
-
42
-
-
0017377714
-
Presenile dementia presenting as aphasia
-
Wechsler A (1977) Presenile dementia presenting as aphasia. J Neurol Neurosurg Psychiatry 40:303-305
-
(1977)
J Neurol Neurosurg Psychiatry
, vol.40
, pp. 303-305
-
-
Wechsler, A.1
|