-
1
-
-
0025989981
-
DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)
-
Bakker E, van Broeckhoven C, Haan J, Voorhoeve E, van Hul W, Levy E, et al. DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type) [see comments]. Am J Hum Genet 1991; 49: 518-21. Comment in: Am J Hum Genet 1991; 49: 507-10.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 518-521
-
-
Bakker, E.1
Van Broeckhoven, C.2
Haan, J.3
Voorhoeve, E.4
Van Hul, W.5
Levy, E.6
-
2
-
-
0026227840
-
-
Bakker E, van Broeckhoven C, Haan J, Voorhoeve E, van Hul W, Levy E, et al. DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type) [see comments]. Am J Hum Genet 1991; 49: 518-21. Comment in: Am J Hum Genet 1991; 49: 507-10.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 507-510
-
-
-
3
-
-
0027970941
-
Are patients with Alzheimer's disease surviving longer in recent years?
-
Beard CM, Kokmen E, O'Brien PC, Kurland LT. Are patients with Alzheimer's disease surviving longer in recent years? Neurology 1994; 44: 1867-71.
-
(1994)
Neurology
, vol.44
, pp. 1867-1871
-
-
Beard, C.M.1
Kokmen, E.2
O'Brien, P.C.3
Kurland, L.T.4
-
4
-
-
0029894227
-
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I-A review of the clinical, radiologic and genetic aspects
-
Bornebroek M, Haan J, Maat-Schieman ML, Van Duinen SG, Roos RA. Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I-A review of the clinical, radiologic and genetic aspects. [Review]. Brain Pathol 1996a; 6: 111-4.
-
(1996)
Brain Pathol
, vol.6
, pp. 111-114
-
-
Bornebroek, M.1
Haan, J.2
Maat-Schieman, M.L.3
Van Duinen, S.G.4
Roos, R.A.5
-
5
-
-
0030064215
-
White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation
-
Bornebroek M, Haan J, van Buchem MA, Lanser JB, de Vries-v.d. Weerd MA, Zoeteweij M, et al. White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation. Arch Neurol 1996b; 53: 43-8.
-
(1996)
Arch Neurol
, vol.53
, pp. 43-48
-
-
Bornebroek, M.1
Haan, J.2
Van Buchem, M.A.3
Lanser, J.B.4
De Vries, V.D.5
Weerd, M.A.6
Zoeteweij, M.7
-
6
-
-
0030919727
-
Dutch hereditary cerebral amyloid angiopathy: Structural lesions and apolipoprotein E genotype
-
Bornebroek M, Haan J, van Duinen SG, Maat-Schieman MLC, van Buchem MA, Bakker E, et al. Dutch hereditary cerebral amyloid angiopathy: structural lesions and apolipoprotein E genotype. Ann Neurol 1997a; 41: 695-8.
-
(1997)
Ann Neurol
, vol.41
, pp. 695-698
-
-
Bornebroek, M.1
Haan, J.2
Van Duinen, S.G.3
Maat-Schieman, M.L.C.4
Van Buchem, M.A.5
Bakker, E.6
-
7
-
-
0030874252
-
Presenilin 1 polymorphism and hereditary cerebral hemorrhage with amyloidosis Dutch type
-
In press
-
Bornebroek M, Haan J, Backhovens H, Deutz P, van Buchem MA, van den Broeck M, et al. Presenilin 1 polymorphism and hereditary cerebral hemorrhage with amyloidosis Dutch type. Ann Neurol 1997b. In press.
-
(1997)
Ann Neurol
-
-
Bornebroek, M.1
Haan, J.2
Backhovens, H.3
Deutz, P.4
Van Buchem, M.A.5
Van Den Broeck, M.6
-
8
-
-
0028917187
-
Parents do matter: Genomic imprinting and parental sex effects in neurological disorders
-
Chatkupt S, Antonowicz M, Johnson WG. Parents do matter: genomic imprinting and parental sex effects in neurological disorders. [Review]. J Neurol Sci 1995; 130: 1-10.
-
(1995)
J Neurol Sci
, vol.130
, pp. 1-10
-
-
Chatkupt, S.1
Antonowicz, M.2
Johnson, W.G.3
-
9
-
-
0030016323
-
Increased risk of dementia in mothers of Alzheimer's disease cases: Evidence for maternal inheritance
-
Edland SD, Silverman JM, Peskind ER, Tsuang D, Wijsman E, Morris JC. Increased risk of dementia in mothers of Alzheimer's disease cases: evidence for maternal inheritance. Neurology 1996; 47: 254-6.
-
(1996)
Neurology
, vol.47
, pp. 254-256
-
-
Edland, S.D.1
Silverman, J.M.2
Peskind, E.R.3
Tsuang, D.4
Wijsman, E.5
Morris, J.C.6
-
10
-
-
0025939678
-
Codon 618 variant of Alzheimer amyloid gene associated with inherited cerebral hemorrhage
-
Fernandez-Madrid I, Levy E, Marder K, Frangione B. Codon 618 variant of Alzheimer amyloid gene associated with inherited cerebral hemorrhage. Ann Neurol 1991; 30: 730-3.
-
(1991)
Ann Neurol
, vol.30
, pp. 730-733
-
-
Fernandez-Madrid, I.1
Levy, E.2
Marder, K.3
Frangione, B.4
-
11
-
-
0025118660
-
Dementia in hereditary cerebral hemorrhage with amyloidosis -Dutch type
-
Haan J, Lanser JB, Zijderveld I, van der Does IG, Roos RA. Dementia in hereditary cerebral hemorrhage with amyloidosis -Dutch type. Arch Neurol 1990; 47: 965-7.
-
(1990)
Arch Neurol
, vol.47
, pp. 965-967
-
-
Haan, J.1
Lanser, J.B.2
Zijderveld, I.3
Van Der Does, I.G.4
Roos, R.A.5
-
12
-
-
0027080784
-
Progressive dementia, without cerebral hemorrhage, in a patient with hereditary cerebral amyloid angiopathy
-
Haan J, Bakker E, Jennekens-Schinkel A, Roos RA. Progressive dementia, without cerebral hemorrhage, in a patient with hereditary cerebral amyloid angiopathy. Clin Neurol Neurosurg 1992; 94: 317-8.
-
(1992)
Clin Neurol Neurosurg
, vol.94
, pp. 317-318
-
-
Haan, J.1
Bakker, E.2
Jennekens-Schinkel, A.3
Roos, R.A.4
-
13
-
-
0028170271
-
The apolipoprotein E ε4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations
-
Haan J, van Broeckhoven C, van Duijn CM, Voorhoeve E, van Harskamp F, van Swieten JC, et al. The apolipoprotein E ε4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations. Ann Neurol 1994; 36: 434-7.
-
(1994)
Ann Neurol
, vol.36
, pp. 434-437
-
-
Haan, J.1
Van Broeckhoven, C.2
Van Duijn, C.M.3
Voorhoeve, E.4
Van Harskamp, F.5
Van Swieten, J.C.6
-
14
-
-
0028095036
-
The neurogenetics genie: Testing for the Huntington's disease mutation
-
Hersch S, Jones R, Koroshetz W, Quaid K. The neurogenetics genie: testing for the Huntington's disease mutation. [Review]. Neurology 1994; 44: 1369-73.
-
(1994)
Neurology
, vol.44
, pp. 1369-1373
-
-
Hersch, S.1
Jones, R.2
Koroshetz, W.3
Quaid, K.4
-
15
-
-
0030000603
-
The consortium to establish a registry for Alzheimer's disease (CERAD). Part XIV: Demographic and clinical predictors of survival in patients with Alzheimer's disease
-
Heyman A, Peterson B, Fillenbaum G, Pieper C. The consortium to establish a registry for Alzheimer's disease (CERAD). Part XIV: demographic and clinical predictors of survival in patients with Alzheimer's disease. Neurology 1996; 46: 656-60.
-
(1996)
Neurology
, vol.46
, pp. 656-660
-
-
Heyman, A.1
Peterson, B.2
Fillenbaum, G.3
Pieper, C.4
-
16
-
-
0027421869
-
Trends in stroke risk factors in the United States
-
Higgins M, Thom T. Trends in stroke risk factors in the United States. Ann Epidemiol 1993; 3: 550-4.
-
(1993)
Ann Epidemiol
, vol.3
, pp. 550-554
-
-
Higgins, M.1
Thom, T.2
-
17
-
-
0028965063
-
Senile dementia-Alzheimer's type and estrogen
-
Honjo H, Tanaka K, Kashiwagi T, Urabe M, Okada H, Hayashi M, et al. Senile dementia-Alzheimer's type and estrogen. [Review]. Horm Metab Res 1995; 27: 204-7.
-
(1995)
Horm Metab Res
, vol.27
, pp. 204-207
-
-
Honjo, H.1
Tanaka, K.2
Kashiwagi, T.3
Urabe, M.4
Okada, H.5
Hayashi, M.6
-
18
-
-
0028342424
-
Estrogen regulates metabolism of Alzheimer amyloid beta precursor protein
-
Jaffe AB, Toran-Allerand CD, Greengard P, Gandy SE. Estrogen regulates metabolism of Alzheimer amyloid beta precursor protein. J Biol Chem 1994; 269: 13065-8.
-
(1994)
J Biol Chem
, vol.269
, pp. 13065-13068
-
-
Jaffe, A.B.1
Toran-Allerand, C.D.2
Greengard, P.3
Gandy, S.E.4
-
19
-
-
0023177469
-
Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage
-
Jensson O, Gudmundsson G, Arnason A, Blondal H, Petursdottir I, Thorsteinsson L, et al. Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage. Acta Neurol Scand 1987; 76: 102-14.
-
(1987)
Acta Neurol Scand
, vol.76
, pp. 102-114
-
-
Jensson, O.1
Gudmundsson, G.2
Arnason, A.3
Blondal, H.4
Petursdottir, I.5
Thorsteinsson, L.6
-
20
-
-
0025296269
-
Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type
-
Levy E, Carman MD, Fernandez-Madrid IJ, Power MD, Lieberburg I, van Duinen SG, et al. Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. Science 1990; 248: 1124-6.
-
(1990)
Science
, vol.248
, pp. 1124-1126
-
-
Levy, E.1
Carman, M.D.2
Fernandez-Madrid, I.J.3
Power, M.D.4
Lieberburg, I.5
Van Duinen, S.G.6
-
21
-
-
0023892051
-
Hereditary cerebral haemorrhage caused by cortical amyloid angiopathy
-
Luyendijk W, Bots GT, Vegter-van der Vlis M, Went LN, Frangione B. Hereditary cerebral haemorrhage caused by cortical amyloid angiopathy. J Neurol Sci 1988; 85: 267-80.
-
(1988)
J Neurol Sci
, vol.85
, pp. 267-280
-
-
Luyendijk, W.1
Bots, G.T.2
Vegter-van Der Vlis, M.3
Went, L.N.4
Frangione, B.5
-
22
-
-
0029927290
-
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II-A review of histopathological aspects
-
Maat-Schieman ML, van Duinen SG, Bornebroek M, Haan J, Roos RA. Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II-A review of histopathological aspects. [Review]. Brain Pathol 1996; 6: 115-20.
-
(1996)
Brain Pathol
, vol.6
, pp. 115-120
-
-
Maat-Schieman, M.L.1
Van Duinen, S.G.2
Bornebroek, M.3
Haan, J.4
Roos, R.A.5
-
23
-
-
0026720105
-
Trends in mortality, morbidity, and risk factor levels for stroke from 1960 through 1990. The Minnesota Heart Survey
-
McGovern PG, Burke GL, Sprafka JM, Xue S, Folsom AR, Blackburn H. Trends in mortality, morbidity, and risk factor levels for stroke from 1960 through 1990. The Minnesota Heart Survey. JAMA 1992; 268: 753-9.
-
(1992)
JAMA
, vol.268
, pp. 753-759
-
-
McGovern, P.G.1
Burke, G.L.2
Sprafka, J.M.3
Xue, S.4
Folsom, A.R.5
Blackburn, H.6
-
24
-
-
0027367513
-
Trends in survival of hospitalized stroke patients between 1970 and 198; The Minnesota heart survey
-
McGovern PG, Pankow JS, Burke GL, Shahar E, Sprafka JM, Folsom AR, et al. Trends in survival of hospitalized stroke patients between 1970 and 198; The Minnesota heart survey. Stroke 1993; 24: 1640-8.
-
(1993)
Stroke
, vol.24
, pp. 1640-1648
-
-
McGovern, P.G.1
Pankow, J.S.2
Burke, G.L.3
Shahar, E.4
Sprafka, J.M.5
Folsom, A.R.6
-
25
-
-
0027532222
-
Explanation for exclusive maternal origin for congenital form of myotonic dystrophy
-
Mulley JC, Staples A, Donnelly A, Gedeon AK, Hecht BK, Nicholson GA, et al. Explanation for exclusive maternal origin for congenital form of myotonic dystrophy [letter] [see comments]. Lancet 1993; 341: 236-7. Comment in: Lancet 1993; 341: 1159-60.
-
(1993)
Lancet
, vol.341
, pp. 236-237
-
-
Mulley, J.C.1
Staples, A.2
Donnelly, A.3
Gedeon, A.K.4
Hecht, B.K.5
Nicholson, G.A.6
-
26
-
-
0027158785
-
-
Mulley JC, Staples A, Donnelly A, Gedeon AK, Hecht BK, Nicholson GA, et al. Explanation for exclusive maternal origin for congenital form of myotonic dystrophy [letter] [see comments]. Lancet 1993; 341: 236-7. Comment in: Lancet 1993; 341: 1159-60.
-
(1993)
Lancet
, vol.341
, pp. 1159-1160
-
-
-
27
-
-
0025775450
-
Age at onset in Huntington's disease: Effect of line of inheritance and patient's sex
-
Roos RA, Vegter-van der Vlis M, Hermans J, Elshove HM, Moll AC, van de Kamp JJ, et al. Age at onset in Huntington's disease: effect of line of inheritance and patient's sex. J Med Genet 1991; 28: 515-9.
-
(1991)
J Med Genet
, vol.28
, pp. 515-519
-
-
Roos, R.A.1
Vegter-van Der Vlis, M.2
Hermans, J.3
Elshove, H.M.4
Moll, A.C.5
Van De Kamp, J.J.6
-
28
-
-
0028906528
-
Improved survival of stroke patients during the 1980s. The Minnesota Stroke Survey
-
Shahar E, McGovern PG, Sprafka JM, Pankow JS, Doliszny KM, Luepker RV, et al. Improved survival of stroke patients during the 1980s. The Minnesota Stroke Survey [see comments]. Stroke 1995; 26: 1-6. Comment in: Stroke 1995; 26: 1302.
-
(1995)
Stroke
, vol.26
, pp. 1-6
-
-
Shahar, E.1
McGovern, P.G.2
Sprafka, J.M.3
Pankow, J.S.4
Doliszny, K.M.5
Luepker, R.V.6
-
29
-
-
0029039017
-
-
Shahar E, McGovern PG, Sprafka JM, Pankow JS, Doliszny KM, Luepker RV, et al. Improved survival of stroke patients during the 1980s. The Minnesota Stroke Survey [see comments]. Stroke 1995; 26: 1-6. Comment in: Stroke 1995; 26: 1302.
-
(1995)
Stroke
, vol.26
, pp. 1302
-
-
-
30
-
-
0025369198
-
Amyloid β-protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)
-
van Broeckhoven C, Haan J, Bakker E, Hardy JA, van Hul W, Wehnert A, et al. Amyloid β-protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch). Science 1990; 248: 1120-2.
-
(1990)
Science
, vol.248
, pp. 1120-1122
-
-
Van Broeckhoven, C.1
Haan, J.2
Bakker, E.3
Hardy, J.A.4
Van Hul, W.5
Wehnert, A.6
-
31
-
-
0019979780
-
Familial cerebral amyloid angiopathy presenting recurrent cerebral haemorrhage
-
Wattendorff AR, Bots GT, Went LN, Endtz LJ. Familial cerebral amyloid angiopathy presenting recurrent cerebral haemorrhage. J Neurol Sci 1982; 55: 121-35.
-
(1982)
J Neurol Sci
, vol.55
, pp. 121-135
-
-
Wattendorff, A.R.1
Bots, G.T.2
Went, L.N.3
Endtz, L.J.4
-
32
-
-
0029039146
-
Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D) : Clinicopathological studies
-
Wattendorf AR, Frangione B, Luyendijk W, Bots GT. Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D) : clinicopathological studies. J Neurol Neurosurg Psychiatry 1995; 58: 699-705.
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.58
, pp. 699-705
-
-
Wattendorf, A.R.1
Frangione, B.2
Luyendijk, W.3
Bots, G.T.4
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