-
1
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group.
-
Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Cell 1993;72:971-83.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
2
-
-
0027162192
-
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
-
Gispert S, Twells R, Orozco G, et al. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Nat Genet 1993;4:295-9.
-
(1993)
Nat Genet
, vol.4
, pp. 295-299
-
-
Gispert, S.1
Twells, R.2
Orozco, G.3
-
3
-
-
0025735626
-
Hereditary cerebral hemorrhage with amyloidosis-Dutch type: Its importance for Alzheimer research
-
Haan J, Hardy JA, Roos RA. Hereditary cerebral hemorrhage with amyloidosis-Dutch type: its importance for Alzheimer research. Trends Neurosci 1991;14:231-4.
-
(1991)
Trends Neurosci
, vol.14
, pp. 231-234
-
-
Haan, J.1
Hardy, J.A.2
Roos, R.A.3
-
5
-
-
0026584805
-
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
-
Buxton J, Shelbourne P, Davies J, et al. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature 1992;355:547-8.
-
(1992)
Nature
, vol.355
, pp. 547-548
-
-
Buxton, J.1
Shelbourne, P.2
Davies, J.3
-
6
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington R, Rogaev EI, Liang Y, et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 1995;375:754-60.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
-
7
-
-
0027759564
-
Characterization and localization of the Huntington disease gene product
-
Hoogeveen AT, Willemsen R, Meyer N, et al. Characterization and localization of the Huntington disease gene product. Hum Mol Genet 1993;2:2069-73.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2069-2073
-
-
Hoogeveen, A.T.1
Willemsen, R.2
Meyer, N.3
-
8
-
-
0026879650
-
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene
-
Hendriks L, van Duijn CM, Cras P, et al. Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene. Nat Genet 1992;1:218-21.
-
(1992)
Nat Genet
, vol.1
, pp. 218-221
-
-
Hendriks, L.1
Van Duijn, C.M.2
Cras, P.3
-
9
-
-
0019957017
-
Age at onset of Pick's and Alzheimer's dementia: Implications for diagnosis and research
-
Heston LL, Mastri AR. Age at onset of Pick's and Alzheimer's dementia: implications for diagnosis and research. J Gerontol 1982;37:422-4.
-
(1982)
J Gerontol
, vol.37
, pp. 422-424
-
-
Heston, L.L.1
Mastri, A.R.2
-
10
-
-
0023194309
-
Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis
-
Gustafson L. Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis. Arch Gerontol Geriatr 1987;6:209-23.
-
(1987)
Arch Gerontol Geriatr
, vol.6
, pp. 209-223
-
-
Gustafson, L.1
-
12
-
-
0027403451
-
Pick's disease versus Alzheimer's disease: A comparison of clinical characteristics
-
Mendez MF, Selwood A, Mastri AR, Frey W. Pick's disease versus Alzheimer's disease: a comparison of clinical characteristics. Neurology 1993;43:289-92.
-
(1993)
Neurology
, vol.43
, pp. 289-292
-
-
Mendez, M.F.1
Selwood, A.2
Mastri, A.R.3
Frey, W.4
-
13
-
-
0026832470
-
Huntington disease and the abuse of genetics
-
Harper PS. Huntington disease and the abuse of genetics. Am J Hum Genet 1992;50:460-4.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 460-464
-
-
Harper, P.S.1
-
14
-
-
0022879806
-
At risk person's attitude toward presymptomatic testing in Huntington disease
-
Markel DS, Young AB, Penney JB. At risk person's attitude toward presymptomatic testing in Huntington disease. Am J Med Genet 1987;26:295-305.
-
(1987)
Am J Med Genet
, vol.26
, pp. 295-305
-
-
Markel, D.S.1
Young, A.B.2
Penney, J.B.3
-
15
-
-
0022860048
-
Intended use of predictive testing by those at risk for Huntington disease
-
Meissen GJ, Berchek RL. Intended use of predictive testing by those at risk for Huntington disease. Am J Med Genet 1987;26:283-93.
-
(1987)
Am J Med Genet
, vol.26
, pp. 283-293
-
-
Meissen, G.J.1
Berchek, R.L.2
-
16
-
-
0022904060
-
Attitudes of persons at risk for Huntington disease toward predictive testing
-
Kessler S, Field T, Worth L, Mosbarger H. Attitudes of persons at risk for Huntington disease toward predictive testing. Am J Med Genet 1987;26:259-70.
-
(1987)
Am J Med Genet
, vol.26
, pp. 259-270
-
-
Kessler, S.1
Field, T.2
Worth, L.3
Mosbarger, H.4
-
17
-
-
0026682523
-
Huntington's disease and the ethics of genetic prediction
-
Terrenoire G. Huntington's disease and the ethics of genetic prediction. J Med Ethics 1992;18:79-85.
-
(1992)
J Med Ethics
, vol.18
, pp. 79-85
-
-
Terrenoire, G.1
|