-
1
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell. 1993;72:971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
3
-
-
0021845212
-
A genetic model for age at onset in Huntington disease
-
Farrer LA, Conneally PM. A genetic model for age at onset in Huntington disease. Am J Hum Genet. 1985;37:350-357.
-
(1985)
Am J Hum Genet
, vol.37
, pp. 350-357
-
-
Farrer, L.A.1
Conneally, P.M.2
-
4
-
-
15844374285
-
Genetic and pathogenetic implications of the age incidence of Huntington's chorea
-
Burch PRJ. Genetic and pathogenetic implications of the age incidence of Huntington's chorea. Adv Neurol. 1973;1:179-190.
-
(1973)
Adv Neurol
, vol.1
, pp. 179-190
-
-
Burch, P.R.J.1
-
5
-
-
0029006808
-
Cognitive scores of Huntington disease gene carriers as compared to non-gene carriers
-
Foroud T, Siemers E, Kleindorfer D, et al. Cognitive scores of Huntington disease gene carriers as compared to non-gene carriers. Ann Neurol. 1995;37:657-664.
-
(1995)
Ann Neurol
, vol.37
, pp. 657-664
-
-
Foroud, T.1
Siemers, E.2
Kleindorfer, D.3
-
6
-
-
0028893812
-
Longitudinal neuropsychological and genetic linkage analysis of persons at risk for Huntington's disease
-
Giordani B, Berent S, Boivin MJ, et al. Longitudinal neuropsychological and genetic linkage analysis of persons at risk for Huntington's disease. Arch Neurol. 1995;552:59-64.
-
(1995)
Arch Neurol
, vol.552
, pp. 59-64
-
-
Giordani, B.1
Berent, S.2
Boivin, M.J.3
-
7
-
-
0021073507
-
The measurement of abnormal movement: Methods developed for Huntington's disease
-
Folstein SE, Jensen B, Leigh RJ, Folstein MF, The measurement of abnormal movement: methods developed for Huntington's disease. Neurobehav Toxicol Teratol. 1983;5:605-609.
-
(1983)
Neurobehav Toxicol Teratol
, vol.5
, pp. 605-609
-
-
Folstein, S.E.1
Jensen, B.2
Leigh, R.J.3
Folstein, M.F.4
-
8
-
-
0025290717
-
Huntington's disease in Venezuela: 7 years of follow-up on symptomatic and asymptomatic individuals
-
Penny JB, Young BM, Shoulson I, et al. Huntington's disease in Venezuela: 7 years of follow-up on symptomatic and asymptomatic individuals. Mov Disord. 1990;5:93-99.
-
(1990)
Mov Disord
, vol.5
, pp. 93-99
-
-
Penny, J.B.1
Young, B.M.2
Shoulson, I.3
-
9
-
-
0027176364
-
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
-
Andrew SE, Goldberg YP, Kremer B, et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nat Genet. 1993;4:398-403.
-
(1993)
Nat Genet
, vol.4
, pp. 398-403
-
-
Andrew, S.E.1
Goldberg, Y.P.2
Kremer, B.3
-
10
-
-
0027261537
-
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
-
Snell RG, MacMillan JC, Cheadle JP, et al. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nat Genet 1993;4:393-397.
-
(1993)
Nat Genet
, vol.4
, pp. 393-397
-
-
Snell, R.G.1
MacMillan, J.C.2
Cheadle, J.P.3
-
11
-
-
0024315678
-
Improving the precision of biological age determinations, II: Automatic human tests, age norms and variability
-
Hochschild R. Improving the precision of biological age determinations, II: automatic human tests, age norms and variability. Exp Gerontol. 1989;24:301-316.
-
(1989)
Exp Gerontol
, vol.24
, pp. 301-316
-
-
Hochschild, R.1
-
13
-
-
0028365786
-
Reduced basal ganglia volume associated with the gene for Huntington's disease in asymptomatic at-risk persons
-
Aylward EH, Brandt J, Codori AM, et al. Reduced basal ganglia volume associated with the gene for Huntington's disease in asymptomatic at-risk persons. Neurology. 1994;44:823-828.
-
(1994)
Neurology
, vol.44
, pp. 823-828
-
-
Aylward, E.H.1
Brandt, J.2
Codori, A.M.3
-
14
-
-
0025009430
-
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease
-
Grafton ST, Mazziotta JC, Pahl JJ, et al. A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease. Ann Neurol. 1990;28:614-621.
-
(1990)
Ann Neurol
, vol.28
, pp. 614-621
-
-
Grafton, S.T.1
Mazziotta, J.C.2
Pahl, J.J.3
-
15
-
-
0027185096
-
Unimpaired verbal memory and oculomotor control in asymptomatic adults with the genetic marker for Huntington's disease
-
Rothlind JC, Brandt J, Zee D, et al. Unimpaired verbal memory and oculomotor control in asymptomatic adults with the genetic marker for Huntington's disease. Arch Neurol. 1993;50:799-802.
-
(1993)
Arch Neurol
, vol.50
, pp. 799-802
-
-
Rothlind, J.C.1
Brandt, J.2
Zee, D.3
-
16
-
-
14444279434
-
PET demonstrates a parallel loss of D1 and D2 dopamine receptors in asymptomatic gene carriers of Huntington's disease
-
Abstract
-
Weeks RA, Harding AE, Brooks DJ, PET demonstrates a parallel loss of D1 and D2 dopamine receptors in asymptomatic gene carriers of Huntington's disease. Neurology. 1995;45(suppl 4):A220. Abstract.
-
(1995)
Neurology
, vol.45
, Issue.4 SUPPL.
-
-
Weeks, R.A.1
Harding, A.E.2
Brooks, D.J.3
-
17
-
-
0027388933
-
Comparison of somatosensory evoked potentials with striatal glucose consumption measured by positron emission tomography in the early diagnosis of Huntington's disease
-
Kuwert T, Noth J, Scholz D, et al. Comparison of somatosensory evoked potentials with striatal glucose consumption measured by positron emission tomography in the early diagnosis of Huntington's disease. Mov Disord. 1993;8:98-106.
-
(1993)
Mov Disord
, vol.8
, pp. 98-106
-
-
Kuwert, T.1
Noth, J.2
Scholz, D.3
-
18
-
-
0023098788
-
Normal caudate glucose metabolism in persons at risk for Huntington's disease
-
Young AB, Penney JB, Starosta-Rubinstein S, et al. Normal caudate glucose metabolism in persons at risk for Huntington's disease. Arch Neurol. 1987; 44:254-257.
-
(1987)
Arch Neurol
, vol.44
, pp. 254-257
-
-
Young, A.B.1
Penney, J.B.2
Starosta-Rubinstein, S.3
-
19
-
-
0022620244
-
Huntington's disease in Venezuela: Neurologic features and functional decline
-
Young AB, Shoulson I, Penney JB, et al. Huntington's disease in Venezuela: neurologic features and functional decline. Neurology. 1986;36:244-249.
-
(1986)
Neurology
, vol.36
, pp. 244-249
-
-
Young, A.B.1
Shoulson, I.2
Penney, J.B.3
-
20
-
-
0026475301
-
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease
-
Grafton ST, Mazziotta JC, Pahl JJ, et al. Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease. Arch Neurol. 1992;49:1161-1167.
-
(1992)
Arch Neurol
, vol.49
, pp. 1161-1167
-
-
Grafton, S.T.1
Mazziotta, J.C.2
Pahl, J.J.3
-
21
-
-
0028099274
-
Trinucleotide repeat length and progression of illness in Huntington's disease
-
Kieburtz K, MacDonald M. Shin C, et al. Trinucleotide repeat length and progression of illness in Huntington's disease. J Med Genet. 1994;31:872-874.
-
(1994)
J Med Genet
, vol.31
, pp. 872-874
-
-
Kieburtz, K.1
MacDonald, M.2
Shin, C.3
|