-
1
-
-
84864749266
-
The incidence and prevalence of Huntington’s disease: A systematic review and meta-analysis
-
Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. The incidence and prevalence of Huntington’s disease: A systematic review and meta-analysis. Mov Disord. 2012;27(9): 1083-91.
-
(2012)
Mov Disord
, vol.27
, Issue.9
, pp. 1083-1091
-
-
Pringsheim, T.1
Wiltshire, K.2
Day, L.3
Dykeman, J.4
Steeves, T.5
Jette, N.6
-
2
-
-
0028715918
-
Huntington’s disease in Hong Kong Chinese: Epidemiology and clinical picture
-
Chang CM, Yu YL, Fong KY, Wong MT, Chan YW, Ng TH, et al. Huntington’s disease in Hong Kong Chinese: Epidemiology and clinical picture. Clinical and Experimental Neurology. 1994;31: 43-51.
-
(1994)
Clinical and Experimental Neurology
, vol.31
, pp. 43-51
-
-
Chang, C.M.1
Yu, Y.L.2
Fong, K.Y.3
Wong, M.T.4
Chan, Y.W.5
Ng, T.H.6
-
3
-
-
15844414681
-
Epidemiological and genetic studies of Huntington’s disease in the San-in area of Japan
-
Nakashima K, Watanabe Y, Kusumi M, Nanba E, Maeoka Y, Nakagawa M, et al. Epidemiological and genetic studies of Huntington’s disease in the San-in area of Japan. Neuroepidemiology. 1996;15: 126-31.
-
(1996)
Neuroepidemiology
, vol.15
, pp. 126-131
-
-
Nakashima, K.1
Watanabe, Y.2
Kusumi, M.3
Nanba, E.4
Maeoka, Y.5
Nakagawa, M.6
-
4
-
-
77957156210
-
Nationwide population-based epidemiologic study of Huntington’s Disease in Taiwan
-
Chen YY, Lai CH. Nationwide population-based epidemiologic study of Huntington’s Disease in Taiwan. Neuroepidemiology. 2010;35: 250-4.
-
(2010)
Neuroepidemiology
, vol.35
, pp. 250-254
-
-
Chen, Y.Y.1
Lai, C.H.2
-
5
-
-
79955758366
-
HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia
-
Warby SC, Visscher H, Collins JA, Doty CN, Carter C, Butland SL, et al. HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia. European Journal of Human Genetics: EJHG. 2011;19: 561-6.
-
(2011)
European Journal of Human Genetics: EJHG
, vol.19
, pp. 561-566
-
-
Warby, S.C.1
Visscher, H.2
Collins, J.A.3
Doty, C.N.4
Carter, C.5
Butland, S.L.6
-
6
-
-
0028316870
-
Aworldwide study of the Huntington’s disease mutation. The sensitivity and specificity of measuring CAG repeats
-
Kremer B, Goldberg P, Andrew SE, Theilmann J, Telenius H, Zeisler J, et al.Aworldwide study of the Huntington’s disease mutation. The sensitivity and specificity of measuring CAG repeats. N Engl J Med. 1994;330: 1401-6.
-
(1994)
N Engl J Med
, vol.330
, pp. 1401-1406
-
-
Kremer, B.1
Goldberg, P.2
Andrew, S.E.3
Theilmann, J.4
Telenius, H.5
Zeisler, J.6
-
7
-
-
79957748358
-
Milestones in huntington disease
-
Shoulson I, Young AB. Milestones in huntington disease.Mov Disord. 2011;26: 1127-33.
-
(2011)
Mov Disord.
, vol.26
, pp. 1127-1133
-
-
Shoulson, I.1
Young, A.B.2
-
8
-
-
84858074593
-
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
-
Lee JM, Ramos EM, Lee JH, Gillis T, Mysore JS, Hayden MR, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012;78: 690-5.
-
(2012)
Neurology
, vol.78
, pp. 690-695
-
-
Lee, J.M.1
Ramos, E.M.2
Lee, J.H.3
Gillis, T.4
Mysore, J.S.5
Hayden, M.R.6
-
9
-
-
78650031174
-
Huntington’s disease: From molecular pathogenesis to clinical treatment
-
Ross CA, Tabrizi SJ. Huntington’s disease: From molecular pathogenesis to clinical treatment. Lancet Neurology. 2011;10: 83-98.
-
(2011)
Lancet Neurology
, vol.10
, pp. 83-98
-
-
Ross, C.A.1
Tabrizi, S.J.2
-
10
-
-
0030691741
-
Epidemiological survey of moyamoya disease in Korea
-
Ikezaki K, Han DH, Kawano T, Inamura T, Fukui M. Epidemiological survey of moyamoya disease in Korea. Clin Neurol Neurosurg. 1997;99(Suppl 2): S6-10.
-
(1997)
Clin Neurol Neurosurg.
, vol.99
, pp. S6-10
-
-
Ikezaki, K.1
Han, D.H.2
Kawano, T.3
Inamura, T.4
Fukui, M.5
-
11
-
-
0034711708
-
Rate of functional decline in Huntington’s disease
-
Marder K, Zhao H, Myers RH, Cudkowicz M, Kayson E, Kieburtz K, et al. Rate of functional decline in Huntington’s disease. Huntington Study Group. Neurology. 2000;54: 452-8.
-
(2000)
Huntington Study Group. Neurology
, vol.54
, pp. 452-458
-
-
Marder, K.1
Zhao, H.2
Myers, R.H.3
Cudkowicz, M.4
Kayson, E.5
Kieburtz, K.6
-
12
-
-
85009332113
-
Unified Huntington’s Disease Rating Scale (UHDRS): Reliability and consistency. Huntington Study Group
-
Unified Huntington’s Disease Rating Scale (UHDRS): Reliability and consistency. Huntington Study Group. Mov Disord. 1996;11: 136-42.
-
(1996)
Mov Disord
, vol.11
, pp. 136-142
-
-
-
13
-
-
0026802299
-
Huntington’s disease in Chinese: Ahypothesis of its origin
-
Leung CM, Chan YW, Chang CM, Yu YL, Chen CN. Huntington’s disease in Chinese: Ahypothesis of its origin. Journal of Neurology, Neurosurgery, and Psychiatry. 1992;55: 681-4.
-
(1992)
Journal of Neurology, Neurosurgery, and Psychiatry
, vol.55
, pp. 681-684
-
-
Leung, C.M.1
Chan, Y.W.2
Chang, C.M.3
Yu, Y.L.4
Chen, C.N.5
-
14
-
-
0028073822
-
Late-onset. Huntington’s disease: A clinical and molecular study
-
James CM, Houlihan GD, Snell RG, Cheadle JP, Harper PS. Late-onset. Huntington’s disease: A clinical and molecular study. Age and Ageing. 1994;23: 445-8.
-
(1994)
Age and Ageing
, vol.23
, pp. 445-448
-
-
James, C.M.1
Houlihan, G.D.2
Snell, R.G.3
Cheadle, J.P.4
Harper, P.S.5
-
15
-
-
58149161719
-
Late onset Huntington Disease: Clinical and genetic characteristics of 34 cases
-
Lipe H, Bird T. Late onset Huntington Disease: Clinical and genetic characteristics of 34 cases. Journal of the Neurological Sciences. 2009;276: 159-62.
-
(2009)
Journal of the Neurological Sciences
, vol.276
, pp. 159-162
-
-
Lipe, H.1
Bird, T.2
-
16
-
-
33745174181
-
Clinical characteristics of childhood-onset (juvenile) Huntington disease: Report of 12 patients and review of the literature
-
Gonzalez-Alegre P, Afifi AK. Clinical characteristics of childhood-onset (juvenile) Huntington disease: Report of 12 patients and review of the literature. J Child Neurol. 2006;21: 223-9.
-
(2006)
J Child Neurol
, vol.21
, pp. 223-229
-
-
Gonzalez-Alegre, P.1
Afifi, A.K.2
-
17
-
-
33646457048
-
Clinical presentation of juvenile Huntington disease
-
Ruocco HH, Lopes-Cendes I, Laurito TL, Li LM, Cendes F. Clinical presentation of juvenile Huntington disease. Arquivos de neuro-psiquiatria. 2006;64: 5-9.
-
(2006)
Arquivos de neuro-psiquiatria
, vol.64
, pp. 5-9
-
-
Ruocco, H.H.1
Lopes-Cendes, I.2
Laurito, T.L.3
Li, L.M.4
Cendes, F.5
-
18
-
-
0034780024
-
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia
-
AlmqvistEW, Elterman DS, MacLeod PM, HaydenMR.High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia. Clinical Genetics. 2001;60: 198-205.
-
(2001)
Clinical Genetics
, vol.60
, pp. 198-205
-
-
Almqvist, E.W.1
Elterman, D.S.2
MacLeod, P.M.3
Hayden, M.R.4
-
19
-
-
14544284039
-
Incidence and mutation rates of Huntington’s disease in Spain: Experience 9 years of direct genetic testing
-
Ramos-Arroyo MA, Moreno S, Valiente A. Incidence and mutation rates of Huntington’s disease in Spain: Experience 9 years of direct genetic testing. Journal of Neurology, Neurosurgery, and Psychiatry. 2005;76: 337-42.
-
(2005)
Journal of Neurology, Neurosurgery, and Psychiatry
, vol.76
, pp. 337-342
-
-
Ramos-Arroyo, M.A.1
Moreno, S.2
Valiente, A.3
-
20
-
-
80054886149
-
Huntington’s disease in Greece: The experience of 14 years
-
Panas M, Karadima G, Vassos E, Kalfakis N, Kladi A, Christodoulou K, et al. Huntington’s disease in Greece: The experience of 14 years. Clinical Genetics. 2011;80: 586-90.
-
(2011)
Clinical Genetics
, vol.80
, pp. 586-590
-
-
Panas, M.1
Karadima, G.2
Vassos, E.3
Kalfakis, N.4
Kladi, A.5
Christodoulou, K.6
-
21
-
-
33644850408
-
Late-onset and typical Huntington disease families from Crete have distinct genetic origins
-
Kartsaki E, Spanaki C, Tzagournissakis M, Petsakou A, Moschonas N, Macdonald M, et al. Late-onset and typical Huntington disease families from Crete have distinct genetic origins. International Journal of Molecular Medicine. 2006;17: 335-46.
-
(2006)
International Journal of Molecular Medicine
, vol.17
, pp. 335-346
-
-
Kartsaki, E.1
Spanaki, C.2
Tzagournissakis, M.3
Petsakou, A.4
Moschonas, N.5
Macdonald, M.6
|