-
1
-
-
84871483440
-
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease
-
Agostinho L de A, Rocha CF, Medina-Acosta E, Barboza HN, et al. (2012). Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease. J. Hum. Genet. 57: 796-803.
-
(2012)
J. Hum. Genet.
, vol.57
, pp. 796-803
-
-
de Agostinho, L.A.1
Rocha, C.F.2
Medina-Acosta, E.3
Barboza, H.N.4
-
2
-
-
0038646365
-
DNA testing for Huntington disease in the Turkish population
-
Akbas F and Erginel-Unaltuna N (2003). DNA testing for Huntington disease in the Turkish population. Eur. Neurol. 50: 20-24.
-
(2003)
Eur. Neurol.
, vol.50
, pp. 20-24
-
-
Akbas, F.1
Erginel-Unaltuna, N.2
-
3
-
-
33846436448
-
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds
-
Andresen JM, Gayán J, Cherny SS, Brocklebank D, et al. (2007). Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. J. Med. Genet. 44: 44-50.
-
(2007)
J. Med. Genet.
, vol.44
, pp. 44-50
-
-
Andresen, J.M.1
Gayán, J.2
Cherny, S.S.3
Brocklebank, D.4
-
4
-
-
0027176364
-
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
-
Andrew SE, Goldberg YP, Kremer B, Telenius H, et al. (1993). The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nat. Genet. 4: 398-403.
-
(1993)
Nat. Genet.
, vol.4
, pp. 398-403
-
-
Andrew, S.E.1
Goldberg, Y.P.2
Kremer, B.3
Telenius, H.4
-
5
-
-
48649083048
-
Huntington's disease as caused by 34 CAG repeats
-
Andrich J, Arning L, Wieczorek S, Kraus PH, et al. (2008). Huntington's disease as caused by 34 CAG repeats. Mov. Disord. 23: 879-881.
-
(2008)
Mov. Disord.
, vol.23
, pp. 879-881
-
-
Andrich, J.1
Arning, L.2
Wieczorek, S.3
Kraus, P.H.4
-
6
-
-
84903019337
-
Huntington's chorea in Michigan. III. Clinical observations
-
Chandler JH, Reed TE and Dejong RN (1960). Huntington's chorea in Michigan. III. Clinical observations. Neurology 10: 148-153.
-
(1960)
Neurology
, vol.10
, pp. 148-153
-
-
Chandler, J.H.1
Reed, T.E.2
Dejong, R.N.3
-
7
-
-
18744410962
-
Ancient origin of the CAG expansion causing Huntington disease in a Spanish population
-
García-Planells J, Burguera JA, Solís P, Millán JM, et al. (2005). Ancient origin of the CAG expansion causing Huntington disease in a Spanish population. Hum. Mutat. 25: 453-459.
-
(2005)
Hum. Mutat.
, vol.25
, pp. 453-459
-
-
García-Planells, J.1
Burguera, J.A.2
Solís, P.3
Millán, J.M.4
-
8
-
-
45149107487
-
Mechanisms of neurodegeneration in Huntington's disease
-
Gil JM and Rego AC (2008). Mechanisms of neurodegeneration in Huntington's disease. Eur. J. Neurosci. 27: 2803-2820.
-
(2008)
Eur. J. Neurosci.
, vol.27
, pp. 2803-2820
-
-
Gil, J.M.1
Rego, A.C.2
-
9
-
-
0036730422
-
Genetic background of Huntington disease in Croatia: Molecular analysis of CAG, CCG, and Delta2642 (E2642del) polymorphisms
-
Hećimović S, Klepac N, Vlasić J, Vojta A, et al. (2002). Genetic background of Huntington disease in Croatia: Molecular analysis of CAG, CCG, and Delta2642 (E2642del) polymorphisms. Hum. Mutat. 20: 233.
-
(2002)
Hum. Mutat.
, vol.20
, pp. 233
-
-
Hećimović, S.1
Klepac, N.2
Vlasić, J.3
Vojta, A.4
-
10
-
-
0035164243
-
The molecular biology of Huntington's disease
-
Ho LW, Carmichael J, Swartz J, Wyttenbach A, et al. (2001). The molecular biology of Huntington's disease. Psychol. Med. 31: 3-14.
-
(2001)
Psychol. Med.
, vol.31
, pp. 3-14
-
-
Ho, L.W.1
Carmichael, J.2
Swartz, J.3
Wyttenbach, A.4
-
11
-
-
12344285383
-
Molecular analysis of the (CAG)n repeat causing Huntington's disease in 34 Iranian families
-
Hormozian F, Houshmand M, Sanati MH, Ghiasvand R, et al. (2004). Molecular analysis of the (CAG)n repeat causing Huntington's disease in 34 Iranian families. Indian J. Hum. Genet. 10: 53-58.
-
(2004)
Indian J. Hum. Genet.
, vol.10
, pp. 53-58
-
-
Hormozian, F.1
Houshmand, M.2
Sanati, M.H.3
Ghiasvand, R.4
-
12
-
-
33644850408
-
Late-onset and typical Huntington disease families from Crete have distinct genetic origins
-
Kartsaki E, Spanaki C, Tzagournissakis M, Petsakou A, et al. (2006). Late-onset and typical Huntington disease families from Crete have distinct genetic origins. Int. J. Mol. Med. 17: 335-346.
-
(2006)
Int. J. Mol. Med.
, vol.17
, pp. 335-346
-
-
Kartsaki, E.1
Spanaki, C.2
Tzagournissakis, M.3
Petsakou, A.4
-
13
-
-
33847694688
-
Autopsy-proven Huntington's disease with 29 trinucleotide repeats
-
Kenney C, Powell S and Jankovic J (2007). Autopsy-proven Huntington's disease with 29 trinucleotide repeats. Mov. Disord. 22: 127-130.
-
(2007)
Mov. Disord.
, vol.22
, pp. 127-130
-
-
Kenney, C.1
Powell, S.2
Jankovic, J.3
-
14
-
-
4444265332
-
Analysis of the IT15 gene in Huntington's disease families
-
Kutuev IA, Khusainova RI, Khidiyatova IM, Magzhanov RV, et al. (2004). Analysis of the IT15 gene in Huntington's disease families. Russian J. Genet. 40: 919-925.
-
(2004)
Russian J. Genet.
, vol.40
, pp. 919-925
-
-
Kutuev, I.A.1
Khusainova, R.I.2
Khidiyatova, I.M.3
Magzhanov, R.V.4
-
15
-
-
0034153618
-
Molecular diagnosis of Huntington disease in Brazilian patients
-
Lima E, Silva TC, Serra HG, Bertuzzo CS and Lopes-Cendes I (2000). Molecular diagnosis of Huntington disease in Brazilian patients. Arq. Neuropsiquiatr. 58: 11-17.
-
(2000)
Arq. Neuropsiquiatr.
, vol.58
, pp. 11-17
-
-
Lima, E.1
Silva, T.C.2
Serra, H.G.3
Bertuzzo, C.S.4
Lopes-Cendes, I.5
-
16
-
-
33746961204
-
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease
-
Metzger S, Bauer P, Tomiuk J, Laccone F, et al. (2006). Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease. Hum. Genet. 120: 285-292.
-
(2006)
Hum. Genet.
, vol.120
, pp. 285-292
-
-
Metzger, S.1
Bauer, P.2
Tomiuk, J.3
Laccone, F.4
-
17
-
-
24344482766
-
Juvenile onset Huntington disease resulting from a very large maternal expansion
-
Nahhas FA, Garbern J, Krajewski KM, Roa BB, et al. (2005). Juvenile onset Huntington disease resulting from a very large maternal expansion. Am. J. Med. Genet. A 137A: 328-331.
-
(2005)
Am. J. Med. Genet. A
, vol.137 A
, pp. 328-331
-
-
Nahhas, F.A.1
Garbern, J.2
Krajewski, K.M.3
Roa, B.B.4
-
18
-
-
0033812250
-
Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India
-
Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, et al. (2000). Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India. Eur. J. Hum. Genet. 8: 678-682.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 678-682
-
-
Pramanik, S.1
Basu, P.2
Gangopadhaya, P.K.3
Sinha, K.K.4
-
19
-
-
0034576049
-
Huntington disease: DNA analysis in Brazilian population
-
Raskin S, Allan N, Teive HA, Cardoso F, et al. (2000). Huntington disease: DNA analysis in Brazilian population. Arq. Neuropsiquiatr. 58: 977-985.
-
(2000)
Arq. Neuropsiquiatr.
, vol.58
, pp. 977-985
-
-
Raskin, S.1
Allan, N.2
Teive, H.A.3
Cardoso, F.4
-
20
-
-
0034045674
-
Family history and DNA analysis in patients with suspected Huntington's disease
-
Siesling S, Vegter-van de Vlis M, Losekoot M, Belfroid RD, et al. (2000). Family history and DNA analysis in patients with suspected Huntington's disease. J. Neurol. Neurosurg. Psychiatry 69: 54-59.
-
(2000)
J. Neurol. Neurosurg. Psychiatry
, vol.69
, pp. 54-59
-
-
Siesling, S.1
van de Vegter-Vlis, M.2
Losekoot, M.3
Belfroid, R.D.4
-
21
-
-
0028564730
-
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
-
Squitieri F, Andrew SE, Goldberg YP, Kremer B, et al. (1994). DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence. Hum. Mol. Genet. 3: 2103-2114.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 2103-2114
-
-
Squitieri, F.1
Andrew, S.E.2
Goldberg, Y.P.3
Kremer, B.4
-
22
-
-
0037819516
-
Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes
-
Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, et al. (2003). Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain 126: 1599-1603.
-
(2003)
Brain
, vol.126
, pp. 1599-1603
-
-
Stevanin, G.1
Fujigasaki, H.2
Lebre, A.S.3
Camuzat, A.4
-
23
-
-
33645970699
-
Intergeneration CAG expansion and contraction in a Chinese HD family
-
Tang Y, Wang Y, Yang P, Liu Y, et al. (2006). Intergeneration CAG expansion and contraction in a Chinese HD family. Am. J. Med. Genet. B Neuropsychiatr. Genet. 141B: 242-244.
-
(2006)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.141 B
, pp. 242-244
-
-
Tang, Y.1
Wang, Y.2
Yang, P.3
Liu, Y.4
-
24
-
-
4644293999
-
DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients
-
Wang CK, Wu YR, Hwu WL, Chen CM, et al. (2004). DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients. Eur. Neurol. 52: 96-100.
-
(2004)
Eur. Neurol.
, vol.52
, pp. 96-100
-
-
Wang, C.K.1
Wu, Y.R.2
Hwu, W.L.3
Chen, C.M.4
-
25
-
-
12144288251
-
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
-
Wexler NS, Lorimer J, Porter J, Gomez F, et al. (2004). Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proc. Natl. Acad. Sci. U. S. A. 101: 3498-3503.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 3498-3503
-
-
Wexler, N.S.1
Lorimer, J.2
Porter, J.3
Gomez, F.4
-
26
-
-
36348940966
-
Factors associated with HD CAG repeat instability in Huntington disease
-
Wheeler VC, Persichetti F, McNeil SM, Mysore JS, et al. (2007). Factors associated with HD CAG repeat instability in Huntington disease. J. Med. Genet. 44: 695-701.
-
(2007)
J. Med. Genet.
, vol.44
, pp. 695-701
-
-
Wheeler, V.C.1
Persichetti, F.2
McNeil, S.M.3
Mysore, J.S.4
|