200 related articles for article (PubMed ID: 18325672)
41. Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7.
Furrer SA; Waldherr SM; Mohanachandran MS; Baughn TD; Nguyen KT; Sopher BL; Damian VA; Garden GA; La Spada AR
Hum Mol Genet; 2013 Mar; 22(5):890-903. PubMed ID: 23197655
[TBL] [Abstract][Full Text] [Related]
42. Massive CAG repeat expansion and somatic instability in maternally transmitted infantile spinocerebellar ataxia type 7.
Trang H; Stanley SY; Thorner P; Faghfoury H; Schulze A; Hawkins C; Pearson CE; Yoon G
JAMA Neurol; 2015 Feb; 72(2):219-23. PubMed ID: 25506882
[TBL] [Abstract][Full Text] [Related]
43. Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7.
Fusco AF; Pucci LA; Switonski PM; Biswas DD; McCall AL; Kahn AF; Dhindsa JS; Strickland LM; La Spada AR; ElMallah MK
Dis Model Mech; 2021 Jul; 14(7):. PubMed ID: 34160002
[TBL] [Abstract][Full Text] [Related]
44. Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Tezenas du Montcel S; Durr A; Bauer P; Figueroa KP; Ichikawa Y; Brussino A; Forlani S; Rakowicz M; Schöls L; Mariotti C; van de Warrenburg BP; Orsi L; Giunti P; Filla A; Szymanski S; Klockgether T; Berciano J; Pandolfo M; Boesch S; Melegh B; Timmann D; Mandich P; Camuzat A; ; ; Goto J; Ashizawa T; Cazeneuve C; Tsuji S; Pulst SM; Brusco A; Riess O; Brice A; Stevanin G
Brain; 2014 Sep; 137(Pt 9):2444-55. PubMed ID: 24972706
[TBL] [Abstract][Full Text] [Related]
45. Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
Mosemiller AK; Dalton JC; Day JW; Ranum LP
Cytogenet Genome Res; 2003; 100(1-4):175-83. PubMed ID: 14526178
[TBL] [Abstract][Full Text] [Related]
46. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
[TBL] [Abstract][Full Text] [Related]
47. Maculopathy and spinocerebellar ataxia type 1: a new association?
Lebranchu P; Le Meur G; Magot A; David A; Verny C; Weber M; Milea D
J Neuroophthalmol; 2013 Sep; 33(3):225-31. PubMed ID: 23584155
[TBL] [Abstract][Full Text] [Related]
48. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483
[TBL] [Abstract][Full Text] [Related]
49. Evidence for a common founder effect amongst South African and Zambian individuals with Spinocerebellar ataxia type 7.
Smith DC; Atadzhanov M; Mwaba M; Greenberg LJ
J Neurol Sci; 2015 Jul; 354(1-2):75-8. PubMed ID: 26003224
[TBL] [Abstract][Full Text] [Related]
50. Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.
Teive HA; Roa BB; Raskin S; Fang P; Arruda WO; Neto YC; Gao R; Werneck LC; Ashizawa T
Neurology; 2004 Oct; 63(8):1509-12. PubMed ID: 15505178
[TBL] [Abstract][Full Text] [Related]
51. Insights into the molecular basis of polyglutamine neurodegeneration from studies of a spinocerebellar ataxia type 7 mouse model.
Grote SK; La Spada AR
Cytogenet Genome Res; 2003; 100(1-4):164-74. PubMed ID: 14526177
[TBL] [Abstract][Full Text] [Related]
52. Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype.
Aleman TS; Cideciyan AV; Volpe NJ; Stevanin G; Brice A; Jacobson SG
Exp Eye Res; 2002 Jun; 74(6):737-45. PubMed ID: 12126946
[TBL] [Abstract][Full Text] [Related]
53. Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect.
Magaña JJ; Tapia-Guerrero YS; Velázquez-Pérez L; Cerecedo-Zapata CM; Maldonado-Rodríguez M; Jano-Ito JS; Leyva-García N; González-Piña R; Martínez-Cruz E; Hernández-Hernández O; Cisneros B
Clin Genet; 2014 Feb; 85(2):159-65. PubMed ID: 23368522
[TBL] [Abstract][Full Text] [Related]
54. [Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Liang XC; Tang JG
Zhonghua Yi Xue Za Zhi; 2006 Jul; 86(25):1755-8. PubMed ID: 17054842
[TBL] [Abstract][Full Text] [Related]
55. Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.
Choubtum L; Witoonpanich P; Hanchaiphiboolkul S; Bhidayasiri R; Jitkritsadakul O; Pongpakdee S; Wetchaphanphesat S; Boonkongchuen P; Pulkes T
BMC Neurol; 2015 Sep; 15():166. PubMed ID: 26374734
[TBL] [Abstract][Full Text] [Related]
56. Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.
Horton LC; Frosch MP; Vangel MG; Weigel-DiFranco C; Berson EL; Schmahmann JD
Cerebellum; 2013 Apr; 12(2):176-93. PubMed ID: 22915085
[TBL] [Abstract][Full Text] [Related]
57. Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations.
Gómez-Coello A; Valadez-Jiménez VM; Cisneros B; Carrillo-Mora P; Parra-Cárdenas M; Hernández-Hernández O; Magaña JJ
J Voice; 2017 Jan; 31(1):123.e1-123.e5. PubMed ID: 26992556
[TBL] [Abstract][Full Text] [Related]
58. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE
J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805
[TBL] [Abstract][Full Text] [Related]
59. Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.
Mittal U; Roy S; Jain S; Srivastava AK; Mukerji M
J Hum Genet; 2005; 50(3):155-157. PubMed ID: 15750685
[TBL] [Abstract][Full Text] [Related]
60. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Alonso E; Martínez-Ruano L; De Biase I; Mader C; Ochoa A; Yescas P; Gutiérrez R; White M; Ruano L; Fragoso-Benítez M; Ashizawa T; Bidichandani SI; Rasmussen A
Mov Disord; 2007 May; 22(7):1050-3. PubMed ID: 17427938
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
