These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 11346374)

  • 41. The clinical diagnosis of autosomal dominant spinocerebellar ataxias.
    Klockgether T
    Cerebellum; 2008; 7(2):101-5. PubMed ID: 18418679
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan.
    Hsieh M; Li SY; Tsai CJ; Chen YY; Liu CS; Chang CY; Ro LS; Chen DF; Chen SS; Li C
    Acta Neurol Scand; 1999 Sep; 100(3):189-94. PubMed ID: 10478584
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by "dual-fluorescence labeled PCR-restriction fragment length analysis".
    Lin JX; Ishikawa K; Sakamoto M; Tsunemi T; Ishiguro T; Amino T; Toru S; Kondo I; Mizusawa H
    J Hum Genet; 2008; 53(4):287-295. PubMed ID: 18301861
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.
    Lin Y; Zheng JY; Jin YH; Xie YC; Jin ZB
    Neurosci Lett; 2008 Mar; 434(2):230-3. PubMed ID: 18325672
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1.
    Platonov FA; Tyryshkin K; Tikhonov DG; Neustroyeva TS; Sivtseva TM; Yakovleva NV; Nikolaev VP; Sidorova OG; Kononova SK; Goldfarb LG; Renwick NM
    Neurogenetics; 2016 Jul; 17(3):179-85. PubMed ID: 27106293
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Detection Methods and Status of CAT Interruption of
    Jang JH; Yoon SJ; Kim SK; Cho JW; Kim JW
    Ann Lab Med; 2022 Mar; 42(2):274-277. PubMed ID: 34635619
    [TBL] [Abstract][Full Text] [Related]  

  • 47. An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia.
    Costanzi-Porrini S; Tessarolo D; Abbruzzese C; Liguori M; Ashizawa T; Giacanelli M
    Neurology; 2000 Jan; 54(2):491-3. PubMed ID: 10668721
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles.
    Zühlke C; Dalski A; Hellenbroich Y; Bubel S; Schwinger E; Bürk K
    Eur J Hum Genet; 2002 Mar; 10(3):204-9. PubMed ID: 11973625
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Jiang H; Tang BS; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
    Chin Med J (Engl); 2005 May; 118(10):837-43. PubMed ID: 15989765
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.
    Takano H; Cancel G; Ikeuchi T; Lorenzetti D; Mawad R; Stevanin G; Didierjean O; Dürr A; Oyake M; Shimohata T; Sasaki R; Koide R; Igarashi S; Hayashi S; Takiyama Y; Nishizawa M; Tanaka H; Zoghbi H; Brice A; Tsuji S
    Am J Hum Genet; 1998 Oct; 63(4):1060-6. PubMed ID: 9758625
    [TBL] [Abstract][Full Text] [Related]  

  • 51. SCA2 trinucleotide expansion in German SCA patients.
    Riess O; Laccone FA; Gispert S; Schöls L; Zühlke C; Vieira-Saecker AM; Herlt S; Wessel K; Epplen JT; Weber BH; Kreuz F; Chahrokh-Zadeh S; Meindl A; Lunkes A; Aguiar J; Macek M; Krebsová A; Macek M; Bürk K; Tinschert S; Schreyer I; Pulst SM; Auburger G
    Neurogenetics; 1997 May; 1(1):59-64. PubMed ID: 10735276
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The hereditary adult-onset ataxias in South Africa.
    Bryer A; Krause A; Bill P; Davids V; Bryant D; Butler J; Heckmann J; Ramesar R; Greenberg J
    J Neurol Sci; 2003 Dec; 216(1):47-54. PubMed ID: 14607302
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Molecular and clinical study of spinocerebellar ataxia type 7 in Chinese kindreds.
    Gu W; Wang Y; Liu X; Zhou B; Zhou Y; Wang G
    Arch Neurol; 2000 Oct; 57(10):1513-8. PubMed ID: 11030806
    [TBL] [Abstract][Full Text] [Related]  

  • 56. SCA1 molecular genetics: a history of a 13 year collaboration against glutamines.
    Orr HT; Zoghbi HY
    Hum Mol Genet; 2001 Oct; 10(20):2307-11. PubMed ID: 11673415
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J; Dalton A; Morrison PJ; Dodge A; Connarty M; Kotze MJ; Rubinsztein DC
    J Med Genet; 1997 Dec; 34(12):982-5. PubMed ID: 9429138
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.
    Juvonen V; Hietala M; Kairisto V; Savontaus ML
    Acta Neurol Scand; 2005 Mar; 111(3):154-62. PubMed ID: 15691283
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan.
    Mori M; Adachi Y; Kusumi M; Nakashima K
    Neuroepidemiology; 2001 May; 20(2):144-9. PubMed ID: 11359084
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 (SCA1) gene in schizophrenic patients.
    Pujana MA; Martorell L; Volpini V; Valero J; Labad A; Vilella E; Estivill X
    Hum Genet; 1997 Jun; 99(6):772-5. PubMed ID: 9187671
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.