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 *

170 related articles for article (PubMed ID: 26336829)

  • 21. Machado-Joseph disease: clinical, molecular, and metabolic characterization in Chinese kindreds.
    Soong B; Cheng C; Liu R; Shan D
    Ann Neurol; 1997 Apr; 41(4):446-52. PubMed ID: 9124801
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.
    Schöls L; Amoiridis G; Epplen JT; Langkafel M; Przuntek H; Riess O
    J Neurol Neurosurg Psychiatry; 1996 Nov; 61(5):466-70. PubMed ID: 8937340
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Investigation on modulation of DNA repair pathways in Chinese MJD patients.
    Wang C; Chen Z; Peng H; Peng Y; Zhou X; Yang H; Wang P; Li T; Hou X; Qiu R; Xia K; Sequeiros J; Tang B; Jiang H
    Neurobiol Aging; 2018 Nov; 71():267.e5-267.e6. PubMed ID: 30033072
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala.
    Martins S; Soong BW; Wong VC; Giunti P; Stevanin G; Ranum LP; Sasaki H; Riess O; Tsuji S; Coutinho P; Amorim A; Sequeiros J; Nicholson GA
    Arch Neurol; 2012 Jun; 69(6):746-51. PubMed ID: 22351852
    [TBL] [Abstract][Full Text] [Related]  

  • 25. CAG repeat expansion of Machado-Joseph disease in the Japanese: analysis of the repeat instability for parental transmission, and correlation with disease phenotype.
    Sasaki H; Wakisaka A; Fukazawa T; Iwabuchi K; Hamada T; Takada A; Mukai E; Matsuura T; Yoshiki T; Tashiro K
    J Neurol Sci; 1995 Nov; 133(1-2):128-33. PubMed ID: 8583215
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease.
    DeStefano AL; Cupples LA; Maciel P; Gaspar C; Radvany J; Dawson DM; Sudarsky L; Corwin L; Coutinho P; MacLeod P
    Am J Hum Genet; 1996 Jul; 59(1):119-27. PubMed ID: 8659514
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Correlation between CAG repeat length and clinical features in Machado-Joseph disease.
    Maciel P; Gaspar C; DeStefano AL; Silveira I; Coutinho P; Radvany J; Dawson DM; Sudarsky L; Guimarães J; Loureiro JE
    Am J Hum Genet; 1995 Jul; 57(1):54-61. PubMed ID: 7611296
    [TBL] [Abstract][Full Text] [Related]  

  • 28. New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3.
    Peng L; Chen Z; Long Z; Liu M; Lei L; Wang C; Peng H; Shi Y; Peng Y; Deng Q; Wang S; Zou G; Wan L; Yuan H; He L; Xie Y; Tang Z; Wan N; Gong Y; Hou X; Shen L; Xia K; Li J; Chen C; Qiu R; Klockgether T; Tang B; Jiang H
    Neurology; 2021 Jun; 96(23):e2885-e2895. PubMed ID: 33893204
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.
    França MC; Emmel VE; D'Abreu A; Maurer-Morelli CV; Secolin R; Bonadia LC; da Silva MS; Nucci A; Jardim LB; Saraiva-Pereira ML; Marques W; Paulson H; Lopes-Cendes I
    Front Neurol; 2012; 3():164. PubMed ID: 23181052
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Selective forces acting on spinocerebellar ataxia type 3/Machado-Joseph disease recurrency: A systematic review and meta-analysis.
    Sena LS; Dos Santos Pinheiro J; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2021 Mar; 99(3):347-358. PubMed ID: 33219521
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The (CAG)n tract of Machado-Joseph Disease gene (ATXN3): a comparison between DNA and mRNA in patients and controls.
    Bettencourt C; Santos C; Montiel R; Kay T; Vasconcelos J; Maciel P; Lima M
    Eur J Hum Genet; 2010 May; 18(5):621-3. PubMed ID: 19935829
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies.
    Mittal U; Srivastava AK; Jain S; Jain S; Mukerji M
    Arch Neurol; 2005 Apr; 62(4):637-40. PubMed ID: 15824265
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.
    Bettencourt C; Santos C; Coutinho P; Rizzu P; Vasconcelos J; Kay T; Cymbron T; Raposo M; Heutink P; Lima M
    BMC Neurol; 2011 Oct; 11():131. PubMed ID: 22023810
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mitochondrial DNA haplogroups and age at onset of Machado-Joseph disease/spinocerebellar ataxia type 3: a study in patients from multiple populations.
    Ramos A; Planchat M; Vieira Melo AR; Raposo M; Shamim U; Suroliya V; Srivastava AK; Faruq M; Morino H; Ohsawa R; Kawakami H; Bannach Jardim L; Saraiva-Pereira ML; Vasconcelos J; Santos C; Lima M
    Eur J Neurol; 2019 Mar; 26(3):506-512. PubMed ID: 30414314
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions.
    Souza GN; Kersting N; Krum-Santos AC; Santos AS; Furtado GV; Pacheco D; Gonçalves TA; Saute JA; Schuler-Faccini L; Mattos EP; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2016 Aug; 90(2):134-40. PubMed ID: 26693702
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract.
    Maciel P; Gaspar C; Guimarães L; Goto J; Lopes-Cendes I; Hayes S; Arvidsson K; Dias A; Sequeiros J; Sousa A; Rouleau GA
    Eur J Hum Genet; 1999; 7(2):147-56. PubMed ID: 10196697
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
    Wang YG; Du J; Wang JL; Chen J; Chen C; Luo YY; Xiao ZQ; Jiang H; Yan XX; Xia K; Pan Q; Tang BS; Shen L
    J Neurol Sci; 2009 Oct; 285(1-2):121-4. PubMed ID: 19608203
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case report.
    Zeng S; Zeng J; He M; Zeng X; Zhou Y; Liu Z; Jiang H; Tang B; Wang J
    J Hum Genet; 2015 Mar; 60(3):157-60. PubMed ID: 25566755
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spastic paraparesis as the first manifestation of Machado-Joseph disease: A case report and review of the literature.
    Lin HC; Chang YY; Chang KH; Chen YF; Lan MY
    Clin Neurol Neurosurg; 2018 Sep; 172():137-140. PubMed ID: 30007589
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Maternal anticipation in Machado-Joseph disease (MJD): some maternal factors independent of the number of CAG repeat units may play a role in genetic anticipation in a Japanese MJD family.
    Takiyama Y; Shimazaki H; Morita M; Soutome M; Sakoe K; Esumi E; Muramatsu S; Yoshida M; Igarashi S; Tanaka H; Tsuji S; Sasaki H; Wakisaka A; Nakano I; Nishizawa M
    J Neurol Sci; 1998 Mar; 155(2):141-5. PubMed ID: 9562258
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.