BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

382 related articles for article (PubMed ID: 16824032)

  • 1. Advances in Huntington's disease diagnostics: development of a standard reference material.
    Levin BC; Richie KL; Jakupciak JP
    Expert Rev Mol Diagn; 2006 Jul; 6(4):587-96. PubMed ID: 16824032
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular genetics of Huntington's disease].
    Goto J; Masuda N; Watanabe M; Kanazawa I
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Importance of the number of trinucleotide repeat expansions in the clinical manifestations of Huntington's chorea].
    Vojvodić N; Culjković B; Romac S; Stojković O; Sternić N; Sokić D; Kostić VS
    Srp Arh Celok Lek; 1998; 126(3-4):77-82. PubMed ID: 9863360
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects].
    Illarioshkin SN; Ivanova-Smolenskaia IA; Markova ED; Nikol'skaia NN; Chabrashvili TZ; Insarova NG
    Genetika; 1996 Jan; 32(1):103-9. PubMed ID: 8647411
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Huntington's chorea: clinical aspects, genetics and current diagnosis].
    Spiegel R
    Ther Umsch; 1995 Dec; 52(12):814-20. PubMed ID: 8539653
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
    Langbehn DR; Brinkman RR; Falush D; Paulsen JS; Hayden MR;
    Clin Genet; 2004 Apr; 65(4):267-77. PubMed ID: 15025718
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease.
    Bat O; Kimmel M; Axelrod DE
    J Theor Biol; 1997 Sep; 188(1):53-67. PubMed ID: 9299309
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A worldwide 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; Squitieri F; Lin B; Bassett A; Almqvist E
    N Engl J Med; 1994 May; 330(20):1401-6. PubMed ID: 8159192
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular analysis of the Huntington's disease gene in New Zealand.
    Whitefield JE; Williams L; Snow K; Dixon J; Winship I; Stapleton PM; Faull RM; Love DR
    N Z Med J; 1996 Feb; 109(1015):27-30. PubMed ID: 8606810
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles.
    Semaka A; Creighton S; Warby S; Hayden MR
    Clin Genet; 2006 Oct; 70(4):283-94. PubMed ID: 16965319
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular diagnosis of Huntington's disease: an analysis of two large families].
    Zeng Y; Chen M; Mao Y
    Zhonghua Yi Xue Za Zhi; 1995 Nov; 75(11):689-93, 711-2. PubMed ID: 8697093
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epidemiology of Huntington's disease in Slovenia.
    Peterlin B; Kobal J; Teran N; Flisar D; Lovrecić L
    Acta Neurol Scand; 2009 Jun; 119(6):371-5. PubMed ID: 18976322
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients.
    Ribaï P; Nguyen K; Hahn-Barma V; Gourfinkel-An I; Vidailhet M; Legout A; Dodé C; Brice A; Dürr A
    Arch Neurol; 2007 Jun; 64(6):813-9. PubMed ID: 17562929
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.
    Margolis RL; O'Hearn E; Rosenblatt A; Willour V; Holmes SE; Franz ML; Callahan C; Hwang HS; Troncoso JC; Ross CA
    Ann Neurol; 2001 Sep; 50(3):373-80. PubMed ID: 11558794
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular diagnosis in Huntington's disease].
    Rosales-Reynoso MA; Barros-Núñez P
    Gac Med Mex; 2008; 144(3):271-3. PubMed ID: 18714598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Huntington's disease.
    Grove M; Vonsattel JP; Mazzoni P; Marder K
    Sci Aging Knowledge Environ; 2003 Oct; 2003(43):dn3. PubMed ID: 14586062
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exploring the correlates of intermediate CAG repeats in Huntington disease.
    Ha AD; Jankovic J
    Postgrad Med; 2011 Sep; 123(5):116-21. PubMed ID: 21904093
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effect of CAG repeat length on psychiatric disorders in Huntington's disease.
    Vassos E; Panas M; Kladi A; Vassilopoulos D
    J Psychiatr Res; 2008 Jun; 42(7):544-9. PubMed ID: 17610899
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
    Veitch NJ; Ennis M; McAbney JP; ; Shelbourne PF; Monckton DG
    DNA Repair (Amst); 2007 Jun; 6(6):789-96. PubMed ID: 17293170
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Huntington's disease: clinical and molecular genetics].
    Warita H; Shiro Y; Kashihara K; Abe K
    Nihon Rinsho; 1999 Apr; 57(4):896-9. PubMed ID: 10222786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.