BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 14571273)

  • 1. Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.
    Costa MC; Magalhães P; Ferreirinha F; Guimarães L; Januário C; Gaspar I; Loureiro L; Vale J; Garrett C; Regateiro F; Magalhães M; Sousa A; Maciel P; Sequeiros J
    Eur J Hum Genet; 2003 Nov; 11(11):872-8. PubMed ID: 14571273
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington disease.
    Alford RL; Ashizawa T; Jankovic J; Caskey CT; Richards CS
    Am J Med Genet; 1996 Dec; 66(3):281-6. PubMed ID: 8985488
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. [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]  

  • 6. 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]  

  • 7. [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]  

  • 8. Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population.
    Sequeiros J; Ramos EM; Cerqueira J; Costa MC; Sousa A; Pinto-Basto J; Alonso I
    Clin Genet; 2010 Oct; 78(4):381-7. PubMed ID: 20236117
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preimplantation genetic diagnosis for Huntington's disease with exclusion testing.
    Sermon K; De Rijcke M; Lissens W; De Vos A; Platteau P; Bonduelle M; Devroey P; Van Steirteghem A; Liebaers I
    Eur J Hum Genet; 2002 Oct; 10(10):591-8. PubMed ID: 12357329
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [DNA diagnosis of Huntington's chorea. Application and genetic counseling in 4 involved families].
    Hammer J; Mächler M; Schmid W
    Schweiz Med Wochenschr; 1987 Dec; 117(51):2074-80. PubMed ID: 2963376
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. [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]  

  • 14. Huntington disease in children: genotype-phenotype correlation.
    Rasmussen A; Macias R; Yescas P; Ochoa A; Davila G; Alonso E
    Neuropediatrics; 2000 Aug; 31(4):190-4. PubMed ID: 11071143
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Pre-symptomatic diagnosis of Huntington disease by polymerase chain reaction].
    Tóth T; Németi M; Papp Z
    Orv Hetil; 1996 Mar; 137(9):451-4. PubMed ID: 8714037
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and genetic characteristics of Mexican Huntington's disease patients.
    Alonso ME; Ochoa A; Boll MC; Sosa AL; Yescas P; López M; Macias R; Familiar I; Rasmussen A
    Mov Disord; 2009 Oct; 24(13):2012-5. PubMed ID: 19672992
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The challenge of juvenile Huntington disease: to test or not to test.
    Koutsis G; Karadima G; Kladi A; Panas M
    Neurology; 2013 Mar; 80(11):990-6. PubMed ID: 23390178
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evidence-based genetic counselling implications for Huntington disease intermediate allele predictive test results.
    Semaka A; Hayden MR
    Clin Genet; 2014 Apr; 85(4):303-11. PubMed ID: 24256063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis].
    Sánchez A; Milà M; Castellví-Bel S; Calopa M; Genís D; Jiménez D; Estivill X
    Med Clin (Barc); 1997 May; 108(18):687-90. PubMed ID: 9324583
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.