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 *

210 related articles for article (PubMed ID: 9153618)

  • 1. Maternal transmission in sporadic Huntington's disease.
    Sánchez A; Milà M; Castellví-Bel S; Rosich M; Jiménez D; Badenas C; Estivill X
    J Neurol Neurosurg Psychiatry; 1997 May; 62(5):535-7. PubMed ID: 9153618
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expansion of a (CAG)n repeat region in a sporadic case of HD.
    Bozza A; Malagù S; Calzolari E; Novelletto A; Pavoni M; del Senno L
    Acta Neurol Scand; 1995 Aug; 92(2):132-4. PubMed ID: 7484060
    [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. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
    De Rooij KE; De Koning Gans PA; Skraastad MI; Belfroid RD; Vegter-Van Der Vlis M; Roos RA; Bakker E; Van Ommen GJ; Den Dunnen JT; Losekoot M
    J Med Genet; 1993 Dec; 30(12):996-1002. PubMed ID: 8133511
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.
    Mandich P; Di Maria E; Bellone E; Ajmar F; Abbruzzese G
    Eur Neurol; 1996; 36(6):348-52. PubMed ID: 8954302
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Diagnosis of "sporadic" Huntington's disease.
    Dürr A; Dodé C; Hahn V; Pêcheux C; Pillon B; Feingold J; Kaplan JC; Agid Y; Brice A
    J Neurol Sci; 1995 Mar; 129(1):51-5. PubMed ID: 7751845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Analysis of the IT15 gene in Huntington's disease families].
    Genetika; 2004 Aug; 40(8):1123-30. PubMed ID: 15523851
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.
    Goldberg YP; Andrew SE; Theilmann J; Kremer B; Squitieri F; Telenius H; Brown JD; Hayden MR
    J Med Genet; 1993 Dec; 30(12):987-90. PubMed ID: 8133509
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.
    MacMillan JC; Morrison PJ; Nevin NC; Shaw DJ; Harper PS; Quarrell OW; Snell RG
    J Med Genet; 1993 Dec; 30(12):1012-3. PubMed ID: 8133497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
    Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N
    Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neuropathological diagnosis and CAG repeat expansion in Huntington's disease.
    Xuereb JH; MacMillan JC; Snell R; Davies P; Harper PS
    J Neurol Neurosurg Psychiatry; 1996 Jan; 60(1):78-81. PubMed ID: 8558157
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Molecular genetic testing in the diagnosis of sporadic cases of Huntington's chorea].
    Ivanova-Smolenskaia IA; Ovchinnikov IV; Illarioshkin SN; Markova ED; Kliushnikov SA; Nikol'skaia NN; Miklina NI
    Zh Nevrol Psikhiatr Im S S Korsakova; 1998; 98(3):19-22. PubMed ID: 9575625
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Huntington's disease: confirmation of diagnosis and presymptomatic testing in Spanish families by genetic analysis.
    Sánchez A; Castellví-Bel S; Milà M; Genis D; Calopa M; Jiménez D; Estivill X
    J Neurol Neurosurg Psychiatry; 1996 Dec; 61(6):625-7. PubMed ID: 8971113
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The DNA test in the diagnosis of Huntington disease].
    Terzić R; Tupković E; Logar N; Sehić A; Duricić E; Sinanović O; Peterlin B
    Med Arh; 2002; 56(4):187-9. PubMed ID: 12518531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.