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 *

117 related articles for article (PubMed ID: 12114488)

  • 1. Predictive testing in the context of pregnancy: experience in Huntington's disease and autosomal dominant cerebellar ataxia.
    Lesca G; Goizet C; Dürr A
    J Med Genet; 2002 Jul; 39(7):522-5. PubMed ID: 12114488
    [No Abstract]   [Full Text] [Related]  

  • 2. Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxias.
    Goizet C; Lesca G; Dürr A;
    Neurology; 2002 Nov; 59(9):1330-6. PubMed ID: 12427879
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An unusual presentation of Huntington's disease.
    Rivkin PR; Pearlson GD
    Psychosomatics; 1998; 39(3):291-4. PubMed ID: 9664778
    [No Abstract]   [Full Text] [Related]  

  • 4. Predictive testing for Huntington's disease.
    Richards M
    Lancet; 2001 Mar; 357(9259):883. PubMed ID: 11265978
    [No Abstract]   [Full Text] [Related]  

  • 5. Associative learning in patients with cerebellar ataxia.
    Tucker J; Harding AE; Jahanshahi M; Nixon PD; Rushworth M; Quinn NP; Thompson PD; Passingham RE
    Behav Neurosci; 1996 Dec; 110(6):1229-34. PubMed ID: 8986327
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Predictive testing for Huntington's disease with linked DNA markers.
    Brock DJ; Mennie M; Curtis A; Millan FA; Barron L; Raeburn JA; Dinwoodie D; Holloway S; Crosbie A; Wright A
    Lancet; 1989 Aug; 2(8661):463-6. PubMed ID: 2570183
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Adult-onset hereditary cerebellar ataxia and neurosensory deafness.
    Schimke RN
    Clin Genet; 1974; 6(5):416-21. PubMed ID: 4434656
    [No Abstract]   [Full Text] [Related]  

  • 8. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
    Onodera Y; Aoki M; Mizuno H; Warita H; Shiga Y; Itoyama Y
    Neurology; 2006 Oct; 67(7):1300-2. PubMed ID: 17030774
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Predictive tests in Huntington's chorea.
    Br Med J; 1978 Mar; 1(6112):528-9. PubMed ID: 147118
    [No Abstract]   [Full Text] [Related]  

  • 10. Huntington's disease in a Coloured family.
    Saffer DS; Nathan DC; Kahle PA; Steingo B
    S Afr Med J; 1974 Nov; 48(58):2399-402. PubMed ID: 4279450
    [No Abstract]   [Full Text] [Related]  

  • 11. International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea. Guidelines for the molecular genetics predictive test in Huntington's disease.
    J Med Genet; 1994 Jul; 31(7):555-9. PubMed ID: 7966192
    [No Abstract]   [Full Text] [Related]  

  • 12. Autosomal dominant spinocerebellar ataxia with slow eye movements-a common hereditary ataxia in Western India.
    Wadia RS; Amin RB; Divate UP; Divate PG; Sainani GS; Sardesai HV
    J Assoc Physicians India; 1976 Jun; 24(6):367-71. PubMed ID: 1022769
    [No Abstract]   [Full Text] [Related]  

  • 13. Psychological effects of predictive testing for Huntington's disease.
    Hayden MR; Bloch M; Wiggins S
    Adv Neurol; 1995; 65():201-10. PubMed ID: 7872141
    [No Abstract]   [Full Text] [Related]  

  • 14. Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.
    Kondo I; Ohta H; Yazaki M; Ikeda JE; Gusella JF; Kanazawa I
    J Med Genet; 1990 Feb; 27(2):105-8. PubMed ID: 1969487
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Observations in a family with dominant type of cerebellar ataxia.
    Frey HJ; Frey ML; Riekkinen PJ; Tuomola H
    Acta Neurol Scand Suppl; 1972; 51():247-8. PubMed ID: 4514343
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia.
    Jen JC; Lee H; Cha YH; Nelson SF; Baloh RW
    Neurology; 2006 Nov; 67(9):1704-6. PubMed ID: 17101914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Differential diagnosis of Huntington's disease: what the clinician should know.
    Cardoso F
    Neurodegener Dis Manag; 2014; 4(1):67-72. PubMed ID: 24640980
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cerebellar ataxia in the eastern and southern parts of Norway.
    Koht J; Tallaksen CM
    Acta Neurol Scand Suppl; 2007; 187():76-9. PubMed ID: 17419835
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Psychodynamic theory and counseling in predictive testing for Huntington's disease.
    Tassicker RJ
    J Genet Couns; 2005 Apr; 14(2):99-107. PubMed ID: 15959641
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Huntington's disease: ethical aspects of presymptomatic testing].
    Gelman-Kohan Z; Chemke J; Nisani R
    Harefuah; 1993 Feb; 124(4):196-8, 247. PubMed ID: 8495897
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.