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 *

113 related articles for article (PubMed ID: 9193167)

  • 1. The genetic basis of hereditary ataxia.
    Klockgether T; Dichgans J
    Prog Brain Res; 1997; 114():569-76. PubMed ID: 9193167
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary ataxias.
    Evidente VG; Gwinn-Hardy KA; Caviness JN; Gilman S
    Mayo Clin Proc; 2000 May; 75(5):475-90. PubMed ID: 10807077
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial cosegregation of manic-depressive illness and a form of hereditary cerebellar ataxia.
    Fernández Piqueras J; Santos J; Visedo G; Pérez de Castro I; Puertollano R; Montejo J; Ramo Tello C; Valle J
    Am J Med Genet; 1995 Jun; 60(3):206-9. PubMed ID: 7573172
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [New insights in the molecular genetics and pathophysiology of hereditary ataxias].
    Bürk K; Klockgether T; Dichgans J
    Nervenarzt; 1999 Jun; 70(6):491-5. PubMed ID: 10412692
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.
    Marzouki N; Benomar A; Yahyaoui M; Birouk N; Elouazzani M; Chkili T; Benlemlih M
    Eur J Med Genet; 2005; 48(1):21-8. PubMed ID: 15953402
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations.
    Chakravarty A; Mukherjee SC
    Neurol India; 2003 Jun; 51(2):227-34. PubMed ID: 14571010
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families.
    Marzouki N; Belal S; Benhamida C; Benlemlih M; Hentati F
    Clin Genet; 2001 Apr; 59(4):257-62. PubMed ID: 11298681
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary ataxia].
    Radojicić BM
    Med Glas; 1972 Aug; 26(8):271-7. PubMed ID: 4121021
    [No Abstract]   [Full Text] [Related]  

  • 9. Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegia.
    Tezenas du Montcel S; Charles P; Goizet C; Marelli C; Ribai P; Vincitorio C; Anheim M; Guyant-Maréchal L; Le Bayon A; Vandenberghe N; Tchikviladzé M; Devos D; Le Ber I; N'Guyen K; Cazeneuve C; Tallaksen C; Brice A; Durr A
    Arch Neurol; 2012 Apr; 69(4):500-8. PubMed ID: 22491195
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The autosomal recessive cerebellar ataxias.
    Anheim M; Tranchant C; Koenig M
    N Engl J Med; 2012 Feb; 366(7):636-46. PubMed ID: 22335741
    [No Abstract]   [Full Text] [Related]  

  • 11. [Ataxias in children. Clinical and genetic aspects].
    Goutieres F
    J Genet Hum; 1981 Sep; 29(3):211-20. PubMed ID: 6801195
    [No Abstract]   [Full Text] [Related]  

  • 12. The inherited ataxias and the new genetics.
    Hammans SR
    J Neurol Neurosurg Psychiatry; 1996 Oct; 61(4):327-32. PubMed ID: 8890766
    [No Abstract]   [Full Text] [Related]  

  • 13. Hereditary ataxia. An unfolded protein.
    Orr HT
    Lancet; 2001 Dec; 358 Suppl():S35. PubMed ID: 11784584
    [No Abstract]   [Full Text] [Related]  

  • 14. SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia.
    Yabe I; Sasaki H; Matsuura T; Takada A; Wakisaka A; Suzuki Y; Fukazawa T; Hamada T; Oda T; Ohnishi A; Tashiro K
    J Neurol Sci; 1998; 156(1):89-95. PubMed ID: 9559993
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Friedreich's ataxia and hereditary vitamin E deficiency. Case study].
    Labauge P; Cavalier L; Ichalalène L; Castelnovo G
    Rev Neurol (Paris); 1998 May; 154(4):339-41. PubMed ID: 9773063
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Autosomal recessive cerebellar ataxias].
    Tranchant C; Anheim M
    Presse Med; 2009 Dec; 38(12):1852-9. PubMed ID: 19442480
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J; Dalton A; Morrison PJ; Dodge A; Connarty M; Kotze MJ; Rubinsztein DC
    J Med Genet; 1997 Dec; 34(12):982-5. PubMed ID: 9429138
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal recessive cerebellar ataxias.
    Palau F; Espinós C
    Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
    Gros-Louis F; Dupré N; Dion P; Fox MA; Laurent S; Verreault S; Sanes JR; Bouchard JP; Rouleau GA
    Nat Genet; 2007 Jan; 39(1):80-5. PubMed ID: 17159980
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.
    Belal S; Hentati F; Ben Hamida C; Ben Hamida M
    Clin Neurosci; 1995; 3(1):39-42. PubMed ID: 7614093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.