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 *

119 related articles for article (PubMed ID: 85351)

  • 1. HLA--determination in families with hereditary ataxia.
    Möller E; Hindfelt B; Olsson JE
    Tissue Antigens; 1978 Nov; 12(5):357-66. PubMed ID: 85351
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage investigations in two families with hereditary ataxia.
    Van Rossum J; Veenema H; Went LN
    J Neurol Neurosurg Psychiatry; 1981 Jun; 44(6):516-22. PubMed ID: 7276965
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic linkage in hereditary ataxia.
    Koeppen AH; Goedde HW; Hirth L; Benkmann HG; Hiller C
    Lancet; 1980 Jan; 1(8159):92-3. PubMed ID: 6101435
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary cerebellar ataxia and genetic linkage with HLA.
    Kumar D; Blank CE; Gelsthorpe K
    Hum Genet; 1986 Apr; 72(4):327-32. PubMed ID: 3457760
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia.
    Pedersen L; Platz P; Ryder LP; Lamm LU; Dissing J
    Hum Genet; 1980; 54(3):371-83. PubMed ID: 6772543
    [No Abstract]   [Full Text] [Related]  

  • 6. Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.
    Belal S; Panayides K; Sirugo G; Ben Hamida C; Ioannou P; Hentati F; Beckmann J; Koenig M; Mandel JL; Ben Hamida M
    Am J Hum Genet; 1992 Dec; 51(6):1372-6. PubMed ID: 1463017
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage between late onset, dominant spinocerebellar ataxia and HLA.
    Werdelin L; Platz P; Lamm LU
    Hum Genet; 1984; 66(1):85-9. PubMed ID: 6698559
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adult onset spinocerebellar ataxia linked to HLA in a South African kindred of mixed ancestry.
    Bryer A; Martell RW; du Toit ED; Beighton P
    Tissue Antigens; 1992 Sep; 40(3):111-5. PubMed ID: 1440565
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.
    Jackson JF; Currier RD; Terasaki PI; Morton NE
    N Engl J Med; 1977 May; 296(20):1138-41. PubMed ID: 857157
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Distribution of dominant hereditary ataxias and Friedreich's ataxia in the Spanish population].
    Mayo Cabrero D; Hernández Cristóbal J; Cantarero Duque S; Martínez Delgado B; Urioste Azcorra M; Robledo Batanero M; García-Ruiz Espiga P; Benítez Ortiz J
    Med Clin (Barc); 2000 Jun; 115(4):121-5. PubMed ID: 10996881
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duffy locus linkage and HLA antigens in hereditary motor-sensory neuropathy.
    Nevsímalová S; Prazák J; Herzog P; Seemanová E
    Schweiz Arch Neurol Psychiatr (1985); 1991; 142(1):19-29. PubMed ID: 1709295
    [TBL] [Abstract][Full Text] [Related]  

  • 12. HLA and complement typing in olivo-ponto-cerebellar atrophy.
    Wastiaux JP; Lamoureux G; Bouchard JP; Durivage A; Barbeau C; Barbeau A
    Can J Neurol Sci; 1978 Feb; 5(1):75-81. PubMed ID: 647501
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus.
    Smeyers P; Monrós E; Vílchez J; Lopez-Arlandis J; Prieto F; Palau F
    Hum Genet; 1996 Jun; 97(6):824-8. PubMed ID: 8641704
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary ataxia and the sixth chromosome.
    Koeppen AH; Goedde HW; Hiller C; Hirth L; Benkmann HG
    Arch Neurol; 1981 Mar; 38(3):158-64. PubMed ID: 6937161
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.
    Ranum LP; Rich SS; Nance MA; Duvick LA; Aita JF; Orr HT; Anton-Johnson S; Schut LJ
    Neurology; 1992 Feb; 42(2):344-7. PubMed ID: 1736163
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
    Bouhlal Y; El-Euch-Fayeche G; Amouri R; Hentati F
    Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system.
    Arruda WO; Petzl-Erler ML; Cardoso MA; Lehner T; Ott J
    Arq Neuropsiquiatr; 1991 Sep; 49(3):285-91. PubMed ID: 1807228
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q.
    Chamberlain S; Farrall M; Shaw J; Wilkes D; Carvajal J; Hillerman R; Doudney K; Harding AE; Williamson R; Sirugo G
    Am J Hum Genet; 1993 Jan; 52(1):99-109. PubMed ID: 8434613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia].
    Sasaki H; Hamada T; Wakisaka A; Tashiro K
    No To Shinkei; 1990 Nov; 42(11):1103-11. PubMed ID: 2076357
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.