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Journal Abstract Search

95 related items for PubMed ID: 7121151

  • 1. [HLA-antigens and sensorineural deafness].
    Gross M, Arndt-Hanser A.
    Laryngol Rhinol Otol (Stuttg); 1982 Jun; 61(6):316-8. PubMed ID: 7121151
    [Abstract] [Full Text] [Related]

  • 2. Influence of human leukocyte antigen in the pathogenesis of Ménière's disease in the South Korean population.
    Yeo SW, Park SN, Jeon EJ, Lee HY, Pyo CW, Kim TG.
    Acta Otolaryngol; 2002 Dec; 122(8):851-6. PubMed ID: 12542204
    [Abstract] [Full Text] [Related]

  • 3. Human leukocyte antigen in childhood unilateral deafness.
    Matsuki K, Harada T, Juji T, Kanzaki J, Koga K, Toriyama M.
    Arch Otolaryngol Head Neck Surg; 1989 Jan; 115(1):46-7. PubMed ID: 2909230
    [Abstract] [Full Text] [Related]

  • 4. [Congenital and hereditary hearing disorders in population of the Nakhichevan Autonomous Republic].
    Panakhiian VM.
    Vestn Otorinolaringol; 2004 Jan; (6):22-4. PubMed ID: 15699983
    [Abstract] [Full Text] [Related]

  • 5. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 6. Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome).
    Desir J, Abramowicz M.
    Orphanet J Rare Dis; 2008 Oct 15; 3():28. PubMed ID: 18922146
    [Abstract] [Full Text] [Related]

  • 7. Inner ear and facial nerve complications of acute otitis media with focus on bacteriology and virology.
    Hydén D, Akerlind B, Peebo M.
    Acta Otolaryngol; 2006 May 15; 126(5):460-6. PubMed ID: 16698694
    [Abstract] [Full Text] [Related]

  • 8. Frequency in Spanish population of familial complement factor 2 type I deficits and associated HLA haplotypes.
    Antolín SC, Del Rey Cerros MJ, Sierra EM, Miñarro DO, Clemente J, Martínez LA, Peña PV, Panete MJ, Pérez PM, Paz-Artal E.
    Hum Immunol; 2005 Oct 15; 66(10):1093-8. PubMed ID: 16386652
    [Abstract] [Full Text] [Related]

  • 9. HLA type and risk of alloimmunization in sickle cell disease.
    Hoppe C, Klitz W, Vichinsky E, Styles L.
    Am J Hematol; 2009 Jul 15; 84(7):462-4. PubMed ID: 19484735
    [No Abstract] [Full Text] [Related]

  • 10. Cochlear implants in deaf children.
    Al-Shaikh AH, Zakzouk SM, Metwalli AA, Dasugi AA.
    Saudi Med J; 2002 Apr 15; 23(4):441-4. PubMed ID: 11953772
    [Abstract] [Full Text] [Related]

  • 11. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
    Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C.
    Eur J Hum Genet; 1998 Apr 15; 6(3):245-50. PubMed ID: 9781028
    [Abstract] [Full Text] [Related]

  • 12. Impact of HLA on the underlying primary diseases in Turkish patients with end-stage renal disease.
    Karahan GE, Seyhun Y, Oguz FS, Kekik C, Onal AE, Yazici H, Turkmen A, Aydin AE, Sever MS, Eldegez U, Carin MN.
    Ren Fail; 2009 Apr 15; 31(1):44-9. PubMed ID: 19142809
    [Abstract] [Full Text] [Related]

  • 13. [Hereditary progressive sensorineural deafness--report of 30 cases in 12 families].
    Wang X.
    Zhonghua Yi Xue Za Zhi; 1983 Nov 15; 63(11):694-8. PubMed ID: 6426737
    [No Abstract] [Full Text] [Related]

  • 14. Profound bilateral sensorineural hearing loss in nigerian children: any shift in etiology?
    Dunmade AD, Segun-Busari S, Olajide TG, Ologe FE.
    J Deaf Stud Deaf Educ; 2007 Nov 15; 12(1):112-8. PubMed ID: 16956969
    [Abstract] [Full Text] [Related]

  • 15. Homozygous status for HLA-E*0103 confers protection from acute graft-versus-host disease and transplant-related mortality in HLA-matched sibling hematopoietic stem cell transplantation.
    Tamouza R, Busson M, Rocha V, Fortier C, Haddad Y, Brun M, Boukouaci W, Bleux H, Socié G, Krishnamoorthy R, Toubert A, Gluckman E, Charron D.
    Transplantation; 2006 Dec 15; 82(11):1436-40. PubMed ID: 17164714
    [Abstract] [Full Text] [Related]

  • 16. Bilateral sensorineural deafness in adenosine deaminase-deficient severe combined immunodeficiency.
    Albuquerque W, Gaspar HB.
    J Pediatr; 2004 Feb 15; 144(2):278-80. PubMed ID: 14760277
    [Abstract] [Full Text] [Related]

  • 17. Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.
    Milman N, Fenger K, Graudal NA, Nielsen LS.
    Dan Med Bull; 1994 Jun 15; 41(3):366-70. PubMed ID: 7924465
    [Abstract] [Full Text] [Related]

  • 18. HLA histocompatibility antigens and meningococcal disease.
    Kristiansen BE, Thorsby E.
    NIPH Ann; 1980 Dec 15; 3(2):75-9. PubMed ID: 7219842
    [Abstract] [Full Text] [Related]

  • 19. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.
    Riga M, Psarommatis I, Lyra Ch, Douniadakis D, Tsakanikos M, Neou P, Apostolopoulos N.
    Int J Pediatr Otorhinolaryngol; 2005 Apr 15; 69(4):449-55. PubMed ID: 15763280
    [Abstract] [Full Text] [Related]

  • 20. [The characteristics of HLA antigen distribution among patients with persistent lambliasis].
    Osipova SO, Niiazova OP, Shimolin AP, Dekhkan-Khodzhaeva NA.
    Med Parazitol (Mosk); 1994 Apr 15; (2):11-3. PubMed ID: 7935180
    [Abstract] [Full Text] [Related]

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