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Journal Abstract Search

140 related items for PubMed ID: 7342672

  • 1. HLA and congenital adrenal hyperplasia.
    Lisá L, Ivasková R, Sajdlová H, Kupková L.
    Acta Paediatr Acad Sci Hung; 1981; 22(4):267-74. PubMed ID: 7342672
    [Abstract] [Full Text] [Related]

  • 2. HLA haplotypes in children with adrenogenital syndrome and their parents.
    László A, Godó B, Kaiser G, Hajdu J, Fazekas C.
    Acta Paediatr Acad Sci Hung; 1981; 22(3):217-22. PubMed ID: 7304161
    [Abstract] [Full Text] [Related]

  • 3. Amniotic 17-alpha hydroxyprogesterone and HLA typing for the prenatal diagnosis of 21-alpha hydroxylase deficiency--congenital adrenal hyperplasia.
    Rosenmann A, Schumert Z, Theodor R, Cohen T, Brautbar C.
    Am J Med Genet; 1980; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 4. [HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population].
    Couillin P, Ravisé N, Hors J, Feingold J, Rappaport R, Kuttenn F, Boué A.
    Pathol Biol (Paris); 1986 Jun; 34(6):789-94. PubMed ID: 3531997
    [Abstract] [Full Text] [Related]

  • 5. Particular interest of HLA typing for genetic counselling in families with congenital adrenal hyperplasia (21-OH deficiency).
    Couillin P, Boué J, Bétuel H, Hors J, Gebuhrer L, Boué A.
    Haematologia (Budap); 1987 Jun; 20(1):25-30. PubMed ID: 3496258
    [Abstract] [Full Text] [Related]

  • 6. [Congenital adrenal hyperplasia and HLA antigens].
    Boué A, Boué J, Couillin P.
    J Genet Hum; 1980 Sep; 28(3):195-200. PubMed ID: 7463017
    [No Abstract] [Full Text] [Related]

  • 7. [Congenital adrenogenital syndrome - its prognosis and immunogenetic aspects].
    Lisá L, Ivasková E, Sajdlová H, Kupková L.
    Cesk Pediatr; 1982 Feb; 37(2):58-61. PubMed ID: 7060198
    [No Abstract] [Full Text] [Related]

  • 8. [Genetic linkage between HLA and virilizing adrenal hyperplasia: study of 12 cases].
    Rochiccioli P, de Mouzon A, Gallegos D, Dutau G, Parra MT, Ohayon E.
    J Genet Hum; 1980 Sep; 28(3):201-5. PubMed ID: 7463018
    [No Abstract] [Full Text] [Related]

  • 9. [Two loci HLA haplotypes in celiac children. Linkage imbalance and haplotype frequencies. Comparative study with a control population].
    Ruiz del Prado MY, Olivares López JL, Lázaro Almarza A, Lasierra Díaz MP.
    An Esp Pediatr; 2001 Jan; 54(1):7-12. PubMed ID: 11181188
    [Abstract] [Full Text] [Related]

  • 10. [The HLA-DR phenotype in Croatian children with gluten enteropathy].
    Jurcić Z, Brkljacić-Surkalović L, Kerhin-Brkljacić V, Kastelan A, Miskić-Musa M, Zobenica M, Pavlović S.
    Lijec Vjesn; 1998 Sep; 120(9):273-7. PubMed ID: 10099667
    [Abstract] [Full Text] [Related]

  • 11. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers].
    Dumić M, Plavsić V, Brkljacić L, Sarnavka V, Mardesić D, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Apr; 105(4):145-9. PubMed ID: 6602259
    [No Abstract] [Full Text] [Related]

  • 12. HLA antigens in juvenile dermatitis herpetiformis.
    Richiardi P, Borelli I, Malavasi F, Curtoni ES, Berti E, Gianotti F, Giannetti A.
    Acta Derm Venereol; 1981 Apr; 61(3):241-4. PubMed ID: 6167108
    [Abstract] [Full Text] [Related]

  • 13. [The eugenic significance of HLA determination in congenital adrenal hyperplasia].
    Li XQ.
    Zhonghua Yi Xue Za Zhi; 1984 Feb; 64(2):105-7. PubMed ID: 6432246
    [No Abstract] [Full Text] [Related]

  • 14. [HLA in the adrenogenital syndrome].
    Ivasková E, Lisá L, Sajdlová H, Kupková L.
    Cas Lek Cesk; 1981 Apr 16; 120(15):442-6. PubMed ID: 7237491
    [No Abstract] [Full Text] [Related]

  • 15. Congenital adrenal hyperplasia.
    New MI, Levine LS.
    Monogr Endocrinol; 1984 Apr 16; 26():1-88. PubMed ID: 6472279
    [Abstract] [Full Text] [Related]

  • 16. 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 16; 66(10):1093-8. PubMed ID: 16386652
    [Abstract] [Full Text] [Related]

  • 17. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A, Stivel M, Zamir R, Kaufman H, Pertzelan A, Laron Z.
    Isr J Med Sci; 1982 Jul 16; 18(7):763-8. PubMed ID: 6980865
    [Abstract] [Full Text] [Related]

  • 18. [Familial membranoproliferative glomerulonephritis].
    Bogdanović RM, Dimitrjević JZ, Nikolić VN, Ognjanović MV, Rodić BD, Slavković BV.
    Srp Arh Celok Lek; 1999 Jul 16; 127(5-6):163-71. PubMed ID: 10500423
    [Abstract] [Full Text] [Related]

  • 19. HLA antigens in multiplex families with isolated congenital heart disease.
    Hafez M, Abdalla A, el-Shennawy F, Tawfik SH.
    Dis Markers; 1986 Dec 16; 4(4):255-60. PubMed ID: 3482990
    [Abstract] [Full Text] [Related]

  • 20. HLA histocompatibility antigens and meningococcal disease.
    Kristiansen BE, Thorsby E.
    NIPH Ann; 1980 Dec 16; 3(2):75-9. PubMed ID: 7219842
    [Abstract] [Full Text] [Related]

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