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331 related items for PubMed ID: 16386652

  • 1. 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; 66(10):1093-8. PubMed ID: 16386652
    [Abstract] [Full Text] [Related]

  • 2. Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II genes.
    Truedsson L, Alper CA, Awdeh ZL, Johansen P, Sjöholm AG, Sturfelt G.
    J Immunol; 1993 Nov 15; 151(10):5856-63. PubMed ID: 7901282
    [Abstract] [Full Text] [Related]

  • 3. [Complete deficiency in the C2 fraction of complement associated with a glomerular nephropathy: apropos of 2 cases].
    Ayed K, Bardi R, Sassi F, Gorgi Y, Ben Maiz H, Haddad S, Ben Ayed H.
    Nephrologie; 1988 Nov 15; 9(5):239-44. PubMed ID: 3216945
    [Abstract] [Full Text] [Related]

  • 4. Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics.
    Matsuki K, Juji T, Tokunaga K, Naohara T, Satake M, Honda Y.
    J Clin Invest; 1985 Dec 15; 76(6):2078-83. PubMed ID: 3865934
    [Abstract] [Full Text] [Related]

  • 5. Studies on the C2-deficiency gene in man.
    Mortensen JP, Buskjaer L, Lamm LU.
    Immunology; 1980 Apr 15; 39(4):541-9. PubMed ID: 7380478
    [Abstract] [Full Text] [Related]

  • 6. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, de Waall LP, Bos JD, Asghar SS.
    Exp Clin Immunogenet; 1996 Apr 15; 13(2):104-11. PubMed ID: 9063702
    [Abstract] [Full Text] [Related]

  • 7. Paroxysmal nocturnal hemoglobinuria: significant association with specific HLA-A, -B, -C, and -DR alleles in an Italian population.
    Lombardi ML, Terrazzano G, Cosentini E, Gargiulo L, Risitano A, Camerlingo R, Sica M, Aufiero D, Poggi A, Pirozzi G, Luzzatto L, Rotoli B, Notaro R, Alfinito F, Ruggiero G.
    Hum Immunol; 2008 Mar 15; 69(3):202-6. PubMed ID: 18396213
    [Abstract] [Full Text] [Related]

  • 8. Studies of HLA, factor B (Bf), complement C2 and C4 haplotypes in type 1 diabetic and control families from northern Sweden.
    Hägglöf B, Holmgren G, Holmlund G, Lindblom B, Olaisen B, Teisberg P.
    Hum Hered; 1986 Mar 15; 36(4):201-12. PubMed ID: 3639057
    [Abstract] [Full Text] [Related]

  • 9. Hereditary C2 deficiency: diagnosis and HLA gene complex associations.
    Gibson DJ, Glass D, Carpenter CB, Schur PH.
    J Immunol; 1976 Apr 15; 116(4):1065-70. PubMed ID: 1082903
    [Abstract] [Full Text] [Related]

  • 10. HLA genotypes in a family with a case of homozygous C2 deficiency and discoid lupus erythematosus.
    Braathen LR, Bratlie A, Teisberg P.
    Acta Derm Venereol; 1986 Apr 15; 66(5):419-22. PubMed ID: 2431580
    [Abstract] [Full Text] [Related]

  • 11. Selective deficiencies in complement component : a family with hereditary C2 deficiency.
    Dantant M, Rivat C, Gilbert D, Fontaine M, Cavelier B, Godin M, Fillastre JP.
    Biomedicine; 1978 Apr 15; 28(3):185-90. PubMed ID: 698338
    [Abstract] [Full Text] [Related]

  • 12. HLA-A, -B, and -DRB1 polymorphism defined by sequence-based typing of the Han population in Northern China.
    Yang G, Deng YJ, Hu SN, Wu DY, Li SB, Zhu J, Zhu BF, Liu Y.
    Tissue Antigens; 2006 Feb 15; 67(2):146-52. PubMed ID: 16441486
    [Abstract] [Full Text] [Related]

  • 13. Polymorphic insertions in 5 Alu loci within the major histocompatibility complex class I region and their linkage disequilibria with HLA alleles in four distinct populations in mainland China.
    Tian W, Wang F, Cai JH, Li LX.
    Tissue Antigens; 2008 Dec 15; 72(6):559-67. PubMed ID: 19054371
    [Abstract] [Full Text] [Related]

  • 14. Serum concentrations of C4 isotypes and factor B in type I C2 deficiency suggest haplotype-dependent quantitative expression of MHC class III complement genes.
    Truedsson L, Gullstrand B, Jönsson T, Klint C.
    Exp Clin Immunogenet; 1995 Dec 15; 12(2):66-73. PubMed ID: 7576717
    [Abstract] [Full Text] [Related]

  • 15. Deficiency of C2, the second complement component, in the family of a patient with SLE-like syndrome: the first case of hereditary C2 deficiency in Czechoslovakia.
    Starsia Z, Zitnan D, Loos M, Stefanovic J, Bosák V, Niks M, Tomanová H, Lukác J, Lulovicová M.
    Haematologia (Budap); 1987 Dec 15; 20(4):215-20. PubMed ID: 3428724
    [Abstract] [Full Text] [Related]

  • 16. HLA class I and class II polymorphism in the population of Rijeka, Croatia.
    Crnić-Martinović M, Vujaklija-Stipanović K, Ristić S, Fućak M, Kapović M, Weiner M, Sepcić J.
    Coll Antropol; 2002 Jun 15; 26(1):69-75. PubMed ID: 12137325
    [Abstract] [Full Text] [Related]

  • 17. [Familial glomerulonephritis and hereditary deficiency of C2].
    Genin C, Freycon MT, Berthoux FC, Lepetit JC, Bétuel H, Freidel C, Freycon F.
    Arch Fr Pediatr; 1978 Dec 15; 35(10):1085-95. PubMed ID: 107905
    [Abstract] [Full Text] [Related]

  • 18. Study of the structure and impact of human leukocyte antigen (HLA)-G-A, HLA-G-B, and HLA-G-DRB1 haplotypes in families with recurrent miscarriage.
    Kolte AM, Steffensen R, Nielsen HS, Hviid TV, Christiansen OB.
    Hum Immunol; 2010 May 15; 71(5):482-8. PubMed ID: 20149831
    [Abstract] [Full Text] [Related]

  • 19. HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiency.
    Clavijo OP, Delgado JC, Awdeh ZL, Fici D, Turbay D, Alper CA, Truedsson L, Yunis EJ.
    Tissue Antigens; 1998 Sep 15; 52(3):282-5. PubMed ID: 9802610
    [Abstract] [Full Text] [Related]

  • 20. C2 deficiency in blood donors and lupus patients: prevalence, clinical characteristics and HLA-associations in the Brazilian population.
    Araújo MN, Silva NP, Andrade LE, Sato EI, Gerbase-DeLima M, Leser PG.
    Lupus; 1997 Sep 15; 6(5):462-6. PubMed ID: 9229366
    [Abstract] [Full Text] [Related]

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