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Journal Abstract Search

102 related items for PubMed ID: 2442945

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  • 6. 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
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  • 9. 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 Oct; 20(4):215-20. PubMed ID: 3428724
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  • 13. [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; 35(10):1085-95. PubMed ID: 107905
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  • 14. [Congenital homozygotic complement deficiency and systemic diseases with skin manifestation: collagenoses and vasculitis].
    Morel P, Civatte J.
    Z Hautkr; 1979 Jul 01; 54(13):625-32. PubMed ID: 483958
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  • 18. [Lupus erythematosus and hereditary lack of complement. Review of about one case of C2 deficit (author's transl)].
    Morel P, Sohier J, Peltier AP, Cottenot F, Civatte J.
    Ann Dermatol Venereol; 1977 Dec 01; 104(12):831-9. PubMed ID: 613949
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