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Journal Abstract Search

251 related items for PubMed ID: 31421540

  • 21. Flow cytometry and immunoblotting analysis of monoclonal antibodies directed to complement regulatory proteins.
    Blanchard D, Navenot JM, Petit-Le Roux Y, Willem C, Loirat MJ.
    Transfus Clin Biol; 1997; 4(1):131-4. PubMed ID: 9095519
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  • 23. Complement activation in diseases presenting with thrombotic microangiopathy.
    Meri S.
    Eur J Intern Med; 2013 Sep; 24(6):496-502. PubMed ID: 23743117
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  • 24. [Complement component deficiencies in human disease].
    Dragon-Durey MA, Fremeaux-Bacchi V.
    Presse Med; 2006 May; 35(5 Pt 2):861-70. PubMed ID: 16710159
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  • 25. Complementopathies.
    Baines AC, Brodsky RA.
    Blood Rev; 2017 Jul; 31(4):213-223. PubMed ID: 28215731
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  • 26. Laboratory tests for disorders of complement and complement regulatory proteins.
    Shih AR, Murali MR.
    Am J Hematol; 2015 Dec; 90(12):1180-6. PubMed ID: 26437749
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  • 27. CHAPLE syndrome uncovers the primary role of complement in a familial form of Waldmann's disease.
    Ozen A.
    Immunol Rev; 2019 Jan; 287(1):20-32. PubMed ID: 30565236
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  • 29. A simplified assay for the specific diagnosis of paroxysmal nocturnal hemoglobinuria: detection of DAF(CD55)- and HRF20(CD59)- erythrocytes in microtyping cards.
    Nilsson B, Hagström U, Englund A, Säfwenberg J.
    Vox Sang; 1993 Jan; 64(1):43-6. PubMed ID: 7680511
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  • 31. Complement the hemostatic system: an intimate relationship.
    Weitz IC.
    Thromb Res; 2014 May; 133 Suppl 2():S117-21. PubMed ID: 24862131
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  • 32. Glycosylphosphatidylinositol (GPI)-anchored membrane proteins in clinical pathophysiology of paroxysmal nocturnal hemoglobinuria (PNH).
    Shichishima T.
    Fukushima J Med Sci; 1995 Jun; 41(1):1-13. PubMed ID: 8606038
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  • 33. Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies.
    El Sissy C, Rosain J, Vieira-Martins P, Bordereau P, Gruber A, Devriese M, de Pontual L, Taha MK, Fieschi C, Picard C, Frémeaux-Bacchi V.
    Front Immunol; 2019 Jun; 10():1936. PubMed ID: 31440263
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  • 34. Relationship between decay accelerating factor deficiency, diminished acetylcholinesterase activity, and defective terminal complement pathway restriction in paroxysmal nocturnal hemoglobinuria erythrocytes.
    Medof ME, Gottlieb A, Kinoshita T, Hall S, Silber R, Nussenzweig V, Rosse WF.
    J Clin Invest; 1987 Jul; 80(1):165-74. PubMed ID: 2439544
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  • 38. Enhanced reactive lysis of paroxysmal nocturnal hemoglobinuria erythrocytes by C5b-9 does not involve increased C7 binding or cell-bound C3b.
    Rosenfeld SI, Jenkins DE, Leddy JP.
    J Immunol; 1985 Jan; 134(1):506-11. PubMed ID: 3964820
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