2000-es idegen nyelvű publikációk

  • Katona, É., Haramura, G., Kárpáti, L., Fachet, J., Muszbek, L.: A simple, quick one-step ELISA assay for the determination of complex plasma factor XIII (a2b2) Thromb. Haemost.  83: 268-73 (2000)
  • Wartiovaara, U., Mikkola, H., Szőke, G., Haramura, G., Kárpáti, L., Balogh, I., Lassila, R., Muszbek, L., Palotie, A.: Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A. Thromb. Haemost.  84: 595-600 (2000)
  • Schlammadinger, Á., Kerényi, A., Muszbek, L., Boda, Z.,.: Comparison of the O’Brien filter test and the PFA-100 platelet analyzer in the laboratory diagnosis of von Willebrand’s disease. Thromb. Haemost. 84: 88-92(2000)
  • Hevessy, Zs., Patthy, A., Kárpáti, L., Muszbek, L.,: a2-plasmin inhibitor: a substrate for tissue transglutaminase. Thromb. Res. 99: 399-406 (2000)
  • Balogh, I., Szőke, G., Kárpáti, L., Wartiovaara, U., Katona, É., Komáromi, I., Haramura, G., Pfliegler, Gy., Mikkola, H., Muszbek, L.: Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia. Blood. 96: 2479-86 (2000)
  • Muszbek, L.: Deficiency causing mutations and common polymorphisms in the Factor XIII-A gene Thromb. Haemost. 84: 524-7 (2000)
  • Kárpáti, L., Penke, B., Katona, É., Balogh, I., Vámosi, Gy., Muszbek, L.: A modified, optimized kinetic photometric assay for he determination of blood coagulation factor XIII activity in plasma Clin. Chem. 46: 1946-55 (2000)
  • Cauwenberghs N, Meiring M, Vauterin S, van Wyk V, Lamprecht S, Roodt JP, Novak L, Harsfalvi J, Deckmyn H, Kotze HF.: Antithrombotic effect of platelet glycoprotein Ib-blocking monoclonal antibody Fab fragments in nonhuman primates. Arterioscler Thromb Vasc Biol. 2000 May;20(5):1347-53.
  • Góth L.: Lipid and carbohydrate metabolism in acatalasemia. Clinical Chemistry. 2000;46:564-566
  • Góth L., Amir Shemirani, Tibor Kalmár: A novel catalase mutation ( a GA insertion) causes the Hungarian type of acatalasemia. Blood Cells, Molecules and Diseases. 2000;26:151-15
  • Góth  L., Gorzsás A., KalmárT.: A simple PCR-heteroduplex screening method for detection of a common mutation of the catalase gene. Clinical Chemistry. 2000;46:1199-1200.
  • Góth L., Eaton J.W.: Hereditary catalase deficiences and increased risk of diabetes.Lancet 2000;356:1820-1821.
  • V. Nagy E, Tóth J, Káldi I., Damjanovich J, Mezősi E, Lenkey Á, Tóth L, Szabó J, Karányi Zs. and Leövey A: Graves’ophthalmopathy: eye muscle involvement in patients with diploplia. European Journal of Endocrinology (2000) 142, 591-597
  • Káplár M, Kappelmayer J, Kiss A, Szabó K, Udvardy M: Increased Leukocyte-Platelet adhesion in chronic myeloproliferative disorders with high platelet counts. Platelets 11: 97-98, 2000
  • Regéczy N, Balogh I, Lakos G, Kappelmayer J, Kiss E: Membranous glomerulonephritis in a patient with inherited activated protein C resistance. Clinical Nephrology 53: 390-393, 2000
  • Kappelmayer J, Gratama J, Karászi É, Menéndez P, Ciudad J, Rivas R, Orfao A. Flow cytometric detection of intracellular myeloperoxidase, CD3 and CD79a. Interaction between monoclonal antibody clones, fluorochromes and sample preparation protocols. Journal of Immunological Methods 242: 53-65, 2000

Frissítés dátuma: 2019.06.27.