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[Thrombocyte dysfunction in children with albinism].
Pap Z, Ajzner E, Kiss C, Emódy J, Závodszky I, Horváth A, Muszbek L. Pap Z, et al. Among authors: kiss c. Orv Hetil. 1997 Feb 23;138(8):467-71. Orv Hetil. 1997. PMID: 9139250 Hungarian.
Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.
Gindele R, Kerényi A, Kállai J, Pfliegler G, Schlammadinger Á, Szegedi I, Major T, Szabó Z, Bagoly Z, Kiss C, Kappelmayer J, Bereczky Z. Gindele R, et al. Among authors: kiss c. Life (Basel). 2021 Mar 5;11(3):202. doi: 10.3390/life11030202. Life (Basel). 2021. PMID: 33807613 Free PMC article.
344 results