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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: kappelmayer j. Life (Basel). 2021 Mar 5;11(3):202. doi: 10.3390/life11030202. Life (Basel). 2021. PMID: 33807613 Free PMC article.
Classical and atypical neuroblastoma--case reports.
Csáthy L, Kappelmayer J, Szegedi I, Kajtár B, Kiss C, Hevessy Z. Csáthy L, et al. Among authors: kappelmayer j. Cytometry B Clin Cytom. 2011 Mar;80(2):134-6. doi: 10.1002/cyto.b.20576. Epub 2010 Dec 2. Cytometry B Clin Cytom. 2011. PMID: 21337495 Free article.
Early relapse after rituximab chemoimmunotherapy.
Kiss F, Buslig J, Szegedi I, Scholtz B, Kappelmayer J, Kiss C. Kiss F, et al. Among authors: kappelmayer j. Pediatr Blood Cancer. 2008 Feb;50(2):372-5. doi: 10.1002/pbc.21388. Pediatr Blood Cancer. 2008. PMID: 17973316
222 results