Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype.

Autor: van Meegeren ME; Hemophilia Treatment Center, Radboud University Medical Center, Nijmegen, The Netherlands., Mancini TL; Unit Thrombosis Hemostasis, Laboratory of Hematology, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands., Schoormans SC; Unit Thrombosis Hemostasis, Laboratory of Hematology, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands., van Haren BJ; Unit Thrombosis Hemostasis, Laboratory of Hematology, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands., van Duren C; Unit Thrombosis Hemostasis, Laboratory of Hematology, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands., Diekstra A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Laros-van Gorkom BA; Hemophilia Treatment Center, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands., Brons PP; Hemophilia Treatment Center, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands., Simons A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Hoefsloot L; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., van Heerde WL; Hemophilia Treatment Center, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands.

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2015 Sep; Vol. 21 (5), pp. e375-83. Date of Electronic Publication: 2015 Jul 24.

Bone cysts in patients with afibrinogenaemia: a literature review and two new cases.

Autor: van Meegeren ME; Haemophilia Treatment Center, Radboud University Medical Center, Nijmegen, The Netherlands., de Rooy JW, Schreuder HW, Brons PP

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2014 Mar; Vol. 20 (2), pp. 244-8. Date of Electronic Publication: 2013 Nov 29.

A short time window to profit from protection of blood-induced cartilage damage by IL-4 plus IL-10.

Autor: van Meegeren ME; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands. M.E.R.vanMeegeren@umcutrecht.nl, Roosendaal G, van Veghel K, Mastbergen SC, Lafeber FP

Publikováno v: Rheumatology (Oxford, England) [Rheumatology (Oxford)] 2013 Sep; Vol. 52 (9), pp. 1563-71. Date of Electronic Publication: 2013 Feb 14.

Joint distraction: a treatment to consider for haemophilic arthropathy.

Autor: van Meegeren ME; Department of Rheumatology and Clinical Immunology, University Medical Center (UMC) Utrecht, Utrecht, The Netherlands., van Vulpen LF, Roosendaal G, Lafeber FP, Mastbergen SC

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2012 Nov; Vol. 18 (6), pp. e418-20. Date of Electronic Publication: 2012 Sep 07.

Joint distraction results in clinical and structural improvement of haemophilic ankle arthropathy: a series of three cases.

Autor: Van Meegeren ME; Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands. m.e.r.vanmeegeren@umcutrecht.nl, Van Veghel K, De Kleijn P, Van Roermund PM, Biesma DH, Lafeber FP, Roosendaal G

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2012 Sep; Vol. 18 (5), pp. 810-7. Date of Electronic Publication: 2012 Apr 25.