Articles

O01 INHERITED ANTITHROMBIN DEFICIENCY AND THROMBOSIS IN CHILDHOOD: DATA FROM A LARGE MULTICENTRIC COHORT

BJH - 2019, issue ?, february 2019

C. Orlando , B. De La Morena-barrio , M.e. De La Morena-barrio , V. Vicente , J. Corral , K. Jochmans MD, PhD

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P01 EVALUATION OF THE COBAS T 711 COAGULATION ANALYSER: A SINGLE CENTER EXPERIENCE

BJH - 2019, issue ?, february 2019

C. Orlando , S. Damiaens , Ö. Belce , K. Jochmans MD, PhD

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P03 PREVALENCE OF HETEROZYGOUS TYPE 2N VON WILLEBRAND DISEASE MUTATIONS IN A BELGIAN SURVEY

BJH - 2019, issue ?, february 2019

I. Vangenechten , J. Jongenotter , K. Jochmans MD, PhD, C. Orlando , A. Gothot MD, PhD, K. Vandenbosch , A. Gadisseur MD, PhD

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A-136 THE p.Arg498Cys MUTATION IN THE CYSTEINE RICH DOMAIN OF ADAMTS13 RESULTS IN A SECRETION DEFICIENCY

BJH - volume 8, issue Abstract Book BSTH, february 2017

A.-S. Schelpe , C. Orlando , C. Geeroms , I. Pareyn , N. VanDePutte , H. Deckmyn PhD, K. Jochmans MD, PhD, S.F. De Meyer PhD, K. VanHoorelbeke PhD

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A-128 PREVALENCE OF HETEROZYGOUS TYPE 2N VON WILLEBRAND DISEASE MUTATIONS IN BELGIUM

BJH - volume 8, issue Abstract Book BSTH, february 2017

J. Jongenotter , I. Vangenechten , K. Jochmans MD, PhD, C. Orlando , A. Gothot MD, PhD, K. Vandenbosch , A. Gadisseur MD, PhD

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A-133 ACQUIRED HAEMOPHILIA A

BJH - volume 8, issue Abstract Book BSTH, february 2017

Y. Van der Beken , C. Orlando , K. Fostier MD, K. Jochmans MD, PhD

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PP2.3 A novel FGA mutation underlying a case of congenital dysfibrinogenemia with unusual clinical presentation

BJH - volume 7, issue Abstract Book BHS, january 2016

M. Tajdar PharmD, M. Herpol , C. Orlando , B. De Bisschop , P. Govaert , K. Jochmans MD, PhD

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