Lize van Vulpen - University Medical Center Utrecht

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A clinical practice guideline for primary care physiotherapy in patients with haemophilia

Johan Blokzijl,Martijn F Pisters,Magnus Aspdahl, Wypke de Boer,Ruth Elise Dybvik Matlary, Danielle Douma-van Riet,Piet de Kleijn,Sébastien Lobet, Paula Loughnane,Paul McLaughlin,Melanie Bladen,Sheila Roche,David Stephensen,Leo van Vlimmeren,Lize F D van Vulpen,Merel A Timmer, EAHAD physiotherapy committee

Haemophilia : the official journal of the World Federation of Hemophilia (2024)

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Quantitative MRI Assessment of Joint Effusion Using T2-relaxometry at 3 Tesla: a Feasibility and Reproducibility Study

Flora H. P. van Leeuwen,Beatrice Lena,Eline D. P. van Bergen, Janoah J. van Klei,Merel A. Timmer,Lize F. D. van Vulpen,Kathelijn Fischer,Pim A. de Jong,Clemens Bos,Wouter Foppen

Skeletal Radiologypp.1-10, (2024)

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Unraveling Facets of MECOM-associated Syndrome: Somatic Genetic Rescue, Clonal Hematopoiesis, and Phenotype Expansion

Blood advancesno. 13 (2024): 3437-3443

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Letter in response to Bounaix et al ‘Management of anticoagulation and factor XIII replacement in a patient with severe factor XIII deficiency and recurrent venous thromboembolic disease’

Lize F.D. van Vulpen,F. Nanne Croles,Roger E.G. Schutgens

Research and Practice in Thrombosis and Haemostasispp.102535, (2024)

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Limited Value of Testing for Factor XIII and Α2-Antiplasmin Deficiency in Patients with a Bleeding Disorder of Unknown Cause

Sander Ariens,Albert Huisman,Idske C. L. Kremer Hovinga,Rolf T. Urbanus,Karin P. M. van Galen,Lize F. D. van Vulpen,Kathelijn Fischer,Roger E. G. Schutgens

HAEMOPHILIAno. 4 (2024): 998-1002

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Navigating the Challenges: a Case Report on Managing a Complicated Postpartum Course in Type 3 Von Willebrand Disease with Alloantibodies

Konrad van der Zwet,Karin P. M. van Galen,Annemiek C. C. Evers,Kathelijn Fischer,Roger E. G. Schutgens,Lize F. D. van Vulpen

RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASISno. 3 (2024)

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Towards Personalized Treatment in Haemophilia: the Role of Genetic Factors in Iron and Heme Control to Identify Patients at Risk for Haemophilic Arthropathy

Lize F. D. van Vulpen,Simon C. Mastbergen,Wouter Foppen,Kathelijn Fischer,Floris P. J. G. Lafeber,Roger E. G. Schutgens

JOURNAL OF PERSONALIZED MEDICINEno. 2 (2024)

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Patients with Moderate Hemophilia A and B with a Severe Bleeding Phenotype Have an Increased Burden of Disease

Marieke J. A. Verhagen,Erna C. van Balen,Nicole M. A. Blijlevens,Michiel Coppens,Waander L. van Heerde,Frank W. G. Leebeek,Sanna R. Rijpma,Lize F. D. van Vulpen,Samantha C. Gouw,Saskia E. M. Schols

JOURNAL OF THROMBOSIS AND HAEMOSTASISno. 1 (2024): 152-162

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Efficacy of a 1:1 Ratio VWF/FVIII Concentrate in Patients with Von Willebrand Disease

Geoffrey Z. L. Kuppens,Kathelijn Fischer,Karin P. M. van Galen,Eduard J. van Beers,Paul R. van der Valk,Idske C. L. Kremer Hovinga,Lize F. D. van Vulpen,Roger E. G. Schutgens

HAEMOPHILIA (2024)

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