Publications by authors named "Wim Terryn"

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Development and validation of a tool for ambulatory monitoring of peripherally inserted central catheter-associated complications.
Sofie Segers, Jodie Langbeen, Stijn Blot, Wim Terryn, Mieke Debrauwere

J Vasc Access· December 2024

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Prosthetic Joint Infection: Case Report and a Review of the Literature.
Stijn Jonckheere, Celestin Mairesse, Patricia Vandecandelaere, Jens Vanbiervliet, Wim Terryn

Pathogens· September 2024

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Intermediate uveitis in common variable immunodeficiency (CVID) associated with a heterozygous variant in the TNFRSF13B gene.
Mathijs Osaer, Wim Terryn, Elfride De Baere, Ciel De Vriendt, Filomeen Haerynck

Retin Cases Brief Rep· July 2024

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Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.
Nika Schuermans, Salima El Chehadeh, Dimitri Hemelsoet, Jérémie Gautheron, Marie-Christine Vantyghem, Wim Terryn

Nat Genet· November 2023

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An expert consensus on practical clinical recommendations and guidance for patients with classic Fabry disease.
Dominique P Germain, Gheona Altarescu, Roberto Barriales-Villa, Renzo Mignani, Krzysztof Pawlaczyk, Wim Terryn

Mol Genet Metab· October 2022

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Efficacy and safety of the investigational complement C5 inhibitor zilucoplan in patients hospitalized with COVID-19: an open-label randomized controlled trial.
Elisabeth De Leeuw, Karel F A Van Damme, Jozefien Declercq, Cedric Bosteels, Bastiaan Maes, Wim Terryn

Respir Res· August 2022

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Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).
Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, Sanne Steyaert, Rudy Van Coster

Orphanet J Rare Dis· May 2022

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Screening for Fabry Disease in Male Patients With Arrhythmia Requiring a Pacemaker or an Implantable Cardioverter-Defibrillator.
Dimitri Hemelsoet, Jan De Keyser, Frederic Van Heuverswyn, Rik Willems, Hans Vandekerckhove, Wim Terryn

Circulation· February 2021

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Chronic intestinal pseudo-obstruction due to β2microglobulin-amyloidosis in a patient on high-flux haemodialysis.
Pieter De Mulder, Kristof Cokelaere, Wim Terryn

BMJ Case Rep· January 2020

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Future perspectives of genome-scale sequencing.
Wouter Steyaert, Steven Callens, Paul Coucke, Bart Dermaut, Dimitri Hemelsoet, Wim Terryn

Acta Clin Belg· February 2018

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Aggressive extensive cardiac mass in an HIV-1-infected patient: should we go for comfort therapy?
Delphine Mtf Vervloet, Michel De Pauw, Laurent Demulier, Jan Vercammen, Wim Terryn

Acta Clin Belg· June 2017

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Gouty arthritis of the spine in a renal transplant patient: a clinical case report: an unusual presentation of a common disorder.
Sofie Dhaese, Marijke Stryckers, Hans Van Der Meersch, Wim Terryn, Steven Van Laecke

Medicine (Baltimore)· April 2015

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Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document.
Marieke Biegstraaten, Reynir Arngrímsson, Frederic Barbey, Lut Boks, Franco Cecchi, Wim Terryn

Orphanet J Rare Dis· March 2015

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Chronic kidney disease and an uncertain diagnosis of Fabry disease: approach to a correct diagnosis.
Linda van der Tol, Einar Svarstad, Alberto Ortiz, Camilla Tøndel, João Paulo Oliveira, Wim Terryn

Mol Genet Metab· February 2015

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Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy.
Wim Terryn, Gert Deschoenmakere, Jan De Keyser, Wouter Meersseman, Wim Van Biesen

Int J Cardiol· September 2013

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Fabry nephropathy: indications for screening and guidance for diagnosis and treatment by the European Renal Best Practice.
Wim Terryn, Pierre Cochat, Roseline Froissart, Alberto Ortiz, Yves Pirson

Nephrol Dial Transplant· March 2013

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Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipients.
Gert De Schoenmakere, Bruce Poppe, Birgitte Wuyts, Kathleen Claes, David Cassiman, Wim Terryn

Nephrol Dial Transplant· December 2008

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Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population.
Wim Terryn, Bruce Poppe, Birgitte Wuyts, Kathleen Claes, Bart Maes

Nephrol Dial Transplant· January 2008

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Goodpasture's syndrome associated with autoimmune thrombotic thrombocytopenic purpura an unusual case.
Wim Terryn, Dominique Benoit, Ann Van Loo, Patrick Peeters, Hans Schepkens

Nephrol Dial Transplant· December 2007

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Phenytoin intoxication in critically ill patients.
Gert De Schoenmakere, Jan De Waele, Wim Terryn, Mieke Deweweire, Alain Verstraete

Am J Kidney Dis· January 2005

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A dramatic case of calciphylaxis 20 years after kidney transplantation.
Hilde Vanbelleghem, Wim Terryn, Leen Van Leuven, Daniel Van Caesbroeck, Pieter Demetter

Nephrol Dial Transplant· December 2004

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Delayed graft function in renal transplantation.
Patrick Peeters, Wim Terryn, Raymond Vanholder, Norbert Lameire

Curr Opin Crit Care· December 2004

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