Research Explorer

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Researcher

Wim Terryn

Awards & Distinctions

7 Results

2023

From gastrointestinal enigma to genetic clarity : unraveling the MYH11 SM2 connection

Steven CallensBart DermautFilomeen HaerynckDimitri HemelsoetLeslie NaessensBruce PoppeSanne SteyaertWim TerrynArnaud VanlanderPATRICK VERLOO et al.

2018

IRF2BPL is associated with neurological phenotypes

Paul C MarcoglieseVandana ShashiRebecca C SpillmannNicholas StongJill A RosenfeldMary Kay KoenigJulian A Martínez-AgostoMatthew HerzogAgnes H ChenPatricia I Dickson et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

2013

Questioning the pathogenic role of the GLA p.Ala143Thr 'mutation' in Fabry disease: implications for screening studies and ERT

Wim TerrynRaymond VanholderDimitri HemelsoetBart LeroyWim Van BiesenG De SchoenmakereBrigitte WuytsKathleen ClaesJulie De BackerAnne De Paepe et al.

Bookchapter in JIMD reports : case and research reports 2012/5

Safety and sample adequacy of renal transplant surveillance biopsies

MARGO LAUTERaymond VanholderDirk VoetPatrick PeetersK CokelaereS DelooseWim Terryn

A1 Journal Article in ACTA CLINICA BELGICA

Screening for Fabry disease: indications, methods and implications

Wim TerrynRaymond VanholderBruce Poppe

2005

Phenytoin intoxication in critically ill patients

Gert De SchoenmakereJan De WaeleWim TerrynMieke DeweweireAlain VerstraeteEric HosteSylvie RotteyNorbert LameireFrancis Colardyn

A1 Journal Article in AMERICAN JOURNAL OF KIDNEY DISEASES

2004

Delayed graft function in renal transplantation

Patrick PeetersWim TerrynRaymond VanholderNorbert Lameire

A2 Journal Article in CURRENT OPINION IN CRITICAL CARE