Research Explorer

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Researcher

Wim Terryn

5 Results

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 DicksonHenry J LinMoin U VeraNoriko SalamonJohn M GrahamDamara OrtizElena InfanteWouter SteyaertBart DermautBruce PoppeHyung-Lok ChungZhongyuan ZuoPei-Tseng LeeOguz KancaFan XiaYapng YangEdward C SmithJoan JasienSujay KansagraGail SpiridigliozziMays El-DairiRobert LarkKacie RileyDwight D KoeberlKatie Golden-GrantShinya YamamotoMichael F WanglerGhayda MirzaaDimitri HemelsoetBrendan LeeStanley F NelsonDavid B GoldsteinHugo J BellenLoren DM Penathe Program for Undiagnosed Diseases (UD-PrOZA)Steven CallensPaul CouckeWim TerrynRudy Van Coster

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 PaepeA FogoMarleen PraetBruce Poppe

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

2004

Delayed graft function in renal transplantation

Patrick PeetersWim TerrynRaymond VanholderNorbert Lameire

A2 Journal Article in CURRENT OPINION IN CRITICAL CARE