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Wim Terryn

Showing results (11-20 of 23) with videos related to

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Molecular Genetics and Metabolism|August 4, 2022
An expert consensus on practical clinical recommendations and guidance for patients with classic Fabry diseaseDominique P Germain, Gheona Altarescu, Roberto Barriales-Villa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 8, 2005
Phenytoin intoxication in critically ill patientsGert De Schoenmakere, Jan De Waele, Wim Terryn, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 14, 2012
Fabry nephropathy: indications for screening and guidance for diagnosis and treatment by the European Renal Best PracticeWim Terryn, Pierre Cochat, Roseline Froissart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 7, 2007
Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis populationWim Terryn, Bruce Poppe, Birgitte Wuyts, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 4, 2008
Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipientsGert De Schoenmakere, Bruce Poppe, Birgitte Wuyts, et al.
International Journal of Cardiology|July 19, 2012
Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophyWim Terryn, Gert Deschoenmakere, Jan De Keyser, et al.
Acta Clinica Belgica|February 17, 2026
A structured proactive penicillin allergy delabeling intervention in adult patients in three non-university hospitalsJodie Langbeen, Evy Desmyttere, Evelien Delaere, et al.
Circulation|February 22, 2021
Screening for Fabry Disease in Male Patients With Arrhythmia Requiring a Pacemaker or an Implantable Cardioverter-DefibrillatorDimitri Hemelsoet, Jan De Keyser, Frederic Van Heuverswyn, et al.
Orphanet Journal of Rare Diseases|May 23, 2022
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, et al.
Molecular Genetics and Metabolism|September 5, 2014
Chronic kidney disease and an uncertain diagnosis of Fabry disease: approach to a correct diagnosisLinda van der Tol, Einar Svarstad, Alberto Ortiz, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|August 4, 2022
An expert consensus on practical clinical recommendations and guidance for patients with classic Fabry diseaseDominique P Germain, Gheona Altarescu, Roberto Barriales-Villa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 8, 2005
Phenytoin intoxication in critically ill patientsGert De Schoenmakere, Jan De Waele, Wim Terryn, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 14, 2012
Fabry nephropathy: indications for screening and guidance for diagnosis and treatment by the European Renal Best PracticeWim Terryn, Pierre Cochat, Roseline Froissart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 7, 2007
Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis populationWim Terryn, Bruce Poppe, Birgitte Wuyts, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 4, 2008
Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipientsGert De Schoenmakere, Bruce Poppe, Birgitte Wuyts, et al.
International Journal of Cardiology|July 19, 2012
Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophyWim Terryn, Gert Deschoenmakere, Jan De Keyser, et al.
Acta Clinica Belgica|February 17, 2026
A structured proactive penicillin allergy delabeling intervention in adult patients in three non-university hospitalsJodie Langbeen, Evy Desmyttere, Evelien Delaere, et al.
Circulation|February 22, 2021
Screening for Fabry Disease in Male Patients With Arrhythmia Requiring a Pacemaker or an Implantable Cardioverter-DefibrillatorDimitri Hemelsoet, Jan De Keyser, Frederic Van Heuverswyn, et al.
Orphanet Journal of Rare Diseases|May 23, 2022
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, et al.
Molecular Genetics and Metabolism|September 5, 2014
Chronic kidney disease and an uncertain diagnosis of Fabry disease: approach to a correct diagnosisLinda van der Tol, Einar Svarstad, Alberto Ortiz, et al.
Pageof 3