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Veerle Labarque

Showing results (21-30 of 76) with videos related to

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Scientific Reports|March 3, 2026
A multiplex allele-specific polymerase chain reaction assay for rapid and affordable detection of APOL1 risk variantsOyindamola Christiana Adebayo, Inge Bongaers, Elena Levtchenko, et al.
Frontiers in Pediatrics|October 11, 2023
Case report: Cardiac intimal sarcoma in a young childSanne Verbeek, Raf Sciot, Maria Debiec-Rychter, et al.
Thrombosis and Haemostasis|November 15, 2021
F11 Gene Duplication Causes Elevated FXI Plasma Levels and Is a Risk for Venous ThrombosisChristine Van Laer, Kathelijne Peerlinck, Marc Jacquemin, et al.
VASA. Zeitschrift Fur Gefasskrankheiten|September 7, 2016
Transarterial embolization of peripheral arteriovenous malformations with ethylenevinyl alcohol copolymer - feasibility, technical outcomes, and clinical outcomesTom De Beule, Jan Vranckx, Peter Verhamme, et al.
Fetal Diagnosis and Therapy|February 17, 2026
Hemoglobin Bart's disease and the Agrinio mutation: A case report of successful fetal interventionKobe Haenen, Emma Van den Eede, Jeroen Breckpot, et al.
Pediatric Nephrology (Berlin, Germany)|December 6, 2022
HIV-associated nephropathy in children: challenges in a resource-limited settingAgathe B Nkoy, Pépé M Ekulu, Veerle Labarque, et al.
Pharmacogenomics|June 9, 2017
The role of the MTHFR C677T polymorphism in methotrexate-induced toxicity in pediatric osteosarcoma patientsLoes Lambrecht, Charlotte Sleurs, Veerle Labarque, et al.
BMC Nephrology|December 16, 2025
APOL1-mediated kidney disease: a narrative review of the lessons learnt from the past 15 yearsOyindamola Christiana Adebayo, Henry Chijindu Okpoli, Joris Vriens, et al.
Pediatric Nephrology (Berlin, Germany)|May 29, 2021
Sickle cell nephropathy: insights into the pediatric populationOyindamola C Adebayo, Lambertus P Van den Heuvel, Wasiu A Olowu, et al.
Research and Practice in Thrombosis and Haemostasis|February 17, 2023
<i>F8/F9</i> variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation ProjectVeerle Labarque, Maria Elisa Mancuso, Mutlu Kartal-Kaess, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
Scientific Reports|March 3, 2026
A multiplex allele-specific polymerase chain reaction assay for rapid and affordable detection of APOL1 risk variantsOyindamola Christiana Adebayo, Inge Bongaers, Elena Levtchenko, et al.
Frontiers in Pediatrics|October 11, 2023
Case report: Cardiac intimal sarcoma in a young childSanne Verbeek, Raf Sciot, Maria Debiec-Rychter, et al.
Thrombosis and Haemostasis|November 15, 2021
F11 Gene Duplication Causes Elevated FXI Plasma Levels and Is a Risk for Venous ThrombosisChristine Van Laer, Kathelijne Peerlinck, Marc Jacquemin, et al.
VASA. Zeitschrift Fur Gefasskrankheiten|September 7, 2016
Transarterial embolization of peripheral arteriovenous malformations with ethylenevinyl alcohol copolymer - feasibility, technical outcomes, and clinical outcomesTom De Beule, Jan Vranckx, Peter Verhamme, et al.
Fetal Diagnosis and Therapy|February 17, 2026
Hemoglobin Bart's disease and the Agrinio mutation: A case report of successful fetal interventionKobe Haenen, Emma Van den Eede, Jeroen Breckpot, et al.
Pediatric Nephrology (Berlin, Germany)|December 6, 2022
HIV-associated nephropathy in children: challenges in a resource-limited settingAgathe B Nkoy, Pépé M Ekulu, Veerle Labarque, et al.
Pharmacogenomics|June 9, 2017
The role of the MTHFR C677T polymorphism in methotrexate-induced toxicity in pediatric osteosarcoma patientsLoes Lambrecht, Charlotte Sleurs, Veerle Labarque, et al.
BMC Nephrology|December 16, 2025
APOL1-mediated kidney disease: a narrative review of the lessons learnt from the past 15 yearsOyindamola Christiana Adebayo, Henry Chijindu Okpoli, Joris Vriens, et al.
Pediatric Nephrology (Berlin, Germany)|May 29, 2021
Sickle cell nephropathy: insights into the pediatric populationOyindamola C Adebayo, Lambertus P Van den Heuvel, Wasiu A Olowu, et al.
Research and Practice in Thrombosis and Haemostasis|February 17, 2023
<i>F8/F9</i> variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation ProjectVeerle Labarque, Maria Elisa Mancuso, Mutlu Kartal-Kaess, et al.
Pageof 8