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Journal of the Belgian Society of Radiology
|
October 25, 2021
Vertebral Tongue-Like Deformity in Mucopolysaccharidosis VI
Michiel Landen, François Eyskens, Filip Vanhoenacker
Molecular Genetics and Metabolism Reports
|
October 11, 2024
Unexplained splenomegaly as a diagnostic marker for a rare but severe disease with an innovative and highly effective new treatment option: A case report
Amber Van Baelen, Stijn Verhulst, François Eyskens
International Journal of Molecular Sciences
|
August 14, 2025
High-Resolution Mass Spectrometry Method for Targeted Screening and Monitoring of Fabry, Gaucher and ASMD Using Dried Blood Spots and Capitainers: Impact of Sample Matrix on Measurement Results
Amber Van Baelen, Stijn Verhulst, François Eyskens
Case Reports in Obstetrics and Gynecology
|
June 27, 2015
Carnitine Deficiency and Pregnancy
Anouk de Bruyn, Yves Jacquemyn, Kristof Kinget, et al.
Acta Cardiologica
|
June 13, 2024
Left ventricular hypertrophy: do not forget Fabry disease. Diagnostic work-up and differential diagnosis
Bernard P Paelinck, Antoine Bondue, Tomas Robyns, et al.
Molecular Genetics and Metabolism Reports
|
August 31, 2023
A new multiplex analysis of glucosylsphingosine and globotriaosylsphingosine in dried blood spots by tandem mass spectrometry
Amber Van Baelen, Laurence Roosens, Sylvie Devos, et al.
Children (Basel, Switzerland)
|
September 28, 2023
What Mothers Know about Newborn Bloodspot Screening and the Sources They Use to Acquire This Knowledge: A Pilot Study in Flanders
Caroline di Gangi, Maren Hermans, Maissa Rayyan, et al.
JIMD Reports
|
March 6, 2023
Severe dilated cardiomyopathy as an unusual clinical presentation in an infant with sialidosis type II
Margot Eyskens, Luc Bruyndonckx, André B P Van Kuilenburg, et al.
Frontiers in Neurology
|
June 6, 2018
Galactosidase Alpha p.A143T Variant Fabry Disease May Result in a Phenotype With Multifocal Microvascular Cerebral Involvement at a Young Age
Lothar Hauth, Jeroen Kerstens, Laetitia Yperzeele, et al.
European Child & Adolescent Psychiatry
|
March 15, 2006
Cognitive functioning and psychiatric disorders in children with a metabolic disease
Annik Simons, François Eyskens, Ann De Groof, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Journal of the Belgian Society of Radiology
|
October 25, 2021
Vertebral Tongue-Like Deformity in Mucopolysaccharidosis VI
Michiel Landen, François Eyskens, Filip Vanhoenacker
Molecular Genetics and Metabolism Reports
|
October 11, 2024
Unexplained splenomegaly as a diagnostic marker for a rare but severe disease with an innovative and highly effective new treatment option: A case report
Amber Van Baelen, Stijn Verhulst, François Eyskens
International Journal of Molecular Sciences
|
August 14, 2025
High-Resolution Mass Spectrometry Method for Targeted Screening and Monitoring of Fabry, Gaucher and ASMD Using Dried Blood Spots and Capitainers: Impact of Sample Matrix on Measurement Results
Amber Van Baelen, Stijn Verhulst, François Eyskens
Case Reports in Obstetrics and Gynecology
|
June 27, 2015
Carnitine Deficiency and Pregnancy
Anouk de Bruyn, Yves Jacquemyn, Kristof Kinget, et al.
Acta Cardiologica
|
June 13, 2024
Left ventricular hypertrophy: do not forget Fabry disease. Diagnostic work-up and differential diagnosis
Bernard P Paelinck, Antoine Bondue, Tomas Robyns, et al.
Molecular Genetics and Metabolism Reports
|
August 31, 2023
A new multiplex analysis of glucosylsphingosine and globotriaosylsphingosine in dried blood spots by tandem mass spectrometry
Amber Van Baelen, Laurence Roosens, Sylvie Devos, et al.
Children (Basel, Switzerland)
|
September 28, 2023
What Mothers Know about Newborn Bloodspot Screening and the Sources They Use to Acquire This Knowledge: A Pilot Study in Flanders
Caroline di Gangi, Maren Hermans, Maissa Rayyan, et al.
JIMD Reports
|
March 6, 2023
Severe dilated cardiomyopathy as an unusual clinical presentation in an infant with sialidosis type II
Margot Eyskens, Luc Bruyndonckx, André B P Van Kuilenburg, et al.
Frontiers in Neurology
|
June 6, 2018
Galactosidase Alpha p.A143T Variant Fabry Disease May Result in a Phenotype With Multifocal Microvascular Cerebral Involvement at a Young Age
Lothar Hauth, Jeroen Kerstens, Laetitia Yperzeele, et al.
European Child & Adolescent Psychiatry
|
March 15, 2006
Cognitive functioning and psychiatric disorders in children with a metabolic disease
Annik Simons, François Eyskens, Ann De Groof, et al.
Page
of 3