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Herzschrittmachertherapie & Elektrophysiologie
|
February 9, 2024
Idiopathic ventricular fibrillation: is it a case for genetic testing?
S N van der Crabben, A A M Wilde
Journal of Inherited Metabolic Disease
|
January 24, 2008
Effect of cysteine dosage on erythrocyte glutathione synthesis rate in a patient with cystathionine beta synthase deficiency
S N van der Crabben, F A Wijburg, M T Ackermans, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 17, 2004
[Qualitative malnutrition due to incorrect complementary feeding in Bush Negro children in Suriname]
S N van der Crabben, H S Heymans, A A van Kempen, et al.
European Journal of Pediatrics
|
October 9, 2025
Genetic evaluation of sudden unexpected death in infants and children
A M Pries, S N van der Crabben, H A Moll, et al.
Journal of Inherited Metabolic Disease
|
March 7, 2013
An update on serine deficiency disorders
S N van der Crabben, N M Verhoeven-Duif, E H Brilstra, et al.
Orphanet Journal of Rare Diseases
|
December 21, 2019
Mandibuloacral dysplasia type B (MADB): a cohort of eight patients from Suriname with a homozygous founder mutation in ZMPSTE24 (FACE1), clinical diagnostic criteria and management guidelines
M M Hitzert, S N van der Crabben, G Baldewsingh, et al.
Hormone Research in Paediatrics
|
November 28, 2013
Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type II
M J E Kempers, S N van der Crabben, M de Vroede, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
February 23, 2008
Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans
M E Stegenga, S N van der Crabben, M C Dessing, et al.
Human Genetics
|
April 8, 2017
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions
G H Renkema, G Visser, F Baertling, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 3, 2021
BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants-design and status
M Jansen, I Christiaans, S N van der Crabben, et al.
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Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Herzschrittmachertherapie & Elektrophysiologie
|
February 9, 2024
Idiopathic ventricular fibrillation: is it a case for genetic testing?
S N van der Crabben, A A M Wilde
Journal of Inherited Metabolic Disease
|
January 24, 2008
Effect of cysteine dosage on erythrocyte glutathione synthesis rate in a patient with cystathionine beta synthase deficiency
S N van der Crabben, F A Wijburg, M T Ackermans, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 17, 2004
[Qualitative malnutrition due to incorrect complementary feeding in Bush Negro children in Suriname]
S N van der Crabben, H S Heymans, A A van Kempen, et al.
European Journal of Pediatrics
|
October 9, 2025
Genetic evaluation of sudden unexpected death in infants and children
A M Pries, S N van der Crabben, H A Moll, et al.
Journal of Inherited Metabolic Disease
|
March 7, 2013
An update on serine deficiency disorders
S N van der Crabben, N M Verhoeven-Duif, E H Brilstra, et al.
Orphanet Journal of Rare Diseases
|
December 21, 2019
Mandibuloacral dysplasia type B (MADB): a cohort of eight patients from Suriname with a homozygous founder mutation in ZMPSTE24 (FACE1), clinical diagnostic criteria and management guidelines
M M Hitzert, S N van der Crabben, G Baldewsingh, et al.
Hormone Research in Paediatrics
|
November 28, 2013
Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type II
M J E Kempers, S N van der Crabben, M de Vroede, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
February 23, 2008
Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans
M E Stegenga, S N van der Crabben, M C Dessing, et al.
Human Genetics
|
April 8, 2017
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions
G H Renkema, G Visser, F Baertling, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 3, 2021
BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants-design and status
M Jansen, I Christiaans, S N van der Crabben, et al.
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of 2