Department of Pediatrics and medical genetics (ceased 1-10-2018)
5407 publications
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Unfortunate oversight
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Quantification of left-ventricular function in patients with abnormal left coronary artery arising from the pulmonary artery late post-repair: a strain and strain rate imaging study
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BRCA1/2 mutation spectrum and frequencies in Belgian breast/ovarian cancer families
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The midwall stress-velocity relationship during manipulation of afterload
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Ehlers-Danlos syndrome, classic type
(2003) GeneReviews®. -
Leber congenital amaurosis
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- Journal Article
- A1
- open access
Use of an event recorder in the decision for pacemaker implantation in a child with syncope
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The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIc)
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Oral manifestations of Marfan syndrome
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Orofacial manifestations in a thirteen-year-old girl with dermatosparaxis (Ehlers-Danos syndrome type VIIc)
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De korte termijn uitkomst van extreem premature pasgeborenen in België (1999-2000)
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Effect of the APOE-491A/T promoter polymorphism on apolipoprotein E levels and risk of Alzheimer disease: the Rotterdam study
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The gene encoding nicastrin, a major γ-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample
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Tau negative frontal lobe dementia at 17q21 : significant finemapping of the candidate region to a 4.8 cM interval
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A population-based study on outcome to discharge for extremely preterm infants born in Belgium during 1999 - 2000 (EPIBEL study)
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Letter to the editor: Meningeal carcinomatosis in a child with Ewing sarcoma
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Continuous flow peritoneal dialysis : an option for future
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Rationalised ACE inhibition (ACE-I) dosing in non-hypertensive children
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Retrospective analysis of efficacy and tolerability of tolterodine in children with overactive bladder
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Nocturnal enuresis (NE) is correlated with an increased nocturnal diuresi/maximal bladder volume ratio
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Referentiewaarden voor uroflow bij kinderen 5-12 jaar
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Critical appraisal of dose-response ACE-I studies in hypertensive patients
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Acute renal failure (ARF) in nephrotic syndrome (NS) is caused by a decreased permeability of the basal membrane
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Proximal tubular hypertrophy during long-term follow-up of children for unilateral Wilm's tumor
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Long term follow up of DDAVP treated enuresis
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Enuresis-incontinentie na levertransplantatie
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Vessel wall tracking based on the modified autocorrelation estimator
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Is DFNA5 a susceptibility gene for age-related hearing impairment?
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Multicollinearity in prognostic factor analyses using the EORTC QLQ-C30 : identification and impact on model selection
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Erythropoietin improves quality of life : a response
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Human recombinant erythropoietin and quality of life : a wonder drug or something to wonder about?
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- Journal Article
- A1
- open access
Complex splicing pattern generates great diversity in human NF1 transcripts
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Evaluatie van stageplaatsen door co-assistenten: papier of internet?
(2002) -
Iood-131 MIBG therapie bij neuro-endocriene tumoren: huidige stand van zaken en indicaties
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Een onderzoek naar de mogelijkheden van asynchrone discussiegroepen bij stage-ondersteuning.
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Discussion group using asynchronous learning network during a clinical rotation in Paediatrics.
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Clinical features of DFNA5
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Meconiaal vruchtwater en het meconiumaspiratiesyndroom
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Evolutie van de indicaties voor hartkatheterisatie bij kinderen.
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Sport: van ontspanning tot competitue
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Nutrition in patients with Cystic Fibrosis : a European consensus
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FOXL2 mutation screening in a large panel of POF patients and XX males
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Homozygous Gly530Ser substitution in COL5A1 causes mild classical Ehlers-Danlos syndrome
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Acute intramural haematoma of the coeliac artery.
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Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).
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Moleculaire genetica bij de vasculaire vorm van het syndroom van Ehlers-Danlos
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- Journal Article
- A1
- open access
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
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CHIRURGISCHE AANPAK EN GENETISCHE DIAGNOSE BIJ EEN KIND MET SYNDROOM VAN MUENKE.
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Meerkleuren fluorescentie in situ hybridisatie: methodologie en toepassingen in diagnostiek en onderzoek
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Wanneer speelt erfelijkheid een rol