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- Journal Article
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Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia
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Joubert syndrome in three siblings
(2015) TIJDSCHRIFT VAN DE BELGISCHE KINDERARTS. In Tijdschrift van de Belgische kinderarts 17(1). p.93-93 -
- Conference Paper
- C3
- open access
Joubert syndrome in three siblings
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A missence mutation in complement factor I associated with recurrent aseptic meningoencephalitis
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Rationalised ACE inhibition (ACE-I) dosing in non-hypertensive children
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Critical appraisal of dose-response ACE-I studies in hypertensive patients
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Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence.
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Rationele aanpak van mictie en continentieproblemen bij kinderen : het Gents model, multidisciplinaire aanpak
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- Conference Paper
- C3
- open access
Les enfants énurétiques avec une capacité vesicale petite comme sele signe clinique : pas d'énurésie nocturne monosymptomatique?