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  1. Article

    Clinical practice recommendations for kidney involvement in tuberous sclerosis complex: a consensus statement by the ERKNet Working Group for Autosomal Dominant Structural Kidney Disorders and the ERA Genes & Kidney Working Group

    Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by the presence of proliferative lesions throughout the body. Management of TSC is challenging because patients have a multiface...

    Djalila Mekahli, Roman-Ulrich Müller, Matko Marlais in Nature Reviews Nephrology (2024)

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    Article

    Low agreement between various eGFR formulae in pediatric and young adult ADPKD patients

    Young autosomal dominant polycystic kidney disease (ADPKD) patients are becoming the new target population for the development of new treatment options. Determination of a reliable equation for estimated glome...

    Pieter Schellekens, Marcelien Verjans, Peter Janssens in Pediatric Nephrology (2023)

  3. Article

    Open Access

    International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people

    These recommendations were systematically developed on behalf of the Network for Early Onset Cystic Kidney Disease (NEOCYST) by an international group of experts in autosomal dominant polycystic kidney disease...

    Charlotte Gimpel, Carsten Bergmann, Detlef Bockenhauer in Nature Reviews Nephrology (2019)

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    Article

    3DUS as an alternative to MRI for measuring renal volume in children with autosomal dominant polycystic kidney disease

    Total kidney volume, measured by magnetic resonance imaging (MRI), is a validated disease progression marker in adults with autosomal dominant polycystic kidney disease (ADPKD). However, in childhood, MRI is b...

    Luc Breysem, Stéphanie De Rechter, Frederik De Keyzer in Pediatric Nephrology (2018)

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    Article

    Multidetector CT of right-sided congenital diaphragmatic hernia associated with hepatopulmonary fusion in a newborn

    We present a neonate with a complex congenital cardiopathy and a right-sided diaphragmatic hernia complicated with hepatopulmonary fusion. Radiography, abdominal US and multidetector CT (MDCT) demonstrated rig...

    Luc Breysem, Sophie Vanhaesebrouck, Marc Gewillig in Pediatric Radiology (2012)

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    Article

    A rare presentation of renal Wegener granulomatosis in a child

    We present a rare case of Wegener granulomatosis of the kidney in childhood. The diagnosis was suggested on imaging due to a combination of clinical symptoms, the lack of improvement with antibiotic therapy, a...

    Riet D’Hauwe, Evelyne Lerut, Luc Breysem, Marleen Smet in Pediatric Radiology (2011)

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    Article

    Tracheal side effects following fetal endoscopic tracheal occlusion for severe congenital diaphragmatic hernia

    Jan Deprest, Luc Breysem, Eduardo Gratacos, Kypros Nicolaides in Pediatric Radiology (2010)

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    Article

    Vallecular cyst as a cause of congenital stridor: report of five patients

    Vallecular cysts are an unusual cause of congenital stridor.

    Luc Breysem, Veerle Goosens, Vincent Vander Poorten in Pediatric Radiology (2009)

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    Article

    High-resolution sonography of a scrotal abscess in a 2-week-old infant

    Scrotal abscess in infancy is rare and, in an otherwise healthy infant, an unexpected pathology. We present a 2-week-old boy with a unilateral scrotal swelling, imaged by high-resolution sonography. Sonography...

    Luc Breysem, Murielle Herman, Philippe Moerman in Pediatric Radiology (2006)

  10. No Access

    Article

    Ultrasound diagnosis of infantile scrotal emphysema

    We report a 4-month-old boy who developed scrotal emphysema following removal of a chest drain. The initial diagnosis was made by ultrasonography. This report describes the sonographic findings, pathophysiolog...

    Maria-Helena Smet, Marleen Palmers, Raymond Oyen, Luc Breysem in Pediatric Radiology (2004)

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    Article

    Fetal trauma: brain imaging in four neonates

    The purpose of this paper is to describe brain pathology in neonates after major traffic trauma in utero during the third trimester. Our patient cohort consisted of four neonates born by emergency cesarean sec...

    Luc Breysem, V. Cossey, E. Mussen, P. Demaerel, W. Van de Voorde in European Radiology (2004)

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    Article

    High-resolution real-time compound ultrasound imaging of transient protein-losing gastropathy of childhood

    We report the case of a 1.5-year-old girl with transient protein-losing gastropathy with hypertrophic gastric folds (PLGH). The diagnosis of PLGH was made by abdominal ultrasound (US) and not by an upper gastr...

    Maria-Helena Smet, Elvier Mussen, Nadine Ectors, Luc Breysem in European Radiology (2003)

  13. Article

    Postnatal cranial ultrasonographic findings in feto-fetal transfusion syndrome

    Our objective was a retrospective evaluation of cranial US in survivors of twin pregnancy with feto-fetal transfusion syndrome (FFTS), with knowledge of prenatal treatment and neonatal/postnatal clinical data...

    Luc Breysem, Gunnar Naulaers, Jan Deprest, Dominique Schoubroeck in European Radiology (2002)

  14. No Access

    Article

    Tuberous sclerosis with cystic renal disease and multifocal renal cell carcinoma in a baby girl

    An infant, in whom the prenatal diagnosis of tuberous sclerosis complex was made, presented with extreme bilateral nephromegaly owing to diffuse cystic changes. Histology of the resected non-functioning left ...

    Luc Breysem, Els Nijs, Willem Proesmans, Maria-Helena Smet in Pediatric Radiology (2002)

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    Article

    Lipoblastoma: a rare mediastinal tumour in a child

    Alain Broeders, Maria-Helena Smet, Luc Breysem, Guy Marchal in Pediatric Radiology (2000)

  16. No Access

    Article

    Erratum: Bronchopulmonary dysplasia: correlation of radiographic and clinical findings; Pediatr Radiol (1997) 27:642–646

    Luc Breysem, Maria-Helena Smet, Stefaan Van Lierde, Hugo Devlieger in Pediatric Radiology (1997)