Publications by authors named "Claudine De Praeter"

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Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisions.
Claudine De Praeter, Arnaud Vanlander, Piet Vanhaesebrouck, Joél Smet, Sara Seneca

Eur J Pediatr· February 2015

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Lactic acidosis in a newborn with adrenal calcifications.
Alexandra Zecic, Joél E Smet, Claudine M De Praeter, Piet Vanhaesebrouck, Carlo Viscomi

Pediatr Res· September 2009

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Unilateral bloody nipple discharge in a two-month-old male.
Claudine De Praeter, Kris De Coen, Katrien Vanneste, Piet Vanhaesebrouck

Eur J Pediatr· April 2008

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Congenital pontocerebellar atrophy and telencephalic defects in three siblings: a new subtype.
Jules G Leroy, Gilles Lyon, Catherine Fallet, Jeanne Amiel, Claudine De Praeter

Acta Neuropathol· October 2007

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Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Gillian Rice, Teresa Patrick, Rekha Parmar, Claire F Taylor, Alec Aeby, Claudine De Praeter

Am J Hum Genet· October 2007

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Transplacental passage of a nonionic contrast agent.
Piet Vanhaesebrouck, Alain G Verstraete, Claudine De Praeter, Koenraad Smets, Alexandra Zecic

Eur J Pediatr· July 2005

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Phototherapy-mediated syndrome of inappropriate secretion of antidiuretic hormone in an in utero selective serotonin reuptake inhibitor-exposed newborn infant.
Piet Vanhaesebrouck, Freia De Bock, Alexandra Zecic, Claudine De Praeter, Koenraad Smets

Pediatrics· May 2005

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Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb).
Christof Völker, Claudine M De Praeter, Birgit Hardt, Willi Breuer, Burga Kalz-Füller

Glycobiology· August 2002

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