Publications by authors named "A Depaepe"

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Complex regional pain syndrome associated with hyperattention rather than neglect for the healthy side: A comprehensive case study.
Laure Christophe, Ludovic Delporte, Patrice Revol, Annick DePaepe, Gilles Rode

Ann Phys Rehabil Med· December 2016

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Compound heterozygous mutations of the TNXB gene cause primary myopathy. Response.
Valérie Allamand, Philippe Beurrier, Ludovic Martin, Fransiska Malfait, Delfien Syx, Anne DePaepe

Neuromuscul Disord· January 2014

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Split hand foot malformation is associated with a reduced level of Dactylin gene expression.
D Basel, A DePaepe, M W Kilpatrick, P Tsipouras

Clin Genet· October 2003

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Acrogeria of the Gottron type in a mother and son.
M Blaszczyk, A Depaepe, L Nuytinck, M Glinska-Ferenz, S Jablonska

Eur J Dermatol· March 2000

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Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: about one-fifth are recurrent.
J Körkkö, H Kuivaniemi, P Paassilta, J Zhuang, G Tromp, A DePaepe

Hum Mutat· May 1997

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