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Acta Orthopaedica Belgica|April 17, 2008
Current limitations to the histopathological diagnosis of some frequently encountered bone tumoursChristine Galant, Jacques Malghem, Catherine Sibille, et al.
Hepatology (Baltimore, Md.)|October 31, 2007
Human skin fibroblasts: From mesodermal to hepatocyte-like differentiationPhilippe A Lysy, Françoise Smets, Catherine Sibille, et al.
Hereditas|November 23, 2007
Partial proximal 10q trisomy: a new case associated with biliary atresiaPhilippe A Lysy, Catherine Sibille, Yves Gillerot, et al.
Pathology, Research and Practice|March 18, 2014
Myofibroblastoma of the breast with smooth muscle differentiation showing deletion of 13q14 region: report of a caseAnne-Laure Trépant, Catherine Sibille, Ana-Maria Frunza, et al.
Pediatric Blood & Cancer|July 21, 2006
Retinoblastoma and deletion of the long arm of chromosome 13: an underestimated diagnosis?Bénédicte Brichard, Christophe Chantrain, Jean-Luc Gala, et al.
Gastroenterology|April 19, 2006
Sustained engraftment and tissue enzyme activity after liver cell transplantation for argininosuccinate lyase deficiencyXavier Stéphenne, Mustapha Najimi, Catherine Sibille, et al.
European Journal of Cancer (Oxford, England : 1990)|December 14, 2005
Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutationBénédicte Brichard, Michel Heusterspreute, Patrick De Potter, et al.
Haematologica|June 14, 2005
6q- is an early and persistent chromosomal aberration in CD3-CD4+ T-cell clones associated with the lymphocytic variant of hypereosinophilic syndromeMarie Ravoet, Catherine Sibille, Florence Roufosse, et al.
Blood|July 18, 2009
Molecular profiling of CD3-CD4+ T cells from patients with the lymphocytic variant of hypereosinophilic syndrome reveals targeting of growth control pathwaysMarie Ravoet, Catherine Sibille, Chunyan Gu, et al.
Experimental Hematology|October 13, 2005
Defective CD3gamma gene transcription is associated with NFATc2 overexpression in the lymphocytic variant of hypereosinophilic syndromeKaren E Willard-Gallo, Bassam M Badran, Marie Ravoet, et al.
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