Publications by authors named "Pascal Vannuffel"

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Correction to: Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLC.
Linea Melchior, Astrid Hirschmann, Paul Hofman, Christophe Bontoux, Angel Concha, Pascal Vannuffel

Virchows Arch· November 2024

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Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLC.
Linea Melchior, Astrid Hirschmann, Paul Hofman, Christophe Bontoux, Angel Concha, Pascal Vannuffel

Virchows Arch· April 2024

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Pathology of the bone marrow and spleen in a case of myelodysplastic/myeloproliferative neoplasm associated with t(8;9)(p22;p24) involving PCM1 and JAK2 genes.
Jean-Louis Dargent, Valérie Mathieux, Sébastien Vidrequin, Xavier Deghorain, Pascal Vannuffel

Eur J Haematol· January 2011

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Identification and characterization of a novel homozygous deletion in the alpha-N-acetylglucosaminidase gene in a patient with Sanfilippo type B syndrome (mucopolysaccharidosis IIIB).
Kristen J Champion, Monica J Basehore, Tim Wood, Anne Destrée, Pascal Vannuffel

Mol Genet Metab· May 2010

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Plasmacytoid dendritic cells in Kimura disease.
Jean-Louis Dargent, Pascal Vannuffel, Jean-Marie Saint-Remy, Simona Fisogni, Fabio Facchetti

Am J Dermatopathol· December 2009

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Impaired up-regulation of polo-like kinase 2 in B-cell chronic lymphocytic leukaemia lymphocytes resistant to fludarabine and 2-chlorodeoxyadenosine: a potential marker of defective damage response.
Emeline de Viron, Laurent Knoops, Thierry Connerotte, Caroline Smal, Lucienne Michaux, Pascal Vannuffel

Br J Haematol· December 2009

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Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin-2 stimulation: A Belgian multicentric study.
Natalie Put, Peter Konings, Katrina Rack, Mauricette Jamar, Nadine Van Roy, Pascal Vannuffel

Genes Chromosomes Cancer· October 2009

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The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset.
Isabelle Maystadt, René Rezsöhazy, Martine Barkats, Sandra Duque, Pascal Vannuffel

Am J Hum Genet· July 2007

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Rapid and easy prenatal diagnosis of sickle cell anemia using double-dye LNA probe technology.
Hakim E Housni, Jo Vandesompele, Pascal Vannuffel, Beatrice Gulbis, Jasmine Parma

Br J Haematol· February 2007

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Activity and safety of combined rituximab with chlorambucil in patients with mantle cell lymphoma.
Deborah Bauwens, Marie Maerevoet, Lucienne Michaux, Ivan Théate, Anne Hagemeijer, Pascal Vannuffel

Br J Haematol· November 2005

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