J. Billiet

发表

Prevalence and Induction of Circulating Antibodies against Recombinant Staphylokinase

P. Declerck, H. Moreau, D. Collen, 1994, Thrombosis and Haemostasis.

High frequency of the JAK2 V617F mutation in patients with thrombocytosis (platelet count>600x109/L) and ringed sideroblasts more than 15% considered as MDS/MPD, unclassifiable.

U. Germing, R. Kronenwett, N. Gattermann, 2007, Blood.

Autologous cord blood use: Clinical and scientific aspects

D. Latinne, A. Ferrant, Y. Benoît, 2011 .

Haptoglobin phenotype 2-2 overrepresentation in Cys282Tyr hemochromatotic patients.

M. Vos, H. Van Vlierberghe, G. Leroux-Roels, 2001, Journal of hepatology.

constitute a new subset of chronic lymphocytic leukemia? 3-21 genes H Do B-cell chronic lymphocytic leukemia patients with Ig V

B. Cauwelier, D. Selleslag, A. Louwagie, 2011 .

Do B-cell chronic lymphocytic leukemia patients with Ig VH3-21 genes constitute a new subset of chronic lymphocytic leukemia?

B. Cauwelier, D. Selleslag, A. Louwagie, 2002, Blood.

Ruxolitinib inhibits transforming JAK2 fusion proteins in vitro and induces complete cytogenetic remission in t(8;9)(p22;p24)/PCM1-JAK2-positive chronic eosinophilic leukemia.

P. Vandenberghe, D. Selleslag, E. Lierman, 2012, Blood.

Leukaemic intermediate lymphocytic lymphomas: analysis of twelve cases diagnosed by morphology.

H. van den Berghe, A. Louwagie, A. Criel, 1992, Leukemia & lymphoma.

Efficacy of Donor Lymphocyte Infusions in Myelodysplastic Syndromes Relapsing after Allogeneic Stem Cell Transplantation: Importance of Karyotype.

D. Selleslag, J. Droogenbroeck, A. Criel, 2004 .

The JAK2V617F mutation can occur in a hematopoietic stem cell that exhibits no proliferative advantage: a case of human allogeneic transplantation.

L. Knoops, D. Selleslag, S. Constantinescu, 2008, Blood.

Further characterization of morphologically defined typical and atypical CLL: a clinical, immunophenotypic, cytogenetic and prognostic study on 390 cases

Robert Vlietinck, Herman Van den Berghe, C. Mecucci, 1997, British journal of haematology.

A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias

P. Marynen, F. Speleman, J. Vandesompele, 2005, Leukemia.

Simultaneous Occurrence of Myelodysplastic Syndrome and Monoclonal B Lymphocytes with a Different Clonal Origin

B. Cauwelier, A. Louwagie, A. Criel, 2002, Leukemia & lymphoma.

X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutation.

G. Mortier, P. Vermeersch, S. Bekri, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Standardisation of multiplex fluorescent short tandem repeat analysis for chimerism testing

A. Criel, F. Nollet, J. Billiet, 2001, Bone Marrow Transplantation.

Analysis of phenotype and outcome in essential thrombocythemia with CALR or JAK2 mutations

P. de Paepe, L. Michaux, T. Tousseyn, 2015, Haematologica.

Evaluation of schistocyte analysis by a novel automated digital cell morphology application

A.-S. Hervent, M. Godefroid, B. Cauwelier, 2014, International journal of laboratory hematology.

Oxidized low-density lipoprotein, iron stores, and haptoglobin polymorphism.

E. Rietzschel, M. D. De Buyzere, J. Delanghe, 2004, Atherosclerosis.

Evaluation of schistocyte analysis by a novel automated digital cell morphology application

B. Cauwelier, J. Emmerechts, J. Billiet, 2015, International journal of laboratory hematology.