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Haematologica
|
April 12, 2012
The different faces of Janus kinase inhibition
Peter Vandenberghe
Haematologica
|
December 10, 2009
New flow cytometry in hematologic malignancies
Jan Cools, Peter Vandenberghe
Haematologica
|
September 2, 2016
Circulating cell-free DNA in hematological malignancies
Lieselot Buedts, Peter Vandenberghe
Pediatric Reports
|
November 5, 2011
Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS
Peter Vandenberghe, Karolien Beel
Haematologica
|
October 2, 2009
G-CSF receptor (CSF3R) mutations in X-linked neutropenia evolving to acute myeloid leukemia or myelodysplasia
Karolien Beel, Peter Vandenberghe
Journal of Immunological Methods
|
February 26, 2004
A flow cytometric method for determination of absolute counts of myeloid precursor dendritic cells in peripheral blood
Ling Ma, Werner Scheers, Peter Vandenberghe
Leukemia Research
|
May 22, 2009
Reduction of BCR-ABL1 mutant clones after discontinuation of TKI therapy
Karolien Beel, Ann Janssens, Gregor Verhoef, et al.
The Open Rheumatology Journal
|
December 1, 2012
Targeted Therapy with Rituximab in Felty's Syndrome: A Case Report
Line Heylen, Daan Dierickx, Peter Vandenberghe, et al.
Cancer Genetics
|
October 4, 2011
FOXP1 and PAX5 are rare but recurrent translocations partners in acute lymphoblastic leukemia
Natalie Put, Dries Deeren, Lucienne Michaux, et al.
Annals of Hematology
|
March 23, 2004
A male with angioimmunoblastic T-cell lymphoma and proliferative glomerulonephritis
Hadewijch De Samblanx, Gregor Verhoef, Pierre Zachée, et al.
Page
of 19
Search research articles
Search
Showing results (1-10 of 185) with videos related to
Sort By:
Page
of 19
Haematologica
|
April 12, 2012
The different faces of Janus kinase inhibition
Peter Vandenberghe
Haematologica
|
December 10, 2009
New flow cytometry in hematologic malignancies
Jan Cools, Peter Vandenberghe
Haematologica
|
September 2, 2016
Circulating cell-free DNA in hematological malignancies
Lieselot Buedts, Peter Vandenberghe
Pediatric Reports
|
November 5, 2011
Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS
Peter Vandenberghe, Karolien Beel
Haematologica
|
October 2, 2009
G-CSF receptor (CSF3R) mutations in X-linked neutropenia evolving to acute myeloid leukemia or myelodysplasia
Karolien Beel, Peter Vandenberghe
Journal of Immunological Methods
|
February 26, 2004
A flow cytometric method for determination of absolute counts of myeloid precursor dendritic cells in peripheral blood
Ling Ma, Werner Scheers, Peter Vandenberghe
Leukemia Research
|
May 22, 2009
Reduction of BCR-ABL1 mutant clones after discontinuation of TKI therapy
Karolien Beel, Ann Janssens, Gregor Verhoef, et al.
The Open Rheumatology Journal
|
December 1, 2012
Targeted Therapy with Rituximab in Felty's Syndrome: A Case Report
Line Heylen, Daan Dierickx, Peter Vandenberghe, et al.
Cancer Genetics
|
October 4, 2011
FOXP1 and PAX5 are rare but recurrent translocations partners in acute lymphoblastic leukemia
Natalie Put, Dries Deeren, Lucienne Michaux, et al.
Annals of Hematology
|
March 23, 2004
A male with angioimmunoblastic T-cell lymphoma and proliferative glomerulonephritis
Hadewijch De Samblanx, Gregor Verhoef, Pierre Zachée, et al.
Page
of 19