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Biomarker Research|December 21, 2021
Daratumumab and venetoclax in combination with chemotherapy provide sustained molecular remission in relapsed/refractory CD19, CD20, and CD22 negative acute B lymphoblastic leukemia with KMT2A-AFF1 transcriptSophie Voruz, Sabine Blum, Laurence de Leval, et al.
The Journal of Clinical Endocrinology and Metabolism|May 17, 2007
Isolated 46,XY gonadal dysgenesis in two sisters caused by a Xp21.2 interstitial duplication containing the DAX1 geneMichela Barbaro, Mikael Oscarson, Jacqueline Schoumans, et al.
European Journal of Haematology|April 16, 2002
Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 casesAnn Nordgren, Mats Heyman, Sigrid Sahlén, et al.
Hematology (Amsterdam, Netherlands)|February 23, 2023
Single-center, observational study of AML/MDS-EB with IDH1/2 mutations: genetic profile, immunophenotypes, mutational kinetics and outcomesVasiliki Papadopoulou, Jacqueline Schoumans, Valentin Basset, et al.
Annals of Hematology|June 20, 2020
Characterization of myelodysplastic syndromes progressing to acute lymphoblastic leukemiaFilipe Martins, Michael Kruszewski, Ilaria Scarpelli, et al.
Current Oncology (Toronto, Ont.)|April 26, 2024
True Donor Cell Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation: Diagnostic and Therapeutic Considerations-Brief ReportMichèle Hoffmann, Yara Banz, Jörg Halter, et al.
Biomedicines|October 26, 2024
Characteristics and Prognosis of "Acute Promyelocytic Leukemia-like" Nucleophosmin-1-Mutated Acute Myeloid Leukemia in a Retrospective Patient CohortVasiliki Papadopoulou, Giulia Schiavini, Gregoire Stalder, et al.
Genes, Chromosomes & Cancer|July 14, 2023
Refined cytogenetic IPSS-R evaluation by the use of SNP array in a cohort of 290 MDS patientsIlaria Scarpelli, Valérie Beyer Stalder, Gerasimos Tsilimidos, et al.
Leukemia & Lymphoma|August 15, 2003
Molecular cytogenetic approach to the diagnosis of splenic lymphoma: a case report of blastoid mantle cell lymphomaErik Björck, Ola Landgren, Jacqueline Schoumans, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairmentBritt-Marie Anderlid, Jacqueline Schoumans, Asa Hallqvist, et al.
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