Detalhe da pesquisa
1.
Routine noninvasive prenatal screening for fetal Rh D in maternal plasma-A 2-year experience from a single center in Belgium.
Transfusion
; 62(5): 1103-1109, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35352833
2.
Mediastinal Myeloid Sarcoma with TP53 Mutation Preceding Acute Myeloid Leukemia with a PICALM-MLLT10 Fusion Gene.
Acta Haematol
; 140(2): 97-104, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30227397
3.
Bias reduction improves accuracy and informativity of high-throughput sequencing chimerism assays.
Clin Chim Acta
; 547: 117452, 2023 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37343694
4.
Chimerism monitoring using biallelic single nucleotide or insertion/deletion polymorphisms: How many markers to screen?
Clin Chim Acta
; 532: 123-129, 2022 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35667475
5.
Reliable and Scalable SARS-CoV-2 qPCR Testing at a High Sample Throughput: Lessons Learned from the Belgian Initiative.
Life (Basel)
; 12(2)2022 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35207446
6.
Nationwide Harmonization Effort for Semi-Quantitative Reporting of SARS-CoV-2 PCR Test Results in Belgium.
Viruses
; 14(6)2022 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35746765
7.
Performance Assessment of the Devyser High-Throughput Sequencing-Based Assay for Chimerism Monitoring in Patients after Allogeneic Hematopoietic Stem Cell Transplantation.
J Mol Diagn
; 23(9): 1116-1126, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34186173
8.
Evaluation of next-generation sequencing-based clonality analysis of T-cell receptor gamma gene rearrangements based on a new interpretation algorithm.
Int J Lab Hematol
; 41(2): 242-249, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30537135
9.
Standardization of Somatic Variant Classifications in Solid and Haematological Tumours by a Two-Level Approach of Biological and Clinical Classes: An Initiative of the Belgian ComPerMed Expert Panel.
Cancers (Basel)
; 11(12)2019 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31888289
10.
The human alphaE-catenin gene CTNNA1: mutational analysis and rare occurrence of a truncated splice variant.
Biochim Biophys Acta
; 1574(3): 262-8, 2002 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-11997091
11.
The JAK2V617F mutation can occur in a hematopoietic stem cell that exhibits no proliferative advantage: a case of human allogeneic transplantation.
Blood
; 112(3): 921-2, 2008 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18650474
12.
Malignant progression of donor-engrafted clonal hematopoiesis in sibling recipients after stem cell transplantation.
Blood Adv
; 4(22): 5631-5634, 2020 11 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33186460
13.
A real-time polymerase chain reaction assay for rapid, sensitive, and specific quantification of the JAK2V617F mutation using a locked nucleic acid-modified oligonucleotide.
J Mol Diagn
; 12(4): 512-9, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20431031
14.
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.
Blood
; 109(3): 1334-5, 2007 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17244688
15.
Do B-cell chronic lymphocytic leukemia patients with Ig VH3-21 genes constitute a new subset of chronic lymphocytic leukemia?
Blood
; 100(3): 1097-8; author reply 1098-9, 2002 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12130479