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Multidrug-resistant Salmonella enterica, Democratic Republic of the Congo

Emerging infectious diseases, 2012-10, Vol.18 (10), p.1692-1694

2012

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Monitoring of SARS‐CoV‐2 concentration and circulation of variants of concern in wastewater of Leuven, Belgium

Journal of medical virology, 2023-02, Vol.95 (2), p.e28587-n/a

2023

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Bleeding control improves after switching to emicizumab: Real-world experience of 177 children in the PedNet registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2024-05, Vol.30 (3), p.685-692

2024

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GATA1 gene variants associated with thrombocytopenia and anemia

Platelets (Edinburgh), 2017-10, Vol.28 (7), p.731-734

2017

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Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes

Haematologica (Roma), 2021-12, Vol.106 (12), p.3206-3210

2021

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Invasive Salmonella Infections at Multiple Surveillance Sites in the Democratic Republic of the Congo, 2011–2014

Clinical infectious diseases, 2015-11, Vol.61 (suppl 4), p.S346-S353

2015

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Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome

Journal of allergy and clinical immunology, 2018-08, Vol.142 (2), p.630-646

2018

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Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-11, Vol.28 (6), p.e248-e250

2022

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Blood platelet research in autism spectrum disorders: In search of biomarkers

Research and practice in thrombosis and haemostasis, 2019-10, Vol.3 (4), p.566-577

2019

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Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia

Haematologica (Roma), 2019-05, Vol.104 (5), p.1036-1045

2019

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The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer

Haematologica (Roma), 2017-04, Vol.102 (4), p.695-706

2017

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Renal Replacement Therapy in children with severe developmental disability: guiding questions for decision-making

European journal of pediatrics, 2018-12, Vol.177 (12), p.1735-1743

2018

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Bortezomib for autoimmune hemolytic anemia after intestinal transplantation

Pediatric transplantation, 2020-06, Vol.24 (4), p.e13700-n/a

2020

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Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding

Blood, 2017-08, Vol.130 (8), p.1026-1030

2017

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De novo variant in tyrosine kinase SRC causes thrombocytopenia: case report of a second family

Platelets (Edinburgh), 2019-10, Vol.30 (7), p.931-934

2019

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Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa

Hematology (Luxembourg), 2023-12, Vol.28 (1), p.2193770-2193770

2023

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No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity

Journal of human genetics, 2012-04, Vol.57 (4), p.277-279

2012

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Value of DNA testing in the diagnosis of sickle‐cell anemia in childhood in an environment with a high prevalence of other causes of anemia

Journal of clinical laboratory analysis, 2022-08, Vol.36 (8), p.e24593-n/a

2022

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Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleeding

Thrombosis and haemostasis, 2001-09, Vol.86 (3), p.733-738

2001

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Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa

EJHaem, 2023-08, Vol.4 (3), p.595-601

2023

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SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles

Human molecular genetics, 2010-04, Vol.19 (7), p.1368-1378

2010

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The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structure

Blood, 2005-10, Vol.106 (7), p.2356-2362

2005

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Regulator of G‐protein signaling 18 controls megakaryopoiesis and the cilia‐mediated vertebrate mechanosensory system

The FASEB journal, 2012-05, Vol.26 (5), p.2125-2136

2012

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PACAP and its receptor VPAC1 regulate megakaryocyte maturation: therapeutic implications

Blood, 2008-02, Vol.111 (4), p.1885-1893

2008

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Multidrug-resistant Salmonella enterica, Democratic Republic of the Congo

Monitoring of SARS‐CoV‐2 concentration and circulation of variants of concern in wastewater of Leuven, Belgium

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome

Bleeding control improves after switching to emicizumab: Real-world experience of 177 children in the PedNet registry

GATA1 gene variants associated with thrombocytopenia and anemia

Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes

Invasive Salmonella Infections at Multiple Surveillance Sites in the Democratic Republic of the Congo, 2011–2014

Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome

Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study

Blood platelet research in autism spectrum disorders: In search of biomarkers

Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia

The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer

Renal Replacement Therapy in children with severe developmental disability: guiding questions for decision-making

Bortezomib for autoimmune hemolytic anemia after intestinal transplantation

Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding

De novo variant in tyrosine kinase SRC causes thrombocytopenia: case report of a second family

Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa

No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity

Value of DNA testing in the diagnosis of sickle‐cell anemia in childhood in an environment with a high prevalence of other causes of anemia

Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleeding

Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles

The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structure

Regulator of G‐protein signaling 18 controls megakaryopoiesis and the cilia‐mediated vertebrate mechanosensory system

PACAP and its receptor VPAC1 regulate megakaryocyte maturation: therapeutic implications

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