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Guillaume Dachy
Guillaume Dachy
MD, PhD
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Cited by
Cited by
Year
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis
FA Arts, R Sciot, B Brichard, M Renard, A de Rocca Serra, G Dachy, ...
Human molecular genetics 26 (10), 1801-1810, 2017
892017
PDGF receptor mutations in human diseases
E Guérit, F Arts, G Dachy, B Boulouadnine, JB Demoulin
Cellular and Molecular Life Sciences 78, 3867-3881, 2021
812021
Association of PDGFRB mutations with pediatric myofibroma and myofibromatosis
G Dachy, RR De Krijger, S Fraitag, I Théate, B Brichard, SB Hoffman, ...
JAMA dermatology 155 (8), 946-950, 2019
492019
Inflammation‐induced cholestasis in cancer cachexia
MM Thibaut, M Sboarina, M Roumain, SA Pötgens, AM Neyrinck, ...
Journal of cachexia, sarcopenia and muscle 12 (1), 70-90, 2021
292021
Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group
S Hettmer, G Dachy, G Seitz, A Agaimy, C Duncan, M Jongmans, S Hirsch, ...
Familial cancer 20, 327-336, 2021
172021
Novel COL4A1‐VEGFD gene fusion in myofibroma
G Dachy, S Fraitag, B Boulouadnine, S Cordi, JB Demoulin
Journal of cellular and molecular medicine 25 (9), 4387-4394, 2021
82021
A germline mutation in the platelet‐derived growth factor receptor beta gene may be implicated in hereditary progressive mucinous histiocytosis
A Onoufriadis, B Boulouadnine, G Dachy, T Higashino, HY Huang, ...
British Journal of Dermatology 184 (5), 967-970, 2021
72021
Severe hypercalcaemia early after kidney transplantation in two patients with severe secondary hyperparathyroidism previously treated with etelcalcetide
G Dachy, JM Pochet, L Labriola, A Buemi, V Gillion, M Jadoul, N Kanaan, ...
Clinical Kidney Journal 14 (8), 1977-1979, 2021
32021
Penttinen syndrome‐associated PDGFRB Val665Ala variant causes aberrant constitutive STAT1 signalling
A Nédélec, EM Guérit, G Dachy, S Lenglez, LS Wong, FA Arts, ...
Journal of cellular and molecular medicine 26 (14), 3902-3912, 2022
22022
Diagnostic limitations and considerations in the imaging evaluation of advanced multicentric infantile myofibromatosis
A Parikh, CAH Driscoll, H Crowley, T York, G Dachy, JB Demoulin, ...
Radiology case reports 15 (11), 2440-2444, 2020
22020
Unwanted acquired mutations in Ba/F3 transformation assays
JB Demoulin, G Dachy, FA Arts
Oncotarget 8 (13), 20523, 2017
12017
Vanishing bile duct syndrome associated with diffuse large B-cell lymphoma.
G Dachy, T Connerotte
British Journal of Haematology 173 (4), 2016
12016
Von Willebrand factor as a potential predictive biomarker of early complications of endothelial origin after allogeneic hematopoietic stem cell transplantation
G Dachy, M Vankeerbergen, N Vanlangendonck, N Straetmans, ...
Bone Marrow Transplantation, 1-3, 2024
2024
VON WILLEBRAND FACTOR AS A POTENTIAL PREDICTIVE BIOMARKER OF EARLY COMPLICATIONS OF ENDOTHELIAL ORIGIN AFTER ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION
G Dachy, M Vankeerbegen, N Vanlangendonck, C Lambert, ...
BONE MARROW TRANSPLANTATION 58 (SUPP 1), 507-508, 2023
2023
Von Willebrand factor as a potential predictive biomarker of early complications of endothelial origin after allogeneic hematopoietic cell transplantation.
M Vankeerbergen, N Vanlangendonck, N Straetmans, C Lambert, ...
2023
Genomic mechanisms of receptor tyrosine kinase activation in myofibroma
G Dachy
UCL-Université Catholique de Louvain, 2020
2020
PDGFRB mutations in sporadic myofibromatosis. 18th BeSHG Annual Meeting “The epigenome in development and disease”
G Dachy, F Arts, R Sciot, B Brichard, M Renard, S Fraitag, C Galant, ...
Abstract book, 17-18, 2015
2015
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Articles 1–17