Theo dõi
Matthieu J. Schlögel
Matthieu J. Schlögel
Ph.D. Student, de Duve Institute, Universite catholique de Louvain, Belgium
Email được xác minh tại uclouvain.be
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
Somatic activating PIK3CA mutations cause venous malformation
N Limaye, J Kangas, A Mendola, C Godfraind, MJ Schlögel, R Helaers, ...
The American Journal of Human Genetics 97 (6), 914-921, 2015
3222015
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema
A Mendola, MJ Schlögel, A Ghalamkarpour, A Irrthum, HL Nguyen, ...
Molecular syndromology 4 (6), 257-266, 2013
1122013
Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations
P Brouillard, MJ Schlögel, N Homayun Sepehr, R Helaers, A Queisser, ...
Orphanet journal of rare diseases 16 (1), 267, 2021
422021
Characterization of ANGPT2 mutations associated with primary lymphedema
VM Leppänen, P Brouillard, EA Korhonen, T Sipilä, SK Jha, N Revencu, ...
Science translational medicine 12 (560), eaax8013, 2020
382020
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
MJ Schlögel, A Mendola, E Fastré, P Vasudevan, K Devriendt, ...
Orphanet Journal of Rare Diseases 10, 1-11, 2015
282015
Genetic causes of lymphedema
MJ Schlögel, P Brouillard, LM Boon, M Vikkula
Lymphedema: presentation, diagnosis, and treatment, 19-31, 2015
72015
Molecular genetics of lymphatic and complex vascular malformations
MJ Schlögel, P Brouillard, LM Boon, M Vikkula
Lymphedema: a concise compendium of theory and practice, 753-763, 2018
52018
No locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
MJ Schlögel, A Mendola, E Fastré, K Devriendt, T de Ravel de l'Argentière, ...
European Journal of Human Genetics 22, 123-123, 2014
12014
Identification of ANGPT2 Mutations as a Novel Cause of Primary Lymphedema
VM Leppänen, P Brouillard, E Korhonen, T Veli Sipilä, S Kumar Jha, ...
ISSVA Workshop, Date: 2020/05/14, Location: virtual, 2020
2020
Identification of novel causes of lymphedema and lymphatic malformation, with phenotypic characterisation of patients
M Schlögel
UCL-Université Catholique de Louvain, 2020
2020
Genetic testing in the diagnostic workup of vascular anomalies
M Vikkula, N Revencu, A Dompmartin, E Khoury, A Mendola, N Limaye, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 654-655, 2019
2019
Lymphatic malformations are caused by somatic mutations in PIK3CA
P Brouillard, MJ Schlogel, E Fastre, LM Boon, M Vikkula
ANGIOGENESIS 17 (4), 969-969, 2014
2014
Mutations in KIF11 cause Microcephaly-Lymphedema-Chorioretinal dysplasia syndrome (MLCRD)
PL Brouillard, M Schlogel, A Mendola, P Ostergaard, A Ghalamkarpour, ...
Abstract book, 31, 2012
2012
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