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Researcher
Elien De Latter
Profile
Projects
Publications
Activities
Awards & Distinctions
9
Results
2017
In-house developed 15-gene sequencing panel for acute myeloid leukemia and myelodysplasia allows robust detection of genetic defects including FLT3-ITD and CEBPA mutations
Joni Van der Meulen
Barbara Denys
Elien De Latter
Steve Lefever
Toon Rosseel
Wouter Steyaert
GRETA VAN DER CRUYSSEN
Isabelle Rottiers
David Creytens
Jo Van Dorpe
et al.
C3
Conference
2017
In-house developed 15-gene sequencing panel for acute myeloid leukemia and myelodysplasia allows robust detection of genetic defects including FLT3-ITD and CEBPA mutations
Joni Van der Meulen
Barbara Denys
Elien De Latter
Steve Lefever
Toon Rosseel
Wouter Steyaert
GRETA VAN DER CRUYSSEN
Isabelle Rottiers
David Creytens
Jo Van Dorpe
et al.
C3
Conference
2017
2016
Clinical, biochemical and genetic spectrum of mitochondrial disorders in Egyptian children : a study of 19 cases
LA Selim
D Mehaney
Rudy Van Coster
SA Hassan
IG Mahmoud
AI El Badawy
Arnaud Vanlander
Joél Smet
Elien De Latter
Katrien Vandemeulebroecke
et al.
C3
Conference
2016
2015
Clinical, biochemical and genetic spectrum of mitochondrial disorders in Egyptian children : a study of 17 cases
Laila Selim
Dina Mehaney
Rudy Van Coster
Sawsan Abdel Hadi
Iman Gamal
Mariane Youssry
Amira El Badawya
Arnaud Vanlander
Joél Smet
Elien De Latter
et al.
C3
Conference
2015
Possible pathogenic mechanism of propofol infusion syndrome involves coenzyme Q
Arnaud Vanlander
Juergen Guenther Okun
ANNIK DE JAEGER
Joél Smet
Elien De Latter
Boel De Paepe
Georges Dacremont
Brigitte Wuyts
Bert Vanheel
Peter De Paepe
et al.
A1
Journal Article
in
ANESTHESIOLOGY
2015
Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2)
Arnaud Vanlander
Björn Menten
Joél Smet
Linda De Meirleir
Tom Sante
Boel De Paepe
Sara Seneca
Sarah F Pearce
Christopher A Powell
Sarah Vergult
et al.
A1
Journal Article
in
HUMAN MUTATION
2015
2013
A homozygous mutation in IBA57 involved in intramitochondrial iron-sulfur cluster synthesis causes severe encephalopathy and mypathy in two neonates
Arnaud Vanlander
Claudia Willbrecht
Nikhita Ajit Bolar
Joél Smet
Boel De Paepe
Elien De Latter
Lut Van Laer
Bart Loeys
Roland Lill
Rudy Van Coster
C3
Conference
2013
Mutation of the iron-sulfur cluster assembly IBA57 gene causes lethal myopathy and encephalopathy
N Ajit Bolar
Arnaud Vanlander
C Wilbrecht
Nathalie Van der Aa
Joél Smet
Boel De Paepe
G Vandeweyer
F Kooy
François Eyskens
Elien De Latter
et al.
C3
Conference
2013
Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy
Nikhita Ajit Bolar
Arnaud Vanlander
Claudia Wilbrecht
Nathalie Van der Aa
Joél Smet
Boel De Paepe
Geert Vandeweyer
Frank Kooy
François Eyskens
Elien De Latter
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2013