Iris M de Lange
6PUBLICATIONS
11CO-AUTHORS
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Publications (6)
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|Feb 27, 2024
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies.Declan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger
|Feb 08, 2020
Modifier genes in SCN1A-related epilepsy syndromes.Iris M de Lange, Flip Mulder, Ruben van 't Slot
|May 31, 2019
Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.Iris M de Lange, Wout Weuring, Ruben van 't Slot
|May 12, 2018
Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in SCN1A-related seizure phenotypes.Iris M de Lange, Boudewijn Gunning, Anja C M Sonsma
|Feb 21, 2018
Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes.Iris M de Lange, Marco J Koudijs, Ruben van 't Slot
|Jul 03, 2017
Male patients affected by mosaic PCDH19 mutations: five new cases.I M de Lange, P Rump, R F Neuteboom
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Frequent Collaborators
1 joint publications
Declan Gallagher
1 joint publications
Christel Depienne
1 joint publications
Davide Mei
1 joint publications
Rikke S Møller
1 joint publications
Rima Nabbout
1 joint publications
Amy L Schneider
1 joint publications
Ingrid E Scheffer
1 joint publications
An-Sofie Schoonjans
1 joint publications
Sameer M Zuberi
1 joint publications
Dennis Lal
