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Author/Creator Sonsma, Anja C. M.

1. A genome‐wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Issue 1 (17th January 2019)

Authors:
Berghuis, Bianca; Stapleton, Caragh; Sonsma, Anja C. M.; Hulst, Janic; de Haan, Gerrit‐Jan; Lindhout, Dick; Demurtas, Rita; Krause, Roland; Depondt, Chantal; Kunz, Wolfram S.; Zara, Federico; Striano, Pasquale; Craig, John; Auce, Pauls; Marson, Anthony G.; Stefansson, Hreinn; O'Brien, Terence J.;...
Other Names:
Avbersek Andreja investigator.; Leu Costin investigator.; Heggeli Kristin investigator.; Willis Joseph investigator.; Speed Douglas investigator.; Sargsyan Narek investigator.; Chinthapalli Krishna investigator.; Borghei Mojgansadat investigator.; Coppola Antonietta investigator.; Gambardella Ant...
Journal:
Epilepsia open
Issue:
Volume 4:Issue 1(2019)
Page Start:
102
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Influence of common SCN1A promoter variants on the severity of SCN1A‐related phenotypes. Issue 7 (29th May 2019)

Authors:
de Lange, Iris M.; Weuring, Wout; van 't Slot, Ruben; Gunning, Boudewijn; Sonsma, Anja C. M.; McCormack, Mark; de Kovel, Carolien; van Gemert, Lisette J. J. M.; Mulder, Flip; van Kempen, Marjan J. A.; Knoers, Nine V. A. M.; Brilstra, Eva H.; Koeleman, Bobby P. C.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 7(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. 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. (11th May 2018)

Authors:
de Lange, Iris M.; Gunning, Boudewijn; Sonsma, Anja C. M.; van Gemert, Lisette; van Kempen, Marjan; Verbeek, Nienke E.; Nicolai, Joost; Knoers, Nine V. A. M.; Koeleman, Bobby P. C.; Brilstra, Eva H.
Journal:
Epilepsia
Issue:
Volume 59:issue 6(2018)
Page Start:
1154
Record Type:
Journal Article
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4. Modifier genes in SCN1A‐related epilepsy syndromes. Issue 4 (7th February 2020)

Authors:
de Lange, Iris M.; Mulder, Flip; van 't Slot, Ruben; Sonsma, Anja C. M.; van Kempen, Marjan J. A.; Nijman, Isaac J.; Ernst, Robert F.; Knoers, Nine V. A. M.; Brilstra, Eva H.; Koeleman, Bobby P. C.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 4(2020)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes. (20th February 2018)

Authors:
de Lange, Iris M.; Koudijs, Marco J.; van 't Slot, Ruben; Gunning, Boudewijn; Sonsma, Anja C. M.; van Gemert, Lisette J. J. M.; Mulder, Flip; Carbo, Ellen C.; van Kempen, Marjan J. A.; Verbeek, Nienke E.; Nijman, Isaac J.; Ernst, Robert F.; Savelberg, Sanne M. C.; Knoers, Nine V. A. M.; Brilstra,...
Journal:
Epilepsia
Issue:
Volume 59:issue 3(2018)
Page Start:
690
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗