Prenatal exome sequencing: A useful tool for the fetal neurologist von Koning, Maayke A., Hoffer, Mariëtte J. V., Nibbeling, Esther A. R., Bijlsma, Emilia K., Toirkens, Menno J. P., Adama‐Scheltema, Phebe N., Verweij, E. Joanne, Veenhof, Marieke B., Santen, Gijs W. E., Peeters‐Scholte, Cacha M. P. C. D.

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From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care von de Koning, Maayke A., Haak, Monique C., Adama van Scheltema, Phebe N., Peeters-Scholte, Cacha M. P. C. D., Koopmann, Tamara T., Nibbeling, Esther A. R., Aten, Emmelien, den Hollander, Nicolette S., Ruivenkamp, Claudia A. L., Hoffer, Mariëtte J. V., Santen, Gijs W. E.

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Associations between Neonatal Magnetic Resonance Imaging and Short- and Long-Term Neurodevelopmental Outcomes in a Longitudinal Cohort of Very Preterm Children von Jansen, Lisette, van Steenis, Andrea, van den Berg-Huysmans, Annette A., Wiggers-de Bruine, Sica T., Rijken, Monique, de Vries, Linda S., Vermeiren, Robert R.J.M., Peeters-Scholte, Cacha M.P.C.D., Steggerda, Sylke J.

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Combining advanced MRI and EEG techniques better explains long-term motor outcome after very preterm birth von van ’t Westende, Charlotte, Steggerda, Sylke J., Jansen, Lisette, van den Berg-Huysmans, Annette A., van de Pol, Laura A., Wiggers-de Bruine, Francisca T., Stam, Cornelis J., Peeters-Scholte, Cacha M. P. C. D.

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Pharmacokinetics and short-term safety of the selective NOS inhibitor 2-iminobiotin in asphyxiated neonates treated with therapeutic hypothermia von Favié, Laurent M. A., Peeters-Scholte, Cacha M. P. C. D., Bakker, Anouk, Tjabbes, Huibert, Egberts, Toine C. G., van Bel, Frank, Rademaker, Carin M. A., Vis, Peter, Groenendaal, Floris

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Efficacy of Levetiracetam as Add-On Therapy in the Treatment of Seizures in Neonates von Rondagh, Mathies, De Vries, Linda S., Peeters-Scholte, Cacha M.P.C.D., Tromp, Selma C., Steggerda, Sylke. J.

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Recurrent Intracranial Hypertension in a Toddler with Graves’ Disease von Vuijk, Floris A., de Bruin, Christiaan, Peeters-Scholte, Cacha M.P.C.D., Notting, Irene C.

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Fetal brain imaging in isolated congenital heart defects - a systematic review and meta-analysis von Jansen, Fenna A. R., Everwijn, Sheila M. P., Scheepjens, Robert, Stijnen, Theo, Peeters-Scholte, Cacha M. P. C. D., van Lith, Jan M. M., Haak, Monique C.

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Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication von Koene, Saskia, Peeters‐Scholte, Cacha M. P. C. D., Knijnenburg, Jeroen, Vries, Linda S., Scheltema, Phebe N. Adama, Meuwissen, Marije E., Steggerda, Sylke J., Santen, Gijs W. E.

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Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders von Stolz, Jacob R., Foote, Kendall M., Veenstra-Knol, Hermine E., Pfundt, Rolph, ten Broeke, Sanne W., de Leeuw, Nicole, Roht, Laura, Pajusalu, Sander, Part, Reelika, Rebane, Ionella, Õunap, Katrin, Stark, Zornitza, Kirk, Edwin P., Lawson, John A., Lunke, Sebastian, Christodoulou, John, Louie, Raymond J., Rogers, R. Curtis, Davis, Jessica M., Innes, A. Micheil, Wei, Xing-Chang, Keren, Boris, Mignot, Cyril, Lebel, Robert Roger, Sperber, Steven M., Sakonju, Ai, Dosa, Nienke, Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M.P.C.D., Ruivenkamp, Claudia A.L., van Bon, Bregje W., Kennedy, Joanna, Low, Karen J., Ellard, Sian, Pang, Lewis, Junewick, Joseph J., Mark, Paul R., Carvill, Gemma L., Swanson, Geoffrey T.

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De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders von Reynhout, Sara, Jansen, Sandra, Haesen, Dorien, van Belle, Siska, de Munnik, Sonja A., Bongers, Ernie M.H.F., Schieving, Jolanda H., Marcelis, Carlo, Amiel, Jeanne, Rio, Marlène, Mclaughlin, Heather, Ladda, Roger, Sell, Susan, Kriek, Marjolein, Peeters-Scholte, Cacha M.P.C.D., Terhal, Paulien A., van Gassen, Koen L., Verbeek, Nienke, Henry, Sonja, Scott Schwoerer, Jessica, Malik, Saleem, Revencu, Nicole, Ferreira, Carlos R., Macnamara, Ellen, Braakman, Hilde M.H., Brimble, Elise, Ruzhnikov, Maura R.Z., Wagner, Matias, Harrer, Philip, Wieczorek, Dagmar, Kuechler, Alma, Tziperman, Barak, Barel, Ortal, de Vries, Bert B.A., Gordon, Christopher T., Janssens, Veerle, Vissers, Lisenka E.L.M.

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Translation from animal to clinical studies, choosing the optimal moment von Favié, Laurent M. A., Peeters-Scholte, Cacha M. P. C. D., Bakker, Anouk, Tjabbes, Huibert, Egberts, Toine C. G., van Bel, Frank, Rademaker, Carin M. A., Vis, Peter, Groenendaal, Floris

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Early recognition of characteristic conventional and amplitude-integrated EEG patterns of seizures in SCN2A and KCNQ3-related epilepsy in neonates von Pijpers, Judith A., Au, Ping Yee Billie, Weeke, Lauren C., Vein, Alla A., Smit, Liesbeth S., Vilan, Ana, Jacobs, Elke, de Vries, Linda S., Steggerda, Sylke J., Cilio, Maria Roberta, Carapancea, Evelina, Cornet, Marie-Coralie, Appendino, Juan P., Peeters-Scholte, Cacha M.P.C.D.

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Nitric Oxide Synthase Inhibition as a Neuroprotective Strategy Following Hypoxic-Ischemic Encephalopathy: Evidence From Animal Studies von Favié, Laurent M A, Cox, Arlette R, van den Hoogen, Agnes, Nijboer, Cora H A, Peeters-Scholte, Cacha M P C D, van Bel, Frank, Egberts, Toine C G, Rademaker, Carin M A, Groenendaal, Floris

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Genotype-phenotype correlation in ATAD3A deletions: not just of scientific relevance von Peeters-Scholte, Cacha M P C D, Adama van Scheltema, Phebe N, Klumper, Frans J C M, Everwijn, Sheila M P, Koopmans, Marije, Hoffer, Mariette J V, Koopmann, Tamara T, Ruivenkamp, Claudia A L, Steggerda, Sylke J, van der Knaap, Marjo S, Santen, Gijs W E

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Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders von Stolz, Jacob R., Foote, Kendall M., Veenstra-Knol, Hermine E., Pfundt, Rolph, ten Broeke, Sanne W., de Leeuw, Nicole, Roht, Laura, Pajusalu, Sander, Part, Reelika, Rebane, Ionella, Õunap, Katrin, Stark, Zornitza, Kirk, Edwin P., Lawson, John A., Lunke, Sebastian, Christodoulou, John, Louie, Raymond J., Rogers, R. Curtis, Davis, Jessica M., Innes, A. Micheil, Wei, Xing-Chang, Keren, Boris, Mignot, Cyril, Lebel, Robert Roger, Sperber, Steven M., Sakonju, Ai, Dosa, Nienke, Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M.P.C.D., Ruivenkamp, Claudia A.L., van Bon, Bregje W., Kennedy, Joanna, Low, Karen J., Ellard, Sian, Pang, Lewis, Junewick, Joseph J., Mark, Paul R., Carvill, Gemma L., Swanson, Geoffrey T.

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The degree of prematurity affects functional brain activity in preterm born children at school-age: An EEG study von van 't Westende, Charlotte, Peeters-Scholte, Cacha M.P.C.D., Jansen, Lisette, van Egmond-van Dam, Janneke C., Tannemaat, Martijn R., de Bruïne, Francisca T., van den Berg-Huysmans, Annette A., Geraedts, Victor J., Gouw, Alida A., Steggerda, Sylke J., Stam, Cornelis J., van de Pol, Laura A.

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Endovascular treatment of patients with stroke caused by anterior cerebral artery occlusions von Vos, Erik M., Kappelhof, Manon, den Hartog, Sanne J., Coutinho, Jonathan M., Emmer, Bart J., Roozenbeek, Bob, van Zwam, Wim H., van Oostenbrugge, Robert J., van der Worp, H. Bart, Uyttenboogaart, Maarten, van Es, Adriaan C. G. M., Majoie, Charles B. L. M., Dippel, Diederik W. J., Peeters-Scholte, Cacha M. P. C. D., van den Wijngaard, Ido R.

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De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders von Reynhout, Sara, Jansen, Sandra, Haesen, Dorien, van Belle, Siska, de Munnik, Sonja A., Bongers, Ernie M.H.F., Schieving, Jolanda H., Marcelis, Carlo, Amiel, Jeanne, Rio, Marlène, Mclaughlin, Heather, Ladda, Roger, Sell, Susan, Kriek, Marjolein, Peeters-Scholte, Cacha M.P.C.D., Terhal, Paulien A., van Gassen, Koen L., Verbeek, Nienke, Henry, Sonja, Schwoerer, Jessica Scott, Malik, Saleem, Revencu, Nicole, Ferreira, Carlos R., Macnamara, Ellen, Braakman, Hilde M.H., Brimble, Elise, Ruzhnikov, Maura R.Z., Wagner, Matias, Harrer, Philip, Wieczorek, Dagmar, Kuechler, Alma, Tziperman, Barak, Barel, Ortal, de Vries, Bert B.A., Gordon, Christopher T., Janssens, Veerle, Vissers, Lisenka E.L.M.

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De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila von Lugtenberg, Dorien, Reijnders, Margot R F, Fenckova, Michaela, Bijlsma, Emilia K, Bernier, Raphael, van Bon, Bregje W M, Smeets, Eric, Vulto-van Silfhout, Anneke T, Bosch, Danielle, Eichler, Evan E, Mefford, Heather C, Carvill, Gemma L, Bongers, Ernie M H F, Schuurs-Hoeijmakers, Janneke Hm, Ruivenkamp, Claudia A, Santen, Gijs W E, van den Maagdenberg, Arn M J M, Peeters-Scholte, Cacha M P C D, Kuenen, Sabine, Verstreken, Patrik, Pfundt, Rolph, Yntema, Helger G, de Vries, Petra F, Veltman, Joris A, Hoischen, Alexander, Gilissen, Christian, de Vries, Bert B A, Schenck, Annette, Kleefstra, Tjitske, Vissers, Lisenka E L M

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