Functional correlates of clinical phenotype and severity in recurrent SCN2A variants von Berecki, Géza, Howell, Katherine B., Heighway, Jacqueline, Olivier, Nelson, Rodda, Jill, Overmars, Isabella, Vlaskamp, Danique R. M., Ware, Tyson L., Ardern-Holmes, Simone, Lesca, Gaetan, Alber, Michael, Veggiotti, Pierangelo, Scheffer, Ingrid E., Berkovic, Samuel F., Wolff, Markus, Petrou, Steven

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Schizophrenia is a later‐onset feature of PCDH19 Girls Clustering Epilepsy von Vlaskamp, Danique R. M., Bassett, Anne S., Sullivan, Joseph E., Robblee, Jennifer, Sadleir, Lynette G., Scheffer, Ingrid E., Andrade, Danielle M.

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Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detection von Cowley, Mark J, Liu, Yu‐Chi, Oliver, Karen L., Carvill, Gemma, Myers, Candace T., Gayevskiy, Velimir, Delatycki, Martin, Vlaskamp, Danique R.M., Zhu, Ying, Mefford, Heather, Buckley, Michael F., Bahlo, Melanie, Scheffer, Ingrid E., Dinger, Marcel E., Roscioli, Tony

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Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome von Buijsse, Nathan, Jansen, Floor E, Ockeloen, Charlotte W, van Kempen, Marjan J A, Zeidler, Shimriet, Willemsen, Marjolein H, Scarano, Emanuela, Monticone, Sonia, Zonneveld-Huijssoon, Evelien, Low, Karen J, Bayat, Allan, Sisodiya, Sanjay M, Samanta, Debopam, Lesca, Gaetan, de Jong, Danielle, Giltay, Jaqcues C, Verbeek, Nienke E, Kleefstra, Tjitske, Brilstra, Eva H, Vlaskamp, Danique R M

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SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy von Vlaskamp, Danique R.M, Shaw, Benjamin J, Burgess, Rosemary, Mei, Davide, Montomoli, Martino, Xie, Han, Myers, Candace T, Bennett, Mark F, XiangWei, Wenshu, Williams, Danielle, Maas, Saskia M, Brooks, Alice S, Mancini, Grazia M.S, van de Laar, Ingrid M.B.H, van Hagen, Johanna M, Ware, Tyson L, Webster, Richard I, Malone, Stephen, Berkovic, Samuel F, Kalnins, Renate M, Sicca, Federico, Korenke, G Christoph, van Ravenswaaij-Arts, Conny M.A, Hildebrand, Michael S, Mefford, Heather C, Jiang, Yuwu, Guerrini, Renzo, Scheffer, Ingrid E

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Author response: SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy von Vlaskamp, Danique R.M., Scheffer, Ingrid E.

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Copy number variation in a hospital-based cohort of children with epilepsy von Vlaskamp, Danique R M, Callenbach, Petra M C, Rump, Patrick, Giannini, Lucia A A, Dijkhuizen, Trijnie, Brouwer, Oebele F, van Ravenswaaij-Arts, Conny M A

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Treatment of prolonged convulsive seizures in children; a single centre, retrospective, observational study von Vlaskamp, Danique R.M, Brouwer, Oebele F, Callenbach, Petra M.C

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Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsy von Vlaskamp, Danique R.M, Rump, Patrick, Callenbach, Petra M.C, Vos, Yvonne J, Sikkema-Raddatz, Birgit, van Ravenswaaij-Arts, Conny M.A, Brouwer, Oebele F

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Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsy von Vlaskamp, Danique R.M., Rump, Patrick, Callenbach, Petra M.C., Brilstra, Eva H., Velthuizen, Mary E., Brouwer, Oebele F., Ranchor, Adelita V., van Ravenswaaij-Arts, Conny M.A.

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PRRT2-related phenotypes in patients with a 16p11.2 deletion von Vlaskamp, Danique R.M., Callenbach, Petra M.C., Rump, Patrick, Giannini, Lucia A.A., Brilstra, Eva H., Dijkhuizen, Trijnie, Vos, Yvonne J., van der Kevie-Kersemaekers, Anne-Marie F., Knijnenburg, Jeroen, de Leeuw, Nicole, van Minkelen, Rick, Ruivenkamp, Claudia A.L., Stegmann, Alexander P.A., Brouwer, Oebele F., van Ravenswaaij-Arts, Conny M.A.

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First autochthonous human West Nile virus infections in the Netherlands, July to August 2020 von Vlaskamp, Danique Rm, Thijsen, Steven Ft, Reimerink, Johan, Hilkens, Pieter, Bouvy, Willem H, Bantjes, Sabine E, Vlaminckx, Bart Jm, Zaaijer, Hans, van den Kerkhof, Hans Htc, Raven, Stijn Fh, Reusken, Chantal Bem

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NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns von Stamberger, Hannah, Hammer, Trine B., Gardella, Elena, Vlaskamp, Danique R. M., Bertelsen, Birgitte, Mandelstam, Simone, de Lange, Iris, Zhang, Jing, Myers, Candace T., Fenger, Christina, Afawi, Zaid, Almanza Fuerte, Edith P., Andrade, Danielle M., Balcik, Yunus, Ben Zeev, Bruria, Bennett, Mark F., Berkovic, Samuel F., Isidor, Bertrand, Bouman, Arjan, Brilstra, Eva, Busk, Øyvind L., Cairns, Anita, Caumes, Roseline, Chatron, Nicolas, Dale, Russell C., de Geus, Christa, Edery, Patrick, Gill, Deepak, Granild-Jensen, Jacob Bie, Gunderson, Lauren, Gunning, Boudewijn, Heimer, Gali, Helle, Johan R., Hildebrand, Michael S., Hollingsworth, Georgie, Kharytonov, Volodymyr, Klee, Eric W., Koeleman, Bobby P. C., Koolen, David A., Korff, Christian, Küry, Sébastien, Lesca, Gaetan, Lev, Dorit, Leventer, Richard J., Mackay, Mark T., Macke, Erica L., McEntagart, Meriel, Mohammad, Shekeeb S., Monin, Pauline, Montomoli, Martino, Morava, Eva, Moutton, Sebastien, Muir, Alison M., Parrini, Elena, Procopis, Peter, Ranza, Emmanuelle, Reed, Laura, Reif, Philipp S., Rosenow, Felix, Rossi, Massimiliano, Sadleir, Lynette G., Sadoway, Tara, Schelhaas, Helenius J., Schneider, Amy L., Shah, Krati, Shalev, Ruth, Sisodiya, Sanjay M., Smol, Thomas, Stumpel, Connie T. R. M., Stuurman, Kyra, Symonds, Joseph D., Mau-Them, Frederic Tran, Verbeek, Nienke, Verhoeven, Judith S., Wallace, Geoffrey, Yosovich, Keren, Zarate, Yuri A., Zerem, Ayelet, Zuberi, Sameer M., Guerrini, Renzo, Mefford, Heather C., Patel, Chirag, Zhang, Yue-Hua, Møller, Rikke S., Scheffer, Ingrid E.

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Schizophrenia is a later‐onset feature of PCDH 19 Girls Clustering Epilepsy von Vlaskamp, Danique R. M., Bassett, Anne S., Sullivan, Joseph E., Robblee, Jennifer, Sadleir, Lynette G., Scheffer, Ingrid E., Andrade, Danielle M.

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Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsy von Vlaskamp, Danique R M, Rump, Patrick, Callenbach, Petra M C, Brilstra, Eva H, Velthuizen, Mary E, Brouwer, Oebele F, Ranchor, Adelita V, van Ravenswaaij-Arts, Conny M A

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Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome von Buijsse, Nathan, Jansen, Floor E, Ockeloen, Charlotte W, van Kempen, Marjan J A, Zeidler, Shimriet, Willemsen, Marjolein H, Scarano, Emanuela, Monticone, Sonia, Zonneveld-Huijssoon, Evelien, Low, Karen J, Bayat, Allan, Sisodiya, Sanjay M, Samanta, Debopam, Lesca, Gaetan, de Jong, Danielle, Giltay, Jaqcues C, Verbeek, Nienke E, Kleefstra, Tjitske, Brilstra, Eva H, Vlaskamp, Danique R M

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Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome von Buijsse, Nathan, Jansen, Floor E, Ockeloen, Charlotte W, van Kempen, Marjan JA, Zeidler, Shimriet, Willemsen, Marjolein H, Scarano, Emanuela, Monticone, Sonia, Zonneveld-Huijssoon, Evelien, Low, Karen J, Bayat, Allan, Sisodiya, Sanjay M, Samanta, Debopam, Lesca, Gaetan, de Jong, Danielle, Giltay, Jaqcues C, Verbeek, Nienke E, Kleefstra, Tjitske, Brilstra, Eva H, Vlaskamp, Danique RM

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