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2022
Borusiak, Peter 
ORCID: 0000-0002-9075-2358, Mazheika, Yuliya, Bauer, Susanne, Haberlandt, Edda, Krois, Ilona, Fricke, Christian, Simon, Liane, Beschoner, Petra, Jerg-Bretzke, Lucia, Geiser, Franziska ORCID: 0000-0002-4212-9692, Hiebel, Nina, Weidner, Kerstin, Albus, Christian, Morawa, Eva and Erim, Yesim
(2022).
The impact of the COVID-19 pandemic on pediatric developmental services: a cross-sectional study on overall burden and mental health status.
Arch. PUblic Health, 80 (1).
LONDON:
BMC.
ISSN 2049-3258
2021
Hofmeister, Benedikt, von Stuelpnagel, Celina, Betzler, Cornelia, Mari, Francesca ORCID: 0000-0003-1992-1654, Renieri, Alessandra ORCID: 0000-0002-0846-9220, Baldassarri, Margherita, Haberlandt, Edda, Jansen, Katrien, Schilling, Stefan, Weber, Peter, Ahlbory, Katja, Tang, Shan, Berweck, Steffen and Kluger, Gerhard
(2021).
Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects.
Neuropediatrics, 52 (2).
S. 109 - 123.
STUTTGART:
GEORG THIEME VERLAG KG.
ISSN 1439-1899
2018
Bobbili, Dheeraj R., Lal, Dennis, May, Patrick ORCID: 0000-0001-8698-3770, Reinthaler, Eva M., Jabbari, Kamel, Thiele, Holger, Nothnagel, Michael ORCID: 0000-0001-8305-7114, Jurkowski, Wiktor, Feucht, Martha, Nuernberg, Peter, Lerche, Holger, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Krause, Roland ORCID: 0000-0001-9938-7126, Neubauer, Bernd A., Reinthaler, Eva M., Zimprich, Fritz ORCID: 0000-0002-6998-5480, Feucht, Martha, Steinboeck, Hannelore, Neophytou, Birgit, Geldner, Julia, Gruber-Sedlmayr, Ursula, Haberlandt, Edda, Ronen, Gabriel M., Altmueller, Janine, Lal, Dennis, Nrnberg, Peter, Sander, Thomas, Thiele, Holger, Krause, Roland ORCID: 0000-0001-9938-7126, May, Patrick ORCID: 0000-0001-8698-3770, Balling, Rudi ORCID: 0000-0003-2902-5650, Lerche, Holger and Neubauer, Bernd A.
(2018).
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
Eur. J. Hum. Genet., 26 (2).
S. 258 - 265.
LONDON:
NATURE PUBLISHING GROUP.
ISSN 1476-5438
2014
Lal, Dennis, Reinthaler, Eva M., Schubert, Julian, Muhle, Hiltrud, Riesch, Erik, Kluger, Gerhard, Jabbari, Kamel, Kawalia, Amit, Baeumel, Christine, Holthausen, Hans, Hahn, Andreas, Feucht, Martha, Neophytou, Birgit, Haberlandt, Edda, Becker, Felicitas, Altmueller, Janine, Thiele, Holger, Lemke, Johannes R., Lerche, Holger, Nuernberg, Peter, Sander, Thomas, Weber, Yvonne, Zimprich, Fritz ORCID: 0000-0002-6998-5480 and Neubauer, Bernd A.
(2014).
DEPDC5 Mutations in Genetic Focal Epilepsies of Childhood.
Ann. Neurol., 75 (5).
S. 788 - 793.
HOBOKEN:
WILEY-BLACKWELL.
ISSN 1531-8249
Reinthaler, Eva M., Lal, Dennis, Jurkowski, Wiktor, Feucht, Martha, Steinboeck, Hannelore, Gruber-Sedlmayr, Ursula, Ronen, Gabriel M., Geldner, Julia, Haberlandt, Edda, Neophytou, Birgit, Hahn, Andreas, Altmueller, Janine, Thiele, Holger, Toliat, Mohammad R., Lerche, Holger, Nuernberg, Peter, Sander, Thomas, Neubauer, Bernd A. and Zimprich, Fritz ORCID: 0000-0002-6998-5480
(2014).
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy.
Epilepsia, 55 (8).
S. E89 - 5.
HOBOKEN:
WILEY-BLACKWELL.
ISSN 1528-1167
Reinthaler, Eva M., Lal, Dennis, Lebon, Sebastien, Hildebrand, Michael S., Dahl, Hans-Henrik M., Regan, Brigid M., Feucht, Martha, Steinboeck, Hannelore, Neophytou, Birgit, Ronen, Gabriel M., Roche, Laurian, Gruber-Sedlmayr, Ursula, Geldner, Julia, Haberlandt, Edda, Hoffmann, Per, Herms, Stefan ORCID: 0000-0002-2786-8200, Gieger, Christian ORCID: 0000-0001-6986-9554, Waldenberger, Melanie ORCID: 0000-0003-0583-5093, Franke, Andre ORCID: 0000-0003-1530-5811, Wittig, Michael, Schoch, Susanne, Becker, Albert J., Hahn, Andreas, Maennik, Katrin, Toliat, Mohammad R., Winterer, Georg, Lerche, Holger, Nuernberg, Peter, Mefford, Heather, Scheffer, Ingrid E., Berkovic, Samuel F., Beckmann, Jacques S., Sander, Thomas, Jacquemont, Sebastien, Reymond, Alexandre, Zimprich, Fritz ORCID: 0000-0002-6998-5480 and Neubauer, Bernd A.
(2014).
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
Hum. Mol. Genet., 23 (22).
S. 6069 - 6081.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2083