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Anzahl der Publikationen: 9
Zeitschriftenartikel
Lersch, Robert; Jannadi, Rawan; Grosse, Leonie; Wagner, Matias; Schneider, Marius Frederik; Stülpnagel, Celina von; Heinen, Florian; Potschka, Heidrun und Borggräfe, Ingo 
ORCID: https://orcid.org/0000-0002-8484-5945
(2023):
Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome.
In: Neuroscientist, Bd. 29, Nr. 6:
732 –750
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-8484-5945
(2023):
Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome.
In: Neuroscientist, Bd. 29, Nr. 6:
732 –750
[PDF, 1MB]
Accogli, Andrea; Wiegand, Gert; Scala, Marcello; Cerminara, Caterina; Iacomino, Michele; Riva, Antonella; Carlini, Barbara; Camerota, Letizia; Belcastro, Vincenzo; Prontera, Paolo; Fernandez-Jaen, Alberto; Bebek, Nerses; Scudieri, Paolo; Baldassari, Simona; Salpietro, Vincenzo; Novelli, Giuseppe; De Luca, Chiara; Stülpnagel, Celina von; Kluger, Felicitas; Kluger, Gerhard Josef; Wohlrab, Gabriele Christine; Ramantani, Georgia; Lewis-Smith, David; Thomas, Rhys H.; Lai, Ming; Verrotti, Alberto; Striano, Salvatore; Depienne, Christel; Minetti, Carlo; Benfenati, Fabio; Brancati, Francesco; Zara, Federico und Striano, Pasquale
(2021):
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy.
In: Neurology, Bd. 97, Nr. 6, E577-E586
Moorhouse, Frederik Jan; Cornell, Sonia; Gerstl, Lucia; Tacke, Moritz; Roser, Timo; Heinen, Florian; Bonfert, Michaela; Stülpnagel, Celina von; Wagner, Matias und Borggraefe, Ingo
(2020):
Cognitive performance and behavior across idiopathic/genetic epilepsies in children and adolescents.
In: Scientific Reports, Bd. 10, Nr. 1, 21543
[PDF, 1MB]
Hofmeister, Benedikt; Stülpnagel, Celina von; Berweck, Steffen; Abicht, Angela; Kluger, Gerhard und Weber, Peter
(2020):
Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome ( SMARCA2 Mutation)-Due to a POLG1 -Related Effect?
In: Neuropediatrics, Bd. 51, Nr. 1: S. 49-52
Willimsky, Eva-Katharina; Munzig, Anna; Mayer, Karin; Biskup, Saskia; Abicht, Angela; Hoertnagel, Konstanze; Voss, Hubertus von; Klein, Hanns-Georg; Rost, Imma; Larsen, Line H. G.; Dahl, Hanns Atli; Hoelz, Hannes; Stülpnagel, Celina von und Borggraefe, Ingo
(2020):
Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.
In: Neuropediatrics, Bd. 52, Nr. 02: S. 92-97
Doering, Jan Henje; Saffari, Afshin; Bast, Thomas; Brockmann, Knut; Ehrhardt, Laura; Fazeli, Walid; Janzarik, Wibke G.; Kluger, Gerhard; Muhle, Hiltrud; Moller, Rikke S.; Platzer, Konrad; Santos, Joana Larupa; Bache, Iben; Bertsche, Astrid; Bonfert, Michaela; Borggraefe, Ingo; Broser, Philip J.; Datta, Alexandre N.; Hammer, Trine Bjorg; Hartmann, Hans; Hasse-Wittmer, Anette; Henneke, Marco; Kuehne, Hermann; Lemke, Johannes R.; Maier, Oliver; Matzker, Eva; Merkenschlager, Andreas; Opp, Joachim; Patzer, Steffi; Rostasy, Kevin; Stark, Birgit; Strzelczyk, Adam; Stülpnagel, Celina von; Weber, Yvonne; Wolff, Markus; Zirn, Birgit; Hoffmann, Georg Friedrich; Koelker, Stefan und Syrbe, Steffen
(2020):
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.
In: Biomedicines, Bd. 8, Nr. 11, 456
Mignot, Cyril; Stülpnagel, Celina von; Nava, Caroline; Ville, Dorothée; Sanlaville, Damien; Lesca, Gaetan; Rastetter, Agnès; Gachet, Benoit; Marie, Yannick; Korenke, G. Christoph; Borggräfe, Ingo; Hoffmann-Zacharska, Dorota; Szczepanik, Elzbieta; Rudzka-Dybala, Mariola; Yiş, Uluç; Çağlayan, Hande; Isapof, Arnaud; Marey, Isabelle; Panagiotakaki, Eleni; Korff, Christian; Rossier, Eva; Riess, Angelika; Beck-Woedl, Stefanie; Rauch, Anita; Zweier, Christiane; Hoyer, Juliane; Reis, André; Mironov, Mikhail; Bobylova, Maria; Mukhin, Konstantin; Hernandez-Hernandez, Laura; Maher, Bridget; Sisodiya, Sanjay; Kuhn, Marius; Glaeser, Dieter; Wechuysen, Sarah; Myers, Candace T.; Mefford, Heather C.; Hörtnagel, Konstanze; Biskup, Saskia; Lemke, Johannes R.; Héron, Delphine; Kluger, Gerhard und Depienne, Christel
(2016):
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.
In: Journal of Medical Genetics, Bd. 53, Nr. 8: S. 511-522
[PDF, 1MB]
Stülpnagel, Celina von; Reilich, Peter; Straube, Andreas; Schäfer, Jan; Blaschek, Astrid; Lee, Seung-Hee; Müller-Felber, Wolfgang; Henschel, Volkmar; Mansmann, Ulrich und Heinen, Florian
(2009):
Myofascial Trigger Points in Children With Tension-Type Headache: A New Diagnostic and Therapeutic Option.
In: Journal of Child Neurology, Bd. 24, Nr. 4: S. 406-409
[PDF, 109kB]
Stülpnagel, Celina von; Reilich, Peter; Straube, Andreas; Schaefer, Jan; Blaschek, Astrid; Lee, Seung-Hee; Müller-Felber, Wolfgang; Henschel, Volkmar; Mansmann, Ulrich und Heinen, Florian
(2009):
Myofascial trigger points in children with tension-type headache: A new diagnostic and therapeutic option.
In: Journal of Child Neurology, Bd. 24, Nr. 4: S. 406-409