Celina von Stülpnagel-Steinbeis

Research output

Research output per year 2001 2020 2021 2023

• 32 Original Article (Journal)
• 5 Case report
• 4 Letter to the editor
• 4 Review article
• 2 More
  • 1 Chapter
  • 1 Correction

Research output per year

Research output per year

Search results

• 2023

  Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration

  Consortium, G. E. R., Vetro, A., Pelorosso, C., Balestrini, S., Masi, A., Hambleton, S., Argilli, E., Conti, V., Giubbolini, S., Barrick, R., Bergant, G., Writzl, K., Bijlsma, E., Brunet, T., Cacheiro, P., Mei, D., Devlin, A., Hoffer, M., Machol, K. & Mannaioni, G. & 26 others, Sakamoto, M., Menezes, M., Courtin, T., Sherr, E., Parra, R., Richardson, R., Roscioli, T., Scala, M., von Stülpnagel, C. (Co-author), Smedley, D., Torella, A., Tohyama, J., Koichihara, R., Hamada, K., Ogata, K., Suzuki, T., Sugie, A., van der Smagt, J., van Gassen, K., Valence, S., Vittery, E., Malone, S., Kato, M., Matsumoto, N., Ratto, G. & Guerrini, R., 3 Aug 2023, In: AMERICAN JOURNAL OF HUMAN GENETICS . 110, 8, p. 1356-1376 21 p.

  Research output: Contribution to journal › Original Article (Journal) › peer-review

  • Stretch-Activated Ion Channel 100%
  • Ectopic Expression 25%
  • Blood Transfusion 25%
  • Macrocytosis 25%
  10 Citations (Web of Science)
• 2022

  Cognitive profiles in pediatric unilobar vs. multilobar epilepsy

  Moorhouse, F., Cornell, S., Gerstl, L., Wagner, J., Tacke, M., Roser, T., Heinen, F., von Stulpnagel, C. (Co-author), Vollmar, C., Kunz, M., Ramantani, G. & Borggraefe, I., 2022, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 41, p. 48-54

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  3 Citations (Web of Science)

• Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome.

  Lersch, R., Jannadi, R., Grosse, L., Wagner, M., Schneider, M. F., von Stülpnagel, C. (Co-author), Heinen, F., Potschka, H. & Borggraefe, I., 2022, In: NEUROSCIENTIST. p. 10738584221088244

  Research output: Contribution to journal › Review article › peer-review
  5 Citations (Web of Science)
• 2021

  Childhood Stroke: Long-Term Outcomes and Health-Related Quality of Life with a Special Focus on the Development of Epilepsy.

  von Stülpnagel, C. (First author), Kutschker, S., Sperl, W. (Co-author), Berweck, S., Staudt, M., Berndt, M. & Kluger, G. (Last author), 2021, In: NEUROPEDIATRICS . 52, 6, p. 469-474

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  2 Citations (Web of Science)

• Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy.

  Accogli, A., Wiegand, G., Scala, M., Cerminara, C., Iacomino, M., Riva, A., Carlini, B., Camerota, L., Belcastro, V., Prontera, P., Fernández-Jaén, A., Bebek, N., Scudieri, P., Baldassari, S., Salpietro, V., Novelli, G., De Luca, C., von Stülpnagel, C. (Co-author), Kluger, F. & Kluger, G. (Co-author) & 13 others, Wohlrab, G. C., Ramantani, G., Lewis-Smith, D., Thomas, R. H., Lai, M., Verrotti, A., Striano, S., Depienne, C., Minetti, C., Benfenati, F., Brancati, F., Zara, F. & Striano, P., 2021, In: NEUROLOGY . 97, 6, p. e577-e586

  Research output: Contribution to journal › Case report › peer-review
  9 Citations (Web of Science)

• Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.

  Wortmann, S., Ziętkiewicz, S., Guerrero-Castillo, S., Feichtinger, R. G., Wagner, M., Russell, J., Ellaway, C., Mróz, D., Wyszkowski, H., Weis, D., Hannibal, I., von Stülpnagel, C. (Co-author), Cabrera-Orefice, A., Lichter-Konecki, U., Gaesser, J., Windreich, R., Myers, K. C., Lorsbach, R., Dale, R. C. & Gersting, S. & 6 others, Prada, C. E., Christodoulou, J., Wolf, N. I., Venselaar, H., Mayr, J. A. & Wevers, R. A., 2021, In: GENETICS IN MEDICINE . 23, 9, p. 1789

  Research output: Contribution to journal › Correction › peer-review

• Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects.

  Hofmeister, B., von Stülpnagel, C. (Co-author), Betzler, C. (Co-author), Mari, F., Renieri, A., Baldassarri, M., Haberlandt, E., Jansen, K., Schilling, S., Weber, P., Ahlbory, K., Tang, S., Berweck, S. & Kluger, G. (Last author), 2021, In: NEUROPEDIATRICS . 52, 2, p. 109-122

  Research output: Contribution to journal › Review article › peer-review
  3 Citations (Web of Science)

• Genetic epilepsies in childhood Exact molecular diagnosis as basis of an individual treatment?

  von Stulpnagel, C. (First author) & Kluger, G. (Last author), 2021, In: Monatsschrift Kinderheilkunde.

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  2 Citations (Web of Science)

• Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.

  Wortmann, S. (First author), Ziętkiewicz, S., Guerrero-Castillo, S., Feichtinger, R. (Co-author), Wagner, M., Russell, J., Ellaway, C., Mróz, D., Wyszkowski, H., Weis, D., Hannibal, I., von Stülpnagel, C. (Co-author), Cabrera-Orefice, A., Lichter-Konecki, U., Gaesser, J., Windreich, R., Myers, K. C., Lorsbach, R., Dale, R. C. & Gersting, S. & 6 others, Prada, C. E., Christodoulou, J., Wolf, N. I., Venselaar, H., Mayr, J. A. (Co-author) & Wevers, R. A., 2021, In: GENETICS IN MEDICINE . 23, 9, p. 1705-1714

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  20 Citations (Web of Science)

• Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.

  Willimsky, E.-K., Munzig, A., Mayer, K., Biskup, S., Abicht, A., Hoertnagel, K., Voss, H. V., Klein, H.-G., Rost, I., Larsen, L. H. G., Dahl, H. A., Hoelz, H., Stuelpnagel, C. V. (Co-author) & Borggraefe, I., 2021, In: NEUROPEDIATRICS . 52, 2, p. 92-97

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  8 Citations (Web of Science)
• 2020

  Antiepileptic therapy approaches in KCNQ2 related epilepsy: A systematic review.

  Kuersten, M., Tacke, M., Gerstl, L., Hoelz, H., Stülpnagel, C. V. (Co-author) & Borggraefe, I., 2020, In: EUROPEAN JOURNAL OF MEDICAL GENETICS. 63, 1, p. 103628

  Research output: Contribution to journal › Review article › peer-review
  48 Citations (Web of Science)

• ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response.

  Gasser, M., Boonsimma, P., Netbaramee, W., Wechapinan, T., Srichomthomg, C., Ittiwut, C., Krenn, M., Zimprich, F., Milenkovic, I., Abicht, A., Biskup, S., Roser, T., Shotelersuk, V., Tacke, M., Kuersten, M., Wagner, M., Borggraefe, I., Suphapeetiporn, K. & von Stülpnagel, C. (Last author), 2020, In: JOURNAL OF CLINICAL NEUROSCIENCE . 72, p. 31-38

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  8 Citations (Web of Science)

• Cognitive performance and behavior across idiopathic/genetic epilepsies in children and adolescents.

  Moorhouse, F. J., Cornell, S., Gerstl, L., Tacke, M., Roser, T., Heinen, F., Bonfert, M., von Stülpnagel, C. (Co-author), Wagner, M. & Borggraefe, I., 2020, In: Scientific reports. 10, 1, p. 21543

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  4 Citations (Web of Science)

• Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome (SMARCA2 Mutation)-Due to a POLG1-Related Effect?

  Hofmeister, B., von Stülpnagel, C. (Co-author), Berweck, S., Abicht, A., Kluger, G. (Co-author) & Weber, P., 2020, In: NEUROPEDIATRICS . 51, 1, p. 49-52

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  5 Citations (Web of Science)

• Impact on Clinical Decision Making of Next-Generation Sequencing in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center.

  Hoelz, H., Herdl, C., Gerstl, L., Tacke, M., Vill, K., von Stuelpnagel, C. (Co-author), Rost, I., Hoertnagel, K., Abicht, A., Hollizeck, S., Larsen, L. H. G. & Borggraefe, I., 2020, In: CLINICAL EEG AND NEUROSCIENCE. 51, 1, p. 61-69

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  24 Citations (Web of Science)

• Network for Therapy in Rare Epilepsies (NETRE): Lessons From the Past 15 Years.

  von, S. C. (First author), van, B. A., Borggraefe, I., Eschermann, K. (Co-author), Hartlieb, T. (Co-author), Kiwull, L. (Co-author), Pringsheim, M. (Co-author), Wolff, M., Kudernatsch, M. (Co-author), Wiegand, G., Striano, P. & Consortium, N., Jan 2020, In: Frontiers in Neurology. 11, p. 622510

  Research output: Contribution to journal › Review article › peer-review
  4 Citations (Web of Science)

• Reader response: SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy

  Wolf, P., von Stülpnagel, C. (Co-author), Hartlieb, T. (Co-author), Møller, R. S. & Kluger, G. (Last author), 2020, In: NEUROLOGY . 94, 8, p. 368-369

  Research output: Contribution to journal › Letter to the editor › peer-review
  2 Citations (Web of Science)

• Response To: Overlapping Phenotype from Double Trouble SMARCA2 and POLG1 Variants c.2556A > C and c.3708G > T, Respectively

  von Stülpnagel, C. (First author), Hofmeister, B., Berweck, S., Kluger, G. (Co-author) & Weber, P., Oct 2020, In: NEUROPEDIATRICS . 51, 5, p. 375-376 2 p.

  Research output: Contribution to journal › Letter to the editor › peer-review

• The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.

  Döring, J. H., Saffari, A., Bast, T., Brockmann, K., Ehrhardt, L., Fazeli, W., Janzarik, W. G., Kluger, G. (Co-author), Muhle, H., Møller, R. S., Platzer, K., Santos, J. L., Bache, I., Bertsche, A., Bonfert, M., Borggräfe, I., Broser, P. J., Datta, A. N., Hammer, T. B. & Hartmann, H. & 19 others, Hasse-Wittmer, A., Henneke, M., Kühne, H., Lemke, J. R., Maier, O., Matzker, E., Merkenschlager, A., Opp, J., Patzer, S., Rostasy, K., Stark, B., Strzelczyk, A., von Stülpnagel, C. (Co-author), Weber, Y., Wolff, M., Zirn, B., Hoffmann, G. F., Kölker, S. & Syrbe, S., 2020, In: BIOMEDICINES. 8, 11

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  27 Citations (Web of Science)
• 2019

  Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies.

  Tiefes, A. M., Hartlieb, T., Tacke, M., von Stülpnagel-Steinbeis, C. (Co-author), Larsen, L. H. G., Hao, Q., Dahl, H. A., Neubauer, B. A., Gerstl, L., Kudernatsch, M. (Co-author), Kluger, G. (Co-author) & Borggraefe, I., 2019, In: CLINICAL EEG AND NEUROSCIENCE. 50, 4, p. 26-272

  Research output: Contribution to journal › Case report › peer-review
  12 Citations (Web of Science)

• Positive Short-Term Effect of Low-Dose Rosuvastatin in a Patient with SYNGAP1-Associated Epilepsy.

  Kluger, G. (First author), von Stülpnagel-Steinbeis, C. (Co-author), Arnold, S., Eschermann, K. & Hartlieb, T., 2019, In: NEUROPEDIATRICS . 50, 4, p. 266-267

  Research output: Contribution to journal › Letter to the editor › peer-review
  5 Citations (Web of Science)

• Unresponsive Wakefulness Syndrome in Children after Near-Drowning: Long-Term Outcome and Impact on the Families.

  Kluger, G. (First author), Kirsch, A., Hessenauer, M., Aust, H., Berweck, S., Sperl, W. (Co-author), Betzler, C. (Co-author), von Stülpnagel-Steinbeis, C. (Co-author) & Staudt, M., 2019, In: NEUROPEDIATRICS . 50, 2, p. 71-79

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  3 Citations (Web of Science)
• 2018

  Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.

  von, S. C. (First author), Hartlieb, T. (First author), Borggräfe, I., Coppola, A., Gennaro, E., Eschermann, K. (Co-author), Kiwull, L. (Co-author), Kluger, F., Krois, I., Møller, R., Rössler, F., Santulli, L. & Kluger, G. (Last author), Dec 2018, In: SEIZURE-EUROPEAN JOURNAL OF EPILEPSY. 65, p. 137

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  27 Citations (Web of Science)

• Kapitel zu Epilepsie nach kindlichem Schlaganfall

  von Stülpnagel-Steinbeis, C., 2018, Pediatric Stroke Manual (Pädiatrische Neurologie) Lucia. Borggräfe, G., Borggräfe, I. & (Hrsg) (eds.).

  Research output: Chapter in Book/Report/Conference proceeding › Chapter
• 2017

  Early seizures predict the development of epilepsy in children and adolescents with stroke.

  Breitweg, I., Stülpnagel, C. V. (Co-author), Pieper, T., Lidzba, K., Holthausen, H., Staudt, M. & Kluger, G. (Last author), 2017, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 21, 3, p. 465-467

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  15 Citations (Web of Science)

• Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.

  von Stülpnagel, C. (First author), Ensslen, M., Møller, R. S., Pal, D. K., Masnada, S., Veggiotti, P., Piazza, E., Dreesmann, M., Hartlieb, T., Herberhold, T. (Co-author), Hughes, E., Koch, M., Kutzer, C., Hoertnagel, K., Nitanda, J., Pohl, M., Rostásy, K., Haack, T. B., Stöhr, K. & Kluger, G. (Co-author) & 1 others, Borggraefe, I., 2017, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 21, 3, p. 530-541

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  34 Citations (Web of Science)

• Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.

  Depienne, C., Nava, C., Keren, B., Heide, S., Rastetter, A., Passemard, S., Chantot-Bastaraud, S., Moutard, M.-L., Agrawal, P. B., VanNoy, G., Stoler, J. M., Amor, D. J., Billette de Villemeur, T., Doummar, D., Alby, C., Cormier-Daire, V., Garel, C., Marzin, P., Scheidecker, S. & de Saint-Martin, A. & 41 others, Hirsch, E., Korff, C., Bottani, A., Faivre, L., Verloes, A., Orzechowski, C., Burglen, L., Leheup, B., Roume, J., Andrieux, J., Sheth, F., Datar, C., Parker, M. J., Pasquier, L., Odent, S., Naudion, S., Delrue, M.-A., Le Caignec, C., Vincent, M., Isidor, B., Renaldo, F., Stewart, F., Toutain, A., Koehler, U., Häckl, B., von Stülpnagel, C. (Co-author), Kluger, G. (Co-author), Møller, R. S., Pal, D., Jonson, T., Soller, M., Verbeek, N. E., van Haelst, M. M., de Kovel, C., Koeleman, B., Monroe, G., van Haaften, G., Attié-Bitach, T., Boutaud, L., Héron, D. & Mignot, C., 2017, In: HUMAN GENETICS . 136, 4, p. 463-479

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  59 Citations (Web of Science)
• 2016

  Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

  Mignot, C., von Stulpnagel, C., Nava, C., Ville, D., Sanlaville, D., Lesca, G., Rastetter, A., Gachet, B., Marie, Y., Korenke, G., Borggraefe, I., Hoffmann-Zacharska, D., Szczepanik, E., Rudzka-Dybala, M., Yis, U., Caglayan, H., Isapof, A., Marey, I., Panagiotakaki, E. & Korff, C. & 24 others, Rossier, E., Riess, A., Beck-Woedl, S., Rauch, A., Zweier, C., Hoyer, J., Reis, A., Mironov, M., Bobylova, M., Mukhin, K., Hernandez-Hernandez, L., Maher, B., Sisodiya, S., Kuhn, M., Glaeser, D., Wechuysen, S., Myers, C., Mefford, H., Hortnagel, K., Biskup, S., Lemke, J., Heron, D., Kluger, G. (Co-author) & Depienne, C., 2016, In: JOURNAL OF MEDICAL GENETICS . 53, 8, p. 511-522

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  109 Citations (Web of Science)

• GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.

  Li, D., Yuan, H., Ortiz-Gonzalez, X. R., Marsh, E. D., Tian, L., McCormick, E. M., Kosobucki, G. J., Chen, W., Schulien, A. J., Chiavacci, R., Tankovic, A., Naase, C., Brueckner, F., von Stülpnagel-Steinbeis, C. (Co-author), Hu, C., Kusumoto, H., Hedrich, U. B. S., Elsen, G., Hörtnagel, K. & Aizenman, E. & 4 others, Lemke, J. R., Hakonarson, H., Traynelis, S. F. & Falk, M. J., 2016, In: AMERICAN JOURNAL OF HUMAN GENETICS . 99, 4, p. 802-816

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  121 Citations (Web of Science)

• MRI-imaging and clinical findings of eleven children with tick-borne encephalitis and review of the literature.

  von Stülpnagel, C. (First author), Winkler, P., Koch, J. (Co-author), Zeches-Kansy, C., Schöttler-Glas, A., Wolf, G., Niller, H. H., Staudt, M., Kluger, G. (Co-author) & Rostasy, K., 2016, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 20, 1, p. 45-52

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  14 Citations (Web of Science)

• Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsy.

  Müller, A., Helbig, I., Jansen, C., Bast, T., Guerrini, R., Jähn, J., Muhle, H., Auvin, S., Korenke, G. C., Philip, S., Keimer, R., Striano, P., Wolf, N. I., Püst, B., Thiels, C., Fogarasi, A., Waltz, S., Kurlemann, G., Kovacevic-Preradovic, T. & Ceulemans, B. & 6 others, Schmitt, B., Philippi, H., Tarquinio, D., Buerki, S., von Stülpnagel, C. (Last author) & Kluger, G. (Last author), 2016, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 20, 1, p. 147-151

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  50 Citations (Web of Science)
• 2015

  SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG.

  von Stülpnagel, C. (First author), Funke, C., Haberl, C., Hörtnagel, K., Jüngling, J., Weber, Y. G., Staudt, M. & Kluger, G. (Last author), 2015, In: NEUROPEDIATRICS . 46, 4, p. 287-291

  Research output: Contribution to journal › Case report › peer-review
  19 Citations (Web of Science)
• 2014

  Current role of rufinamide in the treatment of childhood epilepsy: Literature review and treatment guidelines.

  Coppola, G., Besag, F., Cusmai, R., Dulac, O., Kluger, G. (Co-author), Moavero, R., Nabbout, R., Nikanorova, M., Pisani, F., Verrotti, A., von Stülpnagel, C. (Co-author) & Curatolo, P., 2014, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 18, 6, p. 685-690

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  23 Citations (Web of Science)

• Epilepsy in Aicardi-Goutières syndrome.

  Ramantani, G., Maillard, L. G., Bast, T., Husain, R. A., Niggemann, P., Kohlhase, J., Hertzberg, C., Ungerath, K., Innes, M. A., Walkenhorst, H., Bevot, A., von Stülpnagel, C. (Co-author), Thomas, K., Niemann, F., Ergun, M. A., Tacke, U., Häusler, M., Ikonomidou, C., Korinthenberg, R. & Lee-Kirsch, M. A., 2014, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 18, 1, p. 30-37

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  17 Citations (Web of Science)
• 2013

  Generalized Epilepsy in Two Patients with 5p Duplication

  Kluger, G. (First author), Koehler, U., Neuhann, T. M., Pieper, T., Staudt, M. & von Stülpnagel, C. (Last author), 2013, In: NEUROPEDIATRICS . 44, 4, p. 225-229

  Research output: Contribution to journal › Case report › peer-review
  7 Citations (Web of Science)
• 2012

  First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome).

  von Stülpnagel, C. (First author), Coppola, G., Striano, P., Müller, A., Staudt, M. & Kluger, G. (Last author), 2012, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 16, 5, p. 459-463

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  18 Citations (Web of Science)
• 2011

  Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsy

  Ufer, M., von Stülpnagel, C. (First author), Muhle, H., Haenisch, S., Remmler, C., Majed, A., Plischke, H., Stephani, U., Kluger, G. (Co-author) & Cascorbi, I., 2011, In: PHARMACOGENETICS AND GENOMICS. 21, 10, p. 624-630

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  43 Citations (Web of Science)

• Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome

  Mueller, A., Boor, R., Coppola, G., Striano, P., Dahlin, M., von Stuelpnagel, C. (Co-author), Lotte, J., Staudt, M. & Kluger, G. (Last author), 2011, In: EPILEPSY & BEHAVIOR : E&B. 21, 3, p. 282-284

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  34 Citations (Web of Science)

• Refractory Focal Epilepsy in a Patient with Methylmalonic Aciduria: Case Report on Positive and Long-lasting Effect of Rufinamide

  von Stülpnagel, C. (First author), Leichsenring, M., Müller, A., Staudt, M. & Kluger, G. (Last author), 2011, In: NEUROPEDIATRICS . 42, 2, p. 71-73

  Research output: Contribution to journal › Case report › peer-review
  6 Citations (Web of Science)
• 2010

  Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome.

  Ramantani, G., Kohlhase, J., Hertzberg, C., Innes, A. M., Engel, K., Hunger, S., Borozdin, W., Mah, J. K., Ungerath, K., Walkenhorst, H., Richardt, H.-H., Buckard, J., Bevot, A., Siegel, C., von Stülpnagel, C. (Co-author), Ikonomidou, C., Thomas, K., Proud, V., Niemann, F. & Wieczorek, D. & 6 others, Häusler, M., Niggemann, P., Baltaci, V., Conrad, K., Lebon, P. & Lee-Kirsch, M. A., 2010, In: ARTHRITIS AND RHEUMATISM . 62, 5, p. 1469-1477

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  156 Citations (Web of Science)

• Levetiracetam as add-on therapy in different subgroups of "benign" idiopathic focal epilepsies in childhood

  von Stülpnagel, C. (First author), Kluger, G. (First author), Leiz, S. & Holthausen, H., 2010, In: EPILEPSY & BEHAVIOR : E&B. 17, 2, p. 193-198

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  24 Citations (Web of Science)
• 2009

  Letter: Lack of association between MDR1 polymorphisms and pharmacoresistance to anticonvulsive drugs in patients with childhood-onset epilepsy

  von Stülpnagel, C. (First author), Plischke, H., Zill, P., Bäumel, C., Spiegel, R., Gruber, R. & Kluger, G. (Last author), 2009, In: EPILEPSIA. 50, 7, p. 1835-1837

  Research output: Contribution to journal › Letter to the editor › peer-review
  14 Citations (Web of Science)

• Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option.

  von Stülpnagel, C. (First author), Reilich, P., Straube, A., Schäfer, J., Blaschek, A., Lee, S.-H., Müller-Felber, W., Henschel, V., Mansmann, U. & Heinen, F., 2009, In: JOURNAL OF CHILD NEUROLOGY . 24, 4, p. 406-409

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  22 Citations (Web of Science)
• 2007

  Long-term use of Levetiracetam in patients with severe childhood-onset epilepsy.

  von Stuelpnagel, C. (First author), Holthausen, H. & Kluger, G. (Last author), 2007, In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 11, 6, p. 341-345

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  11 Citations (Web of Science)
• 2006

  [Primary headache in children].

  von Stülpnagel-Steinbeis, C., Blaschek, A., Lee, S. H. & Heinen, F., 2006, In: MMW. MUNCHENER MEDIZINISCHE WOCHENSCHRIFT. 148, 46, p. 39-41

  Research output: Contribution to journal › Original Article (Journal) › peer-review

• Migraine therapy in childhood. Update

  Lee, S., von Stulpnagel, C. & Heinen, F., 2006, In: Monatsschrift Kinderheilkunde. 154, 8, p. 764-+

  Research output: Contribution to journal › Original Article (Journal) › peer-review
  1 Citation (Web of Science)
• 2001

  Association of myocardial infarction with mononuclear cell expression of the cytomegalovirus chemokine receptor US28 in patients with NIDDM.

  Weber, C., von Stülpnagel-Steinbeis, C. (Co-author), Weber, K. S., Hengel, H. & Weber, P. C., 2001, In: EXPERIMENTAL & CLINICAL CARDIOLOGY. 6, 2, p. 105-108

  Research output: Contribution to journal › Original Article (Journal) › peer-review