MUC – Munich University Center for Children with Medical and Developmental Complexity – iSPZ Hauner – integriertes Sozialpädiatrisches Zentrum im Dr. von Haunerschen Kinderspital 
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Fachpublikationen

Stand 05.02.2024

  1. Bartels, F., B. Baumgartner, A. Aigner, G. Cooper, A. Blaschek, E. M. Wendel, A. Bertolini, M. Karenfort, M. Baumann, R. Cleaveland, A. Wegener-Panzer, S. Leiz, M. Salandin, P. Krieg, T. Reindl, M. Reindl, C. Finke, and K. Rostasy. "Impaired Brain Growth in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Acute Disseminated Encephalomyelitis." Neurol Neuroimmunol Neuroinflamm 10, no. 2 (Mar 2023). https://dx.doi.org/10.1212/NXI.0000000000200066.
  2. Blaschek, A., A. Sitzberger, M. Brugger, E. Graf, R. Berutti, M. Zech, and K. Vill. "Taok1-Related Neurodevelopmental Disorder: A New Differential Diagnosis for Childhood-Onset Tremor?", Parkinsonism Relat Disord 109 (Apr 2023): 105320. https://dx.doi.org/10.1016/j.parkreldis.2023.105320.
  3. Boekstegers, A., H. Schmidt, M. Kurzay, T. Vallee, E. Jung, I. Dubinski, R. Maxwell, and I. Schmid. "Cortisol Response in Children with Cancer and Fever During Chemotherapy: A Prospective, Observational Study Using Random Serum Cortisol Levels." Cancer Med 12, no. 8 (Apr 2023): 9247-59. https://dx.doi.org/10.1002/cam4.5667.
  4. Bonfert, M., F. Heinen, P. Kanovsky, A. S. Schroeder, H. G. Chambers, E. Dabrowski, T. L. Geister, A. Hanschmann, M. Althaus, M. Banach, and D. Gaebler-Spira. "Spasticity-Related Pain in Children/Adolescents with Cerebral Palsy. Part 2: Incobotulinumtoxina Efficacy Results from a Pooled Analysis." J Pediatr Rehabil Med 16, no. 1 (2023): 83-98. https://dx.doi.org/10.3233/PRM-220020.
  5. Bonfert, M. V., A. Meuche, G. Urban, C. Borner, U. Breuer, B. Warken, C. Wimmer, H. Strattner, T. Muller, M. Hosl, F. Heinen, S. Berweck, and S. A. Schroder. "Feasibility of Functional Repetitive Neuromuscular Magnetic Stimulation (Frnms) Targeting the Gluteal Muscle in a Child with Cerebral Palsy: A Case Report." Phys Occup Ther Pediatr 43, no. 3 (2023): 338-50. https://dx.doi.org/10.1080/01942638.2022.2138732.
  6. Bonke, E. M., M. V. Bonfert, S. M. Hillmann, J. Seitz-Holland, M. Gaubert, T. L. T. Wiegand, A. De Luca, K. I. K. Cho, S. B. Sandmo, E. Yhang, Y. Tripodis, C. Seer, D. Kaufmann, E. Kaufmann, M. Muehlmann, J. Gooijers, A. P. Lin, A. Leemans, S. P. Swinnen, R. Bahr, M. E. Shenton, O. Pasternak, U. Tacke, F. Heinen, and I. K. Koerte. "Neurological Soft Signs in Adolescents Are Associated with Brain Structure." Cereb Cortex 33, no. 9 (Apr 25 2023): 5547-56. https://dx.doi.org/10.1093/cercor/bhac441.
  7. Bonke, E. M., A. Clauwaert, S. M. Hillmann, U. Tacke, C. Seer, E. Yhang, Y. Tripodis, S. B. Sandmo, T. L. T. Wiegand, D. Kaufmann, E. Kaufmann, S. B. Richmond, M. Gaubert, J. Seitz-Holland, A. Leemans, S. P. Swinnen, R. Bahr, O. Pasternak, F. Heinen, I. K. Koerte, M. V. Bonfert, and J. Gooijers. "Neurological Soft Signs Are Associated with Reduced Medial-Lateral Postural Control in Adolescent Athletes." J Neurol Sci 445 (Feb 15 2023): 120516. https://dx.doi.org/10.1016/j.jns.2022.120516.
  8. Borner-Schroder, C., M. Lang, G. Urban, E. Zaidenstadt, J. Staisch, A. Hauser, I. Hannibal, K. Huss, B. Klose, M. F. Lechner, N. Sollmann, M. N. Landgraf, F. Heinen, and M. V. Bonfert. "Neuromodulation in Pediatric Migraine Using Repetitive Neuromuscular Magnetic Stimulation: A Feasibility Study." Children (Basel) 10, no. 11 (Oct 30 2023). https://dx.doi.org/10.3390/children10111764.
  9. Brunet, T., B. Zott, V. Lieftuchter, D. Lenz, A. Schmidt, P. Peters, R. Kopajtich, M. Zaddach, H. Zimmermann, I. Huning, D. Ballhausen, C. Staufner, A. Bianzano, J. Hughes, R. W. Taylor, R. McFarland, A. Devlin, M. Mihaljevic, N. Barisic, M. Rohlfs, S. Wilfling, N. Sondheimer, S. Hewson, N. M. Marinakis, K. Kosma, J. Traeger-Synodinos, M. Elbracht, M. Begemann, S. Trepels-Kottek, D. Hasan, M. Scala, V. Capra, F. Zara, A. T. van der Ven, J. Driemeyer, C. Apitz, J. Kramer, A. Strong, H. Hakonarson, D. Watson, J. A. Mayr, H. Prokisch, T. Meitinger, I. Borggraefe, J. Spiegler, I. Baric, M. Paolini, L. Gerstl, and M. Wagner. "De Novo Variants in Rnf213 Are Associated with a Clinical Spectrum Ranging from Leigh Syndrome to Early-Onset Stroke." Genet Med 26, no. 2 (Nov 1 2023): 101013. https://dx.doi.org/10.1016/j.gim.2023.101013.
  10. Burgard, C., M. J. Zacherl, A. Todica, J. Hornung, F. Grawe, I. Pekrul, P. Zimmermann, C. Schmid-Tannwald, R. Ladurner, D. Krenz, A. Trupka, J. Wagner, P. Bartenstein, C. Spitzweg, and V. Wenter. "Primary Presentation and Clinical Course of Pediatric and Adolescent Patients with Differentiated Thyroid Carcinoma after Radioiodine Therapy." Front Oncol 13 (2023): 1237472. https://dx.doi.org/10.3389/fonc.2023.1237472.
  11. Cunitz, K., I. Holloway, A. Harzendorf, S. Greving, M. Zeldovich, U. Krenz, D. Timmermann, I. K. Koerte, M. V. Bonfert, S. Berweck, M. Kieslich, K. Brockmann, M. Roediger, A. Buchheim, N. Andelic, M. Lendt, M. Staebler, H. Muehlan, and N. von Steinbuechel. "Health-Related Quality of Life after Pediatric Traumatic Brain Injury: A Quantitative Comparison between Children's and Parents' Perspectives of the Qolibri-Kid/Ado Questionnaire." J Clin Med 12, no. 23 (Nov 30 2023). https://dx.doi.org/10.3390/jcm12237439.
  12. de Sainte Agathe, J. M., B. Pode-Shakked, S. Naudion, V. Michaud, B. Arveiler, P. Fergelot, J. Delmas, B. Keren, C. Poirsier, F. S. Alkuraya, B. Tabarki, E. Bend, K. Davis, M. Bebin, M. L. Thompson, E. M. Bryant, M. Wagner, I. Hannibal, J. Lenberg, M. Krenn, K. M. Wigby, J. R. Friedman, M. Iascone, A. Cereda, T. Miao, E. LeGuern, E. Argilli, E. Sherr, O. Caluseriu, T. Tidwell, P. Bayrak-Toydemir, C. Hagedorn, M. Brugger, K. Vill, F. D. Morneau-Jacob, W. Chung, K. N. Weaver, J. W. Owens, A. Husami, B. P. Chaudhari, B. S. Stone, K. Burns, R. Li, I. M. de Lange, M. Biehler, E. Ginglinger, B. Gerard, R. W. Stottmann, and A. Trimouille. "Arf1-Related Disorder: Phenotypic and Molecular Spectrum." J Med Genet 60, no. 10 (Oct 2023): 999-1005. https://dx.doi.org/10.1136/jmg-2022-108803.
  13. Dzinovic, I., E. Graf, M. Brugger, R. Berutti, I. Prihodova, A. Blaschek, J. Winkelmann, R. Jech, K. Vill, and M. Zech. "Challenges in Establishing the Diagnosis of Prrt2-Related Dystonia: Recurrent Pathogenic Variants in a Homopolymeric Stretch." Mov Disord Clin Pract 10, no. 7 (Jul 2023): 1159-61. https://dx.doi.org/10.1002/mdc3.13793.
  14. Engel, C., S. Valence, G. Delplancq, R. Maroofian, A. Accogli, E. Agolini, F. S. Alkuraya, V. Baglioni, I. Bagnasco, M. Becmeur-Lefebvre, E. Bertini, I. Borggraefe, E. Brischoux-Boucher, A. L. Bruel, A. Brusco, D. K. Bubshait, C. Cabrol, M. R. Cilio, M. C. Cornet, C. Coubes, O. Danhaive, V. Delague, A. S. Denomme-Pichon, M. C. Di Giacomo, M. Doco-Fenzy, H. Engels, K. Cremer, M. Gerard, J. G. Gleeson, D. Heron, J. Goffeney, A. Guimier, F. L. Harms, H. Houlden, M. Iacomino, R. Kaiyrzhanov, B. Kamien, E. G. Karimiani, D. Kraus, P. Kuentz, K. Kutsche, D. Lederer, L. Massingham, C. Mignot, D. Morris-Rosendahl, L. Nagarajan, S. Odent, C. Ormieres, J. N. Partlow, L. Pasquier, L. Penney, C. Philippe, G. Piccolo, C. Poulton, A. Putoux, M. Rio, C. Rougeot, V. Salpietro, I. Scheffer, A. Schneider, S. Srivastava, R. Straussberg, P. Striano, E. M. Valente, P. Venot, L. Villard, A. Vitobello, J. Wagner, M. Wagner, M. S. Zaki, F. Zara, G. Lesca, V. R. Yassaee, M. Miryounesi, F. Hashemi-Gorji, M. Beiraghi, F. Ashrafzadeh, H. Galehdari, C. Walsh, A. Novelli, M. Tacke, D. Sadykova, Y. Maidyrov, K. Koneev, C. Shashkin, V. Capra, M. Zamani, L. Van Maldergem, L. Burglen, and J. Piard. "Brat1-Related Disorders: Phenotypic Spectrum and Phenotype-Genotype Correlations from 97 Patients." Eur J Hum Genet 31, no. 9 (Sep 2023): 1023-31. https://dx.doi.org/10.1038/s41431-023-01410-z.
  15. Esopenko, C., N. Sollmann, E. M. Bonke, T. L. T. Wiegand, F. Heinen, N. L. de Souza, K. M. Breedlove, M. E. Shenton, A. P. Lin, and I. K. Koerte. "Current and Emerging Techniques in Neuroimaging of Sport-Related Concussion." J Clin Neurophysiol 40, no. 5 (Jul 1 2023): 398-407. https://dx.doi.org/10.1097/WNP.0000000000000864.
  16. Gippert, S., M. Wagner, T. Brunet, R. Berruti, M. Brugger, E. M. C. Schwaibold, T. B. Haack, G. F. Hoffmann, M. Bettendorf, and D. Choukair. "Exome Sequencing (Es) of a Pediatric Cohort with Chronic Endocrine Diseases: A Single-Center Study (within the Framework of the Translate-Namse Project)." Endocrine (Nov 8 2023). https://dx.doi.org/10.1007/s12020-023-03581-7.
  17. Grosse, L., V. Lieftuchter, Y. Vollmuth, F. Hoffmann, M. Olivieri, K. Reiter, M. Tacke, F. Heinen, I. Borggraefe, A. Osterman, M. Forstner, J. Hubner, U. von Both, L. Birzele, M. Rohlfs, A. Schomburg, M. M. Bohmer, V. Ruf, D. Cadar, B. Muntau, K. Portner, and D. Tappe. "First Detected Geographical Cluster of Bodv-1 Encephalitis from Same Small Village in Two Children: Therapeutic Considerations and Epidemiological Implications." Infection 51, no. 5 (Oct 2023): 1383-98. https://dx.doi.org/10.1007/s15010-023-01998-w.
  18. Grosse, L., A. C. Meuche, B. Parzefall, C. Borner, J. F. Schnabel, M. A. Spah, P. Klug, N. Sollmann, L. Klich, M. Hosl, F. Heinen, S. Berweck, S. A. Schroder, and M. V. Bonfert. "Functional Repetitive Neuromuscular Magnetic Stimulation (Frnms) Targeting the Tibialis Anterior Muscle in Children with Upper Motor Neuron Syndrome: A Feasibility Study." Children (Basel) 10, no. 10 (Sep 22 2023). https://dx.doi.org/10.3390/children10101584.
  19. Grosse, L., J. F. Schnabel, C. Borner-Schroder, M. A. Spah, A. C. Meuche, N. Sollmann, U. Breuer, B. Warken, M. Hosl, F. Heinen, S. Berweck, S. A. Schroder, and M. V. Bonfert. "Safety and Feasibility of Functional Repetitive Neuromuscular Magnetic Stimulation of the Gluteal Muscles in Children and Adolescents with Bilateral Spastic Cerebral Palsy." Children (Basel) 10, no. 11 (Oct 31 2023). https://dx.doi.org/10.3390/children10111768.
  20. Grosse, L., M. A. Spah, C. Borner, J. F. Schnabel, A. C. Meuche, B. Parzefall, U. Breuer, B. Warken, A. Sitzberger, M. Hosl, F. Heinen, S. Berweck, S. A. Schroder, and M. V. Bonfert. "Addressing Gross Motor Function by Functional Repetitive Neuromuscular Magnetic Stimulation Targeting to the Gluteal Muscles in Children with Bilateral Spastic Cerebral Palsy: Benefits of Functional Repetitive Neuromuscular Magnetic Stimulation Targeting the Gluteal Muscles." Front Neurol 14 (2023): 1161532. https://dx.doi.org/10.3389/fneur.2023.1161532.
  21. Hosl, M., A. Schupfinger, L. Klich, L. Geest, P. Bauer, M. V. Bonfert, F. K. Afifi, S. Nader, and S. Berweck. "Relationship between Kinematic Gait Quality and Caregiver-Reported Everyday Mobility in Children and Youth with Spastic Cerebral Palsy." Eur J Paediatr Neurol 42 (Jan 2023): 88-96. https://dx.doi.org/10.1016/j.ejpn.2022.11.009.
  22. Johannsen, J., D. Weiss, J. Driemeyer, J. Olfe, F. Stute, F. Muller, M. Schutt, R. Trollmann, H. Kolbel, U. Schara-Schmidt, J. Kirschner, A. Pechmann, A. Blaschek, V. Horber, and J. Denecke. "High-Sensitive Cardiac Troponin I (Hs-Ctni) Concentrations in Newborns Diagnosed with Spinal Muscular Atrophy." Front Pediatr 11 (2023): 1259293. https://dx.doi.org/10.3389/fped.2023.1259293.
  23. Jost, W. H., T. Baumer, A. Bevot, U. Birkmann, C. Buhmann, M. Grosheva, O. Guntinas-Lichius, R. Laskawi, S. Paus, C. Pflug, A. S. Schroeder, B. Spittau, A. Steffen, B. Wilken, M. Winterholler, and S. Berweck. "Botulinum Neurotoxin Type a in the Interdisciplinary Treatment of Sialorrhea in Adults and Children-Update and Practice Recommendations." Front Neurol 14 (2023): 1275807. https://dx.doi.org/10.3389/fneur.2023.1275807.
  24. Kaupper, C. S., S. M. Blaauwendraad, C. A. M. Cecil, R. H. Mulder, R. Gaillard, R. Goncalves, I. Borggraefe, B. Koletzko, and V. W. V. Jaddoe. "Cord Blood Metabolite Profiles and Their Association with Autistic Traits in Childhood." Metabolites 13, no. 11 (Nov 9 2023). https://dx.doi.org/10.3390/metabo13111140.
  25. H. E. Klager, B. Nast-Kolb, L. Reuter, F. Hoffmann, S. Juranek, C. Bidlingmaier, N. Fabri, N. K. T. Schonberg, J. Wagner, F. Heinen, O. Muensterer, C. Zeller, A. S. Holler, A. Froba-Pohl, and M. V. Bonfert. "Trends in Pediatric Mild Traumatic Brain Injury During Covid-19-Related Lockdown-a Single-Center Study." Neuropediatrics 54, no. 6 (Dec 2023): 388-96. https://dx.doi.org/10.1055/a-2084-2674.
  26. Kuhne, F., L. L. Becker, T. Bast, A. Bertsche, I. Borggraefe, C. M. Bosselmann, J. Fahrbach, C. Hertzberg, N. A. Herz, M. Hirsch, M. Holtkamp, C. Janello, G. J. Kluger, G. Kurlemann, H. Lerche, K. L. Makridis, F. von Podewils, M. Pringsheim, S. Schubert-Bast, J. Schulz, A. Schulze-Bonhage, D. Steinbart, B. J. Steinhoff, A. Strzelczyk, S. Syrbe, H. De Vries, C. Wagner, J. Wagner, B. Wilken, C. Prager, K. A. Klotz, and A. M. Kaindl. "Real-World Data on Cannabidiol Treatment of Various Epilepsy Subtypes: A Retrospective, Multicenter Study." Epilepsia Open 8, no. 2 (Jun 2023): 360-70. https://dx.doi.org/10.1002/epi4.12699.
  27. Kunz, M., P. Karschnia, I. Borggraefe, S. Noachtar, J. C. Tonn, and C. Vollmar. "Seizure-Free Outcome and Safety of Repeated Epilepsy Surgery for Persistent or Recurrent Seizures." J Neurosurg 138, no. 1 (Jan 1 2023): 9-18. https://dx.doi.org/10.3171/2022.4.JNS212753.
  28. Lawlor, M. W., B. Schoser, M. Margeta, C. A. Sewry, K. A. Jones, P. B. Shieh, N. L. Kuntz, B. K. Smith, J. J. Dowling, W. Muller-Felber, C. G. Bonnemann, A. M. Seferian, A. Blaschek, S. Neuhaus, A. R. Foley, D. N. Saade, E. Tsuchiya, U. R. Qasim, M. Beatka, M. J. Prom, E. Ott, S. Danielson, P. Krakau, S. N. Kumar, H. Meng, M. Vanden Avond, C. Wells, H. Gordish-Dressman, A. H. Beggs, S. Christensen, E. Conner, E. S. James, J. Lee, C. Sadhu, W. Miller, B. Sepulveda, F. Varfaj, S. Prasad, and S. Rico. "Effects of Gene Replacement Therapy with Resamirigene Bilparvovec (At132) on Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Results from a Substudy of the Aspiro Open-Label Clinical Trial." EBioMedicine 99 (Dec 11 2023): 104894. https://dx.doi.org/10.1016/j.ebiom.2023.104894.
  29. Lersch, R., R. Jannadi, L. Grosse, M. Wagner, M. F. Schneider, C. von Stulpnagel, F. Heinen, H. Potschka, and I. Borggraefe. "Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome." Neuroscientist 29, no. 6 (Dec 2023): 732-50. https://dx.doi.org/10.1177/10738584221088244.
  30. Lischka, A., K. Eggermann, C. J. Record, M. F. Dohrn, P. Lassuthova, F. Kraft, M. Begemann, D. Dey, T. Eggermann, D. Beijer, J. Soukalova, M. Laura, A. M. Rossor, R. Mazanec, J. Van Lent, P. J. Tomaselli, M. Ungelenk, K. Y. Debus, S. M. E. Feely, D. Glaser, S. Jagadeesh, M. Martin, G. M. Govindaraj, P. Singhi, R. Baineni, N. Biswal, M. Ibarra-Ramirez, M. Bonduelle, B. Gess, J. Romero Sanchez, R. Suthar, V. Udani, A. Nalini, G. Unnikrishnan, W. Junior Marques, S. Mercier, V. Procaccio, C. Bris, B. Suresh, V. Reddy, M. Skorupinska, N. Bonello-Palot, F. Mochel, G. Dahl, K. Sasidharan, F. M. Devassikutty, S. Nampoothiri, M. J. Rodovalho Doriqui, W. Muller-Felber, K. Vill, T. B. Haack, A. Dufke, M. Abele, R. Stucka, S. Siddiqi, N. Ullah, S. Spranger, D. Chiabrando, B. S. Bolgul, Y. Parman, P. Seeman, A. Lampert, J. B. Schulz, J. N. Wood, J. J. Cox, M. Auer-Grumbach, V. Timmerman, J. de Winter, A. C. Themistocleous, M. Shy, D. L. Bennett, J. Baets, C. A. Hubner, E. Leipold, S. Zuchner, M. Elbracht, A. Cakar, J. Senderek, T. Hornemann, C. G. Woods, M. M. Reilly, and I. Kurth. "Genetic Landscape of Congenital Insensitivity to Pain and Hereditary Sensory and Autonomic Neuropathies." Brain 146, no. 12 (Dec 1 2023): 4880-90. https://dx.doi.org/10.1093/brain/awad328.
  31. Makridis, K. L., K. A. Klotz, G. Ramantani, L. L. Becker, V. San Antonio-Arce, S. Syrbe, K. Wagner, M. J. Shah, U. W. Thomale, A. Tietze, C. E. Elger, I. Borggraefe, and A. M. Kaindl. "Epilepsy Surgery in Early Infancy: A Retrospective, Multicenter Study." Epilepsia Open 8, no. 3 (Sep 2023): 1182-89. https://dx.doi.org/10.1002/epi4.12791.
  32. Melder, A., E. Wittmann, L. Bulubas, B. Dornheim, K. Kerber, U. Vogelmann, M. Campana, J. Hubert, V. Schmidt, F. Heinen, F. Padberg, and M. N. Landgraf. "Transcranial Magnetic Stimulation as a Feasible, Non-Invasive, Neuromodulatory Intervention in Fetal Alcohol Spectrum Disorders. A Very First Proof of Concept." Eur J Paediatr Neurol 47 (Nov 2023): 131-42. https://dx.doi.org/10.1016/j.ejpn.2023.10.004.
  33. Muller-Felber, W., A. Blaschek, O. Schwartz, D. Glaser, U. Nennstiel, I. Brockow, B. Wirth, S. Burggraf, W. Roschinger, M. Becker, J. Durner, K. Eggermann, H. Kolbel, C. Muller, I. Hannibal, B. Olgemoller, U. Schara, A. von Moers, R. Trollmann, J. Johannssen, A. Ziegler, S. Cirak, A. Hahn, M. von der Hagen, C. Weiss, G. Schreiber, M. Flotats-Bastardas, H. Hartmann, S. Illsinger, A. Pechmann, V. Horber, J. Kirschner, C. Kohler, B. Winter, J. Friese, and K. Vill. "Newbornscreening Sma - from Pilot Project to Nationwide Screening in Germany." J Neuromuscul Dis 10, no. 1 (2023): 55-65. https://dx.doi.org/10.3233/JND-221577.
  34. Nissenkorn, A., G. Kluger, S. Schubert-Bast, A. Bayat, M. Bobylova, P. Bonanni, B. Ceulemans, A. Coppola, C. Di Bonaventura, M. Feucht, A. Fuchs, G. Groppel, G. Heimer, B. Herdt, S. Kulikova, K. Mukhin, S. Nicassio, A. Orsini, M. Panagiotou, M. Pringsheim, B. Puest, O. Pylaeva, G. Ramantani, M. Tsekoura, P. Ricciardelli, T. Lerman Sagie, B. Stark, P. Striano, A. van Baalen, M. De Wachter, E. Cerulli Irelli, C. Cuccurullo, C. von Stulpnagel, and A. Russo. "Perampanel as Precision Therapy in Rare Genetic Epilepsies." Epilepsia 64, no. 4 (Apr 2023): 866-74. https://dx.doi.org/10.1111/epi.17530.
  35. Patterson, V., F. Ullah, L. Bryant, J. N. Griffin, A. Sidhu, S. Saliganan, M. Blaile, M. S. Saenz, R. Smith, S. Ellingwood, D. K. Grange, X. Hu, M. Mireguli, Y. Luo, Y. Shen, M. Mulhern, E. Zackai, A. Ritter, K. Izumi, J. Hoefele, M. Wagner, K. M. Riedhammer, B. Seitz, N. H. Robin, D. Goodloe, C. Mignot, B. Keren, H. Cox, J. Jarvis, M. Hempel, C. F. Gibson, F. Tran Mau-Them, A. Vitobello, A. L. Bruel, A. Sorlin, S. Mehta, F. L. Raymond, K. Gilmore, B. C. Powell, K. Weck, C. Li, A. T. Vulto-van Silfhout, T. Giacomini, M. M. Mancardi, A. Accogli, V. Salpietro, F. Zara, N. L. Vora, E. E. Davis, R. Burdine, and E. Bhoj. "Abrogation of Map4k4 Protein Function Causes Congenital Anomalies in Humans and Zebrafish." Sci Adv 9, no. 17 (Apr 28 2023): eade0631. https://dx.doi.org/10.1126/sciadv.ade0631.
  36. Pechmann, A., M. Behrens, K. Dornbrack, A. Tassoni, S. Stein, S. Vogt, D. Zoller, G. Bernert, T. Hagenacker, U. Schara-Schmidt, I. Schwersenz, M. C. Walter, M. Baumann, M. Baumgartner, M. Deschauer, A. Eisenkolbl, M. Flotats-Bastardas, A. Hahn, V. Horber, R. A. Husain, S. Illsinger, J. Johannsen, C. Kohler, H. Kolbel, M. Muller, A. von Moers, K. Schlachter, G. Schreiber, O. Schwartz, M. Smitka, E. Steiner, E. Stogmann, R. Trollmann, K. Vill, C. Weiss, G. Wiegand, A. Ziegler, H. Lochmuller, J. Kirschner, and S. MArtCARE study group. "Effect of Nusinersen on Motor, Respiratory and Bulbar Function in Early-Onset Spinal Muscular Atrophy." Brain 146, no. 2 (Feb 13 2023): 668-77. https://dx.doi.org/10.1093/brain/awac252.
  37. Pechmann, A., M. Behrens, K. Dornbrack, A. Tassoni, F. Wenzel, S. Stein, S. Vogt, D. Zoller, G. Bernert, T. Hagenacker, U. Schara-Schmidt, M. C. Walter, M. Steinbach, A. Blaschek, M. Baumann, M. Baumgartner, B. Becker, M. Flotats-Bastardas, J. Friese, R. Gunther, A. Hahn, H. Kupper, J. Johannsen, C. Kamm, J. C. Koch, C. Kohler, H. Kolbel, K. Kolzter, A. von Moers, S. Naegel, C. Neuwirth, S. Petri, A. Rodiger, M. Schimmel, B. Schrank, G. Schreiber, M. Smitka, C. Stadler, E. Steiner, E. Stogmann, R. Trollmann, M. Turk, M. Weiler, C. Stoltenburg, E. Willichowsky, D. Zeller, A. Ziegler, H. Lochmuller, J. Kirschner, and S. MArtCARE study group. "Improvements in Walking Distance During Nusinersen Treatment - a Prospective 3-Year Smartcare Registry Study." J Neuromuscul Dis 10, no. 1 (2023): 29-40. https://dx.doi.org/10.3233/JND-221600.
  38. Popp, B., M. Brugger, S. Poschmann, T. Bartolomaeus, M. Radtke, J. Hentschel, N. Di Donato, A. Rump, J. Gburek-Augustat, E. Graf, M. Wagner, I. Sorge, J. R. Lemke, T. Meitinger, R. Abou Jamra, V. Strehlow, and T. Brunet. "The Constitutional Gain-of-Function Variant P.Glu1099lys in Nsd2 Is Associated with a Novel Syndrome." Clin Genet 103, no. 2 (Feb 2023): 226-30. https://dx.doi.org/10.1111/cge.14241.
  39. Rossi, A., L. S. Blok, S. Neuser, C. Klockner, K. Platzer, L. O. Faivre, H. Weigand, M. L. Dentici, M. Tartaglia, M. Niceta, P. Alfieri, S. Srivastava, D. Coulter, L. Smith, K. Vinorum, G. Cappuccio, N. Brunetti-Pierri, D. Torun, M. Arslan, M. F. Lauridsen, O. Murch, R. Irving, S. A. Lynch, S. G. Mehta, J. Carmichael, E. Zonneveld-Huijssoon, B. de Vries, T. Kleefstra, K. M. Johannesen, I. T. Westphall, S. S. Hughes, S. Smithson, J. Evans, T. Dudding-Byth, M. Simon, E. van Binsbergen, J. C. Herkert, G. Beunders, H. Oppermann, M. Bakal, R. S. Moller, G. Rubboli, and A. Bayat. "Pou3f3-Related Disorder: Defining the Phenotype and Expanding the Molecular Spectrum." Clin Genet 104, no. 2 (Aug 2023): 186-97. https://dx.doi.org/10.1111/cge.14353.
  40. Rots, D., and T. E. Jakub, and C. Keung, and A. Jackson, and S. Banka, and R. Pfundt, and B. B. A. de Vries, and R. H. van Jaarsveld, and S. M. J. Hopman, and E. van Binsbergen, and I. Valenzuela, and M. Hempel, and T. Bierhals, and F. Kortum, and F. Lecoquierre, and A. Goldenberg, and J. M. Hertz, and C. B. Andersen, and M. Kibaek, and E. J. Prijoles, and R. E. Stevenson, and D. B. Everman, and W. G. Patterson, and L. Meng, and C. Gijavanekar, and K. De Dios, and S. Lakhani, and T. Levy, and M. Wagner, and D. Wieczorek, and P. J. Benke, and M. S. Lopez Garcia, and R. Perrier, and S. B. Sousa, and P. M. Almeida, and M. J. Simoes, and B. Isidor, and W. Deb, and A. A. Schmanski, and O. Abdul-Rahman, and C. Philippe, and A. L. Bruel, and L. Faivre, and A. Vitobello, and C. Thauvin, and J. J. Smits, and L. Garavelli, and S. G. Caraffi, and F. Peluso, and L. Davis-Keppen, and D. Platt, and E. Royer, and L. Leeuwen, and M. Sinnema, and A. P. A. Stegmann, and Ctrm Stumpel, and G. E. Tiller, and D. G. M. Bosch, and S. T. Potgieter, and S. Joss, and M. Splitt, and S. Holden, and M. Prapa, and N. Foulds, and S. Douzgou, and K. Puura, and R. Waltes, and A. G. Chiocchetti, and C. M. Freitag, and F. K. Satterstrom, and S. De Rubeis, and J. Buxbaum, and B. D. Gelb, and A. Branko, and I. Kushima, and J. Howe, and S. W. Scherer, and A. Arado, and C. Baldo, and O. Patat, and D. Benedicte, and D. Lopergolo, and F. M. Santorelli, and T. B. Haack, and A. Dufke, and M. Bertrand, and R. J. Falb, and A. Riess, and P. Krieg, and S. Spranger, and M. F. Bedeschi, and M. Iascone, and S. Josephi-Taylor, and T. Roscioli, and M. F. Buckley, and J. Liebelt, and A. I. Dagli, and E. Aten, and A. C. E. Hurst, and A. Hicks, and M. Suri, and E. Aliu, and S. Naik, and R. Sidlow, and J. Coursimault, and G. Nicolas, and H. Kupper, and F. Petit, and V. Ibrahim, and D. Top, and F. Di Cara, and Consortium Genomics England Research, and R. J. Louie, and E. Stolerman, and H. G. Brunner, and Lelm Vissers, and J. M. Kramer, and T. Kleefstra. "The Clinical and Molecular Spectrum of the Kdm6b-Related Neurodevelopmental Disorder." Am J Hum Genet 110, no. 6 (Jun 1 2023): 963-78. https://dx.doi.org/10.1016/j.ajhg.2023.04.008.
  41. Ruiz Brunner, M. L. M., E. Cuestas, R. von Kries, J. Brooks, C. Wright, F. Heinen, and A. S. Schroeder. "Growth Patterns in Children and Adolescents with Cerebral Palsy from Argentina and Germany." Sci Rep 13, no. 1 (Jun 2 2023): 8947. https://dx.doi.org/10.1038/s41598-023-34634-6.
  42. Schmidlechner, T., M. Zaddach, F. Heinen, S. Cornell, G. Ramantani, J. Remi, C. Vollmar, M. Kunz, and I. Borggraefe. "Iq Changes after Pediatric Epilepsy Surgery: A Systematic Review and Meta-Analysis." J Neurol 271, no. 1 (Jan 2024): 177-87. https://dx.doi.org/10.1007/s00415-023-12002-8.
  43. Schmidt, J., and W. Muller-Felber. "[Myositis: From Diagnosis to Treatment]." Nervenarzt 94, no. 6 (Jun 2023): 510-18. Myositis: von der Diagnose zur Therapie. https://dx.doi.org/10.1007/s00115-023-01490-8.
  44. Schramm, S., C. Borner, M. Reichert, T. Baum, C. Zimmer, F. Heinen, M. V. Bonfert, and N. Sollmann. "Functional Magnetic Resonance Imaging in Migraine: A Systematic Review." Cephalalgia 43, no. 2 (Feb 2023): 3331024221128278. https://dx.doi.org/10.1177/03331024221128278.
  45. Shieh, P. B., N. L. Kuntz, J. J. Dowling, W. Muller-Felber, C. G. Bonnemann, A. M. Seferian, L. Servais, B. K. Smith, F. Muntoni, A. Blaschek, A. R. Foley, D. N. Saade, S. Neuhaus, L. N. Alfano, A. H. Beggs, A. Buj-Bello, M. K. Childers, T. Duong, R. J. Graham, M. Jain, J. Coats, V. MacBean, E. S. James, J. Lee, F. Mavilio, W. Miller, F. Varfaj, M. Murtagh, C. Han, M. Noursalehi, M. W. Lawlor, S. Prasad, and S. Rico. "Safety and Efficacy of Gene Replacement Therapy for X-Linked Myotubular Myopathy (Aspiro): A Multinational, Open-Label, Dose-Escalation Trial." Lancet Neurol 22, no. 12 (Dec 2023): 1125-39. https://dx.doi.org/10.1016/S1474-4422(23)00313-7.
  46. Sollmann, N., G. Hoffmann, S. Schramm, M. Reichert, M. Hernandez Petzsche, J. Strobel, L. Nigris, C. Kloth, J. Rosskopf, C. Borner, M. Bonfert, M. Berndt, G. Gron, H. P. Muller, J. Kassubek, K. Kreiser, I. K. Koerte, H. Liebl, A. Beer, C. Zimmer, M. Beer, and S. Kaczmarz. "Arterial Spin Labeling (Asl) in Neuroradiological Diagnostics - Methodological Overview and Use Cases." Rofo 196, no. 1 (Jan 2024): 36-51. Arterial Spin Labeling (ASL) in der neuroradiologischen Diagnostik - Methodischer Uberblick und Anwendungsfalle. https://dx.doi.org/10.1055/a-2119-5574.
  47. Sollmann, N., P. Schandelmaier, D. Weidlich, J. Stelter, G. B. Joseph, C. Borner, S. Schramm, M. Beer, C. Zimmer, M. N. Landgraf, F. Heinen, D. C. Karampinos, T. Baum, and M. V. Bonfert. "Headache Frequency and Neck Pain Are Associated with Trapezius Muscle T2 in Tension-Type Headache among Young Adults." J Headache Pain 24, no. 1 (Jul 12 2023): 84. https://dx.doi.org/10.1186/s10194-023-01626-w.
  48. Szewczyk, A. K., S. Ulutas, T. Akturk, L. Al-Hassany, C. Borner, F. Cernigliaro, M. Kodounis, S. Lo Cascio, D. Mikolajek, D. Onan, C. Ragaglini, S. Ratti, E. Rivera-Mancilla, S. Tsanoula, R. Villino, K. Messlinger, A. Maassen Van Den Brink, T. de Vries, and Studies European Headache Federation School of Advanced. "Prolactin and Oxytocin: Potential Targets for Migraine Treatment." J Headache Pain 24, no. 1 (Mar 27 2023): 31. https://dx.doi.org/10.1186/s10194-023-01557-6.
  49. Thalwitzer, K. M., J. H. Driedger, J. Xian, A. Saffari, P. Zacher, B. K. Bolsterli, S. M. Ruggiero, K. R. Sullivan, A. N. Datta, C. Kellinghaus, J. Althaus, A. Wiemer-Kruel, A. van Baalen, A. Pampel, M. Alber, H. M. H. Braakman, O. M. Debus, J. Denecke, E. Hobbiebrunken, I. Breitweg, D. Diehl, H. Eitel, J. Gburek-Augustat, M. Preisel, J. U. Schlump, M. Laufs, D. Mammadova, C. Wurst, C. Prager, C. Lohr-Nilles, P. Martin, S. F. Garbade, K. Platzer, I. Benkel-Herrenbrueck, K. Egler, W. Fazeli, J. R. Lemke, E. Runkel, B. Klein, T. Linden, J. Schroter, H. Steffeck, B. Thies, F. von Deimling, S. Illsinger, I. Borggraefe, G. Classen, D. Wieczorek, G. Ramantani, S. Koelker, G. F. Hoffmann, M. Ries, I. Helbig, and S. Syrbe. "Natural History and Developmental Trajectories of Individuals with Disease-Causing Variants in Stxbp1." Neurology 101, no. 9 (Aug 29 2023): e879-e91. https://dx.doi.org/10.1212/WNL.0000000000207550.
  50. Vetro, A., C. Pelorosso, S. Balestrini, A. Masi, S. Hambleton, E. Argilli, V. Conti, S. Giubbolini, R. Barrick, G. Bergant, K. Writzl, E. K. Bijlsma, T. Brunet, P. Cacheiro, D. Mei, A. Devlin, M. J. V. Hoffer, K. Machol, G. Mannaioni, M. Sakamoto, M. P. Menezes, T. Courtin, E. Sherr, R. Parra, R. Richardson, T. Roscioli, M. Scala, C. von Stulpnagel, D. Smedley, Tmem B. collaborators, Consortium Genomics England Research, A. Torella, J. Tohyama, R. Koichihara, K. Hamada, K. Ogata, T. Suzuki, A. Sugie, J. J. van der Smagt, K. van Gassen, S. Valence, E. Vittery, S. Malone, M. Kato, N. Matsumoto, G. M. Ratto, and R. Guerrini. "Stretch-Activated Ion Channel Tmem63b Associates with Developmental and Epileptic Encephalopathies and Progressive Neurodegeneration." Am J Hum Genet 110, no. 8 (Aug 3 2023): 1356-76. https://dx.doi.org/10.1016/j.ajhg.2023.06.008.
  51. von Steinbuechel, N., U. Krenz, F. Bockhop, I. K. Koerte, D. Timmermann, K. Cunitz, M. Zeldovich, N. Andelic, P. Rojczyk, M. V. Bonfert, S. Berweck, M. Kieslich, K. Brockmann, M. Roediger, M. Lendt, A. Buchheim, H. Muehlan, I. Holloway, and L. Olabarrieta-Landa. "A Multidimensional Approach to Assessing Factors Impacting Health-Related Quality of Life after Pediatric Traumatic Brain Injury." J Clin Med 12, no. 12 (Jun 7 2023). https://dx.doi.org/10.3390/jcm12123895.
  52. Von Steinbuechel, N., M. Zeldovich, S. Greving, L. Olabarrieta-Landa, U. Krenz, D. Timmermann, I. K. Koerte, M. V. Bonfert, S. Berweck, M. Kieslich, K. Brockmann, M. Roediger, M. Lendt, M. Staebler, S. Schmidt, H. Muehlan, and K. Cunitz. "Quality of Life after Brain Injury in Children and Adolescents (Qolibri-Kid/Ado)-the First Disease-Specific Self-Report Questionnaire after Traumatic Brain Injury." J Clin Med 12, no. 15 (Jul 26 2023). https://dx.doi.org/10.3390/jcm12154898.
  53. Weinmann, T., L. Finkeldey, E. Wittmann, K. Kerber, J. A. Schlueter, I. Zillinger, A. Maciejok, F. Heinen, and M. N. Landgraf. "Prognostic Factors for Long-Term Outcome in Children with Fetal Alcohol Spectrum Disorders." Res Dev Disabil 136 (May 2023): 104481. https://dx.doi.org/10.1016/j.ridd.2023.104481.
  54. Weinmann, T., L. K. Ordenewitz, J. A. Schluter, J. Jung, K. Kerber, L. Finkeldey, F. Heinen, and M. N. Landgraf. "Establishing a Multidisciplinary Specialist Centre for Fetal Alcohol Spectrum Disorders-Lessons Learned from a Model Project in Germany." Child Care Health Dev (Jun 14 2023). https://dx.doi.org/10.1111/cch.13143.
  55. Weiss, K. J., U. Berger, M. Haider, M. Wagner, E. M. C. Martner, S. Regenauer-Vandewiele, A. Lotz-Havla, E. Schuhmann, W. Roschinger, and E. M. Maier. "Free Carnitine Concentrations and Biochemical Parameters in Medium-Chain Acyl-Coa Dehydrogenase Deficiency: Genotype-Phenotype Correlation." Clin Genet 103, no. 6 (Jun 2023): 644-54. https://dx.doi.org/10.1111/cge.14316.
  56. Werren, E. A., A. Guxholli, N. Jones, M. Wagner, I. Hannibal, J. L. Granadillo, A. V. Tyndall, A. Moccia, R. Kuehl, K. M. Levandoski, D. L. Day-Salvatore, M. Wheeler, Genomics University of Washington Center for Mendelian, J. X. Chong, M. J. Bamshad, A. M. Innes, T. M. Pierson, J. P. Mackay, S. L. Bielas, and D. M. Martin. "De Novo Variants in Gatad2a in Individuals with a Neurodevelopmental Disorder: Gatad2a-Related Neurodevelopmental Disorder." HGG Adv 4, no. 3 (Jul 13 2023): 100198. https://dx.doi.org/10.1016/j.xhgg.2023.100198.
  57. Wiendl, H., A. Abicht, A. Chan, A. Della Marina, T. Hagenacker, K. Hekmat, S. Hoffmann, H. S. Hoffmann, S. Jander, C. Keller, A. Marx, A. Melms, N. Melzer, W. Muller-Felber, M. Pawlitzki, J. C. Ruckert, C. Schneider-Gold, B. Schoser, B. Schreiner, M. Schroeter, B. Schubert, J. P. Sieb, F. Zimprich, and A. Meisel. "Guideline for the Management of Myasthenic Syndromes." Ther Adv Neurol Disord 16 (2023): 17562864231213240. https://dx.doi.org/10.1177/17562864231213240.
  58. von Küstenfeld-Grefenberg, S. I., Strauch, V., Wolter, C., Plank, A., Tacke, M., Borggräfe, I., ... & Hoffmann, F. (2023). Pflegegeführte, interprofessionelle Neuro-AG auf der pädiatrischen Intensivstation: Mehr Verantwortung–mehr Zufriedenheit–mehr Erfolg?. Zeitschrift für Geburtshilfe und Neonatologie, 227(03), e9-e9.
  59. Guo L, Salian S, Xue JY, Rath N, Rousseau J, Kim H, Ehresmann S, Moosa S, Nakagawa N, Kuroda H, Clayton-Smith J, Wang J, Wang Z, Banka S, Jackson A, Zhang YM, Wei ZJ, Hüning I, Brunet T, Ohashi H, Thomas MF, Bupp C, Miyake N, Matsumoto N, Mendoza-Londono R, Costain G, Hahn G, Di Donato N, Yigit G, Yamada T, Nishimura G, Ansel KM, Wollnik B, Hrabě de Angelis M, Mégarbané A, Rosenfeld JA, Heissmeyer V, Ikegawa S, Campeau PM. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans. Am J Hum Genet. 2023 Jul 6;110(7):1068-1085. doi: 10.1016/j.ajhg.2023.06.001. Epub 2023 Jun 22. PMID: 37352860; PMCID: PMC10357479.
  60. Ebstein F, Küry S, Most V, Rosenfelt C, Scott-Boyer MP, van Woerden GM, Besnard T, Papendorf JJ, Studencka-Turski M, Wang T, Hsieh TC, Golnik R, Baldridge D, Forster C, de Konink C, Teurlings SMW, Vignard V, van Jaarsveld RH, Ades L, Cogné B, Mignot C, Deb W, Jongmans MCJ, Cole FS, van den Boogaard MH, Wambach JA, Wegner DJ, Yang S, Hannig V, Brault JA, Zadeh N, Bennetts B, Keren B, Gélineau AC, Powis Z, Towne M, Bachman K, Seeley A, Beck AE, Morrison J, Westman R, Averill K, Brunet T, Haasters J, Carter MT, Osmond M, Wheeler PG, Forzano F, Mohammed S, Trakadis Y, Accogli A, Harrison R, Guo Y, Hakonarson H, Rondeau S, Baujat G, Barcia G, Feichtinger RG, Mayr JA, Preisel M, Laumonnier F, Kallinich T, Knaus A, Isidor B, Krawitz P, Völker U, Hammer E, Droit A, Eichler EE, Elgersma Y, Hildebrand PW, Bolduc F, Krüger E, Bézieau S. PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production. Sci Transl Med. 2023 May 31;15(698):eabo3189. doi: 10.1126/scitranslmed.abo3189. Epub 2023 May 31. PMID: 37256937; PMCID: PMC10506367.
  61. Reijnders MRF, Seibt A, Brugger M, Lamers IJC, Ott T, Klaas O, Horváth J, Rose AMS, Craghill IM, Brunet T, Graf E, Mayerhanser K, Hellebrekers D, Pauck D, Neuen-Jacob E, Rodenburg RJT, Wieczorek D, Klee D, Mayatepek E, Driessen G, Bindermann R, Averdunk L, Lohmeier K, Sinnema M, Stegmann APA, Roepman R, Poulter JA, Distelmaier F. De novo missense variants in RRAGC lead to a fatal mTORopathy of early childhood. Genet Med. 2023 Jul;25(7):100838. doi: 10.1016/j.gim.2023.100838. Epub 2023 Apr 11. PMID: 37057673.
  62. Krenn M, Wagner M, Zulehner G, Weng R, Jäger F, Keritam O, Sener M, Brücke C, Milenkovic I, Langer A, Buchinger D, Habersam R, Mayerhanser K, Brugger M, Brunet T, Jacob M, Graf E, Berutti R, Cetin H, Hoefele J, Winkelmann J, Zimprich F, Rath J. Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnoses. J Neurol. 2024 Apr;271(4):1937-1946. doi: 10.1007/s00415-023-12101-6. Epub 2023 Dec 21. PMID: 38127101; PMCID: PMC10972933.
  63. Borggraefe I, Tacke M, Kunz M, Vollmar C, Rémi J. Epilepsy surgery in pediatric refractory status epilepticus. Clin Epileptol 36, 304–309 (2023). https://doi.org/10.1007/s10309-023-00629-6

  1. Heinen F (13. Juni 2017). NeuroKids - Child Neurology Workbook: Diagnosis and Therapy - Mind Maps. Kohlhammer Verlag
  2. Becker G, Hennicke K, Klein (2015). Suchtgefährdete Erwachsene mit Fetalen Alkoholspektrumstörungen. Diagnostik, Screening-Ansätze und Interventionsmöglichkeiten. Unter Mitarbeit von Mirjam Landgraf. De Gruyter Verlag
  3. Lepke k, Michalowski G (2015). Leit(d)pfade durch das Leben. 16. FASD-Fachtagung. Schulz-Kirchner-Verlag
  4. Müller-Felber W, Schara U. Herausgegeben von Florian Heinen (2015). Neuromuskuläre Erkrankungen bei Kindern und Jugendlichen. Kohlhammer Verlag
  5. Hadders-Algra M, Herausgegeben von Heinen F. (2014). Praxis Entwicklungsneurologie Untersuchung auf Milde Neurologische Dysfunktion (MND).Verlag Kohlhammer
  6. Backmund M (2013). Sucht-Therapie. Grundlagen - Klinik - Standards-Leitfaden für Praxis und Fortbildung. Ecomed Medizin Verlag.
  7. Feldmann R, Michalowski G (2013). Perspektiven für Menschen mit FASD. 14.FASD-Fachtagung. Schulz-Kirchner-Verlag
  8. Landgraf M, Heinen F (2013). Fetales Alkoholsyndrom S3-Leitlinie zur Diagnostik. Reihe Pädiatrische Neurologie. Verlag Kohlhammer
  9. Spohr H (2013). Das Fetale Alkoholsyndrom im Kindes- und Erwachsenenalter. De Gruyter Verlag
  10. Fuchs C, Kurth BM, Scriba PC (2012). Medizinische Versorgung in der Transition, Spezielle Anforderungen beim Übergang von Kindes- und Jugendalter zum Erwachsenenalter. Deutscher Ärzte-Verlag
  11. Heinen F, Krieg S, Borggräfe I, Kieslich M, Böhmer J, Ertl-Wagner B, Pecar A (2012). Neuropharmakologie und Klinische Systematik. Verlag Kohlhammer
  12. Noterdaeme M, Ullrich K, Enders A (2017). Autismus-Spektrum-Störungen (ASS). 2., erweiterte und überarb. Aufl., Verlag Kohlhammer
  13. Heinen F, Böhmer J, Hufschmidt A, Berweck S, Christen HJ, Fietzek U, Kieslich M, Krieg S, Mall V, Müller-Felber W (2009). Pädiatrische Neurologie, Diagnose und Therapie mit Paediatric Clinical Scouts. Verlag Kohlhammer
  14. Fietzek, UM, Berweck S, Wissel J, Heinen, F (2008). Sono´s Anatomy, Focus on Spasticity Targeting Botulinum Toxin Children & Adults. Child & Brain
  15. Heinen F, Berweck S, Fietzek UM, Wissel J (2008). Blue Box Botulinumtoxin. Verlag Hans Huber
  16. Siebner H, Ziemann U (2007). Das TMS-Buch, Transkranielle Magnetstimulation. Springer Verlag
  17. Russel D, Rosenbaum P, Avery L, Lane M (2006). GMFM und GMFCS Messung und Klassifikation motorischer Funktionen. Huber Verlag
  18. Berweck S, Heinen F (2005). Treatment of Cerebral Palsy with Botulinum Toxin, Principles, Clinical Practice, Atlas. Child & Brain
  19. Bourbon F, Rothweiler H, Draeger K (2005). Wartezimmer der Tiere. Child & Brain
  20. Wissel J, Huber M, Fheodoroff K (2004). Rehabilitation und Botulinumtoxin, Grundlagen- Klinik – Atlas – Skalen. Child & Brain