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Publikationen 2015

  • L. Albers, F. Heinen, M. Landgraf, A. Straube, B. Blum, F. Filippopulos, S. Lehmann, U. Mansmann, U. Berger, Y. Akboga and R. von Kries. Headache cessation by an educational intervention in grammar schools: a cluster randomized trial. 2015 Eur J Neurol Volume 222: 270-7,e22
  • A. Blaschek, C. Makowski, C. Stadelmann, S. Pfeiffenbrink, W. Müller-Felber. Pädiatrische MS- Diagnose auf Umwegen (2015). Neuropädiatrie in Klinik und Praxis Volume 3
  • A. Blaschek, K. Vill, W. Müller-FelberTherapiestudien bei Muskeldystrophie Duchenne. 2015 Kinderärztliche Praxis Volume 4 
  • A. Enders. Leitsymptom Muskelhypotonie, Differentialdiagnostik bei Neugeborenen und Säuglingen.2015Pädiat. prax. Volume 84:633-645
  • A. Hilgendorff, M. A. O'ReillyBronchopulmonary dysplasia early changes leading to long-term consequences. 2015 Front Med (Lausanne). Volume 2:2 
  • A. Hilgendorff, K. Parai, R. Ertsey, E. Navarro, N. Jain, F. Carandang, J. Peterson, L. Mokres, C. Milla, S. Preuss, M. A. Alcazar, S. Khan, J. Masumi, N. Ferreira-Tojais, S. Mujahid, B. Starcher, M. Rabinovitch and R. Bland . Lung matrix and vascular remodeling in mechanically ventilated elastin haploinsufficient newborn mice. 2015 Am J Physiol Lung Cell Mol Physiol. Volume 3085:L464-78 
  • A. Tabea, B. Warken, J. V. Graser, T. Ulrich, I. Borggraefe, F. Heinen, A. Meyer-Heim, H. J. van Hedel and A. S. Schroeder. Practical Recommendations for Robot-Assisted Treadmill Therapy (Lokomat) in Children with Cerebral Palsy: Indications, Goal Setting, and Clinical Implementation within the WHO-ICF Framework. 2015. Neuropediatrics Volume 464:248-60 
  • I. K. Koerte, A. P. Lin, M. Muehlmann, S. Merugumala, H. Liao, T. Starr, D. Kaufmann, M. Mayinger, D. Steffinger, B. Fisch, S. Karch, F. Heinen, B. Ertl-Wagner, M. Reiser, R. A. Stern, R. Zafonte and M. E. Shenton . Altered Neurochemistry in Former Professional Soccer Players without a History of Concussion. 2015J Neurotrauma. 2015 Volume 3217:1287-93
  • I. K. Koerte, A. Willems, M. Muehlmann, K. Moll, S. Cornell, S. Pixner, D. Steffinger, D. Keeser, F. Heinen, M. Kubicki, M. E. Shenton, B. Ertl-Wagner and G. Schulte-Korne. Mathematical abilities in dyslexic children: a diffusion tensor imaging study.. 2015. Brain Imaging Behav 
  • I. K. Koerte, J. Hufschmidt, M. Muehlmann, Y. Tripodis, J. M. Stamm, O. Pasternak, M. Y. Giwerc, M. J. Coleman, C. M. Baugh, N. G. Fritts, F. Heinen, A. P. Lin, R. Stern and M. E. Shenton Cavum Septi Pellucidi in Symptomatic Former Professional Football Players. 2015. J Neurotrauma 
  • I. K. Koerte, M. Mayinger, M. Muehlmann, D. Kaufmann, A. P. Lin, D. Steffinger, B. Fisch, B. S. Rauchmann, S. Immler, S. Karch, F. R. Heinen, B. Ertl-Wagner, M. Reiser, R. A. Stern, R. Zafonte and M. E. Shenton. Cortical thinning in former professional soccer players. 2015. Brain Imaging Behav
  • J. Reunert, A. S. Lotz-Havla, G. Polo, F. Kannenberg, M. Fobker, M. Griese, E. Mengel, A. C. Muntau, P. Schnabel, O. Sommerburg, I. Borggraefe, A. Dardis, A. P. Burlina, M. A. Mall, G. Ciana, B. Bembi, A. B. Burlina and T. Marquardt Niemann-Pick Type C-2 Disease: Identification by Analysis of Plasma Cholestane-3beta,5alpha,6beta-Triol and Further Insight into the Clinical Phenotype. 2015. JIMP Rep. Volume 23:17-26
  • K. Jahn, T. Langhagen and F. Heinen. Vertigo and dizziness in children. 2015. Curr. Opin Neurol. Volume 281:78-82 
  • K. M. Forster, S. Immler, M. Ensslen, A. Flemmer, A. Schulze, M. von Poblotzki, O. Genzel-Boroviczeny, F. Heinen and A. Hilgendorff [Indications and concept of follow-up care of home-monitoring for premature and risk infants]. 2015 Klin Padiatr. Volume 2272:72-9 
  • K. Vill, J. Schessl, V. Teusch, S. Schroeder, A. Blaschek, B. Schoser and W. Muller-Felber. Muscle ultrasound in classic infantile and adult Pompe disease: a useful screening tool in adults but not in infants. 2015 Neuromuscul Disord. Volume252:120-6 
  • K. Vill, L. Ille, S. A. Schroeder, A. Blaschek and W. Muller-Felber. Six-minute walk test versus two-minute walk test in children with Duchenne muscular dystrophy: Is more time more information. 2015. Eur J Paediatr Neurol. Volume196:640-6
  • K. Vill, M. Kuhn, D. Glaser and W. Muller-Felber Overlap phenotype between CMT1A and hereditary neuropathy with liability to pressure palsies caused by the novel small in-frame deletion c.407_418del12 in PMP22 gene. 2015. Neuropediatrics. Volume 461:44-8
  • K. Vill, M. Kuhn, D. Glaser, M. C. Walter and W. Muller-Felber. Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene. 2015 neuropdiatrics. . Volume 464:282-6
  • K. Vill, W. Müller-Felber. Kongenitale Myopathien: Diagnosestellung, Patientenversorgung und differenzialdiagnostische Abgrenzung.2015 Kinderärztliche Praxis. Volume 4:227-231 
  • L. Albers, A. Straube, M. N. Landgraf, F. Filippopulos, F. Heinen and R. von Kries. Migraine and tension type headache in adolescents at grammar school in Germany - burden of disease and health care utilization. 2015. J Headache Pain. Volume 16:534 
  • L. Albers, R. von Kries, F. Heinen and A. StraubeHeadache in school children: is the prevalence increasing? 2015. Curr Pain Headache Rep. Voulme 193:4 
  • M. Baumann, K. Sahin, C. Lechner, E. M. Hennes, K. Schanda, S. Mader, M. Karenfort, C. Selch, M. Hausler, A. Eisenkolbl, M. Salandin, U. Gruber-Sedlmayr, A. Blaschek, V. Kraus, S. Leiz, J. Finsterwalder, T. Gotwald, G. Kuchukhidze, T. Berger, M. Reindl and K. Rostasy. Clinical and neuroradiological differences of paediatric acute disseminating encephalomyelitis with and without antibodies to the myelin oligodendrocyte glycoprotein . 2015. J Neurol Neurosurg Psychiatry. Volume 863:265-72.
  • M. C. Walter, M. Rossius, M. Zitzelsberger, M. Vorgerd, W. Muller-Felber, B. Ertl-Wagner, Y. Zhang, H. Brinkmeier, J. Senderek and B. Schoser50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation. 2015. Neuromuscul Disord. Volume 257:577-84
  • M. N. Landgraf, B. Ertl-Wagner, I. K. Koerte, J. Thienel, T. Langhagen, A. Straube, R. von Kries, P. Reilich, A. Pomschar and F. Heinen. Alterations in the trapezius muscle in young patients with migraine--a pilot case series with MRI2015. Eur J Paediatr Neurol. Volume 193:372-6 
  • M. N. Landgraf, R. von Kries, F. Heinen, T. Langhagen, A. Straube and L. AlbersSelf-reported neck and shoulder pain in adolescents is associated with episodic and chronic migraine. 2015. Cephalgia 
  • M. Tacke and I. Borggraefe. No clinically significant lymphocyte count change in pediatric patients treated with levetiracetam. 2015. Epilepsy Res. Volume114:147-8
  • M.N. Landgraf, C. Seubert, F. Heinen, T. Nicolai. Verdacht auf Kindesmisshandlung - Procedere in der Notaufnahme. 2015. Notfall. Volume 18:17-21
  • N. Heussinger, E. Kontopantelis, J. Gburek-Augustat, A. Jenke, G. Vollrath, R. Korinthenberg, P. Hofstetter, S. Meyer, I. Brecht, B. Kornek, P. Herkenrath, M. Schimmel, K. Wenner, M. Hausler, S. Lutz, M. Karenfort, A. Blaschek, M. Smitka, S. Karch, M. Piepkorn, K. Rostasy, T. Lucke, P. Weber, R. Trollmann, J. Klepper, M. Haussler, R. Hofmann, R. Weissert, A. Merkenschlager, M. Buttmann and G.-M. for. Oligoclonal bands predict multiple sclerosis in children with optic neuritis. 2015. Ann Neurol. Volume 574:393-6 
  • N. J. Nedergaard, F. Heinen, S. Sloth, H. C. Holmberg and U. G. Kersting. Biomechanics of the ski cross start indoors on a customised training ramp and outdoors on snow. 2015. Sports Biomech. Volume 5143:273-86. 
  • N. Lehnen, T. Langhagen, F. Heinen, D. Huppert, T. Brandt and K. Jahn. Vestibular paroxysmia in children: a treatable cause of short vertigo attacks. 2015. Dev Med Child Neurol. Volume 574:393-6
  • S. M. Herbst, C. R. Proepper, T. Geis, I. Borggraefe, A. Hahn, O. Debus, M. Haeussler, G. von Gersdorff, G. Kurlemann, M. Ensslen, N. Beaud, J. Budde, M. Gilbert, R. Heiming, R. Morgner, H. Philippi, S. Ross, G. Strobl-Wildemann, K. Muelleder, P. Vosschulte, D. J. Morris-Rosendahl, G. Schuierer and U. HehrLIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs. 2015: Brain Dev.
  • S. Niedermaier and A. Hilgendorff. Bronchopulmonary dysplasia - an overview about pathophysiologic concepts. 2015. Mol Cell Peditr. Volume 21:2 
  • S. Rudnik-Schoneborn, D. Tolle, J. Senderek, K. Eggermann, M. Elbracht, U. Kornak, M. von der Hagen, J. Kirschner, B. Leube, W. Muller-Felber, U. . Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients. 2015. Clin Genet
  • T. Langhagen, L. Albers, F. Heinen, A. Straube, F. Filippopulos, M. N. Landgraf, L. Gerstl, K. Jahn and R. von Kries. Period Prevalence of Dizziness and Vertigo in Adolescents. 2015. PLoS One. Volume 109 e0136512
  • W Müller-Felber. Diagnostik von Polyneuropathien im Kindes- und Jugendalter. 2015. Kinderärztliche Praxis. Volume 4:221-6
 
 

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