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Publikationen 2011-2013

  • Albers L, Milde-Busch A, Bayer O, Lehmann S, Riedel C, Bonfert M, Heinen F, Straube A, von Kries R. Prevention of headache in adolescents: population-attributable risk fraction for risk factors amenable to intervention. Neuropediatrics. 2013 Feb;44(1):40-5.

  • Bernhard MK, Syrbe S, Landgraf M, Merkenschlager A. Persistierende Wolfsmilchgewächs-Intoxikation. Chronisches Erschöpfungs- und Schmerzsyndrom bei einer 12-jährigen Patientin. Kinder- und Jugendmedizin 2011; 11: 211-212

  • Blaschek A, Milde-Busch A, Straube A, Schankin C, Langhagen T, Jahn K, Schröder SA, Reiter K, von Kries R, Heinen F. Self-reported muscle pain in adolescents with migraine and tension-type headache. Cephalalgia. 2012, Feb;32(3):241-9.

  • Blaschek A, Storm van's Gravesande K, Heinen F, Pritsch M, Mall V, Calabrese P. Neuropsychological aspects of childhood multiple sclerosis: an overview. Neuropediatrics. 2012 Aug;43(4):176-83.

  • Blaschek et al. Early white matter changes in childhood multiple sclerosis: A diffusion tensor imaging study. AJNR 2013 Oct; 34(10): 2015-20

  • Blaschek A, Kümpfel T, Hohlfeld R, Ertl-Wagner B, Müller-Felber  W, Heinen F. Transition als Kernaufgabe der Pädiatrischen Neurologie Beispiel iSPZLMU - Multiple Sklerose (MS). Report Versorgungsforschung, 2012; 187-192

  • Bonfert M, Straube A, Schroeder AS, Reilich P, Ebinger F, Heinen F. Primary headache in children and adolescents: update on pharmacotherapy of migraine and tension-type headache. Neuropediatrics. 2013 Feb;44(1):3-19.

  • Borggraefe, I., Heinen, F., and Noachtar, S. (2011). Anforderungen an ein Epilepsiezentrum für Kinder und Jugendliche. Zeitschrift für Epileptologie 24, 167-171.

  • Borggraefe I, Bonfert M, Bast T, Neubauer BA, Schotten KJ, Maßmann K, Noachtar S, Tuxhorn I, May TW, Heinen F; German HEAD Study Group. Levetiracetam vs. sulthiame in benign epilepsy with entrotemporal spikes in childhood: a double-blinded, randomized, controlled trial (German HEAD Study). Eur J Paediatr Neurol. 2013 Sep;17(5):507-14.

  • Byrne BJ, Kishnani PS, Case LE, Merlini L, Müller-Felber W, Prasad S, van der Ploeg A. Pompe disease: design, methodology, and early findings from the Pompe Registry. Mol Genet Metab. 2011 May;103(1):1-11. doi:10.1016/j.ymgme.2011.02.004. Epub 2011 Feb 11. Erratum in: Mol Genet Metab. 2011, Nov;104(3):424. PubMed PMID: 21439876.

  • Cornell SA, Lahiri A, Eulitz C. (2011). "What you encode is not necessarily what you store": evidence for sparse feature representations from mismatch negativity. Brain Research; 1394:79-89.

  • Enders A. Neurobiologische Grundlagen zum Verständnis des therapeutischen Vorgehens im Castillo Morales-Konzept. Medizinsch-Therapeutische Grundlagen: Das Kind mit muskulärer Hypotonie, Das Kind mit Trisomie 21, Kinder mit orofazialen Problemen, Das Kind mit Cerebralparese. In Türk C, Söhlemann S, Rummel H (Hrsg.): Das Castillo Morales-Konzept, Thieme Verlag 2012

  • Ensslen M, Blaschek A, Penzien J, Borggräfe I (2011). Epileptischer Phänotyp der Anti-NMDAR-Enzephalitis. 37. Jahrestagung der Gesellschaft für Neuropädiatrie. Garmisch-Partenkirchen.

  • Ensslen, M, Wörnle M, Weber L, Heinen F, Borggräfe I. (2012). Akuttherapieder NMDAR-Enzephalitis: Immunadsorption im Rahmen eines therapierefrsktären Status epilepticus. 38. Jahrestagung der Gesellschaft für Neuropädiatrie Münster.

  • Ensslen, M., Mehrkens, J.H., Bötzel, K., Schröder, A.S., Müller-Felber, W., Heinen, F., and Borggraefe, I. (2011). Dystonien im Kindesalter. Monatsschrift Kinderheilkunde 159, 17-24.

  • Ertl-Wagner B, Koerte I, Kuempfel T, Blaschek A et al. (2011). Non-specific alterations of craniocervical venous drainage in multiple sclerosis assessed by cardiac-gated phase-contrast MR imaging.  Multiple Scler. Epub ahead of print

  • Ertl-Wagner B, Koerte I, Kümpfel T, Blaschek A, Laubender RP, Schick M, Steffinger D, Kaufmann D, Heinen F, Reiser M, Alperin N, Hohlfeld R. Non-specific alterations of craniocervical venous drainage in multiple sclerosis revealed by cardiac-gated phase-contrast MRI. Mult Scler. 2012 Jul;18(7):1000-7.

  • Frühe B, Allgaier AK, Pietsch K, Baethmann M, Peters J, Kellnar S, Heep A, Burdach S, von Schweinitz D, Schulte-Körne G (2012). Children's Depression Screener (ChilD-S): development and validation of a depression screening instrument for children in pediatric care. Child Psychiatry and Human Development, 43 (1): 137-151

  • Frühe B, Allgaier AK, Pietsch K, Schulte-Körne G (2012). Depressions-Screening bei pädiatrischen Patienten: Ein Vergleich der konkurrenten Validität des Depressionsinventars für Kinder und Jugendliche, des Depressionstest für Kinder und des Childrens Depression Screeners. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 40 (3): 161-169

  • Gallenmüller C, Felber WM, Dusl M, Stucka R, Guergueltcheva V, Blaschek A, von der Hagen M, Huebner A, Müller JS, Lochmüller H, Abicht A. Salbutamol-responsivelimb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK. Neuromuscul Disord. 2013 Aug 7. doi:pii:S0960-8966(13)00933-4. 10.1016/j.nmd.2013.08.002. [Epub ahead of print] PubMed PMID: 24183479.

  • Goebel HH, Blaschek A. Protein aggregation in congenital myopathies. Semin Pediatr Neurol. 2011; 18(4): 272-6

  • Hartig MB, Iuso A, Haack T, Kmiec T, Jurkiewicz E, Heim K, Roeber S, Tarabin V, Dusi S, Krajewska-Walasek M, Jozwiak S, Hempel M, Winkelmann J, Elstner M, Oexle K, Klopstock T, Mueller-Felber W, Gasser T, Trenkwalder C, Tiranti V, Kretzschmar H, Schmitz G, Strom TM, Meitinger T, Prokisch H. Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. Am J Hum Genet. 2011 Oct 7;89(4):543-50. doi: 10.1016/j.ajhg.2011.09.007. PubMed PMID: 21981780; PubMedCentral PMCID: PMC3188837.

  • Heinen F. Headaches in childhood and adolescence. Neuropediatrics. 2013 Feb;44(1):1-2.

  • Hilgendorff A, Parai K, Ertsey R, Rey-Parra GJ, Thebaud B, Tamosiuniene R, Jain N, Navarro EF, Starcher BC, Nicolls MR, Rabinovitch M, Bland RD (2012). Neonatal Mice Genetically Modified to Express the Elastase Inhibitor Elafin are Protected Against the Adverse Effects of Mechanical Ventilation on Lung Growth. Am J Physiol Lung Cell Mol Physiol. Epub ahead of print

  • Hilgendorff A, Parai K, Ertsey R, Jain N, Navarro EF, Peterson JL, Tamosiuniene R, Nicolls MR, Starcher BC, Rabinovitch M, Bland RD (2011). Inhibiting lung elastase activity enables lung growth in mechanically ventilated newborn mice. Am J Respir Crit Care Med. 1;184(5):537-46.

  • Holdenried M, Schenck TL, Akpaloo J, Müller-Felber W, Holzbach T, Giunta RE. [Quality of life after brachial plexus lesions in adults]. Handchir Mikrochir Plast Chir. 2013 Aug;45(4):229-34. doi: 10.1055/s-0033-1353161. Epub 2013 Aug 22. German. PubMed PMID: 23970402.

  • Jahn K, Langhagen T, Schroeder AS, Heinen F (2011). Vertigo and dizziness in childhood - update on diagnosis and treatment. Neuropediatrics. 42(4):129-34. Epub 2011 Jul 15. Review.

  • Kirschner J, Schorling D, Hauschke D, Rensing-Zimmermann C, Wein U, Grieben U, Schottmann G, Schara U, Konrad K, Müller-Felber W, Thiele S, Wilichowski E, Hobbiebrunken E, Stettner GM, Korinthenberg R. Somatropin treatment of spinal muscular atrophy: A placebo-controlled, double-blind crossover pilot study. Neuromuscul Disord. 2013 Nov 13. doi:pii: S0960-8966(13)00991-7.10.1016/j.nmd.2013.10.011. [Epub ahead of print] PubMed PMID: 24300782.

  • Koerte IK, Schroeder AS, Fietzek UM, Borggraefe I, Kerscher M, Berweck S, Reiser M, Ertl-Wagner B, Heinen F. Muscle atrophy beyond the clinical effect after a single dose of OnabotulinumtoxinA injected in the procerus muscle: a study with magnetic resonance imaging. Dermatol Surg. 2013 May;39(5):761-5.

  • Koerte IK, Schankin CJ, Immler S, Lee S, Laubender RP, Grosse C, Eftimov L, Milde-Busch A, Reiser M, Straube A, Heinen F, Alperin N, Ertl-Wagner B. Altered cerebrovenous drainage in patients with migraine as assessed by phase-contrast magnetic resonance imaging. Invest Radiol. 2011 Jul;46(7):434-40.

  • Koerte I, Pelavin P, Kirmess B, Fuchs T, Berweck S, Laubender RP, et al. Anisotropy of transcallosal motor fibres indicates functional impairment in children with periventricular leukomalacia. Dev Med Child Neurol 2011; 53: 179-86.

  • Kornek B, Aboul-Enei F, Rostasy K, Milos RI, Steiner I, Penzie P, Hellwig K  , Pitarokoili K, Storm van's Gravesande K, Karenfor M, Blaschek A, Meyer A, Seidl R, Debelic D, Vass K, Prayer D, Kristoferitsch W and Bayas A. Natalizumab therapy in highly active pediatric multiple sclerosis. JAMA Neurol. 2013 April; 70(4): 469-75

  • Kornek B, Schmitl B, Vass K, Zehetmayer S, Prtisch M, Penzin J, Karenfort M, Blaschek A, Seidl R, Prayer D, Rostasy K. Evaluation of the 2010 McDonald multiple sclerosis criteria in children with a clinically isolated syndrome. Mult.Scler. 2012, 18 (12): 1768-74

  • Kropp P, Meyer B, Landgraf M, Ruscheweyh R, Ebinger F, Straube A. Headache in children: update on biobehavioral treatments. Neuropediatrics. 2013;44(1):20-4

  • Kunz M, Lehner M, Heger A,Armbrust L, Weigand H, Peraud A. Neurodevelopmental and esthetic resultsbin children after surgical corrsction of metopic suture synostosis: a single institutional experience. Child Nerv Syst. 2013 Dec 13 (Epub ahead).
  • Kümpfel  T, Gerdes LA, Wacker T, Blaschek A, et al. Familial Mediterranean fever-associated mutation pyrin E148Q as a potential risk factor for multiple sclerosis.  Mult.Scler. 2012, 18(9):1229-38

  • Landgraf M, Heinen F (2012). Development of an evidence- and consensus-based guideline for the diagnosis of fetal alcohol syndrome in Germany. Neuropediatrics 43.

  • Landgraf M, Heinen F. Entwicklung einer Evidenz- und Konsens- basierten Leitlinie zur Diagnose des fetalen Alkoholsyndroms in Deutschland. Neuropädiatrie in Klinik und Praxis 2012.

  • Landgraf MN, Nothacker M, Kopp IB, Heinen F. The Diagnosis of Fetal Alcohol Syndrome. Dtsch Arztebl Int. 2013 Oct;110(42):703-710.

  • Landgraf MN, Nothacker M, Heinen F. Diagnosis of fetal alcohol syndrome (FAS): German guideline version 2013. Eur J Paediatr Neurol. 2013 Sep;17(5):437-46.

  • Landgraf M, Heinen F. S3-Leitlinie:  Fetales Alkoholsyndrom -  Diagnostik. http://www.awmf.org/leitlinien/detail/ll/022-025.html

  • Landgraf MN, Nothacker M., Heinen F. Diagnosis of Fetal Alcohol Syndrome (FAS): German Guideline Version 2013. Eur J Paediatr Neurol. 2013;17(5):437-46.

  • Landgraf M, Bernhard M. K., Syrbe S, Sorge I, Hirsch W, Schmiedek P, Merkenschlager A. Moyamoya-Erkrankungen - eine seltene Gefäßerkrankung mit neurologischen Ausfällen bei Manifestation. Fallbericht über einen acht Jahre alten Jungen vietnamesischer Herkunft. Kinder- und Jugendmedizin 2012; 12: 115-119.

  • Langhagen T, Schroeder AS, Rettinger N, Borggraefe I, Jahn K. Migraine-related vertigo and somatoform vertigo frequently occur in children and are often associated. Neuropediatrics 2013; 44: 55-8.

  • Lehmann S, Milde-Busch A, Straube A, von Kries R, Heinen F. How specific are risk factors for headache in adolescents? Results from a cross-sectional study in Germany. Neuropediatrics. 2013 Feb;44(1):46-54.

  • Mainberger F, Zenker M, Jung NH, Delvendahl I, Brandt A, Freudenberg L, Heinen F, Mall V. Impaired motor cortex plasticity in patients with Noonan syndrome. Clin Neurophysiol. 2013 Dec;124(12):2439-44.

  • Mainberger F, Jung NH, Zenker M, Wahlländer U, Freudenberg L, Langer S, Berweck S, Winkler T, Straube A, Heinen F, Granström S, Mautner VF, Lidzba K, Mall V. Lovastatin improves impaired synaptic plasticity and phasic alertness in patients with neurofibromatosis type 1. BMC Neurol. 2013 Oct 2;13:131. doi: 10.1186/1471-2377-13-131.

  • Merkl M, Beblo S, Wand D, Nickel P, Bigl A, Landgraf M, Merkenschlager A, Bernhard MK. Coumarin embryopathy and palmo-plantar hyperkeratosis in an 8-year-old boy. Kinder- und Jugendmedizin 2011; 11: 213-215.

  • Milde-Busch A, Straube A, Heinen F, von Kries R. Identified risk factors and adolescents' beliefs about triggers for headaches: results from a cross-sectional study. J Headache Pain. 2012 Nov;13(8):639-43.

  • Milde-Busch A, Blaschek A, Heinen F et al. Associations between stress and migraine and tension-type headache: results from a school-based study in adolescents from grammar schools in Germany. Cephalagia 2011, 31: 774-785

  • Muehlmann M, Koerte IK, Laubender RP, Steffinger D, Lehner M, Peraud A, Heinen F, Kiefer M, Reiser M, Ertl-Wagner B. Magnetic resonance-based estimation of intracranial pressure correlates with ventriculoperitoneal shunt valve opening pressure setting in children with hydrocephalus. Invest Radiol. 2013 Jul;48(7):543-7.

  • Muller-Felber W, Wanschitz J, Vill K, Baumann M. Pediatric idiopathic inflammatory myopathies: an update on diagnostic and treatment strategies. Neuropediatrics. 2013 Dec;44(6):314-23. doi: 10.1055/s-0033-1358600. Epub 2013 Nov 7. PubMed PMID: 24203857.

  • Olivieri M, Bidlingmaier C, Schetzeck S, Borggrafe I, Geisen C, Kurnik K. Arterial thrombosis in homozygous antithrombin deficiency. Hamostaseologie 2012; 32 Suppl 1: S79-82.

  • Pietsch K, Allgaier AK, Frühe B, Rohde S, Hosie S, Heinrich M, Schulte-Körne G (2011). Screening for depression in adolescent paediatric patients: validity of the new Depression Screener for Teenagers (DesTeen). Journal of Affective Disorders, 133 (1-2): 69-75

  • Pomschar A, Koerte I, Lee S, Laubender RP, Straube A, Heinen F, Ertl-Wagner B, Alperin N. MRI evidence for altered venous drainage and intracranial compliance in mild traumatic brain injury. PLoS One. 2013;8(2):e55447.

  • Proebstel AK, Dormmair K, Bittner R. et al. Antibodies to MOG are transient in childhodd acute disseminated encephalomyelitis. Neurology 2011,77: 580-8

  • Regnery C, Kornblum C, Hanisch F, Vielhaber S, Strigl-Pill N, Grunert B, Müller-Felber W, Glocker FX, Spranger M, Deschauer M, Mengel E, Schoser B. 36 months observational clinical study of 38 adult Pompe disease patients under alglucosidase alfa enzyme replacement therapy. J Inherit Metab Dis. 2012 Sep;35(5):837-45. Epub 2012 Jan 31. PubMed PMID: 22290025.

  • Roberts M, Kishnani PS, van der Ploeg AT, Müller-Felber W, Merlini L, Prasad S, Case LE. The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe Registry. Mol Genet Metab. 2011 Dec;104(4):574-82. doi: 10.1016/j.ymgme.2011.08.011. Epub 2011 Aug 16. PubMed PMID: 21930409.

  • Roser T, Bonfert M, Ebinger F, Blankenburg M, Ertl-Wagner B, Heinen F. Primary versus secondary headache in children: a frequent diagnostic challenge in clinical routine. Neuropediatrics. 2013 Feb;44(1):34-9.

  • Rostasy K, Mader S, Schanda K, Huppke P, Gärtner J, Busch V, Karenfurt M, Tibussek D, Blaschek A, Kornek B, Leitz YS, Schimmel M, DiPauli F, Berger T, Reindl M. Anti-myelin oligodendrocyte glycoprotein antibodies in pediatric patients with optic neuritis. Arch Neurology 2012, 69(6): 752-6

  • Rostasy K, Mader S, Hennes E, Schanda K, Gredler V, Guenther A, Blaschek A, Korenke C, Pritsch M, Pohl D, Maier O, Kuchukhidze G, Brunner-Krainz M, Berger T, Reindl M. Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica. Mult.Scler.2012 July; 19(8): 1052-9

  • Schenck TL, Bayer T, Enders A, Marton MA, Machens HG, Müller-Felber W, Giunta RE. [Splints in birth-related brachial plexus injuries]. Handchir Mikrochir Plast Chir. 2011 Apr;43(2):105-11. doi: 10.1055/s-0031-1271660. Epub 2011 Apr 20. German. PubMed PMID: 21509702.

  • Schetzek S, Heinen F, Kruse S, Borggraefe I, Bonfert M, Gaul C, Gottschling S, Ebinger F. Headache in children: update on complementary treatments. Neuropediatrics. 2013 Feb;44(1):25-33.

  • Schroeder AS, Fietzek UM, Pavicic T, Stehr M, Baumann AC, Ruzicka T, Heinen F (2011). Botulinum toxin--the all-rounder in medicine. MMW Fortschr Med. 27;153(4):33-9; German. No abstract available.

  • Schmidt B, Anderson PJ, Doyle LW, Dewey D, Grunau RE, Asztalos EV, Davis PG, Tin W, Moddemann D, Solimano A, Ohlsson A, Barrington KJ, Roberts RS (2012). Survival without disability to age 5 years after neonatal caffeine therapy for apnea of prematurity. Caffeine for Apnea of Prematurity (CAP) Trial Investigators. JAMA 18;307(3):275-82.

  • Schroeder AS, Kling T, Huss K, Borggraefe I, Koerte IK, Blaschek A, Jahn K, Heinen F, Berweck S. Botulinum toxin type A and B for the reduction of hypersalivation in children with neurological disorders: a focus on effectiveness and therapy adherence. Neuropediatrics. 2012 Feb;43(1):27-36

  • Schroeder AS, Huss K, Blaschek A, Koerte IK, Zeykan B, Roser T, Langhagen T, Schwerin A, Berweck S, Reilich P, Schaefer J, Straube A, Heinen F. Ten-year follow-up in a case series of integrative botulinum toxin intervention in adolescents with chronic daily headache and associated muscle pain. Neuropediatrics. 2012 Dec;43(6):339-45

  • Schroeder AS, Kappler M, Bonfert M, Borggraefe I, Schoen C, Reiter K. Seizures and stupor during intravenous mannose therapy in a patient with CDG syndrome type 1b (MPI-CDG). J Inherit Metab Dis 2010; 33 Suppl 3: S497-502.

  • Stavrinou P, Kunz M, Lehner M, Heger A, Müller-Felber W, Tonn JC, Peraud A. Children with tethered cord syndrome of different etiology benefit from microsurgery-a single institution experience. Childs Nerv Syst. 2011 May;27(5):803-10. doi: 10.1007/s00381-010-1374-9. Epub 2011 Jan 6. PubMed PMID: 21210127.

  • Tezer FI, Agan K, Borggraefe I, Noachtar S. Seizure semiology reflects spread from frontal to temporal lobe: evolution of hyperkinetic to automotor seizures as documented by invasive EEG video recordings. Epileptic Disord 2013; 15: 338-41.

 
 

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