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Items: 1 to 50 of 62

1.

Effect and safety of treatment with ACE-inhibitor Enalapril and β-blocker metoprolol on the onset of left ventricular dysfunction in Duchenne muscular dystrophy - a randomized, double-blind, placebo-controlled trial.

Dittrich S, Graf E, Trollmann R, Neudorf U, Schara U, Heilmann A, von der Hagen M, Stiller B, Kirschner J, Pozza RD, Müller-Felber W, Weiss K, von Au K, Khalil M, Motz R, Korenke C, Lange M, Wilichowski E, Pattathu J, Ebinger F, Wiechmann N, Schröder R; German Competence Network for Congenital Heart Defects and the Treat-NMD Neuromuscular Network Investigators list of additional local Investigators and co-workers of the German Competence Network for Congenital Heart Defects and the Treat-NMD Neuromuscular Network.

Orphanet J Rare Dis. 2019 May 10;14(1):105. doi: 10.1186/s13023-019-1066-9.

2.

[Migraine in children and adolescents-brain and muscle? : Another example of why children are not small adults].

Landgraf MN, König H, Hannibal I, Langhagen T, Bonfert MV, Klose B, Rahmsdorf B, Giese RM, Straube A, von Kries R, Albers L, Ebinger F, Ertl-Wagner B, Kammer B, Körte I, Sollmann N, Krieg S, Heinen F.

Nervenarzt. 2017 Dec;88(12):1402-1410. doi: 10.1007/s00115-017-0428-6. Review. German.

PMID:
28956079
3.

[Definition, diagnostics and therapy of chronic widespread pain and the (so-called) fibromyalgia syndrome in children and adolescents : Updated guidelines 2017].

Draheim N, Ebinger F, Schnöbel-Müller E, Wolf B, Häuser W.

Schmerz. 2017 Jun;31(3):296-307. doi: 10.1007/s00482-017-0208-z. Review. German.

PMID:
28493225
4.

B-cell populations discriminate between pediatric- and adult-onset multiple sclerosis.

Schwarz A, Balint B, Korporal-Kuhnke M, Jarius S, von Engelhardt K, Fürwentsches A, Bussmann C, Ebinger F, Wildemann B, Haas J.

Neurol Neuroimmunol Neuroinflamm. 2016 Dec 15;4(1):e309. doi: 10.1212/NXI.0000000000000309. eCollection 2017 Jan.

5.

[Abdominal pain in children and adolescents].

Ebinger F.

MMW Fortschr Med. 2014 Nov 6;156(19):66-8. Review. German. No abstract available.

PMID:
25510029
6.

Efficacy and tolerability of methylprednisolone pulse therapy in childhood epilepsies other than infantile spasms.

Bast T, Richter S, Ebinger F, Rating D, Wiemer-Kruel A, Schubert-Bast S.

Neuropediatrics. 2014 Dec;45(6):378-85. doi: 10.1055/s-0034-1387817. Epub 2014 Sep 3.

PMID:
25184741
7.

Headache in school children: prevalence and risk factors.

Straube A, Heinen F, Ebinger F, von Kries R.

Dtsch Arztebl Int. 2013 Nov 29;110(48):811-8. doi: 10.3238/arztebl.2013.0811. Review.

8.

Differences in use of complementary and alternative medicine between children and adolescents with cancer in Germany: a population based survey.

Gottschling S, Meyer S, Längler A, Scharifi G, Ebinger F, Gronwald B.

Pediatr Blood Cancer. 2014 Mar;61(3):488-92. doi: 10.1002/pbc.24769. Epub 2013 Sep 13.

PMID:
24038864
9.

T-cell homeostasis in pediatric multiple sclerosis: old cells in young patients.

Balint B, Haas J, Schwarz A, Jarius S, Fürwentsches A, Engelhardt K, Bussmann C, Ebinger F, Fritzsching B, Paul F, Seidel U, Vlaho S, Huppke P, Gärtner J, Wildemann B.

Neurology. 2013 Aug 27;81(9):784-92. doi: 10.1212/WNL.0b013e3182a2ce0e. Epub 2013 Aug 2.

PMID:
23911752
10.

Headache in pediatric practice.

Caviness V, Ebinger F.

Handb Clin Neurol. 2013;112:827-38. doi: 10.1016/B978-0-444-52910-7.00002-7. Review. No abstract available.

PMID:
23622290
11.

Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency.

De Franco E, Shaw-Smith C, Flanagan SE, Edghill EL, Wolf J, Otte V, Ebinger F, Varthakavi P, Vasanthi T, Edvardsson S, Hattersley AT, Ellard S.

Diabet Med. 2013 May;30(5):e197-200. doi: 10.1111/dme.12122. Epub 2013 Feb 28.

12.

Headache in children: update on complementary treatments.

Schetzek S, Heinen F, Kruse S, Borggraefe I, Bonfert M, Gaul C, Gottschling S, Ebinger F.

Neuropediatrics. 2013 Feb;44(1):25-33. doi: 10.1055/s-0032-1333435. Epub 2013 Jan 11. Review.

PMID:
23315555
13.

Headache in children: update on biobehavioral treatments.

Kropp P, Meyer B, Landgraf M, Ruscheweyh R, Ebinger F, Straube A.

Neuropediatrics. 2013 Feb;44(1):20-4. doi: 10.1055/s-0032-1333434. Epub 2013 Jan 9. Review.

PMID:
23303552
14.

Primary headache in children and adolescents: update on pharmacotherapy of migraine and tension-type headache.

Bonfert M, Straube A, Schroeder AS, Reilich P, Ebinger F, Heinen F.

Neuropediatrics. 2013 Feb;44(1):3-19. doi: 10.1055/s-0032-1330856. Epub 2013 Jan 9. Review.

PMID:
23303551
15.

Primary versus secondary headache in children: a frequent diagnostic challenge in clinical routine.

Roser T, Bonfert M, Ebinger F, Blankenburg M, Ertl-Wagner B, Heinen F.

Neuropediatrics. 2013 Feb;44(1):34-9. doi: 10.1055/s-0032-1332743. Epub 2013 Jan 3. Review.

PMID:
23288699
16.

Aspartylglucosaminuria: unusual neonatal presentation in Qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family.

Opladen T, Ebinger F, Zschocke J, Sengupta D, Ben-Omran T, Shahbeck N, Moog U, Fischer C, Bürger F, Haas D, Ruef P, Harting I, Al-Rifai H, Hoffmann GF.

J Child Neurol. 2014 Jan;29(1):36-42. doi: 10.1177/0883073812469049. Epub 2012 Dec 26.

PMID:
23271757
17.

An unusual case of paralytic ileus.

Seessle J, Stremmel W, Ebinger F, Merle U.

Z Gastroenterol. 2012 Nov;50(11):1161-5. doi: 10.1055/s-0032-1313125. Epub 2012 Nov 13.

PMID:
23150108
18.

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.

Rosewich H, Thiele H, Ohlenbusch A, Maschke U, Altmüller J, Frommolt P, Zirn B, Ebinger F, Siemes H, Nürnberg P, Brockmann K, Gärtner J.

Lancet Neurol. 2012 Sep;11(9):764-73. doi: 10.1016/S1474-4422(12)70182-5. Epub 2012 Jul 30.

PMID:
22850527
19.

Glucose transporter-1 (GLUT1) deficiency syndrome: diagnosis and treatment in late childhood.

Gramer G, Wolf NI, Vater D, Bast T, Santer R, Kamsteeg EJ, Wevers RA, Ebinger F.

Neuropediatrics. 2012 Jun;43(3):168-71. doi: 10.1055/s-0032-1315433. Epub 2012 May 23.

PMID:
22622956
20.

Use of linezolid in neonatal and pediatric inpatient facilities--results of a retrospective multicenter survey.

Simon A, Müllenborn E, Prelog M, Schenk W, Holzapfel J, Ebinger F, Klabunde-Cherwon A, Faber J, Groll AH, Masjosthusmann K, Dohna-Schwake C, Beutel K, Dirkwinkel E, Lehrnbecher T, Ammann RA, Müller A.

Eur J Clin Microbiol Infect Dis. 2012 Jul;31(7):1435-42. doi: 10.1007/s10096-011-1461-1. Epub 2011 Nov 3.

PMID:
22048844
21.

Alternating hemiplegia of childhood: metabolic studies in the largest European series of patients.

Fons C, Campistol J, Panagiotakaki E, Giannotta M, Arzimanoglou A, Gobbi G, Neville B, Ebinger F, Nevšímalová S, Laan L, Casaer P, Spiel G, Ninan M, Sange G, Artuch R, Schyns T, Vavassori R, Poncelin D; ENRAH Consortium.

Eur J Paediatr Neurol. 2012 Jan;16(1):10-4. doi: 10.1016/j.ejpn.2011.08.006. Epub 2011 Sep 25.

PMID:
21945173
22.

[Migraine variants and unusual types of migraine in childhood].

Gaul C, Kraya T, Holle D, Benkel-Herrenbrück I, Schara U, Ebinger F.

Schmerz. 2011 Apr;25(2):148-56. doi: 10.1007/s00482-011-1021-8. Review. German.

PMID:
21431964
23.

Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults.

Panagiotakaki E, Gobbi G, Neville B, Ebinger F, Campistol J, Nevsímalová S, Laan L, Casaer P, Spiel G, Giannotta M, Fons C, Ninan M, Sange G, Schyns T, Vavassori R, Poncelin D; ENRAH Consortium, Arzimanoglou A.

Brain. 2010 Dec;133(Pt 12):3598-610. doi: 10.1093/brain/awq295. Epub 2010 Oct 24.

PMID:
20974617
24.

Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotype.

Yis U, Uyanik G, Heck PB, Smitka M, Nobel H, Ebinger F, Dirik E, Feng L, Kurul SH, Brocke K, Unalp A, Özer E, Cakmakci H, Sewry C, Cirak S, Muntoni F, Hehr U, Morris-Rosendahl DJ.

Neuromuscul Disord. 2011 Jan;21(1):20-30. doi: 10.1016/j.nmd.2010.08.007. Epub 2010 Oct 18.

PMID:
20961758
25.

Prospective pilot intervention study to prevent medication errors in drugs administered to children by mouth or gastric tube: a programme for nurses, physicians and parents.

Bertsche T, Bertsche A, Krieg EM, Kunz N, Bergmann K, Hanke G, Hoppe-Tichy T, Ebinger F, Haefeli WE.

Qual Saf Health Care. 2010 Oct;19(5):e26. doi: 10.1136/qshc.2009.033753. Epub 2010 Apr 8.

PMID:
20378618
26.

Levetiracetam in the treatment of neonatal seizures: a pilot study.

Fürwentsches A, Bussmann C, Ramantani G, Ebinger F, Philippi H, Pöschl J, Schubert S, Rating D, Bast T.

Seizure. 2010 Apr;19(3):185-9. doi: 10.1016/j.seizure.2010.01.003. Epub 2010 Feb 4.

27.

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.

Leen WG, Klepper J, Verbeek MM, Leferink M, Hofste T, van Engelen BG, Wevers RA, Arthur T, Bahi-Buisson N, Ballhausen D, Bekhof J, van Bogaert P, Carrilho I, Chabrol B, Champion MP, Coldwell J, Clayton P, Donner E, Evangeliou A, Ebinger F, Farrell K, Forsyth RJ, de Goede CG, Gross S, Grunewald S, Holthausen H, Jayawant S, Lachlan K, Laugel V, Leppig K, Lim MJ, Mancini G, Marina AD, Martorell L, McMenamin J, Meuwissen ME, Mundy H, Nilsson NO, Panzer A, Poll-The BT, Rauscher C, Rouselle CM, Sandvig I, Scheffner T, Sheridan E, Simpson N, Sykora P, Tomlinson R, Trounce J, Webb D, Weschke B, Scheffer H, Willemsen MA.

Brain. 2010 Mar;133(Pt 3):655-70. doi: 10.1093/brain/awp336. Epub 2010 Feb 2.

PMID:
20129935
28.

GAPO syndrome associated with craniofacial vascular malformation.

Castrillon-Oberndorfer G, Seeberger R, Bacon C, Engel M, Ebinger F, Thiele OC.

Am J Med Genet A. 2010 Jan;152A(1):225-7. doi: 10.1002/ajmg.a.33192. No abstract available.

PMID:
20034076
29.

Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features.

Wolf NI, Rahman S, Schmitt B, Taanman JW, Duncan AJ, Harting I, Wohlrab G, Ebinger F, Rating D, Bast T.

Epilepsia. 2009 Jun;50(6):1596-607. doi: 10.1111/j.1528-1167.2008.01877.x. Epub 2008 Nov 19.

30.

Band-like intracranial calcification with simplified gyration and polymicrogyria: a distinct "pseudo-TORCH" phenotype.

Briggs TA, Wolf NI, D'Arrigo S, Ebinger F, Harting I, Dobyns WB, Livingston JH, Rice GI, Crooks D, Rowland-Hill CA, Squier W, Stoodley N, Pilz DT, Crow YJ.

Am J Med Genet A. 2008 Dec 15;146A(24):3173-80. doi: 10.1002/ajmg.a.32614.

PMID:
19012351
31.

Posaconazole concentrations in the central nervous system.

Rüping MJ, Albermann N, Ebinger F, Burckhardt I, Beisel C, Müller C, Vehreschild JJ, Kochanek M, Fätkenheuer G, Bangard C, Ullmann AJ, Herr W, Kolbe K, Hallek M, Cornely OA.

J Antimicrob Chemother. 2008 Dec;62(6):1468-70. doi: 10.1093/jac/dkn409. Epub 2008 Sep 28. No abstract available.

PMID:
18824458
32.

Inhibition of voriconazole metabolism by chloramphenicol in an adolescent with central nervous system aspergillosis.

Hafner V, Albermann N, Haefeli WE, Ebinger F.

Antimicrob Agents Chemother. 2008 Nov;52(11):4172-4. doi: 10.1128/AAC.00805-08. Epub 2008 Sep 15.

33.

Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.

Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, Decock C, Delbeke P, Ensenauer R, Ebinger F, Gillessen-Kaesbach G, Hendriks Y, Kimonis V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E.

Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819.

PMID:
18642388
34.

Abnormal myelination in Angelman syndrome.

Harting I, Seitz A, Rating D, Sartor K, Zschocke J, Janssen B, Ebinger F, Wolf NI.

Eur J Paediatr Neurol. 2009 May;13(3):271-6. doi: 10.1016/j.ejpn.2008.04.005. Epub 2008 Jun 24.

PMID:
18573670
35.

Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy.

Wolf NI, Harting I, Innes AM, Patzer S, Zeitler P, Schneider A, Wolff A, Baier K, Zschocke J, Ebinger F, Boltshauser E, Rating D.

Neuropediatrics. 2007 Apr;38(2):64-70.

PMID:
17712733
36.

A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brain.

Shimomura K, Hörster F, de Wet H, Flanagan SE, Ellard S, Hattersley AT, Wolf NI, Ashcroft F, Ebinger F.

Neurology. 2007 Sep 25;69(13):1342-9. Epub 2007 Jul 25.

PMID:
17652641
37.

The assessment of pain coping and pain-related cognitions in children and adolescents: current methods and further development.

Hermann C, Hohmeister J, Zohsel K, Ebinger F, Flor H.

J Pain. 2007 Oct;8(10):802-13. Epub 2007 Jul 12.

PMID:
17631054
38.

Unusual clinical presentation of primary hypothyroidism in a very young infant caused by autoimmune thyroiditis: case report and update of the literature.

Mittnacht J, Schmidt F, Ebinger F, Bettendorf M.

Eur J Pediatr. 2007 Aug;166(8):881-3. Epub 2006 Nov 21.

PMID:
17120037
39.

Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination.

Wolf NI, Cundall M, Rutland P, Rosser E, Surtees R, Benton S, Chong WK, Malcolm S, Ebinger F, Bitner-Glindzicz M, Woodward KJ.

Neurogenetics. 2007 Jan;8(1):39-44. Epub 2006 Sep 13.

PMID:
16969684
40.
41.

Cardiorespiratory regulation in migraine. Results in children and adolescents and review of the literature.

Ebinger F, Kruse M, Just U, Rating D.

Cephalalgia. 2006 Mar;26(3):295-309.

PMID:
16472336
42.

Intraoperative MRI for interventional neurosurgical procedures and tumor resection control in children.

Kremer P, Tronnier V, Steiner HH, Metzner R, Ebinger F, Rating D, Hartmann M, Seitz A, Unterberg A, Wirtz CR.

Childs Nerv Syst. 2006 Jul;22(7):674-8. Epub 2006 Feb 1.

PMID:
16450131
43.

Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy.

Senderek J, Krieger M, Stendel C, Bergmann C, Moser M, Breitbach-Faller N, Rudnik-Schöneborn S, Blaschek A, Wolf NI, Harting I, North K, Smith J, Muntoni F, Brockington M, Quijano-Roy S, Renault F, Herrmann R, Hendershot LM, Schröder JM, Lochmüller H, Topaloglu H, Voit T, Weis J, Ebinger F, Zerres K.

Nat Genet. 2005 Dec;37(12):1312-4. Epub 2005 Nov 13.

PMID:
16282977
44.

Diffuse cortical necrosis in a neonate with incontinentia pigmenti and an encephalitis-like presentation.

Wolf NI, Krämer N, Harting I, Seitz A, Ebinger F, Pöschl J, Rating D.

AJNR Am J Neuroradiol. 2005 Jun-Jul;26(6):1580-2.

45.

Beta-sarcoglycan gene mutations in Turkey.

Balci B, Wilichowski E, Haliloğlu G, Talim B, Aurino S, Kremer E, Ebinger F, Senbil N, Anlar B, Kale G, Nigro V, Topaloğlu H, Bonnemann C, Dinçer P.

Acta Myol. 2004 Dec;23(3):154-8.

PMID:
15938573
46.

Leukoencephalopathy with ataxia, hypodontia, and hypomyelination.

Wolf NI, Harting I, Boltshauser E, Wiegand G, Koch MJ, Schmitt-Mechelke T, Martin E, Zschocke J, Uhlenberg B, Hoffmann GF, Weber L, Ebinger F, Rating D.

Neurology. 2005 Apr 26;64(8):1461-4.

PMID:
15851747
47.

T2-hyperintense cerebellar cortex in Marinesco-Sjögren syndrome.

Harting I, Blaschek A, Wolf NI, Seitz A, Haupt M, Goebel HH, Rating D, Sartor K, Ebinger F.

Neurology. 2004 Dec 28;63(12):2448-9. No abstract available.

PMID:
15623732
48.

Headache and backache after lumbar puncture in children and adolescents: a prospective study.

Ebinger F, Kosel C, Pietz J, Rating D.

Pediatrics. 2004 Jun;113(6):1588-92.

PMID:
15173478
49.

Strict bed rest following lumbar puncture in children and adolescents is of no benefit.

Ebinger F, Kosel C, Pietz J, Rating D.

Neurology. 2004 Mar 23;62(6):1003-5.

PMID:
15037713
50.

Phenylalanine can be detected in brain tissue of healthy subjects by 1H magnetic resonance spectroscopy.

Pietz J, Lutz T, Zwygart K, Hoffmann GF, Ebinger F, Boesch C, Kreis R.

J Inherit Metab Dis. 2003;26(7):683-92.

PMID:
14707517

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