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Items: 1 to 50 of 87

1.

Adherence to Guidelines in the Treatment of Diabetic Ketoacidosis in Children: An Austrian Survey.

Weinberger K, Seick Barbarini D, Simma B.

Pediatr Emerg Care. 2018 Jul 24. doi: 10.1097/PEC.0000000000001551. [Epub ahead of print]

PMID:
30045350
2.

High Prevalence and Incidence of Diabetic Peripheral Neuropathy in Children and Adolescents With Type 1 Diabetes Mellitus: Results From a Five-Year Prospective Cohort Study.

Walter-Höliner I, Barbarini DS, Lütschg J, Blassnig-Ezeh A, Zanier U, Saely CH, Simma B.

Pediatr Neurol. 2018 Mar;80:51-60. doi: 10.1016/j.pediatrneurol.2017.11.017. Epub 2017 Dec 13.

PMID:
29429781
3.

Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages.

Schieck M, Schouten JP, Michel S, Suttner K, Toncheva AA, Gaertner VD, Illig T, Lipinski S, Franke A, Klintschar M, Kalayci O, Sahiner UM, Birben E, Melén E, Pershagen G, Freidin MB, Ogorodova LM, Granell R, Henderson J, Brunekreef B, Smit HA, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Genuneit J, Jonigk D, Postma DS, Koppelman GH, Vonk JM, Timens W, Boezen HM, Kabesch M.

J Allergy Clin Immunol. 2016 Aug;138(2):421-31. doi: 10.1016/j.jaci.2015.12.1305. Epub 2016 Feb 20.

PMID:
26906082
4.

Cross-sectional study to evaluate the longitudinal development of child and adolescent psychiatric diagnoses of inpatients in Vorarlberg, Austria.

Schwarz K, Fuchs M, Veraar M, Menz W, Kemmler G, Simma B.

Eur J Pediatr. 2016 Feb;175(2):221-8. doi: 10.1007/s00431-015-2612-7. Epub 2015 Aug 29.

PMID:
26319008
5.

Confirmation of Host Genetic Determinants in the CFH Region and Susceptibility to Meningococcal Disease in a Central European Study Sample.

Biebl A, Muendlein A, Kinz E, Drexel H, Kabesch M, Zenz W, Elling R, Müller C, Keil T, Lau S, Simma B.

Pediatr Infect Dis J. 2015 Oct;34(10):1115-7. doi: 10.1097/INF.0000000000000823.

PMID:
26135246
6.

Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact.

Toncheva AA, Potaczek DP, Schedel M, Gersting SW, Michel S, Krajnov N, Gaertner VD, Klingbeil JM, Illig T, Franke A, Winkler C, Hohlfeld JM, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Genuneit J, Muntau AC, Kabesch M.

Allergy. 2015 Oct;70(10):1288-99. doi: 10.1111/all.12652. Epub 2015 Jul 20.

PMID:
26011647
7.

Polymorphisms related to ORMDL3 are associated with asthma susceptibility, alterations in transcriptional regulation of ORMDL3, and changes in TH2 cytokine levels.

Schedel M, Michel S, Gaertner VD, Toncheva AA, Depner M, Binia A, Schieck M, Rieger MT, Klopp N, von Berg A, Bufe A, Laub O, Rietschel E, Heinzmann A, Simma B, Vogelberg C, Genuneit J, Illig T, Kabesch M.

J Allergy Clin Immunol. 2015 Oct;136(4):893-903.e14. doi: 10.1016/j.jaci.2015.03.014. Epub 2015 Apr 28.

PMID:
25930191
8.

Neonatal assessment in the delivery room--Trial to Evaluate a Specified Type of Apgar (TEST-Apgar).

Rüdiger M, Braun N, Aranda J, Aguar M, Bergert R, Bystricka A, Dimitriou G, El-Atawi K, Ifflaender S, Jung P, Matasova K, Ojinaga V, Petruskeviciene Z, Roll C, Schwindt J, Simma B, Staal N, Valencia G, Vasconcellos MG, Veinla M, Vento M, Weber B, Wendt A, Yigit S, Zotter H, Küster H; TEST-Apgar Study-Group.

BMC Pediatr. 2015 Mar 8;15:18. doi: 10.1186/s12887-015-0334-7.

9.

Hypoglycemia in Newborn Infants at Risk.

Jonas D, Dietz W, Simma B.

Klin Padiatr. 2014 Sep 5. [Epub ahead of print] No abstract available.

PMID:
25192404
10.

Hypoglycemia in newborn infants at risk.

Jonas D, Dietz W, Simma B.

Klin Padiatr. 2014 Sep;226(5):287-91. doi: 10.1055/s-0034-1385928. Epub 2014 Aug 25.

PMID:
25153912
11.

Fine-mapping of IgE-associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project data.

Sharma V, Michel S, Gaertner V, Franke A, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Frischer T, Genuneit J, Zeilinger S, Illig T, Schedel M, Potaczek DP, Kabesch M.

Allergy. 2014 Aug;69(8):1077-84. doi: 10.1111/all.12431. Epub 2014 Jun 14.

PMID:
24930997
12.

Compliance with guidelines recommending the use of simulation for neonatal and infant resuscitation training in Austria.

Mileder LP, Urlesberger B, Schwindt J, Simma B, Schmölzer GM.

Klin Padiatr. 2014 Jan;226(1):24-8. doi: 10.1055/s-0033-1361106. Epub 2014 Jan 16.

PMID:
24435789
13.

The burden of pneumococcal meningitis in Austrian children between 2001 and 2008.

Klobassa DS, Zoehrer B, Paulke-Korinek M, Gruber-Sedlmayr U, Pfurtscheller K, Strenger V, Sonnleitner A, Kerbl R, Ausserer B, Arocker W, Kaulfersch W, Hausberger B, Covi B, Eitelberger F, Vécsei A, Simma B, Birnbacher R, Kurz H, Zwiauer K, Weghuber D, Heuberger S, Quehenberger F, Kollaritsch H, Zenz W.

Eur J Pediatr. 2014 Jul;173(7):871-8. doi: 10.1007/s00431-013-2260-8. Epub 2014 Jan 14.

PMID:
24419336
14.

A role of FCER1A and FCER2 polymorphisms in IgE regulation.

Sharma V, Michel S, Gaertner V, Franke A, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Frischer T, Genuneit J, Potaczek DP, Kabesch M.

Allergy. 2014 Feb;69(2):231-6. doi: 10.1111/all.12336. Epub 2013 Dec 20.

PMID:
24354852
15.

Genetic variation in TH17 pathway genes, childhood asthma, and total serum IgE levels.

Schieck M, Michel S, Suttner K, Illig T, Zeilinger S, Franke A, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Frischer T, Genuneit J, Kerzel S, Kabesch M.

J Allergy Clin Immunol. 2014 Mar;133(3):888-91. doi: 10.1016/j.jaci.2013.08.048. Epub 2013 Nov 1. No abstract available.

PMID:
24184148
16.

Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22.

Blassnig-Ezeh A, Bandelier C, Frühmesser A, Revencu N, Krabichler B, Beauloye V, Ravoet M, Fauth C, Zschocke J, Simma B, Kotzot D.

Am J Med Genet A. 2013 Dec;161A(12):3176-81. doi: 10.1002/ajmg.a.36176. Epub 2013 Sep 24.

PMID:
24115558
17.

Polymorphisms in the IRF-4 gene, asthma and recurrent bronchitis in children.

Pinto LA, Michel S, Klopp N, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Simma B, Frischer T, Genuneit J, Gorski M, Illig T, Kabesch M.

Clin Exp Allergy. 2013 Oct;43(10):1152-9. doi: 10.1111/cea.12175.

PMID:
24074333
18.

Sodium bicarbonate--the swings and roundabouts will not stop without randomized evidence.

Simma B, Kirpalani H.

Crit Care Med. 2013 Sep;41(9):2242-3. doi: 10.1097/CCM.0b013e31828e9098. No abstract available.

PMID:
23979378
19.

Validity of the neurological examination in diagnosing diabetic peripheral neuropathy.

Höliner I, Haslinger V, Lütschg J, Müller G, Barbarini DS, Fussenegger J, Zanier U, Saely CH, Drexel H, Simma B.

Pediatr Neurol. 2013 Sep;49(3):171-7. doi: 10.1016/j.pediatrneurol.2013.03.014. Epub 2013 Jul 4.

PMID:
23831248
20.

Different FCER1A polymorphisms influence IgE levels in asthmatics and non-asthmatics.

Potaczek DP, Michel S, Sharma V, Zeilinger S, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Frischer T, Genuneit J, Illig T, Kabesch M.

Pediatr Allergy Immunol. 2013 Aug;24(5):441-9. doi: 10.1111/pai.12083. Epub 2013 Jun 3.

PMID:
23725541
21.

Mild head injury in pediatrics: algorithms for management in the ED and in young athletes.

Simma B, Lütschg J, Callahan JM.

Am J Emerg Med. 2013 Jul;31(7):1133-8. doi: 10.1016/j.ajem.2013.04.007. Epub 2013 May 20. Review.

PMID:
23702075
22.

[Evaluation of a child protecting team by an independent cooperation partner - suggestions for an optimized procedure].

Verocai E, Kitzelmann I, Juen F, Simma B.

Klin Padiatr. 2013 Jul;225(4):234-8. doi: 10.1055/s-0033-1333753. Epub 2013 Apr 4. German.

PMID:
23559432
23.

Two cases of unusual Lyme infection presenting as central nervous system Lyme disease.

Blassnig-Ezeh A, Schober H, Luetschg J, Jäger A, Simma B.

Klin Padiatr. 2013 Mar;225(2):91-92. doi: 10.1055/s-0033-1333764. Epub 2013 Mar 21. No abstract available.

PMID:
23519747
24.

Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma.

Pandey RC, Michel S, Schieck M, Binia A, Liang L, Klopp N, Franke A, von Berg A, Bufe A, Rietschel E, Heinzmann A, Laub O, Simma B, Frischer T, Genuneit J, Illig T, Kabesch M.

J Allergy Clin Immunol. 2013 Apr;131(4):1245-7. doi: 10.1016/j.jaci.2012.12.675. Epub 2013 Feb 4. No abstract available.

PMID:
23384682
25.

Genetic variation in the Toll-like receptor signaling pathway is associated with childhood asthma.

Pandey RC, Michel S, Tesse R, Binia A, Schedel M, Liang L, Klopp N, Franke A, von Berg A, Bufe A, Rietschel E, Heinzmann A, Laub O, Simma B, Frischer T, Genuneit J, Illig T, Kabesch M.

J Allergy Clin Immunol. 2013 Feb;131(2):602-5. doi: 10.1016/j.jaci.2012.10.061. Epub 2012 Dec 28. No abstract available.

PMID:
23273951
26.

Therapy in pediatric stroke.

Simma B, Höliner I, Luetschg J.

Eur J Pediatr. 2013 Jul;172(7):867-75. doi: 10.1007/s00431-012-1863-9. Epub 2012 Nov 6. Review.

PMID:
23129344
27.

Genetic variants in Protocadherin-1, bronchial hyper-responsiveness, and asthma subphenotypes in German children.

Toncheva AA, Suttner K, Michel S, Klopp N, Illig T, Balschun T, Vogelberg C, von Berg A, Bufe A, Heinzmann A, Laub O, Rietschel E, Simma B, Frischer T, Genuneit J, von Mutius E, Kabesch M.

Pediatr Allergy Immunol. 2012 Nov;23(7):636-41. doi: 10.1111/j.1399-3038.2012.01334.x. Epub 2012 Oct 11.

PMID:
23050600
28.

Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU).

Huemer M, Simma B, Mayr D, Möslinger D, Mühl A, Schmid I, Ulmer H, Bodamer OA.

J Inherit Metab Dis. 2012 Sep;35(5):817-21. Epub 2012 Jan 31.

PMID:
22290024
29.

[The Fetal Tobacco Syndrome - A statement of the Austrian Societies for General- and Family Medicine (ÖGAM), Gynecology and Obstetrics (ÖGGG), Hygiene, Microbiology and Preventive Medicine (ÖGHMP), Pediatrics and Adolescence Medicine (ÖGKJ) as well as Pneumology (ÖGP)].

Horak F Jr, Fazekas T, Zacharasiewicz A, Eber E, Kiss H, Lichtenschopf A, Neuberger M, Schmitzberger R, Simma B, Wilhelm-Mitteräcker A, Riedler J.

Wien Klin Wochenschr. 2012 Mar;124(5-6):129-45. doi: 10.1007/s00508-011-0106-9. Epub 2011 Dec 22. Review. German.

PMID:
22189489
30.

Salicylate intoxication with symptoms of septicaemia in a 17-month-old girl.

Haslinger V, Dietz W, Bartsch M, Simma B.

Klin Padiatr. 2011 Dec;223(7):436-7. doi: 10.1055/s-0031-1287821. Epub 2011 Sep 29. No abstract available.

PMID:
21959649
31.

Canavan disease: a novel mutation.

Schober H, Luetschg J, Hoeliner I, Kalb S, Simma B.

Pediatr Neurol. 2011 Oct;45(4):256-8. doi: 10.1016/j.pediatrneurol.2011.06.011.

PMID:
21907889
32.

Unifying candidate gene and GWAS Approaches in Asthma.

Michel S, Liang L, Depner M, Klopp N, Ruether A, Kumar A, Schedel M, Vogelberg C, von Mutius E, von Berg A, Bufe A, Rietschel E, Heinzmann A, Laub O, Simma B, Frischer T, Genuneit J, Gut IG, Schreiber S, Lathrop M, Illig T, Kabesch M.

PLoS One. 2010 Nov 12;5(11):e13894. doi: 10.1371/journal.pone.0013894.

33.

Low levels of asymmetric dimethylarginine in children with diabetes mellitus type I compared with healthy children.

Huemer M, Simma B, Mayr D, Mühl A, Rami B, Schober E, Ulmer H, Zanier U, Bodamer OA.

J Pediatr. 2011 Apr;158(4):602-606.e1. doi: 10.1016/j.jpeds.2010.09.058. Epub 2010 Nov 12.

PMID:
21074173
34.

Compliance to clinical guidelines determines outcome in glutaric aciduria type I in the era of newborn screening.

Höliner I, Simma B, Reiter A, Sass JO, Zschocke J, Huemer M.

Klin Padiatr. 2010 Jan-Feb;222(1):35-7. doi: 10.1055/s-0029-1239525. Epub 2010 Jan 18.

PMID:
20084589
35.

CD14 C-159T and toll-like receptor 4 Asp299Gly polymorphisms in surviving meningococcal disease patients.

Biebl A, Muendlein A, Kazakbaeva Z, Heuberger S, Sonderegger G, Drexel H, Lau S, Nickel R, Kabesch M, Simma B.

PLoS One. 2009 Oct 7;4(10):e7374. doi: 10.1371/journal.pone.0007374.

36.

Variations of Apgar score of very low birth weight infants in different neonatal intensive care units.

Rüdiger M, Küster H, Herting E, Berger A, Müller C, Urlesberger B, Simma B, Poets CF, Wauer RR, Tschirch E.

Acta Paediatr. 2009 Sep;98(9):1433-6. doi: 10.1111/j.1651-2227.2009.01347.x. Epub 2009 Jun 25.

PMID:
19558600
37.

Neonatal diabetes mellitus due to pancreas agenesis: a new case report and review of the literature.

Barbarini DS, Haslinger V, Schmidt K, Patch AM, Müller G, Simma B.

Pediatr Diabetes. 2009 Nov;10(7):487-91. doi: 10.1111/j.1399-5448.2009.00523.x. Epub 2009 Jun 3. Review.

PMID:
19496968
38.

Nasal continuous positive airway pressure (n-CPAP) does not change cardiac output in preterm infants.

Moritz B, Fritz M, Mann C, Simma B.

Am J Perinatol. 2008 Feb;25(2):105-9. doi: 10.1055/s-2008-1040341. Epub 2008 Jan 31.

PMID:
18240105
39.

Risk factors for pediatric stroke: consequences for therapy and quality of life.

Simma B, Martin G, Müller T, Huemer M.

Pediatr Neurol. 2007 Aug;37(2):121-6.

PMID:
17675027
40.

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.

Moffatt MF, Kabesch M, Liang L, Dixon AL, Strachan D, Heath S, Depner M, von Berg A, Bufe A, Rietschel E, Heinzmann A, Simma B, Frischer T, Willis-Owen SA, Wong KC, Illig T, Vogelberg C, Weiland SK, von Mutius E, Abecasis GR, Farrall M, Gut IG, Lathrop GM, Cookson WO.

Nature. 2007 Jul 26;448(7152):470-3. Epub 2007 Jul 4.

41.

Total homocysteine, folate, and cobalamin, and their relation to genetic polymorphisms, lifestyle and body mass index in healthy children and adolescents.

Huemer M, Vonblon K, Födinger M, Krumpholz R, Hubmann M, Ulmer H, Simma B.

Pediatr Res. 2006 Dec;60(6):764-9. Epub 2006 Oct 25.

PMID:
17065574
42.

Prenatal and postnatal treatment in cobalamin C defect.

Huemer M, Simma B, Fowler B, Suormala T, Bodamer OA, Sass JO.

J Pediatr. 2005 Oct;147(4):469-72.

PMID:
16227032
43.

Hyperhomocysteinemia in children treated with antiepileptic drugs is normalized by folic acid supplementation.

Huemer M, Ausserer B, Graninger G, Hubmann M, Huemer C, Schlachter K, Tscharre A, Ulmer H, Simma B.

Epilepsia. 2005 Oct;46(10):1677-83.

44.

Vaccine strategies of meningococcal disease: results of a 10-year population-based study.

Biebl A, Hartmann G, Bernhard C, Bechter E, Luckner-Hornischer A, Frühwirth M, Heuberger S, Offner F, Barbieri V, Simma B.

Eur J Pediatr. 2005 Dec;164(12):735-40. Epub 2005 Aug 27.

PMID:
16133244
45.

Loss of intrahepatic bile ducts: an important feature of familial hemophagocytic lymphohistiocytosis.

Kapelari K, Fruehwirth M, Heitger A, Königsrainer A, Margreiter R, Simma B, Offner FA.

Virchows Arch. 2005 Jun;446(6):619-25. Epub 2005 May 20.

PMID:
15906086
46.

Successful treatment of ARDS and severe pulmonary hypertension in a child with Bordetella pertussis infection.

Skladal D, Horak E, Frühwirth M, Maurer H, Simma B.

Wien Klin Wochenschr. 2004 Nov 30;116(21-22):760-2.

PMID:
15628648
47.

Neonatal type IV glycogen storage disease associated with "null" mutations in glycogen branching enzyme 1.

Janecke AR, Dertinger S, Ketelsen UP, Bereuter L, Simma B, Müller T, Vogel W, Offner FA.

J Pediatr. 2004 Nov;145(5):705-9.

PMID:
15520786
48.

Congenital cutaneous mastocytosis.

Mann C, Sepp N, Simma B.

J Pediatr. 2004 Jul;145(1):134. No abstract available.

PMID:
15238925
49.

Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies.

Petek E, Windpassinger C, Simma B, Mueller T, Wagner K, Kroisel PM.

J Hum Genet. 2003;48(6):283-7. Epub 2003 Apr 24.

PMID:
12836054
50.

Congenital cystic lung disease: diagnostic and therapeutic considerations.

Horak E, Bodner J, Gassner I, Schmid T, Simma B, Grässl G, Sawyer SM.

Clin Pediatr (Phila). 2003 Apr;42(3):251-61. Review.

PMID:
12739924

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