Haberlandt E - Search Results

1

Predictive validity of attentional functions in differentiating children with and without ADHD: a componential analysis.

Kaufmann L, Zieren N, Zotter S, Karall D, Scholl-Bürgi S, Haberlandt E, Fimm B. Kaufmann L, et al. Among authors: haberlandt e. Dev Med Child Neurol. 2010 Apr;52(4):371-8. doi: 10.1111/j.1469-8749.2009.03560.x. Epub 2010 Jan 5. Dev Med Child Neurol. 2010. PMID: 20059511 Free article.

2

Brief report: CANTAB performance and brain structure in pediatric patients with Asperger syndrome.

Kaufmann L, Zotter S, Pixner S, Starke M, Haberlandt E, Steinmayr-Gensluckner M, Egger K, Schocke M, Weiss EM, Marksteiner J. Kaufmann L, et al. Among authors: haberlandt e. J Autism Dev Disord. 2013 Jun;43(6):1483-90. doi: 10.1007/s10803-012-1686-6. J Autism Dev Disord. 2013. PMID: 23117423

3

Adrenocorticotropic hormone versus pulsatile dexamethasone in the treatment of infantile epilepsy syndromes.

Haberlandt E, Weger C, Sigl SB, Rauchenzauner M, Scholl-Bürgi S, Rostásy K, Karall D. Haberlandt E, et al. Pediatr Neurol. 2010 Jan;42(1):21-7. doi: 10.1016/j.pediatrneurol.2009.07.011. Pediatr Neurol. 2010. PMID: 20004858

4

Glucose transporter type 1 deficiency syndrome effectively treated with modified Atkins diet.

Haberlandt E, Karall D, Jud V, Baumgartner SS, Zotter S, Rostasy K, Baumann M, Scholl-Buergi S. Haberlandt E, et al. Neuropediatrics. 2014 Apr;45(2):117-9. doi: 10.1055/s-0033-1349225. Epub 2013 Jul 25. Neuropediatrics. 2014. PMID: 23888468

5

Adiponectin and visfatin concentrations in children treated with valproic acid.

Rauchenzauner M, Haberlandt E, Scholl-Bürgi S, Ernst B, Hoppichler F, Karall D, Ebenbichler CF, Rostasy K, Luef G. Rauchenzauner M, et al. Among authors: haberlandt e. Epilepsia. 2008 Feb;49(2):353-7. doi: 10.1111/j.1528-1167.2007.01460.x. Epub 2007 Dec 6. Epilepsia. 2008. PMID: 18070089 Free article.

6

Homozygosity for MECP2 gene in a girl with classical Rett syndrome.

Karall D, Haberlandt E, Scholl-Bürgi S, Baumgartner S, Naudó M, Martorell L. Karall D, et al. Among authors: haberlandt e. Eur J Med Genet. 2007 Nov-Dec;50(6):465-8. doi: 10.1016/j.ejmg.2007.07.001. Epub 2007 Aug 6. Eur J Med Genet. 2007. PMID: 17881312

7

Unrecognized citrullinemia mimicking encephalitis in a 14-year-old boy: unexpected result through the use of a standardized lumbar puncture protocol.

Karall D, Haberlandt E, Albrecht U, Rostasy K, Häberle J, Scholl-Bürgi S. Karall D, et al. Among authors: haberlandt e. Neuropediatrics. 2012 Apr;43(2):59-63. doi: 10.1055/s-0032-1307453. Epub 2012 Apr 3. Neuropediatrics. 2012. PMID: 22473243

8

Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy.

Krabichler B, Rostasy K, Baumann M, Karall D, Scholl-Bürgi S, Schwarzer C, Gautsch K, Spreiz A, Kotzot D, Zschocke J, Fauth C, Haberlandt E. Krabichler B, et al. Among authors: haberlandt e. Ann Hum Genet. 2012 Jul;76(4):326-31. doi: 10.1111/j.1469-1809.2012.00710.x. Epub 2012 May 21. Ann Hum Genet. 2012. PMID: 22606975

9

Matrix-metalloproteinases and proinflammatory cytokines in children with febrile convulsions and epilepsy--cause or consequence?

Haberlandt E, Rauchenzauner M, Morass M, Wondrak P, Scholl-Bürgi S, Rostásy K, Karall D. Haberlandt E, et al. Epilepsy Res. 2013 Jul;105(1-2):225-8. doi: 10.1016/j.eplepsyres.2012.12.003. Epub 2013 Jan 10. Epilepsy Res. 2013. PMID: 23313321

10

Ketogenic diet in a patient with refractory status epilepticus due to POLG mutation.

Koessler M, Haberlandt E, Karall D, Baumann M, Höller A, Scholl-Bürgi S. Koessler M, et al. Among authors: haberlandt e. JIMD Rep. 2020 Oct 1;57(1):3-8. doi: 10.1002/jmd2.12169. eCollection 2021 Jan. JIMD Rep. 2020. PMID: 33473333 Free PMC article.

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