Plecko B - Search Results

1

Late-onset miliary pneumonitis after near drowning.

Mangge H, Plecko B, Grubbauer HM, Popper H, Smolle-Jüttner F, Zach M. Mangge H, et al. Among authors: plecko b. Pediatr Pulmonol. 1993 Feb;15(2):122-4. doi: 10.1002/ppul.1950150210. Pediatr Pulmonol. 1993. PMID: 8474784

2

Oral beta-hydroxybutyrate supplementation in two patients with hyperinsulinemic hypoglycemia: monitoring of beta-hydroxybutyrate levels in blood and cerebrospinal fluid, and in the brain by in vivo magnetic resonance spectroscopy.

Plecko B, Stoeckler-Ipsiroglu S, Schober E, Harrer G, Mlynarik V, Gruber S, Moser E, Moeslinger D, Silgoner H, Ipsiroglu O. Plecko B, et al. Pediatr Res. 2002 Aug;52(2):301-6. doi: 10.1203/00006450-200208000-00025. Pediatr Res. 2002. PMID: 12149510 Clinical Trial.

3

Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus Merzbacher phenotype.

Plecko B, Stöckler-Ipsiroglu S, Gruber S, Mlynarik V, Moser E, Simbrunner J, Ebner F, Bernert G, Harrer G, Gal A, Prayer D. Plecko B, et al. Neuropediatrics. 2003 Jun;34(3):127-36. doi: 10.1055/s-2003-41276. Neuropediatrics. 2003. PMID: 12910435

4

Pipecolic acid concentrations in brain tissue of nutritionally pyridoxine-deficient rats.

Plecko B, Hoeger H, Jakobs C, Struys E, Stromberger C, Leschnik M, Muehl A, Stoeckler-Ipsiroglu S. Plecko B, et al. J Inherit Metab Dis. 2005;28(5):689-93. doi: 10.1007/s10545-005-0071-4. J Inherit Metab Dis. 2005. PMID: 16151899

5

Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene.

Plecko B, Paul K, Paschke E, Stoeckler-Ipsiroglu S, Struys E, Jakobs C, Hartmann H, Luecke T, di Capua M, Korenke C, Hikel C, Reutershahn E, Freilinger M, Baumeister F, Bosch F, Erwa W. Plecko B, et al. Hum Mutat. 2007 Jan;28(1):19-26. doi: 10.1002/humu.20433. Hum Mutat. 2007. PMID: 17068770

6

Pipecolic acid elevation in plasma and cerebrospinal fluid of two patients with pyridoxine-dependent epilepsy.

Plecko B, Stöckler-Ipsiroglu S, Paschke E, Erwa W, Struys EA, Jakobs C. Plecko B, et al. Ann Neurol. 2000 Jul;48(1):121-5. Ann Neurol. 2000. PMID: 10894227

7

Liposomal amphotericin-B (AmBisome) for treatment of cutaneous widespread candidosis in an infant with methylmalonic acidaemia.

Stöckler S, Lackner H, Ginter G, Schwinger W, Plecko B, Müller W. Stöckler S, et al. Among authors: plecko b. Eur J Pediatr. 1993 Dec;152(12):981-3. doi: 10.1007/BF01957220. Eur J Pediatr. 1993. PMID: 8131816

8

Unrelated CD3/CD19-depleted peripheral stem cell transplantation for Hurler syndrome.

Schwinger W, Sovinz P, Benesch M, Lackner H, Seidel M, Strenger V, Sperl D, Raicht A, Brunner-Krainz M, Paschke E, Plecko B, Urban C. Schwinger W, et al. Among authors: plecko b. Pediatr Hematol Oncol. 2014 Nov;31(8):723-30. doi: 10.3109/08880018.2014.939794. Epub 2014 Aug 12. Pediatr Hematol Oncol. 2014. PMID: 25116402

9

Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings.

Srinivasaraghavan R, Parameswaran N, Mathis D, Bürer C, Plecko B. Srinivasaraghavan R, et al. Among authors: plecko b. Neuropediatrics. 2018 Apr;49(2):154-157. doi: 10.1055/s-0037-1621721. Epub 2018 Feb 5. Neuropediatrics. 2018. PMID: 29401530

10

Copper concentration of liver tissue under long-term copper-histidine therapy in a patient with Menkes disease.

Kroepfl T, Mair E, Deutsch J, Brunner-Krainz M, Paschke E, Plecko B. Kroepfl T, et al. Among authors: plecko b. J Inherit Metab Dis. 2006 Aug;29(4):593. doi: 10.1007/s10545-006-0312-1. Epub 2006 Jun 19. J Inherit Metab Dis. 2006. PMID: 16786254

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