Bodamer OA - Search Results

1

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. Huemer M, et al. Among authors: bodamer oa. J Inherit Metab Dis. 2012 Sep;35(5):817-21. doi: 10.1007/s10545-011-9448-8. Epub 2012 Jan 31. J Inherit Metab Dis. 2012. PMID: 22290024

2

Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria.

Huemer M, Födinger M, Bodamer OA, Mühl A, Herle M, Weigmann C, Ulmer H, Stöckler-Ipsiroglu S, Möslinger D. Huemer M, et al. Among authors: bodamer oa. Mol Genet Metab. 2008 May;94(1):46-51. doi: 10.1016/j.ymgme.2007.12.001. Epub 2008 Jan 14. Mol Genet Metab. 2008. PMID: 18249021

3

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. Huemer M, et al. Among authors: bodamer oa. J Pediatr. 2011 Apr;158(4):602-606.e1. doi: 10.1016/j.jpeds.2010.09.058. Epub 2010 Nov 12. J Pediatr. 2011. PMID: 21074173

4

Prenatal and postnatal treatment in cobalamin C defect.

Huemer M, Simma B, Fowler B, Suormala T, Bodamer OA, Sass JO. Huemer M, et al. Among authors: bodamer oa. J Pediatr. 2005 Oct;147(4):469-72. doi: 10.1016/j.jpeds.2005.04.040. J Pediatr. 2005. PMID: 16227032

5

Comparison of tetrahydrofuran and ethyl acetate as extraction solvents for urinary organic acid analysis.

Wittmann G, Karg E, Mühl A, Bodamer OA, Túri S. Wittmann G, et al. Among authors: bodamer oa. J Inherit Metab Dis. 2008 Feb;31(1):73-80. doi: 10.1007/s10545-007-0767-8. Epub 2008 Jan 14. J Inherit Metab Dis. 2008. PMID: 18188678

6

Rapid analysis of total plasma homocysteine by tandem mass spectrometry.

Tuschl K, Bodamer OA, Erwa W, Mühl A. Tuschl K, et al. Among authors: bodamer oa. Clin Chim Acta. 2005 Jan;351(1-2):139-41. doi: 10.1016/j.cccn.2004.08.016. Clin Chim Acta. 2005. PMID: 15563882

7

Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?

Holub M, Bodamer OA, Item C, Mühl A, Pollak A, Stöckler-Ipsiroglu S. Holub M, et al. Among authors: bodamer oa. Acta Paediatr. 2005 Jan;94(1):48-52. doi: 10.1111/j.1651-2227.2005.tb01787.x. Acta Paediatr. 2005. PMID: 15858960

8

Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type I.

Crone J, Möslinger D, Bodamer OA, Schima W, Huber WD, Holme E, Stöckler Ipsiroglu S. Crone J, et al. Among authors: bodamer oa. Acta Paediatr. 2003 May;92(5):625-8. Acta Paediatr. 2003. PMID: 12839296

9

Low creatinine: the diagnostic clue for a treatable neurologic disorder.

Bodamer OA, Iqbal F, Mühl A, Hung C, Prayer D, Ratschmann R, Item BC. Bodamer OA, et al. Neurology. 2009 Mar 3;72(9):854-5. doi: 10.1212/01.wnl.0000343955.66292.07. Neurology. 2009. PMID: 19255414 No abstract available.

10

Characterization of seven novel mutations in seven patients with GAMT deficiency.

Item CB, Mercimek-Mahmutoglu S, Battini R, Edlinger-Horvat C, Stromberger C, Bodamer O, Mühl A, Vilaseca MA, Korall H, Stöckler-Ipsiroglu S. Item CB, et al. Hum Mutat. 2004 May;23(5):524. doi: 10.1002/humu.9238. Hum Mutat. 2004. PMID: 15108290

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