Muntau AC - Search Results

1

First-trimester increased nuchal translucency as a prenatal sign of Zellweger syndrome.

Strenge S, Froster UG, Wanders RJ, Gartner J, Maier EM, Muntau AC, Faber R. Strenge S, et al. Among authors: muntau ac. Prenat Diagn. 2004 Feb;24(2):151-3. doi: 10.1002/pd.805. Prenat Diagn. 2004. PMID: 14974126 No abstract available.

2

PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease.

Preuss N, Brosius U, Biermanns M, Muntau AC, Conzelmann E, Gartner J. Preuss N, et al. Among authors: muntau ac. Pediatr Res. 2002 Jun;51(6):706-14. doi: 10.1203/00006450-200206000-00008. Pediatr Res. 2002. PMID: 12032265

3

[Breaking bad news--a video-based training unit for medical students].

Kopecky-Wenzel M, Maier EM, Muntau AC, Reinhardt D, Frank R. Kopecky-Wenzel M, et al. Among authors: muntau ac. Z Kinder Jugendpsychiatr Psychother. 2009 Mar;37(2):139-44. doi: 10.1024/1422-4917.37.2.139. Z Kinder Jugendpsychiatr Psychother. 2009. PMID: 19402001 German.

4

Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation.

Maier EM, Kammerer S, Muntau AC, Wichers M, Braun A, Roscher AA. Maier EM, et al. Among authors: muntau ac. Ann Neurol. 2002 Nov;52(5):683-8. doi: 10.1002/ana.10376. Ann Neurol. 2002. PMID: 12402273

5

What are effects of a spaced activation of virtual patients in a pediatric course?

Maier EM, Hege I, Muntau AC, Huber J, Fischer MR. Maier EM, et al. Among authors: muntau ac. BMC Med Educ. 2013 Mar 28;13:45. doi: 10.1186/1472-6920-13-45. BMC Med Educ. 2013. PMID: 23537162 Free PMC article.

6

The domain-specific and temperature-dependent protein misfolding phenotype of variant medium-chain acyl-CoA dehydrogenase.

Jank JM, Maier EM, Reiβ DD, Haslbeck M, Kemter KF, Truger MS, Sommerhoff CP, Ferdinandusse S, Wanders RJ, Gersting SW, Muntau AC. Jank JM, et al. Among authors: muntau ac. PLoS One. 2014 Apr 9;9(4):e93852. doi: 10.1371/journal.pone.0093852. eCollection 2014. PLoS One. 2014. PMID: 24718418 Free PMC article.

7

Disease manifestations and X inactivation in heterozygous females with Fabry disease.

Maier EM, Osterrieder S, Whybra C, Ries M, Gal A, Beck M, Roscher AA, Muntau AC. Maier EM, et al. Among authors: muntau ac. Acta Paediatr Suppl. 2006 Apr;95(451):30-8. doi: 10.1080/08035320600618809. Acta Paediatr Suppl. 2006. PMID: 16720462

8

Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected].

Maier EM, Pongratz J, Muntau AC, Liebl B, Nennstiel-Ratzel U, Busch U, Fingerhut R, Olgemöller B, Roscher AA, Röschinger W. Maier EM, et al. Among authors: muntau ac. Clin Genet. 2009 Aug;76(2):179-87. doi: 10.1111/j.1399-0004.2009.01217.x. Clin Genet. 2009. PMID: 19780764

9

Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.

Coenen MJ, van den Heuvel LP, Ugalde C, Ten Brinke M, Nijtmans LG, Trijbels FJ, Beblo S, Maier EM, Muntau AC, Smeitink JA. Coenen MJ, et al. Among authors: muntau ac. Ann Neurol. 2004 Oct;56(4):560-4. doi: 10.1002/ana.20229. Ann Neurol. 2004. PMID: 15455402

10

Role of Pex19p in the targeting of PMP70 to peroxisome.

Kashiwayama Y, Asahina K, Shibata H, Morita M, Muntau AC, Roscher AA, Wanders RJ, Shimozawa N, Sakaguchi M, Kato H, Imanaka T. Kashiwayama Y, et al. Among authors: muntau ac. Biochim Biophys Acta. 2005 Dec 15;1746(2):116-28. doi: 10.1016/j.bbamcr.2005.10.006. Epub 2005 Nov 14. Biochim Biophys Acta. 2005. PMID: 16344115 Free article.

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