Meissner T - Search Results

1

Malonic aciduria: long-term follow-up of new patients detected by newborn screening.

Baertling F, Mayatepek E, Thimm E, Schlune A, Kovacevic A, Distelmaier F, Salomons GS, Meissner T. Baertling F, et al. Among authors: meissner t. Eur J Pediatr. 2014 Dec;173(12):1719-22. doi: 10.1007/s00431-014-2421-4. Epub 2014 Sep 20. Eur J Pediatr. 2014. PMID: 25233985

2

Chronic pancreatitis in branched-chain organic acidurias--a case of methylmalonic aciduria and an overview of the literature.

Marquard J, El Scheich T, Klee D, Schmitt M, Meissner T, Mayatepek E, Oh J. Marquard J, et al. Among authors: meissner t. Eur J Pediatr. 2011 Feb;170(2):241-5. doi: 10.1007/s00431-010-1313-5. Epub 2010 Oct 6. Eur J Pediatr. 2011. PMID: 20924605 Review.

3

Clinical and genetic heterogeneity in congenital hyperinsulinism.

Meissner T, Mayatepek E. Meissner T, et al. Eur J Pediatr. 2002 Jan;161(1):6-20. doi: 10.1007/s004310100850. Eur J Pediatr. 2002. PMID: 11808881 Review.

4

Long-term follow-up of 114 patients with congenital hyperinsulinism.

Meissner T, Wendel U, Burgard P, Schaetzle S, Mayatepek E. Meissner T, et al. Eur J Endocrinol. 2003 Jul;149(1):43-51. doi: 10.1530/eje.0.1490043. Eur J Endocrinol. 2003. PMID: 12824865

5

Odd-numbered long-chain fatty acids in erythrocyte phospholipids as long-term follow-up parameter in propionic acidemia.

Meissner T, Leichsenring M, Mayatepek E. Meissner T, et al. Clin Chem Lab Med. 2004;42(9):1005-8. doi: 10.1515/CCLM.2004.203. Clin Chem Lab Med. 2004. PMID: 15497464

6

Inborn errors of carbohydrate metabolism.

Mayatepek E, Hoffmann B, Meissner T. Mayatepek E, et al. Among authors: meissner t. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):607-18. doi: 10.1016/j.bpg.2010.07.012. Best Pract Res Clin Gastroenterol. 2010. PMID: 20955963 Review.

7

Liver cirrhosis in glycogen storage disease Ib.

Baertling F, Mayatepek E, Gerner P, Baba HA, Franzel J, Schlune A, Meissner T. Baertling F, et al. Among authors: meissner t. Mol Genet Metab. 2013 Mar;108(3):198-200. doi: 10.1016/j.ymgme.2013.01.003. Epub 2013 Jan 11. Mol Genet Metab. 2013. PMID: 23357201

8

Screening for non-alcoholic fatty liver disease in children and adolescents with type 1 diabetes mellitus: a cross-sectional analysis.

Kummer S, Klee D, Kircheis G, Friedt M, Schaper J, Häussinger D, Mayatepek E, Meissner T. Kummer S, et al. Among authors: meissner t. Eur J Pediatr. 2017 Apr;176(4):529-536. doi: 10.1007/s00431-017-2876-1. Epub 2017 Feb 17. Eur J Pediatr. 2017. PMID: 28213828

9

Persistent hyperinsulinaemic hypoglycaemia of infancy: therapy, clinical outcome and mutational analysis.

Meissner T, Brune W, Mayatepek E. Meissner T, et al. Eur J Pediatr. 1997 Oct;156(10):754-7. doi: 10.1007/s004310050706. Eur J Pediatr. 1997. PMID: 9365062

10

Richner-Hanhart syndrome detected by expanded newborn screening.

Meissner T, Betz RC, Pasternack SM, Eigelshoven S, Ruzicka T, Kruse R, Laitenberger G, Mayatepek E. Meissner T, et al. Pediatr Dermatol. 2008 May-Jun;25(3):378-80. doi: 10.1111/j.1525-1470.2008.00687.x. Pediatr Dermatol. 2008. PMID: 18577048

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