Meissner T - Search Results

1

Diagnostic difficulties in glucokinase hyperinsulinism.

Meissner T, Marquard J, Cobo-Vuilleumier N, Maringa M, Rodríguez-Bada P, García-Gimeno MA, Baixeras E, Weber J, Olek K, Sanz P, Mayatepek E, Cuesta-Muñoz AL. Meissner T, et al. Horm Metab Res. 2009 Apr;41(4):320-6. doi: 10.1055/s-0028-1102922. Epub 2008 Dec 3. Horm Metab Res. 2009. PMID: 19053014 Free article.

2

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.

3

Rare forms of congenital hyperinsulinism.

Marquard J, Palladino AA, Stanley CA, Mayatepek E, Meissner T. Marquard J, et al. Among authors: meissner t. Semin Pediatr Surg. 2011 Feb;20(1):38-44. doi: 10.1053/j.sempedsurg.2010.10.006. Semin Pediatr Surg. 2011. PMID: 21186003 Review.

4

Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism.

Meissner T, Friedmann B, Okun JG, Schwab MA, Otonkoski T, Bauer T, Bärtsch P, Mayatepek E. Meissner T, et al. Horm Metab Res. 2005 Nov;37(11):690-4. doi: 10.1055/s-2005-870583. Horm Metab Res. 2005. PMID: 16308838

5

Urinary alpha-ketoglutarate is elevated in patients with hyperinsulinism-hyperammonemia syndrome.

Meissner T, Mayatepek E, Kinner M, Santer R. Meissner T, et al. Clin Chim Acta. 2004 Mar;341(1-2):23-6. doi: 10.1016/j.cccn.2003.10.023. Clin Chim Acta. 2004. PMID: 14967154

6

Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant.

Hennewig U, Hadzik B, Vogel M, Meissner T, Goecke T, Peters H, Selzer G, Mayatepek E, Hoehn T. Hennewig U, et al. Among authors: meissner t. J Hum Genet. 2008;53(6):573-577. doi: 10.1007/s10038-008-0275-1. Epub 2008 Mar 14. J Hum Genet. 2008. PMID: 18340402

7

Long-term medical treatment in congenital hyperinsulinism: a descriptive analysis in a large cohort of patients from different clinical centers.

Welters A, Lerch C, Kummer S, Marquard J, Salgin B, Mayatepek E, Meissner T. Welters A, et al. Among authors: meissner t. Orphanet J Rare Dis. 2015 Nov 25;10:150. doi: 10.1186/s13023-015-0367-x. Orphanet J Rare Dis. 2015. PMID: 26608306 Free PMC article. Review.

8

Congenital hyperinsulinism: molecular basis of a heterogeneous disease.

Meissner T, Beinbrech B, Mayatepek E. Meissner T, et al. Hum Mutat. 1999;13(5):351-61. doi: 10.1002/(SICI)1098-1004(1999)13:5<351::AID-HUMU3>3.0.CO;2-R. Hum Mutat. 1999. PMID: 10338089 Review.

9

Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome.

Santer R, Kinner M, Passarge M, Superti-Furga A, Mayatepek E, Meissner T, Schneppenheim R, Schaub J. Santer R, et al. Among authors: meissner t. Hum Genet. 2001 Jan;108(1):66-71. doi: 10.1007/s004390000432. Hum Genet. 2001. PMID: 11214910

10

Hyperinsulinism in syndromal disorders.

Meissner T, Rabl W, Mohnike K, Scholl S, Santer R, Mayatepek E. Meissner T, et al. Acta Paediatr. 2001 Aug;90(8):856-9. Acta Paediatr. 2001. PMID: 11529530

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