Lücke T - Search Results

1

Glutaric aciduria type I: pathomechanisms of neurodegeneration.

Ullrich K, Flott-Rahmel B, Schluff P, Musshoff U, Das A, Lücke T, Steinfeld R, Christensen E, Jakobs C, Ludolph A, Neu A, Röper R. Ullrich K, et al. Among authors: lucke t. J Inherit Metab Dis. 1999 Jun;22(4):392-403. doi: 10.1023/a:1005595921323. J Inherit Metab Dis. 1999. PMID: 10407776

2

Glutaric aciduria I: creatine supplementation restores creatinephosphate levels in mixed cortex cells from rat incubated with 3-hydroxyglutarate.

Das AM, Lücke T, Ullrich K. Das AM, et al. Among authors: lucke t. Mol Genet Metab. 2003 Feb;78(2):108-11. doi: 10.1016/s1096-7192(02)00227-5. Mol Genet Metab. 2003. PMID: 12618082

3

Mitochondrial function in schimke-immunoosseous dysplasia.

Lücke T, Ehrich JH, Das AM. Lücke T, et al. Metab Brain Dis. 2005 Sep;20(3):237-42. doi: 10.1007/s11011-005-7211-7. Metab Brain Dis. 2005. PMID: 16167201

4

Developmental changes of oxalate excretion in enterally fed preterm infants.

Illsinger S, Lücke T, Vaske B, Schmidt KH, Bohnhorst B, Das AM. Illsinger S, et al. Among authors: lucke t. J Inherit Metab Dis. 2009 Feb;32(1):102-8. doi: 10.1007/s10545-008-1024-5. Epub 2008 Dec 12. J Inherit Metab Dis. 2009. PMID: 19067228

5

Scheie syndrome: enzyme replacement therapy does not prevent progression of cervical myelopathy due to spinal cord compression.

Illsinger S, Lücke T, Hartmann H, Mengel E, Müller-Forell W, Donnerstag F, Das AM. Illsinger S, et al. Among authors: lucke t. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S321-5. doi: 10.1007/s10545-009-1265-y. Epub 2009 Nov 4. J Inherit Metab Dis. 2009. PMID: 19894140

6

3-methylglutaconic aciduria type I in a boy with fever-associated seizures.

Illsinger S, Lücke T, Zschocke J, Gibson KM, Das AM. Illsinger S, et al. Among authors: lucke t. Pediatr Neurol. 2004 Mar;30(3):213-5. doi: 10.1016/j.pediatrneurol.2003.09.016. Pediatr Neurol. 2004. PMID: 15033206

7

Low lysine diet in glutaric aciduria type I--effect on anthropometric and biochemical follow-up parameters.

Boy N, Haege G, Heringer J, Assmann B, Mühlhausen C, Ensenauer R, Maier EM, Lücke T, Hoffmann GF, Müller E, Burgard P, Kölker S. Boy N, et al. Among authors: lucke t. J Inherit Metab Dis. 2013 May;36(3):525-33. doi: 10.1007/s10545-012-9517-7. Epub 2012 Sep 13. J Inherit Metab Dis. 2013. PMID: 22971958 Clinical Trial.

8

Fabry disease: reduced activities of respiratory chain enzymes with decreased levels of energy-rich phosphates in fibroblasts.

Lücke T, Höppner W, Schmidt E, Illsinger S, Das AM. Lücke T, et al. Mol Genet Metab. 2004 May;82(1):93-7. doi: 10.1016/j.ymgme.2004.01.011. Mol Genet Metab. 2004. PMID: 15110329

9

Elevated plasma concentrations of the endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine in citrullinemia.

Lücke T, Tsikas D, Kanzelmeyer N, Vaske B, Das AM. Lücke T, et al. Metabolism. 2006 Dec;55(12):1599-603. doi: 10.1016/j.metabol.2006.07.020. Metabolism. 2006. PMID: 17142130

10

Developmental changes in the L-arginine/nitric oxide pathway from infancy to adulthood: plasma asymmetric dimethylarginine levels decrease with age.

Lücke T, Kanzelmeyer N, Kemper MJ, Tsikas D, Das AM. Lücke T, et al. Clin Chem Lab Med. 2007;45(11):1525-30. doi: 10.1515/CCLM.2007.300. Clin Chem Lab Med. 2007. PMID: 17892438

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