Das, A. M., S. Illsinger, H. Hartmann, K. Oehler, B. Bohnhorst, W. N. Kuhn-Velten and T. Lücke (2009). „Prenatal benzoate treatment in urea cycle defects.“ Arch Dis Child Fetal Neonatal Ed 94(3): F216-217.

Hartmann, H., A. M. Das and T. Lücke (2009). „Correspondence (letter to the editor): Risk group includes infants.“ Dtsch Arztebl Int 106(17): 290-291; author reply 291.

Houtkooper, R. H., R. J. Rodenburg, C. Thiels, H. van Lenthe, F. Stet, B. T. Poll-The, J. E. Stone, C. G. Steward, R. J. Wanders, J. Smeitink, W. Kulik and F. M. Vaz (2009). „Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome.“ Anal Biochem 387(2): 230-237.

Illsinger, S., T. Lücke, H. Hartmann, E. Mengel, W. Muller-Forell, F. Donnerstag and A. M. Das (2009). „Scheie syndrome: Enzyme replacement therapy does not prevent progression of cervical myelopathy due to spinal cord compression.“ J Inherit Metab Dis.

Illsinger, S., T. Lücke, B. Vaske, K. H. Schmidt, B. Bohnhorst and A. M. Das (2009). „Developmental changes of oxalate excretion in enterally fed preterm infants.“ J Inherit Metab Dis 32(1): 102-108.

Lücke, T., M. Keiser, S. Illsinger, M. J. Lentze, H. Y. Naim and A. M. Das (2009). „Congenital and putatively acquired forms of sucrase-isomaltase deficiency in infancy: effects of sacrosidase therapy.“ J Pediatr Gastroenterol Nutr 49(4): 485-487.

Meyburg, J., A. M. Das, F. Hoerster, M. Lindner, H. Kriegbaum, G. Engelmann, J. Schmidt, M. Ott, A. Pettenazzo, T. Lücke, H. Bertram, G. F. Hoffmann and A. Burlina (2009). „One liver for four children: first clinical series of liver cell transplantation for severe neonatal urea cycle defects.“ Transplantation 87(5): 636-641.

Sauer, M., B. Meissner, D. Fuchs, B. Gruhn, H. Kabisch, R. Erttmann, M. Suttorp, A. Beilken, T. Lücke, K. Welte, L. Grigull and K. W. Sykora (2009). „Allogeneic blood SCT for children with Hurler’s syndrome: results from the German multicenter approach MPS-HCT 2005.“ Bone Marrow Transplant 43(5): 375-381.

Das, A. M., T. Lücke, U. Meyer, H. Hartmann and S. Illsinger (2010). „Glycogen storage disease type 1: impact of medium-chain triglycerides on metabolic control and growth.“ Ann Nutr Metab 56(3): 225-232.

Heringer, J., S. P. Boy, R. Ensenauer, B. Assmann, J. Zschocke, I. Harting, T. Lücke, E. M. Maier, C. Muhlhausen, G. Haege, G. F. Hoffmann, P. Burgard and S. Kolker (2010). „Use of guidelines improves the neurological outcome in glutaric aciduria type I.“ Ann Neurol 68(5): 743-752.

Hunter, K. B., T. Lücke, J. Spranger, S. F. Smithson, H. Alpay, J. L. Andre, Y. Asakura, R. Bogdanovic, D. Bonneau, R. Cairns, K. Cransberg, S. Frund, H. Fryssira, D. Goodman, K. Helmke, B. Hinkelmann, G. Lama, P. Lamfers, C. Loirat, S. Majore, C. Mayfield, B. F. Pontz, C. Rusu, J. M. Saraiva, B. Schmidt, L. Shoemaker, S. Sigaudy, N. Stajic, D. Taha and C. F. Boerkoel (2010). „Schimke immunoosseous dysplasia: defining skeletal features.“ Eur J Pediatr 169(7): 801-811.

Illsinger, S., N. Janzen, S. Sander, K. H. Schmidt, J. Bednarczyk, L. Mallunat, J. Bode, F. Hagebolling, L. Hoy, T. Lücke, R. Hass and A. M. Das (2010). „Preeclampsia and HELLP syndrome: impaired mitochondrial function in umbilical endothelial cells.“ Reprod Sci 17(3): 219-226.

Illsinger, S., K. H. Schmidt, T. Lücke, B. Vaske, B. Bohnhorst and A. M. Das (2010). „Plasma and urine amino acid pattern in preterm infants on enteral nutrition: impact of gestational age.“ Amino Acids 38(3): 959-972.

Stankov, M. V., T. Lücke, A. M. Das, R. E. Schmidt and G. M. Behrens (2010). „Mitochondrial DNA depletion and respiratory chain activity in primary human subcutaneous adipocytes treated with nucleoside analogue reverse transcriptase inhibitors.“ Antimicrob Agents Chemother 54(1): 280-287.

Witt, L., W. A. Osthaus, T. Lücke, B. Juttner, N. Teich, S. Janisch, A. S. Debertin and R. Sumpelmann (2010). „Safety of glucose-containing solutions during accidental hyperinfusion in piglets.“ Br J Anaesth 105(5): 635-639.

Chobanyan-Jurgens, K., A. J. Fuchs, D. Tsikas, N. Kanzelmeyer, A. M. Das, S. Illsinger, B. Vaske, J. Jordan and T. Lücke (2011). „Increased asymmetric dimethylarginine (ADMA) dimethylaminohydrolase (DDAH) activity in childhood hypercholesterolemia type II.“ Amino Acids epub.

Grigull, L., K. W. Sykora, A. Tenger, H. Bertram, M. Meyer-Marcotty, H. Hartmann, E. Bultmann, A. Beilken, M. Zivicnjak, M. Mynarek, A. W. Osthaus, R. Schilke, K. Kollewe and T. Lücke (2011). „Variable disease progression after successful stem cell transplantation: prospective follow-up investigations in eight patients with Hurler syndrome.“ Pediatr Transplant 15(8): 861-869.

Hartmann, H., A. M. Das and T. Lücke (2011). „Re: Honzik T, Adamovicova A, Smolka V, Magner M, Hruba E, Zeman J. Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B12 deficiency–what have we learned? Eur Jour Ped Neurol 14 (2010) 488-495.“ Eur J Paediatr Neurol 15(4): 377; author reply 378.

Illsinger, S., C. Goken, M. Brockmann, I. Thiemann, J. Bednarczyk, K. H. Schmidt, T. Lücke, L. Hoy, N. Janzen and A. Das (2011). „Effect of tacrolimus on energy metabolism in human umbilical endothelial cells.“ Ann Transplant 16(2): 68-75.

Illsinger, S., N. Janzen, T. Lücke, J. Bednarczyk, K. H. Schmidt, L. Hoy, J. Sander and A. M. Das (2011). „Cyclosporine A: impact on mitochondrial function in endothelial cells.“ Clin Transplant 25(4): 584-593.

Illsinger, S., N. Janzen, S. Sander, J. Bode, L. Mallunat, R. Thomasmeyer, F. Hagebolling, K. H. Schmidt, J. Bednarczyk, B. Vaske, T. Lücke and A. M. Das (2011). „Energy metabolism in umbilical endothelial cells from preterm and term neonates.“ J Perinat Med 39(5): 587-593.

Janzen, N., S. Illsinger, U. Meyer, Y. S. Shin, J. Sander, T. Lücke and A. M. Das (2011). „Early Cataract Formation Due to Galactokinase Deficiency: Impact of Newborn Screening.“ Arch Med Res 42(7): 608-612.

Kanzelmeyer, N., D. Tsikas, K. Chobanyan-Jurgens, B. Beckmann, B. Vaske, S. Illsinger, A. M. Das and T. Lücke (2011). „Asymmetric dimethylarginine in children with homocystinuria or phenylketonuria.“ Amino Acids epub.

Lücke, T., S. Illsinger, A. Jensen, A. M. Das, H. Hartmann, K. W. Sykora, M. Mynarek and L. Grigull (2011). „Das Therapieverfahren der Stammzelltransplantation aus der Sicht des Neuropädiaters.“ Neuropädiatrie in Klinik und Praxis 10(4): 108-120.

Mynarek, M., J. Tolar, M. H. Albert, M. L. Escolar, J. J. Boelens, M. J. Cowan, N. Finnegan, A. Glomstein, D. A. Jacobsohn, J. S. Kuhl, H. Yabe, J. Kurtzberg, D. Malm, P. J. Orchard, C. Klein, T. Lücke and K. W. Sykora (2011). „Allogeneic hematopoietic SCT for alpha-mannosidosis: an analysis of 17 patients.“ Bone Marrow Transplant.

Thiel, C., N. Rind, D. Popovici, G. F. Hoffmann, K. Hanson, R. L. Conway, C. R. Adamski, E. Butler, R. Scanlon, M. Lambert, N. Apeshiotis, C. Thiels, G. Matthijs and C. Korner (2011). „Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip.“ Hum Mutat.

Grapp, M., I. A. Just, T. Linnankivi, P. Wolf, T. Lücke, M. Hausler, J. Gartner and R. Steinfeld (2012). „Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiency.“ Brain.