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Molecular and functional characterisation of mild MCAD deficiency.
Zschocke J, Schulze A, Lindner M, Fiesel S, Olgemöller K, Hoffmann GF, Penzien J, Ruiter JP, Wanders RJ, Mayatepek E. Zschocke J, et al. Among authors: lindner m. Hum Genet. 2001 May;108(5):404-8. doi: 10.1007/s004390100501. Hum Genet. 2001. PMID: 11409868
Emergency management of inherited metabolic diseases.
Prietsch V, Lindner M, Zschocke J, Nyhan WL, Hoffmann GF. Prietsch V, et al. Among authors: lindner m. J Inherit Metab Dis. 2002 Nov;25(7):531-46. doi: 10.1023/a:1022040422590. J Inherit Metab Dis. 2002. PMID: 12638937 Review.
Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.
Schulze-Bergkamen A, Okun JG, Spiekerkötter U, Lindner M, Haas D, Kohlmüller D, Mayatepek E, Schulze-Bergkamen H, Greenberg CR, Zschocke J, Hoffmann GF, Kölker S. Schulze-Bergkamen A, et al. Among authors: lindner m. Pediatr Res. 2005 Nov;58(5):873-80. doi: 10.1203/01.PDR.0000181378.98593.3E. Epub 2005 Sep 23. Pediatr Res. 2005. PMID: 16183823
636 results