Trefz KF - Search Results

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Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims data.

Trefz KF, Muntau AC, Kohlscheen KM, Altevers J, Jacob C, Braun S, Greiner W, Jha A, Jain M, Alvarez I, Lane P, Schröder C, Rutsch F. Trefz KF, et al. Orphanet J Rare Dis. 2019 Jul 22;14(1):181. doi: 10.1186/s13023-019-1153-y. Orphanet J Rare Dis. 2019. PMID: 31331350 Free PMC article.

Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase gene.

Seidel J, Streck S, Bellstedt K, Vianey-Saban C, Pedersen CB, Vockley J, Korall H, Roskos M, Deufel T, Trefz KF, Sewell AC, Kauf E, Zintl F, Lehnert W, Gregersen N. Seidel J, et al. Among authors: trefz kf. J Inherit Metab Dis. 2003;26(1):37-42. doi: 10.1023/a:1024019311933. J Inherit Metab Dis. 2003. PMID: 12872838

Indolic tryptophan metabolism in uraemia.

Byrd DJ, Berthold HW, Trefz KF, Kochen W, Gilli G, Schärer K, Schüler HW, Asbach HW. Byrd DJ, et al. Among authors: trefz kf. Proc Eur Dial Transplant Assoc. 1976;12:347-54. Proc Eur Dial Transplant Assoc. 1976. PMID: 935125

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