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Geburtshilfe Und Frauenheilkunde|November 1, 1990
[Alpha-thalassemia as a rare differential diagnosis of hydrops fetalis et placentae]A Luttkus, E Kattner, E U GrieseJournal of Cancer Research and Clinical Oncology|January 1, 1994
Competitive nested polymerase chain reaction for quantification of human MDR1 gene expressionF Grünebach, E U Griese, K SchumacherNaunyn-Schmiedeberg'S Archives of Pharmacology|October 1, 1994
A missense mutation in exon 6 of the CYP2D6 gene leading to a histidine 324 to proline exchange is associated with the poor metabolizer phenotype of sparteineB Evert, E U Griese, M EichelbaumHuman Genetics|January 1, 1985
Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected familiesE U Griese, E Kohne, J HorstHuman Genetics|January 1, 1985
Detection of a restriction site polymorphism within the human alpha-globin gene complexG Assum, E U Griese, J HorstHuman Genetics|January 1, 1984
Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German familiesJ Horst, E U Griese, E Kleihauer, et al.Clinical Pharmacology and Therapeutics|October 1, 1995
Dihydrocodeine: a new opioid substrate for the polymorphic CYP2D6 in humansM F Fromm, U Hofmann, E U Griese, et al.British Journal of Clinical Pharmacology|October 6, 1999
Pharmacokinetics of dihydrocodeine and its active metabolite after single and multiple oral dosingS Ammon, U Hofmann, E U Griese, et al.Pediatric Research|February 7, 2001
Telomeres in neonates: new insights in fetal hematopoiesisU Friedrich, M Schwab, E U Griese, et al.Clinical Neuropharmacology|May 14, 1998
Interaction of modafinil and clomipramine as comedication in a narcoleptic patientM Grözinger, S Härtter, C Hiemke, et al.Pageof 3