✦ LIBER ✦

Pharmacogenetics of mephenytoin: A new drug hydroxylation polymorphism in man

✍ Scribed by A. Küpfer; R. Preisig

Publisher: Springer
Year: 1984
Tongue: English
Weight: 972 KB
Volume: 26
Category: Article
ISSN: 0031-6970
DOI: 10.1007/bf00541938

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Analysis of mephenytoin, 4-hydroxymephen

Analysis of mephenytoin, 4-hydroxymephenytoin and 4-hydroxyphenytoin enantiomers in human urine by cyclodextrin micellar electrokinetic capillary chromatography: Simple determination of a hydroxylation polymorphism in man

✍ Claudia Desiderio; Salvatore Fanali; Adrian Küpfer; Dr. Wolfgang Thormann 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 649 KB

Defective N-oxidation of sparteine in ma

Defective N-oxidation of sparteine in man: A new pharmacogenetic defect

✍ M. Eichelbaum; N. Spannbrucker; Barbara Steincke; H. J. Dengler 📂 Article 📅 1979 🏛 Springer 🌐 English ⚖ 558 KB

Genetics of humanS-adenosylhomocysteine

Genetics of humanS-adenosylhomocysteine hydrolase. A new polymorphism in man

✍ S. Bissbort; K. Bender; T. F. Wienker; K. H. Grzeschik 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 405 KB

Pharmacokinetics in man of a new antiarr

Pharmacokinetics in man of a new antiarrhythmic drug, cibenzoline

✍ M. Canal; B. Flouvat; D. Tremblay; A. Dufour 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 676 KB

Relevance of genetic polymorphism in dru

Relevance of genetic polymorphism in drug metabolism in the development of new drugs

✍ L. P. Balant; U. Gundert-Remy; A. R. Boobis; Ch. Bahr 📂 Article 📅 1989 🏛 Springer 🌐 English ⚖ 483 KB

Polymorphism of red cell glyoxalase I (E

Polymorphism of red cell glyoxalase I (E.C.: 4.4.1.5). A new genetic marker in man

✍ J. Kömpf; S. Bissbort; S. Gussmann; H. Ritter 📂 Article 📅 1975 🏛 Springer 🌐 English ⚖ 151 KB

The polymorphism of glyoxalase I was investigated in 169 mother-child combinations from southwestern Germany. Glyoxalase I (GLO) has 3 common phenotypes: GLO 1, GLO 2-1, and GLO 2. The results are in good agreement with the formal hypothesis: Two alleles GLO1 and GLO2 at an autosomal locus. The GLO1