Zobrazeno 1 - 10
of 118
pro vyhledávání: '"O, Borud"'
Publikováno v:
Acta Pharmacologica et Toxicologica. 31:540-549
Urine from germ-free and normal rats were investigated both before and after oral L-DOPA administration. Two neutral L-DOPA metabolites were tentatively identified as (N-acetyl)-3-methoxy-4-hydroxyphenylethylamine and 3-methoxy-4-hydroxyphenylethanol
Publikováno v:
Acta Pharmacologica et Toxicologica. 30:185-192
Rat urines were investigated for phenolic acids, phenolic amines and neutral phenolic compounds while under dietary control, and also after the oral administration of L-DOPA. Germ-free, mono-associated and conventional rats were used. No major differ
Publikováno v:
Acta Pharmacologica et Toxicologica. 33:308-316
Urine and faeces of rats were investigated for phenolic compounds after oral administration of 14C-L-DOPA. Germ-free and conventional rats were used. The urinary radioactive metabolites detected were: 3-methoxy-4-hydroxyphenylethylamine, 3-methoxy-4-
Publikováno v:
Journal of Intellectual Disability Research. 31:299-301
This article describes a profoundly mentally retarded woman with spastic tetraplegia, deafness and abnormal liver function tests with a secondary Cystathioninuria. The Cystathioninuria could be corrected with vitamin B6 supplementation.
Publikováno v:
Ultrastructural Pathology. 16:263-275
From 1986 to 1991, 472 muscle biopsy specimens from patients from different hospitals in Norway were examined. Of these, 364 were embedded for electron microscopy, and 194 were examined with electron microscopy. Ultrastructural alterations in the mit
Publikováno v:
International journal of cancer. 88(3)
Glutathione plays an important role in drug resistance of tumor cells and in their ability to resist oxidative stress. Improved salvage of glutathione can be obtained through increased activity of gamma-glutamyltransferase (GGT), which is of importan
Autor:
Shimpei Tada, E.N.H. Jansen, U. Harte, A. Engelhardt, G. Nappi, Juan A. Vargas, Sigurd Lindal, Nezihe Ertekin, Emilia Martignoni, J. Aasly, Masao Honda, Claudio Pacchetti, Ariel Villagra, F. Grahmann, Cumhur Ertekin, O. Borud, A. Goldfarb, T. Torbergsen, Svein Ivar Mellgren, Tapani Kallanranta, Sait Almis, D. Städt, R. Heun, A.R. Rozeboom, Yuhichi Hata, E. Rohrbach, L. Sibilla, Hiroshi Tsukagoshi, Atsuo Ishimoto, Helinä Mononen, A. Mendelowitsch, E. Rosenmann, Ludwig Kappos, P.F. Ippel, Sadayoshi Ohbu, Y. Shapira, Masayuki Ikeda, Martti Lepojärvi, M. Ratzka, B. Glick, Bernhard Neundörfer, A. Finsterbush, Elena Rodríguez, E.W. Radue, Antonio García-Merino, Hiroyuki Fukuda, M. Turla, G. Hageman, P. Bruggi, Otmar Gratzl
Publikováno v:
European Neurology. 30:356-358
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 83(9)
Using high pressure liquid chromatography on strong cation exchange column, we analyzed capillary blood from 141 healthy full-term newborns for lactate and pyruvate concentrations. Total range of lactate was 367-3245 mumol/l and reference interval (m
Publikováno v:
Journal of medical genetics. 31(5)
Aspartylglucosaminuria (AGU, McKusick 208400) is an autosomal recessive lysosomal storage disorder. Ninety percent of all patients are from Finland and only sporadic cases have been reported from elsewhere. In northern Norway, however, nine patients