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Scandinavian Journal of Clinical and Laboratory Investigation|February 24, 2001
Porphyrins, porphyrin metabolism and porphyrias. II. Diagnosis and monitoring in the acute porphyriasS Thunell, P Harper, A Brock, et al.Physiological Research|February 15, 2007
The difficult clinical diagnosis of erythropoietic protoporphyriaS Wahlin, Y Floderus, A-M Ros, et al.Human Genetics|August 1, 1988
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyriaJ S Lee, M Anvret, J Lindsten, et al.Lakartidningen|August 13, 1998
[Porphyria cutanea tarda is the most common type of porphyria. Medical control is a team work]P Harper, S Thunell, R Hultcrantz, et al.Journal of Medical Genetics|December 1, 1995
Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyriaG Lundin, J Hashemi, Y Floderus, et al.Blood|May 9, 2001
Highly heterogeneous nature of delta-aminolevulinate dehydratase (ALAD) deficiencies in ALAD porphyriaM Maruno, K Furuyama, R Akagi, et al.Journal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.Lakartidningen|July 29, 1998
[Risk of liver failure in erythropoietic protoporphyria. Be alert for sings of cholestatic development!]P Harper, S Thunell, B G Ericzon, et al.Physiological Research|February 15, 2007
(Far) Outside the box: genomic approach to acute porphyriaS ThunellJournal of Chromatography|January 11, 1977
Thin-layer chromatographic procedure for the detection, isolation and identification of basic psychotropic drugs in urineS ThunellPageof 32