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Y Floderus

Showing results (11-20 of 34) with videos related to

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Lakartidningen|July 23, 1998
[Porphyria--a metabolic mine field]Y Floderus, P Harper, A Henrichson, et al.
Clinical Genetics|January 15, 2011
Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyriaM Barbaro, M Kotajärvi, P Harper, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 24, 2001
The W198X and R173W mutations in the porphobilinogen deaminase gene in acute intermittent porphyria have higher clinical penetrance than R167W. A population-based studyC Andersson, Y Floderus, A Wikberg, et al.
Upsala Journal of Medical Sciences|January 1, 1981
Catechol-O-methyltransferase activity in human erythrocytes: methodological aspectsY Floderus, J Sääf, S B Ross, et al.
Biochemical Pharmacology|November 4, 2010
Ionic influence on human erythrocyte catechol-O-methyltransferase activityY Floderus, J Sääf, S B Ross, et al.
Clinical Genetics|December 1, 1983
Genetic regulation of the red cell uroporphyrinogen-I-synthetase level in families with acute intermittent porphyriaL Wetterberg, Y Floderus, S Thunell, et al.
Clinical Genetics|February 1, 1985
The dysequilibrium syndrome: a study of the etiology and pathogenesisF Rasmussen, K H Gustavson, V R Sara, et al.
Journal of Internal Medicine|May 19, 2004
Enrichment of HFE mutations in Swedish patients with familial and sporadic form of porphyria cutanea tardaP Harper, Y Floderus, P Holmström, et al.
Lakartidningen|July 29, 1998
[Prevention of acute intermittent porphyria is the best solution. Most important are early diagnosis and counseling]Y Floderus, P Harper, A Henrichson, et al.
Physiological Research|February 15, 2007
The difficult clinical diagnosis of erythropoietic protoporphyriaS Wahlin, Y Floderus, A-M Ros, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Lakartidningen|July 23, 1998
[Porphyria--a metabolic mine field]Y Floderus, P Harper, A Henrichson, et al.
Clinical Genetics|January 15, 2011
Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyriaM Barbaro, M Kotajärvi, P Harper, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 24, 2001
The W198X and R173W mutations in the porphobilinogen deaminase gene in acute intermittent porphyria have higher clinical penetrance than R167W. A population-based studyC Andersson, Y Floderus, A Wikberg, et al.
Upsala Journal of Medical Sciences|January 1, 1981
Catechol-O-methyltransferase activity in human erythrocytes: methodological aspectsY Floderus, J Sääf, S B Ross, et al.
Biochemical Pharmacology|November 4, 2010
Ionic influence on human erythrocyte catechol-O-methyltransferase activityY Floderus, J Sääf, S B Ross, et al.
Clinical Genetics|December 1, 1983
Genetic regulation of the red cell uroporphyrinogen-I-synthetase level in families with acute intermittent porphyriaL Wetterberg, Y Floderus, S Thunell, et al.
Clinical Genetics|February 1, 1985
The dysequilibrium syndrome: a study of the etiology and pathogenesisF Rasmussen, K H Gustavson, V R Sara, et al.
Journal of Internal Medicine|May 19, 2004
Enrichment of HFE mutations in Swedish patients with familial and sporadic form of porphyria cutanea tardaP Harper, Y Floderus, P Holmström, et al.
Lakartidningen|July 29, 1998
[Prevention of acute intermittent porphyria is the best solution. Most important are early diagnosis and counseling]Y Floderus, P Harper, A Henrichson, et al.
Physiological Research|February 15, 2007
The difficult clinical diagnosis of erythropoietic protoporphyriaS Wahlin, Y Floderus, A-M Ros, et al.
Pageof 4