Family evaluations in acute intermittent porphyria using red cell uroporphyrinogen I synthetase.-Reference-Cited by-同舟云学术

Family evaluations in acute intermittent porphyria using red cell uroporphyrinogen I synthetase.

Published:1979-04-01 Issue:2 Volume:16 Page:134-139
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Lamon J M,Frykholm B C,Tschudy D P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. Evaluation of kindreds with acute intermittent porphyria: progress and problems;Bonkowsky, H.L.; Bottomley, S.S.;Clinical Research,1977

2. Porphyrin synthesis and mitochondrial respiration in acute intermittent porphyria. Studies using cultured human fibroblasts;Bonkowsky, H.L.; Tschudy, D.P.; Weinbach, E.C.; Ebert, P.S.; Doherty, J.M.;Journal ofLaboratory and Clinical Medicine,1975

3. Urinary 8-aminolaevulinic acid andporphobilinogen in different types of porphyria;Haeger-Aronsen, B.;Lancet,1958

4. A red cell enzyme method for the diagnosis of acute intermittent porphyria;Magnussen, C.R.; Levine, J.B.; Doherty, J.M.; Chessman, J.O.; Tschudy, D.P.;Blood,1974

5. The determination of aminoketones in biological fluids;Marver, H.S.; Tschudy, D.P.; Perlroth, M.G.; Collins, A.; Hunter, Jr, G.;Analytical Biochemistry,1966

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