Plumboporphyria (ALAD deficiency) in a lead worker: a scenario for potential diagnostic confusion.

Author:

Dyer J,Garrick D P,Inglis A,Pye I F

Publisher

BMJ

Subject

Public Health, Environmental and Occupational Health

Reference9 articles.

1. Modified erythrocyte uroporphyrinogen. I synthase assay, and its clinical interpretation;Piepkorn, M.W.; Hamemyik, P.; Labbe, R.F.;Clin Chem,1978

2. A study of the determination of a ALA dehydratase activity in haemolysates of human erythrocytes;Collier, H.B.;Clin Biochem,1971

3. Determination of lead in blood using electrothermal atomisation atomic absorption spectrometry with a l'vov platform and matrix modifier;Miller, D.T.; Paschal, D.C.; Gunter, E.W.; Stroud, P.E.; D'Angelo, J.;Analyst,1987

4. New type of hepatic porphyria with porphobilinogen synthase defect and intermittent acute clinical manifestation;Doss, M.; von Tiepermann, R.; Schneider, J.; Schmid, H.;Klin Wochenschr,1979

5. Lead poisoning in inherited 8-aminolevulinic acid dehydratase deficiency;Doss, M.; Laubenthal, F.; Stoeppler, M.;Int Arch Occup Environ Health,1984

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