Literature DB >> 5630168

The porphyrias: a genetic problem.

J Waldenström, B Haeger-Aronsen.   

Abstract

Mesh:

Year:  1967        PMID: 5630168     DOI: 10.1016/b978-1-4831-6757-2.50006-3

Source DB:  PubMed          Journal:  Prog Med Genet        ISSN: 0079-6441


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  5 in total

1.  Porphyria variegata and porphyria cutanea tarda in siblings: chemical and genetic aspects.

Authors:  C J Watson; R A Cardinal; I Bossenmaier; Z J Petryka
Journal:  Proc Natl Acad Sci U S A       Date:  1975-12       Impact factor: 11.205

Review 2.  The porphyrias: a review.

Authors:  G H Elder; C H Gray; D C Nicholson
Journal:  J Clin Pathol       Date:  1972-12       Impact factor: 3.411

3.  Decreased red cell uroporphyrinogen I synthetase activity in intermittent acute porphyria.

Authors:  L J Strand; U A Meyer; B F Felsher; A G Redeker; H S Marver
Journal:  J Clin Invest       Date:  1972-10       Impact factor: 14.808

4.  An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.

Authors:  J P Kushner; A J Barbuto; G R Lee
Journal:  J Clin Invest       Date:  1976-11       Impact factor: 14.808

5.  Heme biosynthesis in intermittent acute prophyria: decreased hepatic conversion of porphobilinogen to porphyrins and increased delta aminolevulinic acid synthetase activity.

Authors:  L J Strand; B F Felsher; A G Redeker; H S Marver
Journal:  Proc Natl Acad Sci U S A       Date:  1970-11       Impact factor: 11.205

  5 in total

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