Literature DB >> 5667765

Hereditary coproporphyria. Study of a Swedish family.

B Haeger-Aronsen, G Stathers, G Swahn.   

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Year:  1968        PMID: 5667765     DOI: 10.7326/0003-4819-69-2-221

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


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  8 in total

1.  Aucte intermittent porphyria and epilepsy.

Authors:  R Biagini; R Tignani; A R Fifi; L Nappini
Journal:  Arch Dis Child       Date:  1979-08       Impact factor: 3.791

2.  Catecholamine uptake, accumulation, and release in acute porphyria.

Authors:  M F Beal; N O Atuk; T C Westfall; S M Turner
Journal:  J Clin Invest       Date:  1977-11       Impact factor: 14.808

Review 3.  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

4.  Production and characterization of erythropoietic protoporphyric heterodimeric ferrochelatases.

Authors:  Wided Najahi-Missaoui; Harry A Dailey
Journal:  Blood       Date:  2005-04-14       Impact factor: 22.113

5.  Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.

Authors:  M Doss; R von Tiepermann; K H Pflüger
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

6.  Hereditary coproporphyria: unusual nervous system involvement in two cases.

Authors:  C Casali; M Lo Monaco; L D'Alessandro; D Griso; A Amantea; G C Topi; P Tonali
Journal:  J Neurol       Date:  1984       Impact factor: 4.849

7.  Hereditary coproporphyria: incidence in a large English family.

Authors:  J Andrews; H Erdjument; D C Nicholson
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

8.  Hereditary coproporphyria and epilepsy.

Authors:  A B Houston; M J Brodie; M R Moore; G G Thompson; J B Stephenson
Journal:  Arch Dis Child       Date:  1977-08       Impact factor: 3.791

  8 in total

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