Literature DB >> 744295

Relationships between acute hepatic porphyrias due to genetic variability of primary enzyme defects and limiting function of uroporphyrinogen synthase.

M Doss.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 744295     DOI: 10.1016/0020-711x(78)90069-1

Source DB:  PubMed          Journal:  Int J Biochem        ISSN: 0020-711X


× No keyword cloud information.
  11 in total

1.  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

Review 2.  Erythropoietic and hepatic porphyrias.

Authors:  U Gross; G F Hoffmann; M O Doss
Journal:  J Inherit Metab Dis       Date:  2000-11       Impact factor: 4.982

3.  Lead poisoning in inherited delta-aminolevulinic acid dehydratase deficiency.

Authors:  M Doss; F Laubenthal; M Stoeppler
Journal:  Int Arch Occup Environ Health       Date:  1984       Impact factor: 3.015

4.  A molecular, enzymatic and clinical study in a family with hereditary coproporphyria.

Authors:  U Gross; H Puy; U Meissauer; J Lamoril; J C Deybach; M Doss; Y Nordmann; M O Doss
Journal:  J Inherit Metab Dis       Date:  2002-08       Impact factor: 4.982

5.  The "glucose effect" in acute hepatic porphyrias and in experimental porphyria.

Authors:  M Doss; F Verspohl
Journal:  Klin Wochenschr       Date:  1981-07-01

6.  Correction of the biochemical defect in porphobilinogen deaminase deficient cells by non-viral gene delivery.

Authors:  Annika Johansson; Christer Möller; Pauline Harper
Journal:  Mol Cell Biochem       Date:  2003-08       Impact factor: 3.396

7.  Porphobilinogen-synthase (delta-aminolevulinic acid dehydratase) deficiency in bone marrow cells of two patients with porphobilinogen-synthase defect acute porphyria.

Authors:  M Doss; R V Tiepermann; J Schneider
Journal:  Klin Wochenschr       Date:  1983-07-15

8.  Hereditary prophobilinogen synthase deficiency in human associated with acute hepatic porphyria.

Authors:  A Brandt; M Doss
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Conversion of 5-aminolaevulinate into haem by liver homogenates. Comparison of rat and chick embryo.

Authors:  J F Healey; H L Bonkowsky; P R Sinclair; J F Sinclair
Journal:  Biochem J       Date:  1981-09-15       Impact factor: 3.857

10.  Persistent protoporphyrinemia in hereditary porphobilinogen synthase (delta-aminolevulinic acid dehydrase) deficiency under low lead exposure. A new molecular basis for the pathogenesis of lead intoxication.

Authors:  M Doss; U Becker; F Sixel; S Geisse; H Solcher; J Schneider; G Kufner; H Schlegel; M Stoeppler
Journal:  Klin Wochenschr       Date:  1982-06-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.