Literature DB >> 16695698

STUDIES OF COPROPORPHYRIN. III. IDIOPATHIC COPROPORPHYRINURIA; A HITHERTO UNRECOGNIZED FORM CHARACTERIZED BY LACK OF SYMPTOMS IN SPITE OF THE EXCRETION OF LARGE AMOUNTS OF COPROPORPHYRIN.

C J Watson1, S Schwartz, W Schulze, L O Jacobson, R Zagaria.   

Abstract

Entities:  

Year:  1949        PMID: 16695698      PMCID: PMC439622          DOI: 10.1172/JCI102091

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


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  2 in total

1.  CONCERNING THE NATURALLY OCCURRING PORPHYRINS: I. The Isolation of Coproporphyrin I from the Urine in a Case of Cincophen Cirrhosis.

Authors:  C J Watson
Journal:  J Clin Invest       Date:  1935-01       Impact factor: 14.808

2.  STUDIES OF COPROPORPHYRIN. I. THE PER DIEM EXCRETION AND ISOMER DISTRIBUTION OF COPROPORPHYRIN IN NORMAL HUMAN URINE.

Authors:  C J Watson; V Hawkinson; S Schwartz; D Sutherland
Journal:  J Clin Invest       Date:  1949-05       Impact factor: 14.808

  2 in total
  9 in total

1.  [New data on porphyrin metabolism and porphyrin diseases].

Authors:  W STICH
Journal:  Klin Wochenschr       Date:  1959-07-01

2.  Hereditary coproporphyria.

Authors:  H BERGER; A GOLDBERG
Journal:  Br Med J       Date:  1955-07-09

3.  Normal human urinary porphyrins.

Authors:  A COMFORT; H MOORE; M WEATHERALL
Journal:  Biochem J       Date:  1954-10       Impact factor: 3.857

Review 4.  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

5.  Hereditary coproporphyria with acute intermittent manifestations.

Authors:  H D Barnes; N Whittaker
Journal:  Br Med J       Date:  1965-11-06

6.  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

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

Review 8.  [Neurocutaneous porphyrias].

Authors:  J Frank
Journal:  Hautarzt       Date:  2016-03       Impact factor: 0.751

9.  Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria.

Authors:  J L Hawk; I A Magnus; A Parkes; G H Elder; M Doyle
Journal:  J R Soc Med       Date:  1978-10       Impact factor: 18.000

  9 in total

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