Literature DB >> 12994898

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

I H SCHEINBERG, D GITLIN.   

Abstract

Entities:  

Keywords:  BLOOD PROTEINS; HEPATOLENTICULAR DEGENERATION/blood in

Mesh:

Substances:

Year:  1952        PMID: 12994898     DOI: 10.1126/science.116.3018.484

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


× No keyword cloud information.
  81 in total

1.  Wilson's Disease.

Authors: 
Journal:  Curr Treat Options Gastroenterol       Date:  1999-02

2.  ABSORPTION OF COPPER IN MALABSORPTION SYNDROMES.

Authors:  I STERNLIEB; H D JANOWITZ
Journal:  J Clin Invest       Date:  1964-06       Impact factor: 14.808

3.  [A CONTRIBUTION TO WILSON'S DISEASE FROM A CLINICAL AND MORPHOLOGICAL VIEWPOINT].

Authors:  R SCHEDIFKA; A TENNSTEDT
Journal:  Dtsch Z Nervenheilkd       Date:  1964-07-06

4.  [PROTEIN-CHEMICAL AND IMMUNOLOGIC STUDIES IN PATIENTS WITH SKIN DISEASES].

Authors:  G BREHM
Journal:  Arch Klin Exp Dermatol       Date:  1965-01-13

5.  [Disorders of copper and amino acid metabolism in hepato-cerebral degeneration and their treatment with BAL].

Authors:  J STEGER; R STEGER
Journal:  Dtsch Z Nervenheilkd       Date:  1954

6.  Blood copper and its relationship to the globulins.

Authors:  J N CUMINGS; H J GOODWIN; C J EARL
Journal:  J Clin Pathol       Date:  1955-02       Impact factor: 3.411

7.  [Clinical significance of the relations between iron and protein metabolism].

Authors:  F WUHRMANN; B JASINSKI
Journal:  Klin Wochenschr       Date:  1955-02-01

8.  Copper metabolism and the liver.

Authors:  J M WALSHE
Journal:  Postgrad Med J       Date:  1963-04       Impact factor: 2.401

9.  Ceruloplasmin reduces the adhesion and scavenges superoxide during the interaction of activated polymorphonuclear leukocytes with endothelial cells.

Authors:  C Broadley; R L Hoover
Journal:  Am J Pathol       Date:  1989-10       Impact factor: 4.307

Review 10.  Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

Authors:  P de Bie; P Muller; C Wijmenga; L W J Klomp
Journal:  J Med Genet       Date:  2007-08-23       Impact factor: 6.318

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.