Document Detail

Genetic studies in etiologically different chronic liver diseases
MedLine Citation:
PMID:  3788223     Owner:  NLM     Status:  MEDLINE    
In 198 patients with chronic liver diseases of different etiology 16 genetic feature systems were investigated (blood groups, erythrocytic enzymes, immunoglobulin allotypes, proteins). In comparison to a representative normal population significant differences of the frequency of the distribution of phenotypes of various systems were found. In these cases is remarkable that association between genetic markers and hepatopathies were above all proved in their classification according to etiopathogenetic criteria. We evaluate our findings as a reference to the importance of genetic factors in the development of chronic liver diseases.
R Nilius; W Schmidt; E Scheibe; B Zipprich; D Kämpfe; N Schulz
Publication Detail:
Type:  English Abstract; Journal Article    
Journal Detail:
Title:  Zeitschrift für die gesamte innere Medizin und ihre Grenzgebiete     Volume:  41     ISSN:  0044-2542     ISO Abbreviation:  Z Gesamte Inn Med     Publication Date:  1986 Sep 
Date Detail:
Created Date:  1987-01-08     Completed Date:  1987-01-08     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  21730470R     Medline TA:  Z Gesamte Inn Med     Country:  GERMANY, EAST    
Other Details:
Languages:  ger     Pagination:  482-5     Citation Subset:  IM    
Vernacular Title:
Genetische Untersuchungen bei ätiologisch unterschiedlichen chronischen Leberkrankheiten.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Blood Group Antigens / genetics
Chronic Disease
Haptoglobins / genetics
Immunoglobulin Allotypes / genetics
Liver Diseases / genetics*
Reg. No./Substance:
0/Blood Group Antigens; 0/Haptoglobins; 0/Immunoglobulin Allotypes

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  The characteristics of acute renal failure in cardiogenic shock in the elderly.
Next Document:  Effect of various sclerosing drugs on the rat esophagus