Načítá se...

α(1) Antitrypsin deficiency and liver disease in childhood: genetic, immunochemical, histological, and ultrastructural diagnosis

α(1) Antitrypsin deficiency is a significant factor in the pathogenesis of neonatal cholestasis and progressive juvenile cirrhosis. The diagnosis may be suggested by the liver biopsy appearances and confirmed by immunochemical analysis of the serum. Genetic counselling of affected families is of imp...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Milford, A., Underwood, J. C. E.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1974
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC478157/
https://ncbi.nlm.nih.gov/pubmed/4212921
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!