๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Wherefore art thou liver disease associated with alpha- 1 antitrypsin deficiency?

โœ Scribed by Harvey L. Sharp


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
333 KB
Volume
22
Category
Article
ISSN
0270-9139

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Molecular pathogenesis of alpha-1-antitr
โœ David H. Perlmutter; Jeffrey L. Brodsky; William F. Balistreri; Bruce C. Trapnel ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 321 KB

In recent years, we have witnessed several important paradigm shifts in understanding the molecular basis of liver disease in alpha-1-antitrypsin (AT) deficiency. These shifts have become possible as a result of a number of advances in research on the cell biology of aggregation-prone mutant protein

Liver disease in children with pizz ฮฑ1-a
โœ Fayez K. Ghishan; Harry L. Greene ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 446 KB

We present our experience with 18 pediatric patients with a,-antitrypsin deficiency of the PiZZ phenotype. Fifteen patients (83%) presented with neonatal cholestatic jaundice at a mean age of 2 f 0.6 months (2S.D.). The ma1e:female ratio was 15:3, indicating a male predominance. All metabolic, infec

Genetic study of a family with two membe
โœ Clark, Peggy ;Breit, S. N. ;Dawkins, R. L. ;Penny, R. ;Opitz, John M. ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 317 KB ๐Ÿ‘ 1 views

## Abstract Alpha 1 antitrypsin phenotypes and serum levels are presented for a family in which two brothers have Weber Christian disease and ฮฑ1 antitrypsin (PI) Z phenotypes. Clinical histories are described for these two men. A younger brother has the PI Z phenotype but does not have the disease,