نتایج جستجو برای: 1 antitrypsin deficiency

تعداد نتایج: 2853876  

Journal: :Archives of internal medicine 1983
N D Phung R J Harbeck C Helbling-Muntges

2007
Dawn L DeMeo Robert A Sandhaus Alan F Barker Mark L Brantly Edward Eden Gerard McElvaney Stephen Rennard Esteban Burchard James M Stocks James K Stoller Charlie Strange Gerard M Turino Edward J Campbell Edwin K Silverman

Dawn L DeMeo, Robert A Sandhaus, Alan F Barker, Mark L Brantly, Edward Eden, N Gerard McElvaney, Stephen Rennard, Esteban Burchard, James M Stocks, James K Stoller, Charlie Strange, Gerard M Turino, Edward J Campbell, Edwin K Silverman . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ....

Journal: :The British journal of ophthalmology 1994
R M Manners M L Donaldson C Low P J Fenton

Journal: :Pulmonology 2017
J M Figueira Gonçalves F Martínez Bugallo D Díaz Pérez M D Martín Martínez I García-Talavera R Pitti Pérez

Journal: :GE Portuguese Journal of Gastroenterology 2023

Alpha-1 antitrypsin deficiency (AATD) is one of the most common genetic diseases and caused by mutations in SERPINA1 gene. The homozygous Pi*Z variant responsible for majority classic severe form alpha-1 deficiency, which characterized markedly decreased levels serum (AAT) with a strong predisposition to lung liver disease. diagnosis early treatment AATD-associated disease are challenges clinic...

Journal: :Bioorganic & Medicinal Chemistry Letters 2021

?1-antitrypsin deficiency is characterised by the misfolding and intracellular polymerisation of mutant protein within endoplasmic reticulum (ER) hepatocytes. Small molecules that bind stabilise Z were identified via a DNA-encoded library screen. A subsequent structure based optimisation led to series highly potent, selective cellular active correctors.

Journal: :Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace 1995
D M Geddes M A Beckles

Alpha 1-antitrypsin deficiency is associated with pulmonary emphysema and liver cirrhosis. The pathogenesis and treatment is reviewed with particular emphasis on gene therapy for emphysema. The technology of gene transfer using viruses and liposomes is developing fast and animal experiments have confirmed the feasibility of gene therapy for alpha 1-antitrypsin deficiency (AATD). So far only sub...

Journal: :Hepatology 1983
S Anand R R Schade C Bendetti R Kelly B S Rabin J Krause T E Starzl S Iwatsuki D H Van Thiel

A patient with coexistent hemochromatosis and alpha-1-antitrypsin deficiency which led to cirrhosis and death despite adequate therapy for hemochromatosis is reported. Evaluation of the family revealed first degree relatives with iron overload and others with alpha-1-antitrypsin deficiency but none with both conditions. The role of family studies in the early recognition and possible prevention...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید