Results 121 to 130 of about 24,735 (239)
Introduction: Alpha-1 antitrypsin (AAT) is a glycoprotein produced by liver, belonging to the serine protease inhibitor family. Alpha-1 antitrypsin deficiency (AATD) is very common autosomal recessive genetic disease caused by point mutation in ...
Dawid Kościołek +9 more
doaj +1 more source
Alpha-1-Antitrypsin Deficiency Panniculitis [PDF]
C, Irvine +3 more
openaire +2 more sources
Volumetric Single‐Molecule Tracking Inside Subcellular Structures
This correlative microscopy approach integrates single‐molecule light‐field microscopy (SMLFM) with widefield Fourier light‐field microscopy (FLFM) to enable 3D single‐molecule tracking within the organelles of living mammalian cells. Instantaneous volumetric segmentation enhances the sensitivity of molecular organization and diffusion measurements ...
Sam Daly +8 more
wiley +1 more source
Long-term augmentation therapy with Alpha-1 Antitrypsin in an MZ-AAT severe persistent asthma [PDF]
A young Caucasian female with severe bronchial asthma and Alpha1-antitrypsin (AAT) deficiency, MZ phenotype, experienced a quick and severe limitation of her physical capacity, which negatively affected her psychological state and social life, though she
Blanco, Ignacio +7 more
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Remote Pancreatic Response to Severe Polytrauma Correlates With Clinical Outcome
ABSTRACT Background Acute pancreatic injury can result from blunt or sharp force trauma, often leading to serious complications. While direct pancreatic trauma is associated with high rates of infection, organ failure, and mortality, little is known about the pancreas as a potential secondary target and remote trauma organ and thereby as a booster of ...
Rebecca Halbgebauer +17 more
wiley +1 more source
Long-term augmentation therapy with Alpha-1 Antitrypsin in an MZ-AAT severe persistent asthma [PDF]
Long-term augmentation therapy with Alpha- 1 Antitrypsin in an MZ-AAT severe persistent asthma. I. Blanco, H. Canto, J. Flóres, C. Camblor, V. Cárcaba, F.J. de Serres,S. Janciauskiene, E.F. Bustillo.
Blanco, Ignacio
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In a multi‐centre study of obeticholic acid in primary biliary cholangitis, 45% discontinued the drug over 4 years, with 11% moving to combination therapy (fibrates). Of those continuing, response rates increased from 37% (1 year) to 55% (4 years). Non‐response at 12 months and cirrhosis were independent predictors of liver‐related events.
Nadir Abbas +18 more
wiley +1 more source
ABSTRACT Background Postoperative atrial arrhythmia (POAA) is common after lung transplant, but data on its implications and management are limited. This study assessed POAA incidence and timing, its association with mortality and rehospitalizations, and outcomes related to postoperative beta‐blocker use.
Daniel M. Chen +11 more
wiley +1 more source
Portacaval shunt in three children with alpha‐1‐antitrypsin deficiency and cirrhosis: 9 to 12⅓ years later [PDF]
Busuttil, RW +3 more
core +1 more source
Deficiência de alfa-1-antitripsina na doença pulmonar obstrutiva crónica [PDF]
Introdução – A deficiência de alfa-1-antitripsina é uma das alterações genéticas graves encontradas por todo o mundo. Porém, permanece subdiagnosticada, apesar da forte predisposição à doença pulmonar obstrutiva crónica que condiciona.
Cardoso, Patrícia Neves
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