نتایج جستجو برای: antitrypsin deficiency

تعداد نتایج: 139573  

Journal: :COPD 2006
Frederick J de Serres Ignacio Blanco Enrique Fernández-Bustillo

Alpha-1 antitrypsin deficiency is known as a significant genetic risk factor for COPD for carriers of phenotype PIMZ, and for phenotypes PIZZ and PISZ. Genetic epidemiological studies for alpha-1 antitrypsin deficiency conducted by others on both COPD patients and concurrent non-COPD controls were used to estimate the risk factors for all six phenotypic classes (namely, the normal phenotype PIM...

Journal: :Pneumologia 2012
Danielius Serapinas Raimundas Sakalauskas

BACKGROUND AND OBJECTIVE Alpha-1 antitrypsin deficiency is an underdiagnosed condition in patients with chronic obstructive pulmonary disease. Diagnosis of this genetic condition is confirmed by genetic verification of pathology, but for screening purposes quantitative methods can be useful. The aim of our study was to evaluate sensitivity and specificity of quantitative methods for alpha-1 ant...

2012
Danielius Serapinas Brigita Sitkauskiene Raimundas Sakalauskas

INTRODUCTION Chronic obstructive pulmonary disease (COPD) has been recently defined as a systemic pulmonary inflammatory disease, and congenital α1 antitrypsin deficiency is one of the well-established genetic risk factors for chronic obstructive pulmonary disease. The aim of our study was to evaluate the possible associations of α1 antitrypsin with inflammatory markers - CRP, sCD14, TNF-α, sTN...

Mitra Samareh Fekri Mohammad Rahmatian, Nasrin Bazargan Harandi Nasrollah Jamshidi Gohari, Sayed Mehdi Hashemi Bajgani,

Background: One of the genetic risk factors for chronic obstructive pulmonary disease (COPD) is deficiency of Alpha-1 Antitrypsin (A1AT). There is no exact statistics about the prevalence of this disease in different regions of Iran. The present study aimed to determine the prevalence of alpha-1 antitrypsin (A1AT) deficiency in COPD patients in Kerman, Iran. Metho...

ژورنال: :hepatitis monthly 0
aleksandra topic university of belgrade, faculty of pharmacy, department of medical biochemistry, vojvode stepe, 45011221, serbia +38-1113951283, [email protected]; university of belgrade, faculty of pharmacy, department of medical biochemistry, vojvode stepe, 45011221, serbia +38-1113951283, [email protected] mila ljujic university of belgrade, institute of molecular genetics and genetic engineering, serbia dragica radojkovic university of belgrade, institute of molecular genetics and genetic engineering, serbia

context alpha-1-antitrypsin (a1at) is the most abundant liver-derived, highly polymorphic, glycoprotein in plasma. hereditary deficiency of alpha-1-antitrypsin in plasma (a1atd) is a consequence of accumulation of polymers of a1at mutants in endoplasmic reticulum of hepatocytes and other a1at-producing cells. one of the clinical manifestations of a1atd is liver disease in childhood and cirrhosi...

2013
Bita Geramizadeh Zahra Jowkar Leila Karami Masoum Masoumpour Samrad Mehrabi Mohammad-Ali Ghayoumi

BACKGROUND Alpha-1 antitrypsin deficiency is a genetic disease which affects both lung and liver. This disease is a recognized factor for chronic obstructive pulmonary disease (COPD). However its importance as the cause of COPD in a country such as Iran is unclear. OBJECTIVES This study was conducted to find out the role of α-1 antitrypsin deficiency as a cause of COPD in Iranian patients. ...

Journal: :Gastroentérologie Clinique et Biologique 2010

Journal: :New England Journal of Medicine 2020

Journal: :Chest 1996
R J Browne D M Mannino M J Khoury

OBJECTIVE To describe trends of reported alpha 1-antitrypsin deficiency mortality in the United States from 1979-1991. METHODS We analyzed death certificate reports in the multiple-cause mortality files compiled by the National Center for Health Statistics. RESULTS Of the 26,866,600 deaths that occurred during the 13-year period, 1,930 had alpha 1-antitrypsin deficiency listed as a cause of...

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