A family study of the variability of pulmonary function in alpha 1-antitrypsin deficiency. Quantitative phenotypes.
about
Liver injury in alpha1-antitrypsin deficiency: an aggregated protein induces mitochondrial injuryAlpha 1-antitrypsin deficiency. 3: Clinical manifestations and natural historyAlpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema riskCausal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels.Alpha-1-antitrypsin augmentation therapy in deficient individuals enrolled in the Alpha-1 Foundation DNA and Tissue Bankα₁-Antitrypsin protease inhibitor MZ heterozygosity is associated with airflow obstruction in two large cohorts.Gender-related differences in severe, early-onset chronic obstructive pulmonary disease.Chronic obstructive pulmonary disease in alpha1-antitrypsin PI MZ heterozygotes: a meta-analysis.Effect of age and occupational exposure to airway irritants on lung function in non-smoking individuals with alpha 1-antitrypsin deficiency (PiZZ).Plasma levels of elastase-specific fibrinopeptides correlate with proteinase inhibitor phenotype. Evidence for increased elastase activity in subjects with homozygous and heterozygous deficiency of alpha 1-proteinase inhibitorAssociation of IREB2 and CHRNA3 polymorphisms with airflow obstruction in severe alpha-1 antitrypsin deficiencySystemic inflammation in COPD in relation to smoking statusThe selective advantage of alpha1-antitrypsin deficiency.Pathogenesis of chronic liver injury and hepatocellular carcinoma in alpha-1-antitrypsin deficiency.Circulating alpha1-antitrypsin in the general population: determinants and association with lung function.Alpha one antitrypsin deficiency: from gene to treatment.Recent advances in α-1-antitrypsin deficiency-related lung disease.Inflammatory markers in chronic obstructive pulmonary disease patients with different α1 antitrypsin genotypesWell-Known and Less Well-Known Functions of Alpha-1 Antitrypsin. Its Role in Chronic Obstructive Pulmonary Disease and Other Disease Developments.American Thoracic Society/European Respiratory Society statement: standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency.Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis.Alpha-1 Antitrypsin PiMZ Genotype Is Associated with Chronic Obstructive Pulmonary Disease in Two Racial Groups
P2860
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P2860
A family study of the variability of pulmonary function in alpha 1-antitrypsin deficiency. Quantitative phenotypes.
description
1990 nî lūn-bûn
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1990年の論文
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1990年学术文章
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1990年学术文章
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1990年学术文章
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1990年学术文章
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1990年学术文章
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1990年學術文章
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name
A family study of the variabil ...... ency. Quantitative phenotypes.
@en
A family study of the variabil ...... ency. Quantitative phenotypes.
@nl
type
label
A family study of the variabil ...... ency. Quantitative phenotypes.
@en
A family study of the variabil ...... ency. Quantitative phenotypes.
@nl
prefLabel
A family study of the variabil ...... ency. Quantitative phenotypes.
@en
A family study of the variabil ...... ency. Quantitative phenotypes.
@nl
P2093
P2860
P356
P1476
A family study of the variabil ...... ency. Quantitative phenotypes.
@en
P2093
Campbell EJ
Province MA
Silverman EK
P2860
P304
P356
10.1164/AJRCCM/142.5.1015
P577
1990-11-01T00:00:00Z