about
Genetic interstitial lung diseaseAn official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancyDiagnostic criteria and follow-up in neuroendocrine cell hyperplasia of infancy: a case series.A standardized blood test for the routine clinical diagnosis of impaired GM-CSF signaling using flow cytometry.Pathogenesis of Interstitial Lung Disease in Children and AdultsInfants and Young Children with Children's Interstitial Lung Disease.Expanding Our Understanding of Children's Interstitial Lung Disease.Recurrence of alveolar capillary dysplasia with misalignment of pulmonary veins in two consecutive siblingsA disorder of surfactant metabolism without identified genetic mutationsBronchoalveolar lavage fluid cytokine profiles in neuroendocrine cell hyperplasia of infancy and follicular bronchiolitis.Childhood interstitial lung disease due to surfactant protein C deficiency: frequent use and costs of hospital services for a single case in Australia.Imaging of Childhood Interstitial Lung DiseaseInterstitial lung disease in infants: new classification system, imaging technique, clinical presentation and imaging findings.Regulation of lung development and regeneration by the vascular system.Rare Lung Diseases: Interstitial Lung Diseases and Lung Manifestations of Rheumatological Diseases.Update on Diffuse Lung Disease in Children.Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: a decade's experience.Genetic disorders of surfactant protein dysfunction: when to consider and how to investigate.Gene Editing and Genetic Lung Disease. Basic Research Meets Therapeutic Application.Rapid and progressive pulmonary fibrosis in 2 families with DNA repair deficiencies of undetermined etiology.Interstitial lung disease in two brothers with novel compound heterozygous ABCA3 mutations.Insights from human genetic studies of lung and organ fibrosis.EMC3 coordinates surfactant protein and lipid homeostasis required for respiration.A novel surfactant protein C mutation resulting in aberrant protein processing and altered subcellular localization causes infantile interstitial lung disease.New clinical practice guidelines on the classification, evaluation and management of childhood interstitial lung disease in infants: what do they mean?ILDgenDB: integrated genetic knowledge resource for interstitial lung diseases (ILDs).
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description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Genetic Basis of Children's Interstitial Lung Disease.
@ast
Genetic Basis of Children's Interstitial Lung Disease.
@en
type
label
Genetic Basis of Children's Interstitial Lung Disease.
@ast
Genetic Basis of Children's Interstitial Lung Disease.
@en
prefLabel
Genetic Basis of Children's Interstitial Lung Disease.
@ast
Genetic Basis of Children's Interstitial Lung Disease.
@en
P2860
P356
P1476
Genetic Basis of Children's Interstitial Lung Disease.
@en
P2093
Lawrence M Nogee
P2860
P356
10.1089/PED.2009.0024
P577
2010-03-01T00:00:00Z