An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy - Test2 - elhamkhani - TriplyDB

An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy

An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy

http://www.wikidata.org/entity/Q26824718

about

Interstitial Lung Disease in Childhood: Clinical and Genetic Aspects Interstitial lung disease in children Diffuse lung disease of infancy: a pattern-based, algorithmic approach to histological diagnosis Alveolar development and disease Pulmonary hypertension in childhood interstitial lung disease: A systematic review of the literature.Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?The molecular era of surfactant biology.Interstitial lung disease: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.Diseases of pulmonary surfactant homeostasis.Genotype-phenotype correlations for infants and children with ABCA3 deficiency Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations "A remarkable experience of god, shaping us as a family": parents' use of faith following child's rare disease diagnosis.Surfactant lipidomics in healthy children and childhood interstitial lung disease Categorizing diffuse parenchymal lung disease in children.Lost after translation: insights from pulmonary surfactant for understanding the role of alveolar epithelial dysfunction and cellular quality control in fibrotic lung disease.Diffuse Lung Disease in Biopsied Children 2 to 18 Years of Age. Application of the chILD Classification Scheme A disorder of surfactant metabolism without identified genetic mutations Surfactant Protein C-associated interstitial lung disease; three different phenotypes of the same SFTPC mutation.Assessing the feasibility of a web-based registry for multiple orphan lung diseases: the Australasian Registry Network for Orphan Lung Disease (ARNOLD) experience.Childhood interstitial lung disease due to surfactant protein C deficiency: frequent use and costs of hospital services for a single case in Australia.Pediatric lung transplantation: indications and outcomes.Hydroxychloroquine in children with interstitial (diffuse parenchymal) lung diseases.CT chest under general anesthesia: pulmonary, anesthetic and radiologic dilemmas.Diffuse lung disease in infants less than 1 year of age: Histopathological diagnoses and clinical outcome.Cellular mechanisms of alveolar pathology in childhood interstitial lung diseases: current insights from mouse genetics.LungMAP: The Molecular Atlas of Lung Development Program.Childhood interstitial lung disease: A systematic review.European protocols for the diagnosis and initial treatment of interstitial lung disease in children.Rare Lung Diseases: Interstitial Lung Diseases and Lung Manifestations of Rheumatological Diseases.Recent advances in paediatric respiratory medicine.Children's Interstitial and Diffuse Lung Disease. Progress and Future Horizons.Update on Diffuse Lung Disease in Children.Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: a decade's experience.Pulmonary Vasculopathy Associated with FIGF Gene Mutation.Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health-NHLBI Workshop, September 3 and 4, 2015.Interstitial lung disease in infancy: A general approach.A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy.Genetic disorders of surfactant protein dysfunction: when to consider and how to investigate.Childhood interstitial lung disease: Family experiences.Interstitial lung disease in newborns.

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An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy

http://www.wikidata.org/entity/Q26824718

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2013 nî lūn-bûn

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2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2013 թվականի օգոստոսին հրատարակված գիտական հոդված

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2013年の論文

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Aaron Hamvas

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Alan S. Brody

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Bettina C. Hilman

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Claire Langston

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Geoffrey Kurland

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Gregory J. Redding

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Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency

Mutations in TITF-1 are associated with benign hereditary chorea

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice

A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds

Radiation exposure from CT scans in childhood and subsequent risk of leukaemia and brain tumours: a retrospective cohort study

Diagnosis of severe combined immunodeficiency

A mutation in the surfactant protein C gene associated with familial interstitial lung disease

American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Soci

Genetic disorders of surfactant dysfunction

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