Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy. - Wikidata - awgldk - TriplyDB

Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.

Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.

http://www.wikidata.org/entity/Q34402453

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Genetic interstitial lung disease G-CSF and GM-CSF in Neutropenia An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy Respiratory epithelial cells orchestrate pulmonary innate immunity.Assessment and management of pulmonary alveolar proteinosis in a reference center Autoimmune pulmonary proteinosis in a Chilean teenager, a rare aetiology of interstitial lung disease.Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?The molecular era of surfactant biology.Long-term follow-up and treatment of congenital alveolar proteinosis.The GM-CSF/IL-3/IL-5 cytokine receptor family: from ligand recognition to initiation of signaling.Diseases of pulmonary surfactant homeostasis.Pulmonary macrophage transplantation therapy Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.Regional ventilation changes in severe asthma after bronchial thermoplasty with (3)He MR imaging and CT.A standardized blood test for the routine clinical diagnosis of impaired GM-CSF signaling using flow cytometry.Surfactant dysfunction.Elderly-onset hereditary pulmonary alveolar proteinosis and its cytokine profile.The parallel lives of alpha1-antitrypsin deficiency and pulmonary alveolar proteinosis.Use of induced pluripotent stem cells to recapitulate pulmonary alveolar proteinosis pathogenesis.Update in pediatric lung disease 2010.The GM-CSF receptor family: mechanism of activation and implications for disease.Autoimmune pulmonary alveolar proteinosis: treatment options in year 2013.Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review.Pulmonary alveolar proteinosis: time to shift?Facts and promises on lung biomarkers in interstitial lung diseases.Update on Diffuse Lung Disease in Children.Function and safety of lentivirus-mediated gene transfer for CSF2RA-deficiency.Does dust-associated pulmonary alveolar proteinosis represent an autoimmune disorder?Pulmonary Alveolar Proteinosis Syndrome.Recurrence of pulmonary alveolar proteinosis after bilateral lung transplantation in a patient with a nonsense mutation in CSF2RB.Whole-Genome Sequencing of a Family with Hereditary Pulmonary Alveolar Proteinosis Identifies a Rare Structural Variant Involving CSF2RA/CRLF2/IL3RA Gene Disruption.Targeting cholesterol homeostasis in lung diseases.T-cell-restricted T-bet overexpression induces aberrant hematopoiesis of myeloid cells and impairs function of macrophages in the lung.A newly identified novel variant in the CSF2RA gene in a child with pulmonary alveolar proteinosis: a case report.Primary pulmonary alveolar proteinosis: computed tomography features at diagnosis.TALEN-mediated functional correction of human iPSC-derived macrophages in context of hereditary pulmonary alveolar proteinosis.Pulmonary transplantation of macrophage progenitors as effective and long-lasting therapy for hereditary pulmonary alveolar proteinosis.Whole-lung lavage for pediatric patients with pulmonary alveolar proteinosis.Hematopoietic stem cell transplantation for pulmonary alveolar proteinosis associated with primary immunodeficiency disease.Long-term inhaled granulocyte macrophage-colony-stimulating factor in autoimmune pulmonary alveolar proteinosis: effectiveness, safety, and lowest effective dose.

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P2860

Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.

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2010年の論文

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Hereditary pulmonary alveolar ...... ation, diagnosis, and therapy.

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RCCM.201002-0271OC

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American Journal of Respiratory and Critical Care Medicine

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Hereditary pulmonary alveolar ...... ation, diagnosis, and therapy.

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Brenna C Carey

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Bruce C Trapnell

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Bruce K Rubin

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Carrie Stevens

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Claudia Chalk

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Ilaria Campo

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Jeffrey A Whitsett

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Katharine Kevill

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Lawrence M Nogee

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Lisa R Young

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P2860

The structure of the GM-CSF receptor complex reveals a distinct mode of cytokine receptor activation

Granulocyte/macrophage colony-stimulating factor-deficient mice show no major perturbation of hematopoiesis but develop a characteristic pulmonary pathology

Characteristics of a large cohort of patients with autoimmune pulmonary alveolar proteinosis in Japan.

Standard mutation nomenclature in molecular diagnostics: practical and educational challenges

Critical cytoplasmic domains of the common beta subunit of the human GM-CSF, IL-3 and IL-5 receptors for growth signal transduction and tyrosine phosphorylation

Hematopoietic and lung abnormalities in mice with a null mutation of the common beta subunit of the receptors for granulocyte-macrophage colony-stimulating factor and interleukins 3 and 5.

Pulmonary alveolar proteinosis: progress in the first 44 years.

The pulmonary collectins and surfactant metabolism.

Human GM-CSF autoantibodies and reproduction of pulmonary alveolar proteinosis.

Gm-CSF regulates pulmonary surfactant homeostasis and alveolar macrophage-mediated innate host defense.

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1292-1304

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