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American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 11/2010, Volume 182, Issue 10, pp. 1292 - 1304
Rationale We identified a 6 year old girl with pulmonary alveolar proteinosis (PAP), impaired granulocyte macrophage colony stimulating factor (GM CSF)... 
Surfactant | Gm-csf receptor | Alveolar macrophage | Whole lung lavage | Genetic disease | alveolar macrophage | INTERLEUKIN-3 | COLONY-STIMULATING FACTOR | GM CSF | DISORDERS | COMMON BETA-SUBUNIT | DEFICIENT MICE | GM-CSF AUTOANTIBODIES | receptor | whole lung lavage | LUNG LAVAGE | GENE | RESPIRATORY SYSTEM | genetic disease | MACROPHAGE DIFFERENTIATION | surfactant | CRITICAL CARE MEDICINE | Humans | Genetic Diseases, Inborn - genetics | Child, Preschool | Infant | Male | Dyspnea - etiology | Receptors, Granulocyte Colony-Stimulating Factor - genetics | Genetic Diseases, Inborn - therapy | Receptors, Granulocyte-Macrophage Colony-Stimulating Factor - genetics | Pulmonary Alveolar Proteinosis - genetics | Receptors, Granulocyte Colony-Stimulating Factor - blood | Female | Genetic Diseases, Inborn - etiology | Child | Genetic Diseases, Inborn - diagnosis | Granulocyte-Macrophage Colony-Stimulating Factor - blood | Lung - pathology | Pulmonary Alveolar Proteinosis - therapy | Genotype | Disease Progression | Pulmonary Alveolar Proteinosis - pathology | Receptors, Granulocyte Colony-Stimulating Factor - physiology | Autoantibodies - physiology | Receptors, Granulocyte-Macrophage Colony-Stimulating Factor - physiology | Pedigree | Genetic Markers - genetics | Age of Onset | Mutation | Pulmonary Alveolar Proteinosis - diagnosis | F. Pediatrics and Lung Development | GM-CSF receptor
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