Hereditary surfactant protein B deficiency resulting from a novel mutation

Intensive Care Medicine

Volumn 26, Issue 1, 2000, Pages 97-100

  Somaschini, Marco ^a,d   Wert, S ^b   Mangili, G ^a   Colombo, A ^a   Nogee, L ^c  

^a OSPEDALI RIUNITI   (Italy)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d SAN RAFFAELE HOSPITAL   (Italy)

Author keywords

Congenital pulmonary alveolar proteinosis; Respiratory distress syndrome; Surfactant protein B deficiency

Indexed keywords

DEXAMETHASONE; DOBUTAMINE; DOPAMINE; LUNG SURFACTANT EXTRACT; NITRIC OXIDE; PROSTACYCLIN; SURFACTANT PROTEIN B;

ARTICLE; ARTIFICIAL VENTILATION; CASE REPORT; FEMALE; FRAMESHIFT MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOXEMIA; INFANT; LUNG ALVEOLUS PROTEINOSIS; NEONATAL RESPIRATORY DISTRESS SYNDROME; NEWBORN INTENSIVE CARE; OXYGEN THERAPY; PROTEIN DEFICIENCY; PULMONARY HYPERTENSION; RESPIRATORY ACIDOSIS;

EID: 0034027164     PISSN: 03424642     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001340050019     Document Type: Article

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