We present a case of recurrent pulmonary alveolar proteinosis after heart-lung transplantation in a child with lysinuric protein intolerance. The recurrence of the pulmonary disease provides further insight regarding the possible pathogenesis of pulmonary alveolar proteinosis and therapeutic options for this complication
Pulmonary alveolar proteinosis (PAP) is a rare pulmonary syndrome that is characterized by the accum...
Hereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB, which encod...
Background: Pulmonary alveolar proteinosis (PAP) is very rare in children. Only a few small series h...
We present a case of recurrent pulmonary alveolar proteinosis after heart-lung transplantation in a ...
Pulmonary alveolar proteinosis (PAP) is characterized by the accumulation of surfactant derived mate...
Pulmonary alveolar proteinosis (PAP) affecting transplanted lungs is not well recognized. Herein, we...
We report the case of a 69-year-old man five-month post double lung transplant for idiopathic pulmon...
Pulmonary alveolar proteinosis (PAP) is a pulmonary disease characterized by disruption of surfactan...
BACKGROUND: Pulmonary alveolar proteinosis (PAP) is a rare disease characterised by accumulation of ...
Pulmonary alveolar proteinosis (PAP) is a progressive lung disease characterized by accumulated surf...
Pulmonary alveolar proteinosis is a rare condition characterized by the abnormal accumulation of sur...
Pulmonary alveolar proteinosis, (PAP) is a rare disease of unknown etiology, characterized by accumu...
AbstractHereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB, whi...
PAP is a rare alveolointerstitial lung disorder characterized histologically by the intra-alveolar a...
Pulmonary alveolar proteinosis is a rare condition characterized by accumulation of intra-alveolar s...
Pulmonary alveolar proteinosis (PAP) is a rare pulmonary syndrome that is characterized by the accum...
Hereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB, which encod...
Background: Pulmonary alveolar proteinosis (PAP) is very rare in children. Only a few small series h...
We present a case of recurrent pulmonary alveolar proteinosis after heart-lung transplantation in a ...
Pulmonary alveolar proteinosis (PAP) is characterized by the accumulation of surfactant derived mate...
Pulmonary alveolar proteinosis (PAP) affecting transplanted lungs is not well recognized. Herein, we...
We report the case of a 69-year-old man five-month post double lung transplant for idiopathic pulmon...
Pulmonary alveolar proteinosis (PAP) is a pulmonary disease characterized by disruption of surfactan...
BACKGROUND: Pulmonary alveolar proteinosis (PAP) is a rare disease characterised by accumulation of ...
Pulmonary alveolar proteinosis (PAP) is a progressive lung disease characterized by accumulated surf...
Pulmonary alveolar proteinosis is a rare condition characterized by the abnormal accumulation of sur...
Pulmonary alveolar proteinosis, (PAP) is a rare disease of unknown etiology, characterized by accumu...
AbstractHereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB, whi...
PAP is a rare alveolointerstitial lung disorder characterized histologically by the intra-alveolar a...
Pulmonary alveolar proteinosis is a rare condition characterized by accumulation of intra-alveolar s...
Pulmonary alveolar proteinosis (PAP) is a rare pulmonary syndrome that is characterized by the accum...
Hereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB, which encod...
Background: Pulmonary alveolar proteinosis (PAP) is very rare in children. Only a few small series h...