pulmonary alveolar proteinosis and alveolar microlithiasis. Wegeners granulomatosis is vasculitis that is associated with pulmonary manifestations in most of the cases. ILD: Interstitial lung disease.

offering a groundbreaking solution for diagnosing autoimmune pulmonary alveolar proteinosis (aPAP), a rare lung disease. The test requires just a finger-prick blood sample and builds upon the ...

Pulmonary alveolar proteinosis (PAP) is a rare respiratory disease that affects somewhere between 4 and 40 people per million worldwide. The condition causes substances such as fats and proteins ...

has announced the publication of a manuscript detailing long-term outcomes for molgramostim inhalation solution in patients ...

His father had received a diagnosis of myelodysplastic syndrome at age 33 years and had died from pulmonary alveolar proteinosis and invasive pulmonary aspergillosis at age 36 years. Clinical images ...

Our lead program, MOLBREEVI*, is a recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) in Phase 3 development for autoimmune pulmonary alveolar proteinosis (aPAP).