×
About 1,206 results

ALLMedicine™ Pulmonary Alveolar Proteinosis Center

Research & Reviews  599 results

Expression profiles and potential functions of long noncoding RNAs and mRNAs in autoimm...
https://doi.org/10.18632/aging.202818
Aging Yang Y, Xu W et. al.

Apr 6th, 2021 - Autoimmune pulmonary alveolar proteinosis (APAP) is a rare lung disease that may be associated with surfactant overaccumulation. To assess the function of long noncoding RNAs (lncRNAs) in APAP, we performed microarray analyses to identify differen...

Autoimmune pulmonary alveolar proteinosis and idiopathic pulmonary haemosiderosis: a du...
https://doi.org/10.1136/bcr-2020-241048
BMJ Case Reports; Walsh L, McCarthy C et. al.

Apr 3rd, 2021 - Pulmonary alveolar proteinosis (PAP) is a rare pulmonary condition which leads to excessive accumulation of proteinaceous material within the alveoli. Idiopathic pulmonary haemosiderosis (IPH) is another orphan lung disease and results in recurren...

B cell-activating factors in autoimmune pulmonary alveolar proteinosis.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923513
Orphanet Journal of Rare Diseases; Hirose M, Arai T et. al.

Mar 3rd, 2021 - Autoimmune pulmonary alveolar proteinosis (APAP) results from the suppression of granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling by a neutralizing autoantibody against GM-CSF. B cell-activating factor (BAFF) and a proliferation...

Hereditary pulmonary alveolar proteinosis as collateral damage from a large chromosomal...
https://doi.org/10.1002/ppul.25336
Pediatric Pulmonology; Schmidt A, Kenia P et. al.

Feb 25th, 2021 - A girl with a known chromosomal deletion at Xp22.33, learning difficulties and short stature presented with dyspnea and dry cough and an abnormal chest X-ray. Computed tomography was typical for pulmonary alveolar proteinosis (PAP), and the diagno...

Genetic determinants of risk in autoimmune pulmonary alveolar proteinosis.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884840
Nature Communications; Sakaue S, Yamaguchi E et. al.

Feb 16th, 2021 - Pulmonary alveolar proteinosis (PAP) is a devastating lung disease caused by abnormal surfactant homeostasis, with a prevalence of 6-7 cases per million population worldwide. While mutations causing hereditary PAP have been reported, the genetic b...

see more →

Clinicaltrials.gov  603 results

Expression profiles and potential functions of long noncoding RNAs and mRNAs in autoimm...
https://doi.org/10.18632/aging.202818
Aging Yang Y, Xu W et. al.

Apr 6th, 2021 - Autoimmune pulmonary alveolar proteinosis (APAP) is a rare lung disease that may be associated with surfactant overaccumulation. To assess the function of long noncoding RNAs (lncRNAs) in APAP, we performed microarray analyses to identify differen...

Autoimmune pulmonary alveolar proteinosis and idiopathic pulmonary haemosiderosis: a du...
https://doi.org/10.1136/bcr-2020-241048
BMJ Case Reports; Walsh L, McCarthy C et. al.

Apr 3rd, 2021 - Pulmonary alveolar proteinosis (PAP) is a rare pulmonary condition which leads to excessive accumulation of proteinaceous material within the alveoli. Idiopathic pulmonary haemosiderosis (IPH) is another orphan lung disease and results in recurren...

B cell-activating factors in autoimmune pulmonary alveolar proteinosis.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923513
Orphanet Journal of Rare Diseases; Hirose M, Arai T et. al.

Mar 3rd, 2021 - Autoimmune pulmonary alveolar proteinosis (APAP) results from the suppression of granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling by a neutralizing autoantibody against GM-CSF. B cell-activating factor (BAFF) and a proliferation...

Hereditary pulmonary alveolar proteinosis as collateral damage from a large chromosomal...
https://doi.org/10.1002/ppul.25336
Pediatric Pulmonology; Schmidt A, Kenia P et. al.

Feb 25th, 2021 - A girl with a known chromosomal deletion at Xp22.33, learning difficulties and short stature presented with dyspnea and dry cough and an abnormal chest X-ray. Computed tomography was typical for pulmonary alveolar proteinosis (PAP), and the diagno...

Genetic determinants of risk in autoimmune pulmonary alveolar proteinosis.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884840
Nature Communications; Sakaue S, Yamaguchi E et. al.

Feb 16th, 2021 - Pulmonary alveolar proteinosis (PAP) is a devastating lung disease caused by abnormal surfactant homeostasis, with a prevalence of 6-7 cases per million population worldwide. While mutations causing hereditary PAP have been reported, the genetic b...

see more →

News  4 results

Growth Factors Associated with Neutrophil Function
https://www.medpagetoday.com/pulmonology/smokingcopd/5026

Feb 8th, 2007 - Action Points Explain to patients who ask that pulmonary alveolar proteinosis is a rare disease characterized by the accumulation of surfactant debris in the lungs. About one in five deaths attributed to the disease are the result of opportunistic...

Pulmonary Opacities in a Patient With Essential Thrombocythemia
https://www.medscape.com/viewarticle/405329_2

Nov 26th, 2001 - Discussion Since the HRCT findings in this case were not typical for nontuberculous mycobacterial pulmonary infection, the patient underwent thoracoscopic lung biopsy, which provided the diagnosis of pulmonary alveolar proteinosis (PAP). Due to th...

Our new understanding of pulmonary alveolar proteinosis: What an internist needs to know
https://www.mdedge.com/ccjm/article/93615/pulmonology/our-new-understanding-pulmonary-alveolar-proteinosis-what-internist
Peter Mazzone, MD, Mary Jane Thomassen, PhD et. al.

ABSTRACTPulmonary alveolar proteinosis (PAP; the accumulation of surfactant lipids and proteins in the alveoli) has a number of infectious and environmental causes but is usually idiopathic. The clinical presentation of PAP is nonspecific; thus, t.

see more →