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2008 1
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2014 7
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2022 9
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Page 1
Autoimmune Pulmonary Alveolar Proteinosis.
McCarthy C, Carey BC, Trapnell BC. McCarthy C, et al. Am J Respir Crit Care Med. 2022 May 1;205(9):1016-1035. doi: 10.1164/rccm.202112-2742SO. Am J Respir Crit Care Med. 2022. PMID: 35227171 Free PMC article.
Autoimmune pulmonary alveolar proteinosis (PAP) is a rare disease characterized by myeloid cell dysfunction, abnormal pulmonary surfactant accumulation, and innate immune deficiency. ...
Autoimmune pulmonary alveolar proteinosis (PAP) is a rare disease characterized by myeloid cell dysfunction, abn …
Infections in autoimmune pulmonary alveolar proteinosis: a large retrospective cohort.
Mabo A, Borie R, Wemeau-Stervinou L, Uzunhan Y, Gomez E, Prevot G, Reynaud-Gaubert M, Traclet J, Bergot E, Cadranel J, Marchand-Adam S, Bergeron A, Blanchard E, Bondue B, Bonniaud P, Bourdin A, Burgel PR, Hirschi S, Marquette CH, Quétant S, Nunes H, Chenivesse C, Crestani B, Guirriec Y, Monnier D, Ménard C, Tattevin P, Cottin V, Luque Paz D, Jouneau S; OrphaLung Network. Mabo A, et al. Thorax. 2023 Dec 15;79(1):68-74. doi: 10.1136/thorax-2023-220040. Thorax. 2023. PMID: 37758458 Free article.
BACKGROUND: Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare disease, predisposing to an increased risk of infection. ...
BACKGROUND: Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare disease, predisposing to an increased ris …
Upper Lobe-predominant Autoimmune Pulmonary Alveolar Proteinosis.
Goda M, Takigawa Y, Fujiwara K, Shinno Y. Goda M, et al. Intern Med. 2023 May 15;62(10):1569-1570. doi: 10.2169/internalmedicine.0226-22. Epub 2022 Oct 12. Intern Med. 2023. PMID: 36223923 Free PMC article. No abstract available.
Nebulised granulocyte-macrophage colony-stimulating factor (GM-CSF) in autoimmune pulmonary alveolar proteinosis: a systematic review and meta-analysis.
Munsif M, Sweeney D, Leong TL, Stirling RG. Munsif M, et al. Eur Respir Rev. 2023 Nov 22;32(170):230080. doi: 10.1183/16000617.0080-2023. Print 2023 Dec 31. Eur Respir Rev. 2023. PMID: 37993127 Free PMC article. Review.
BACKGROUND: Autoimmune pulmonary alveolar proteinosis (aPAP) results from impaired macrophage-mediated clearance of alveolar surfactant lipoproteins. ...
BACKGROUND: Autoimmune pulmonary alveolar proteinosis (aPAP) results from impaired macrophage-mediated clearance …
A dried blood spot test for diagnosis of autoimmune pulmonary alveolar proteinosis.
Carey B, Chalk C, Stock J, Toth A, Klingler M, Greenberg H, Uchida K, Arumugam P, Trapnell BC. Carey B, et al. J Immunol Methods. 2022 Dec;511:113366. doi: 10.1016/j.jim.2022.113366. Epub 2022 Oct 2. J Immunol Methods. 2022. PMID: 36198356 Free PMC article.
Granulocyte/macrophage colony-stimulating factor autoantibodies (GMAbs) mediate the pathogenesis of autoimmune pulmonary alveolar proteinosis (autoimmune PAP) and their quantification in serum by enzyme-linked immunosorbent assay (ELISA) - the serum GM …
Granulocyte/macrophage colony-stimulating factor autoantibodies (GMAbs) mediate the pathogenesis of autoimmune pulmonary al …
An exploratory study investigating biomarkers associated with autoimmune pulmonary alveolar proteinosis (aPAP).
Campo I, Meloni F, Gahlemann M, Sauter W, Ittrich C, Schoelch C, Trapnell BC, Gupta A. Campo I, et al. Sci Rep. 2022 May 24;12(1):8708. doi: 10.1038/s41598-022-11446-8. Sci Rep. 2022. PMID: 35610268 Free PMC article.
Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disorder involving production of autoantibodies against endogenous granulocyte-macrophage colony-stimulating factor (GM-CSF). ...
Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disorder involving production of autoantibodies …
CYFRA21-1 is a more sensitive biomarker to assess the severity of pulmonary alveolar proteinosis.
Bai JW, Gu SY, Sun XL, Lu HW, Liang S, Xu JF. Bai JW, et al. BMC Pulm Med. 2022 Jan 3;22(1):2. doi: 10.1186/s12890-021-01795-x. BMC Pulm Med. 2022. PMID: 34980056 Free PMC article.
BACKGROUND: Serum lactate dehydrogenase (LDH), carcinoembryonic antigen (CEA) and CYFRA21-1 are the commonly used biomarkers to identify patients with autoimmune pulmonary alveolar proteinosis (APAP). However, it is not clear which of the biomarkers is …
BACKGROUND: Serum lactate dehydrogenase (LDH), carcinoembryonic antigen (CEA) and CYFRA21-1 are the commonly used biomarkers to identify pat …
48 results