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Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine.
Adegunsoye A, Kropski JA, Behr J, Blackwell TS, Corte TJ, Cottin V, Glanville A, Glassberg MK, Griese M, Hunninghake GM, Johannson KA, Keane MP, Kim JS, Kolb M, Maher TM, Oldham JM, Podolanczuk AJ, Rosas IO, Martinez FJ, Noth I, Schwartz DA. Adegunsoye A, et al. Among authors: griese m. Am J Respir Crit Care Med. 2024 Apr 4. doi: 10.1164/rccm.202401-0238SO. Online ahead of print. Am J Respir Crit Care Med. 2024. PMID: 38573068
A roadmap to precision treatments for familial pulmonary fibrosis.
Hurley K, Ozaki M, Philippot Q, Galvin L, Crosby D, Kirwan M, Gill DR, Alysandratos KD, Jenkins G, Griese M, Nathan N, Borie R; COST Open-ILD Group Management Committee. Hurley K, et al. Among authors: griese m. EBioMedicine. 2024 May 7;104:105135. doi: 10.1016/j.ebiom.2024.105135. Online ahead of print. EBioMedicine. 2024. PMID: 38718684 Free PMC article. Review.
Whole lung lavage therapy for pulmonary alveolar proteinosis: a global survey of current practices and procedures.
Campo I, Luisetti M, Griese M, Trapnell BC, Bonella F, Grutters J, Nakata K, Van Moorsel CH, Costabel U, Cottin V, Ichiwata T, Inoue Y, Braschi A, Bonizzoni G, Iotti GA, Tinelli C, Rodi G; WLL International Study Group. Campo I, et al. Among authors: griese m. Orphanet J Rare Dis. 2016 Aug 31;11(1):115. doi: 10.1186/s13023-016-0497-9. Orphanet J Rare Dis. 2016. PMID: 27577926 Free PMC article.
Successful atorvastatin treatment of pulmonary alveolar proteinosis in a child with GM-CSF receptor deficiency.
Nayır Büyükşahin H, Yalçın E, Özdemir A, Haliloglu M, Orhan D, Griese M, Gothe F, Rapp C, Hardenberg SGV, Debbağ S, Güzelkaş İ, Emiralioğlu N, Doğru D, Özçelik U, Kiper N. Nayır Büyükşahin H, et al. Among authors: griese m. Pediatr Pulmonol. 2024 Jun;59(6):1777-1780. doi: 10.1002/ppul.26946. Epub 2024 Feb 27. Pediatr Pulmonol. 2024. PMID: 38411295 No abstract available.
Multivalent, calcium-independent binding of surfactant protein A and D to sulfated glycosaminoglycans of the alveolar epithelial glycocalyx.
Avcibas R, Vermul A, Gluhovic V, Boback N, Arroyo R, Kingma P, Isasi-Campillo M, Garcia-Ortega L, Griese M, Kuebler WM, Ochs M, Lauster D, Lopez-Rodriguez E. Avcibas R, et al. Among authors: griese m. Am J Physiol Lung Cell Mol Physiol. 2024 May 1;326(5):L524-L538. doi: 10.1152/ajplung.00283.2023. Epub 2024 Feb 20. Am J Physiol Lung Cell Mol Physiol. 2024. PMID: 38375572 Free article.
Estimating the effect of nintedanib on forced vital capacity in children and adolescents with fibrosing interstitial lung disease using a Bayesian dynamic borrowing approach.
Maher TM, Brown KK, Cunningham S, DeBoer EM, Deterding R, Fiorino EK, Griese M, Schwerk N, Warburton D, Young LR, Gahlemann M, Voss F, Stock C; InPedILD trial investigators. Maher TM, et al. Among authors: griese m. Pediatr Pulmonol. 2024 Apr;59(4):1038-1046. doi: 10.1002/ppul.26882. Epub 2024 Jan 30. Pediatr Pulmonol. 2024. PMID: 38289091
Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension.
Postma AV, Rapp CK, Knoflach K, Volk AE, Lemke JR, Ackermann M, Regamey N, Latzin P, Celant L, Jansen SMA, Bogaard HJ, Ilgun A, Alders M, van Spaendonck-Zwarts KY, Jonigk D, Klein C, Gräf S, Kubisch C, Houweling AC, Griese M. Postma AV, et al. Among authors: griese m. Genet Med Open. 2023;1(1):100811. doi: 10.1016/j.gimo.2023.100811. Genet Med Open. 2023. PMID: 38230350 Free PMC article.
An evaluation of an open access iPSC training course: "How to model interstitial lung disease using patient-derived iPSCs".
Schweikert A, Kenny S, Oglesby I, Glasgow A, de Santi C, Gensch I, Lachmann N, Desroziers T, Fletcher C, Snijders D, Nathan N, Hurley K; COST Open-ILD Group Management Committee. Schweikert A, et al. Stem Cell Res Ther. 2023 Dec 20;14(1):377. doi: 10.1186/s13287-023-03598-9. Stem Cell Res Ther. 2023. PMID: 38124115 Free PMC article.
402 results