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Page 1
Pulmonary storage.
Šterclová M. Šterclová M. Vnitr Lek. 2022 Winter;68(8):525-531. doi: 10.36290/vnl.2022.111. Vnitr Lek. 2022. PMID: 36575071 English.
In a broader context, however, the accumulation of various substances in the lung tissue is also encountered in cases of pediatric pulmonary interstitial glycogenosis (PIG), alveolar lipoproteinosis or pulmonary amyloidosis. The cause of PIG is not clear. The diseas …
In a broader context, however, the accumulation of various substances in the lung tissue is also encountered in cases of pediatric pulmonary …
Amyloidosis of the Lung.
Khoor A, Colby TV. Khoor A, et al. Arch Pathol Lab Med. 2017 Feb;141(2):247-254. doi: 10.5858/arpa.2016-0102-RA. Arch Pathol Lab Med. 2017. PMID: 28134587 Free article. Review.
Three different clinicopathologic forms of amyloidosis can be seen in the lungs: diffuse alveolar-septal amyloidosis, nodular pulmonary amyloidosis, and tracheobronchial amyloidosis. OBJECTIVE: -To clarify the relationship between the fibril protein-based amyloidosi …
Three different clinicopathologic forms of amyloidosis can be seen in the lungs: diffuse alveolar-septal amyloidosis, nodular pulmonary
Clinical, radiologic, and pathologic features and outcomes of pulmonary transthyretin amyloidosis.
Eggleston RH, Hartman TE, Walkoff LA, Yi ES, Ryu JH, Baqir M. Eggleston RH, et al. Respir Med. 2022 Apr;194:106761. doi: 10.1016/j.rmed.2022.106761. Epub 2022 Feb 8. Respir Med. 2022. PMID: 35217402 Free article. Review.
INTRODUCTION: Amyloid transthyretin amyloidosis (ATTR) is characterized by deposition of a misfolded conformation of the transport protein TTR, most commonly in cardiac and nerve tissue, causing clinical disease. Pulmonary amyloidosis, or deposition of ATTR in lung …
INTRODUCTION: Amyloid transthyretin amyloidosis (ATTR) is characterized by deposition of a misfolded conformation of the transport protein T …
Senile pulmonary amyloidosis.
Kunze WP. Kunze WP. Pathol Res Pract. 1979 Aug;164(4):413-22. doi: 10.1016/S0344-0338(79)80058-8. Pathol Res Pract. 1979. PMID: 514902
Lung tissue obtained from 340 necropsies of persons aged 80 years and over was investigated for the occurrence of pulmonary amyloid deposits by means of a sensitive fluorescence technique. The incidence of pulmonary amyloidosis was about 2% below the age of 80, near …
Lung tissue obtained from 340 necropsies of persons aged 80 years and over was investigated for the occurrence of pulmonary amyloid deposits …
Amyloid-associated Cystic Lung Disease.
Zamora AC, White DB, Sykes AM, Hoskote SS, Moua T, Yi ES, Ryu JH. Zamora AC, et al. Chest. 2016 May;149(5):1223-33. doi: 10.1378/chest.15-1539. Epub 2016 Jan 12. Chest. 2016. PMID: 26513525
METHODS: We reviewed the records of subjects having biopsy-proven pulmonary amyloidosis with cystic lung disease demonstrated at high-resolution computed tomography (HRCT). ...RESULTS: Twenty-one subjects (13 female, eight male; median age, 61 years) with cystic …
METHODS: We reviewed the records of subjects having biopsy-proven pulmonary amyloidosis with cystic lung disease demonstrated …
18F-FDG PET/CT in patients with amyloid light-chain amyloidosis: case-series and literature review.
Mekinian A, Jaccard A, Soussan M, Launay D, Berthier S, Federici L, Lefèvre G, Valeyre D, Dhote R, Fain O; Centre de Référence des Amyloses immunoglobulinémiques et autres maladies liées aux dépots des immunoglobulines monoclonales. Mekinian A, et al. Amyloid. 2012 Jun;19(2):94-8. doi: 10.3109/13506129.2012.682833. Epub 2012 May 16. Amyloid. 2012. PMID: 22587492 Review.
PET was negative in the patient with cardiac amyloidosis and two patients with pulmonary amyloidosis. CONCLUSION: High FDG uptake may be present in patients with AL amyloidosis, however prospective studies are needed in order to determine the place of FDG PET in AL …
PET was negative in the patient with cardiac amyloidosis and two patients with pulmonary amyloidosis. CONCLUSION: High FDG upt …
Pulmonary amyloidosis in Sjogren's syndrome: a case report and systematic review of the literature.
Rajagopala S, Singh N, Gupta K, Gupta D. Rajagopala S, et al. Respirology. 2010 Jul;15(5):860-6. doi: 10.1111/j.1440-1843.2010.01772.x. Epub 2010 Jun 4. Respirology. 2010. PMID: 20546191 Review.
Cough and dyspnoea (56%) were the most common symptoms. The diagnosis of pulmonary amyloidosis was made subsequent to that of SS, with a median delay of 7 years. ...There is no data to support any definitive therapeutic intervention for SS-related pulmonary
Cough and dyspnoea (56%) were the most common symptoms. The diagnosis of pulmonary amyloidosis was made subsequent to that of …
18F-FDG PET scanning in pulmonary amyloidosis.
Baqir M, Lowe V, Yi ES, Ryu JH. Baqir M, et al. J Nucl Med. 2014 Apr;55(4):565-8. doi: 10.2967/jnumed.113.130823. Epub 2014 Feb 20. J Nucl Med. 2014. PMID: 24556593 Free article.
METHODS: A computer-assisted search of medical records was conducted to identify subjects with pulmonary amyloidosis (confirmed by biopsy) who were seen at the Mayo Clinic during a 15-y period between January 1, 1997, and December 31, 2011, and had a PET scan availa …
METHODS: A computer-assisted search of medical records was conducted to identify subjects with pulmonary amyloidosis (confirme …
Common variable immunodeficiency and pulmonary amyloidosis: a case report.
Arslan S, Ucar R, Yavsan DM, Esen H, Maden E, Reisli I, Calıskaner AZ. Arslan S, et al. J Clin Immunol. 2015 May;35(4):344-7. doi: 10.1007/s10875-015-0151-7. Epub 2015 Mar 14. J Clin Immunol. 2015. PMID: 25773572
We describe the first case of pulmonary hypertension secondary to pulmonary amyloidosis in a patient with CVID....
We describe the first case of pulmonary hypertension secondary to pulmonary amyloidosis in a patient with CVID....
27 results