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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 2
1964 1
1965 1
1967 1
1970 1
1971 2
1973 2
1974 3
1975 1
1976 3
1977 3
1978 1
1979 1
1980 1
1981 5
1982 1
1983 4
1984 2
1985 5
1986 5
1987 8
1988 19
1989 28
1990 16
1991 17
1992 18
1993 19
1994 15
1995 38
1996 24
1997 17
1998 22
1999 24
2000 32
2001 38
2002 26
2003 43
2004 25
2005 42
2006 23
2007 23
2008 20
2009 21
2010 15
2011 18
2012 23
2013 21
2014 19
2015 25
2016 28
2017 23
2018 21
2019 23
2020 35
2021 21
2022 26
2023 29
2024 4

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885 results

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Page 1
Renal AA amyloidosis: presentation, diagnosis, and current therapeutic options: a review.
Karam S, Haidous M, Royal V, Leung N. Karam S, et al. Kidney Int. 2023 Mar;103(3):473-484. doi: 10.1016/j.kint.2022.10.028. Epub 2022 Dec 9. Kidney Int. 2023. PMID: 36502873 Review.
Amyloid A amyloidosis is thought to be the second most common form of systemic amyloidosis behind amyloidosis secondary to monoclonal Ig. ...
Amyloid A amyloidosis is thought to be the second most common form of systemic amyloidosis behind amyloidosis secondary …
Diagnosis and Treatment of AL Amyloidosis.
Palladini G, Milani P. Palladini G, et al. Drugs. 2023 Feb;83(3):203-216. doi: 10.1007/s40265-022-01830-z. Epub 2023 Jan 18. Drugs. 2023. PMID: 36652193 Review.
Systemic light chain (AL) amyloidosis is caused by an usually small B cell clone that produces a toxic light chain forming amyloid deposits in tissue. ...Stagings are based on cardiac and renal biomarkers and guides the choice of treatment. The combination of daratu …
Systemic light chain (AL) amyloidosis is caused by an usually small B cell clone that produces a toxic light chain forming amyloid de …
Secondary, AA, Amyloidosis.
Papa R, Lachmann HJ. Papa R, et al. Rheum Dis Clin North Am. 2018 Nov;44(4):585-603. doi: 10.1016/j.rdc.2018.06.004. Epub 2018 Sep 7. Rheum Dis Clin North Am. 2018. PMID: 30274625 Review.
Secondary, AA, amyloidosis is a rare systemic complication that can develop in any long-term inflammatory disorder, and is characterized by the extracellular deposition of fibrils derived from serum amyloid A (SAA) protein. ...The kidney is the major involved organ with pr …
Secondary, AA, amyloidosis is a rare systemic complication that can develop in any long-term inflammatory disorder, and is characteri …
Amyloidosis and the Kidney: An Update.
Nader R, Angel-Korman A, Havasi A. Nader R, et al. Semin Nephrol. 2022 Nov;42(6):151343. doi: 10.1016/j.semnephrol.2023.151343. Epub 2023 May 4. Semin Nephrol. 2022. PMID: 37148782 Review.
Various types of systemic amyloidosis can wreak havoc on the architecture and functioning of the kidneys. ...Amyloid renal staging in light chain amyloidosis amyloidosis helps inform prognosis and risk for end-stage kidney disease. ...
Various types of systemic amyloidosis can wreak havoc on the architecture and functioning of the kidneys. ...Amyloid renal sta …
Renal amyloidosis: an update on diagnosis and pathogenesis.
Gupta N, Kaur H, Wajid S. Gupta N, et al. Protoplasma. 2020 Sep;257(5):1259-1276. doi: 10.1007/s00709-020-01513-0. Epub 2020 May 24. Protoplasma. 2020. PMID: 32447467 Review.
Renal amyloidosis is characterized by the acellular Congo red-positive pathologic deposition of amyloid fibrils within glomeruli and/or the interstitium. ...This in-depth review emphasizes on the clinical features, renal pathological findings, and diagnosis o
Renal amyloidosis is characterized by the acellular Congo red-positive pathologic deposition of amyloid fibrils within glomeru
Systemic immunoglobulin light chain amyloidosis.
Merlini G, Dispenzieri A, Sanchorawala V, Schönland SO, Palladini G, Hawkins PN, Gertz MA. Merlini G, et al. Nat Rev Dis Primers. 2018 Oct 25;4(1):38. doi: 10.1038/s41572-018-0034-3. Nat Rev Dis Primers. 2018. PMID: 30361521 Review.
Systemic immunoglobulin light chain amyloidosis is a protein misfolding disease caused by the conversion of immunoglobulin light chains from their soluble functional states into highly organized amyloid fibrillar aggregates that lead to organ dysfunction. The disease is pr …
Systemic immunoglobulin light chain amyloidosis is a protein misfolding disease caused by the conversion of immunoglobulin light chai …
An Update on Familial Mediterranean Fever.
Lancieri M, Bustaffa M, Palmeri S, Prigione I, Penco F, Papa R, Volpi S, Caorsi R, Gattorno M. Lancieri M, et al. Int J Mol Sci. 2023 May 31;24(11):9584. doi: 10.3390/ijms24119584. Int J Mol Sci. 2023. PMID: 37298536 Free PMC article. Review.
(1) Background: Familial Mediterranean Fever (FMF) is the prototypal autoinflammatory disease, characterized by recurrent bursts of neutrophilic inflammation. (2) Methods: In this study we look at the most recent literature on this condition and integrate it with novel informatio …
(1) Background: Familial Mediterranean Fever (FMF) is the prototypal autoinflammatory disease, characterized by recurrent bursts of neutroph …
Renal amyloidosis: a new time for a complete diagnosis.
Feitosa VA, Neves PDMM, Jorge LB, Noronha IL, Onuchic LF. Feitosa VA, et al. Braz J Med Biol Res. 2022 Oct 3;55:e12284. doi: 10.1590/1414-431X2022e12284. eCollection 2022. Braz J Med Biol Res. 2022. PMID: 36197414 Free PMC article. Review.
The kidney is the organ most frequently involved in systemic amyloidosis. Renal amyloidosis is characterized by acellular pathologic Congo red-positive deposition of amyloid fibrils in glomeruli, vessels, and/or interstitium. ...Of note, laser microdissection …
The kidney is the organ most frequently involved in systemic amyloidosis. Renal amyloidosis is characterized by acellul …
Systemic AL amyloidosis: current approach and future direction.
Bou Zerdan M, Nasr L, Khalid F, Allam S, Bouferraa Y, Batool S, Tayyeb M, Adroja S, Mammadii M, Anwer F, Raza S, Chaulagain CP. Bou Zerdan M, et al. Oncotarget. 2023 Apr 26;14:384-394. doi: 10.18632/oncotarget.28415. Oncotarget. 2023. PMID: 37185672 Free PMC article. Review.
The autologous hematopoietic cell transplantation (HCT) after high dose melphalan therapy is an effective strategy which is usually done after initial bortezomib induction therapy. Unfortunately, most systemic AL amyloidosis patients are not candidate for HCT due to frailt …
The autologous hematopoietic cell transplantation (HCT) after high dose melphalan therapy is an effective strategy which is usually done aft …
AL amyloidosis: advances in diagnostics and treatment.
Ryšavá R. Ryšavá R. Nephrol Dial Transplant. 2019 Sep 1;34(9):1460-1466. doi: 10.1093/ndt/gfy291. Nephrol Dial Transplant. 2019. PMID: 30299492 Review.
The monoclonal light chains kappa (kappa) or lambda (lambda) or their fragments form the fibrils that deposit and accumulate in different tissues. Renal involvement is very frequent in AL amyloidosis and can lead to the development of nephrotic syndrome followed by …
The monoclonal light chains kappa (kappa) or lambda (lambda) or their fragments form the fibrils that deposit and accumulate in different ti …
885 results