Disappearance of immunoglobulins from persistent renal amyloid deposits following stem cell transplantation for heavy-and light-chain amyloidosis-Reference-Cited by-同舟云学术

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Disappearance of immunoglobulins from persistent renal amyloid deposits following stem cell transplantation for heavy-and light-chain amyloidosis

Published:2015-03-21 Issue:7 Volume:30 Page:1151-1155
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrol. Dial. Transplant.

Author:

Safadi Sami,Saad Ahmed,Quint Patrick S.,Sethi Sanjeev,Leung Nelson,Kurtin Paul,Nasr Samih H.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/30/7/1151/6838381/gfv018.pdf

Reference24 articles.

1. Kyle RA Linos A Beard CM Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989 [see comments]. Blood 1992; 79: 1817–1822

2. The diagnosis and characteristics of renal heavy-chain and heavy/light-chain amyloidosis and their comparison with renal light-chain amyloidosis

3. Primary Systemic Amyloidosis

4. A patient with persistent renal AL amyloid deposition after clinical remission by HDM/SCT therapy

5. No regression of renal AL amyloid in monoclonal gammopathy after successful autologous blood stem cell transplantation and significant clinical improvement

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1. Congophilic fibrils in the glomeruli with polyclonal immunoglobulin gamma staining - another cause for diagnostic overlap: A case report;World Journal of Clinical Cases;2024-06-16

2. Light and heavy chain deposition disease with focal amyloid deposition diagnosed with mass spectrometry: a case report;BMC Nephrology;2023-06-26

3. Light and heavy chain deposition disease with focal amyloid deposition diagnosed with mass spectrometry: A case report;2023-01-16

4. Electron Microscopy of Renal Involvement in Hematopoietic Stem-Cell Transplantation;Atlas of Renal Ultrastructural Pathology;2023

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