Results 131 to 140 of about 27,127 (159)

Summary of Papers Presented at the 45th Annual McGuire Lecture Series [PDF]

, 1974
It is the purpose of this presentation to quickly review some of the important points of the papers which were presented at the 45th Annual McGuire Lecture Series on the subject of immunology and rheumatic ...
Irby, Robert
core   +1 more source

Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis

American journal of hematology/oncology, 2005
M. Gertz, R. Comenzo, R. Falk, J. Fermand, B. Hazenberg, P. Hawkins, G. Merlini, P. Moreau, P. Ronco, V. Sanchorawala, O. Sezer, A. Solomon, G. Grateau   +12 more
semanticscholar   +1 more source

Renal amyloidosis revisited: amyloid distribution, dynamics and biochemical type [PDF]

, 2017
Background. Renal amyloidosis results from protein misfolding and leads to progressive renal insufficiency. Few data are available concerning the relevance of the histomorphological patterns and the dynamics of the disease process. Methods.
Hopfer, Helmut, Mihatsch, Michael J., Wiech, Thorsten   +2 more
core  

A case of pulmonary transthyretin amyloidosis with concurrent mycobacterial tuberculosis infection

Respirology Case Reports
Amyloidosis is a pathological deposition disease that causes a spectrum of organ dysfunction. Pulmonary involvement is generally associated with immunoglobulin light chain type (AL) amyloid. Transthyretin (ATTR) amyloid build up in the lung is thought to
Hanson Siu, Ari Mond, James Shaw, Ruth Chin, Patrick Hosking, Hari Wimaleswaran   +5 more
doaj   +1 more source

Amyloid Neuropathy: From Pathophysiology to Treatment in Light‐Chain Amyloidosis and Hereditary Transthyretin Amyloidosis

Annals of Neurology
Amyloid neuropathy is caused by deposition of insoluble β‐pleated amyloid sheets in the peripheral nervous system. It is most common in: (1) light‐chain amyloidosis, a clonal non‐proliferative plasma cell disorder in which fragments of immunoglobulin ...
Pitcha Chompoopong, M. Mauermann, Hasan K. Siddiqi, Amanda Peltier   +3 more
semanticscholar   +1 more source

Hyperimmunoglobulinemia D and periodic fever : A new syndrome [PDF]

, 1984
Contains fulltext : 4434.pdf (publisher's version ) (Open ...
Furth, R. van, Lobatto, S., Meer, J.W.M. van der, Meijer, C.J.L.M., Nieuwkoop, J.A. van, Radl, J., Vossen, J.M.   +6 more
core   +1 more source

Treatment Options For Relapsed/refractory Systemic Light-Chain (AL) Amyloidosis: Current Perspectives

Journal of Blood Medicine, 2019
Shayna Sarosiek, Vaishali Sanchorawala Amyloidosis Center, Boston University School of Medicine and Boston Medical Center, Boston, MA, USACorrespondence: Shayna Sarosiek; Vaishali SanchorawalaAmyloidosis Center, Boston University School of Medicine and ...
Sarosiek S, Sanchorawala V
doaj  

Chinese consensus on the diagnosis and treatment of immunoglobulin light-chain cardiac amyloidosis

Chinese Medical Journal, 2023
Kaini Shen, Zhuang Tian, Yajuan Gao, Yining Wang, Li Huo, Jian Li, Yun Zhang, Shuyang Zhang   +7 more
semanticscholar   +1 more source

Clarifying immunoglobulin gene usage in systemic and localized immunoglobulin light-chain amyloidosis by mass spectrometry.

Blood, 2017
T. Kourelis, S. Dasari, J. Theis, M. Ramirez-Alvarado, Paul J. Kurtin, M. Gertz, S. Zeldenrust, Roman M. Ženka, A. Dogan, A. Dispenzieri   +9 more
semanticscholar   +1 more source

An Unusual Cardiac Manifestation of Multiple Myeloma [PDF]

, 2011
Chehab, Bassem, Tadros, Peter, Wiley, Mark   +2 more
core   +2 more sources