Results 231 to 240 of about 3,969,240 (284)

Amyloid-Like Immunoglobulin Deposition Neuropathy. [PDF]

J Peripher Nerv Syst
Sawaya C, Fabian M, Saldaña AS, Osman C, Hadden R, Katifi H.   +5 more
europepmc   +1 more source

Biclonal gammopathy with coexistent proximal tubulopathy and cast nephropathy in multiple myeloma: a rare case report. [PDF]

BMC Nephrol
Yu S, Sun J, Mei X.
europepmc   +1 more source

Using Synthetic Glycans to Investigate Anti‐Glycan Antibodies and Explore Their Medical Potential

Angewandte Chemie International Edition, EarlyView.
Anti‐glycan antibodies are essential in health and disease. Access to novel glycan structures paves the way for progress in antibody profiling for biomarker discovery, antibody development, and vaccine design. We summarize the strategies to synthesize and utilize synthetic glycans for the development and application of anti‐glycan antibodies in basic ...
Fabienne Weber, Aina Valenti, Jiří Ledvinka, Oren Moscovitz, Peter H. Seeberger   +4 more
wiley   +1 more source

Host specificity and horizontal gene transfer in the MIB-MIP immunoglobulin evasion system in Mycoplasma gallisepticum. [PDF]

Vet Res
Ekanayake D, Vaz P, Legione AR, Wawegama NK, Browning GF, Tivendale KA.   +5 more
europepmc   +1 more source

Development and Preliminary Validation of a MALDI-TOF MS Assay Using KTI as an Internal Standard for Serum M-Protein Light Chain Analysis in Multiple Myeloma: A Pilot Study. [PDF]

Medicina (Kaunas)
Wang J, Zhao Y, Xie S, Liu H, Di M, Wang B, Tang B, Xie W, Yang X, Lai Z, Dong Y.   +10 more
europepmc   +1 more source

Early-stage IgM kappa proliferative glomerulonephritis with monoclonal immunoglobulin deposition presenting with atypical renal insufficiency: a case report and literature review. [PDF]

Front Med (Lausanne)
Cui A, Yu J, Pan T, Xu H, Xu Z.
europepmc   +1 more source

Proliferative glomerulonephritis with monoclonal IgG3 deposits: A case series. [PDF]

J Transl Autoimmun
Zhang R, Xu L, Xu J, Zhou X, Guo Z, Yu H, Song W, Feng Z, Bao Y, Yan R.   +9 more
europepmc   +1 more source

Light chain deposition disease masquerading as hypophosphatemic osteomalacia: a case report. [PDF]

Front Med (Lausanne)
Chen J, Bing Q, Liu M, Zhao S, Wang Q, Hu Q, Zhao Z.   +6 more
europepmc   +1 more source

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Immunoglobulin light chain amyloidosis

Expert Review of Hematology, 2013
Primary light chain amyloidosis is the most common form of systemic amyloidosis and is caused by misfolded light chains that cause proteotoxicity and rapid decline of vital organ function. Early diagnosis is essential in order to deliver effective therapy and prevent irreversible organ damage.
MERLINI, GIAMPAOLO, Comenzo RL, Seldin DC, Wechalekar A, Gertz MA   +4 more
openaire   +3 more sources