Results 1 to 10 of about 1,107 (143)

Clinical Determinants of Urinary Podocyte Biomarkers and Their Feasibility in Paraprotein-Related Kidney Disease [PDF]

open access: yesDiagnostics
Background/Objectives: Kidney injury is a frequent complication of multiple myeloma (MM) and monoclonal gammopathies. Podocyte stress markers, such as urinary nephrin and podocin, have been studied in other renal diseases but their utility in paraprotein-
Oliver Helk   +6 more
doaj   +2 more sources

Systematic Review of Kidney Transplant Outcomes in Monoclonal Ig Deposition Disease [PDF]

open access: yesKidney International Reports
Introduction: Historical case series of monoclonal Ig deposition disease (MIDD) after kidney transplantation (KTx) reported unfavorable outcomes. Recent case series support more acceptable outcomes in selected patients.
Cihan Heybeli, Nelson Leung
doaj   +2 more sources

Dysproteinemia-Associated Kidney Disease: A Single-Center Observational Study [PDF]

open access: yesRevista Portuguesa de Nefrologia e Hipertensão, 2022
Introduction: Dysproteinemia is associated with kidney damage and treatment of underlying conditions is crucial to minimize kidney damage. The aim of this study was to describe and analyze the characteristics and outcome of the patients diagnosed with ...
João Bernardo   +7 more
doaj   +1 more source

Macroglobulinemia de Waldenström: primer caso con confirmación molecular en Honduras [PDF]

open access: yesRevista Médica Hondureña, 2021
Antecedentes: La Macroglobulinemia de Waldens tröm (MW) es un desorden proliferativo en el cual está presente un Linfoma Linfoplasmocitoide (LLP) en la médula ósea y asociado a una gammapatía monoclonal IgM.
Flora Duarte   +5 more
doaj   +1 more source

Paraproteinemia and neuropathy

open access: yesNeurological Sciences, 2021
Paraproteinemia is associated with different peripheral neuropathies. The major causes of neuropathy correlated with paraproteinemia are the deposition of immunoglobulin in the myelin, represented by anti-myelin-associated glycoprotein (MAG) neuropathy; deposition of immunoglobulin or its fragment in the interstitium, represented by immunoglobulin ...
Haruki Koike, Masahisa Katsuno
openaire   +2 more sources

Data on the clinical, analytical, and laboratory factors associated with negative anion gaps at an academic medical center

open access: yesData in Brief, 2022
The anion gap is a calculated parameter derived from the difference between the major plasma cations and anions in serum/plasma or whole blood, with a widely used simple equation utilizing concentrations of sodium, chloride, and bicarbonate.
Joseph M. Laakman   +2 more
doaj   +1 more source

Ileo-ileal Intussusception and Bowel Obstruction Caused by Plasmablastic Lymphoma of Small Bowel- A Rare Entity in Rare Location [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Intussusception of small bowel is considered a rare cause of bowel obstruction in adults accounting for only about 1% of bowel obstruction in adults. Intussusception in adults is uncommon with 95% cases of intussusceptions occurring in children.
Aditya Atul Kulkarni, Sanjiv S. Thakur
doaj   +1 more source

Identification of Monoclonal Immunoglobulins by Immunofixation Electrophoresis - Some Questions

open access: yesActa Medica, 1999
In the series of 2413 paraproteins analyzed by immunoelectrophoresis during 30 years, doubled paraproteinemias were found 42 times, i.e. a frequence of 1.7%.
Miloš Tichý
doaj   +1 more source

Spectacular skin nodules: Cutaneous necrobiotic xanthogranuloma without paraproteinemia

open access: yesIndian Journal of Dermatology, 2012
Necrobiotic xanthogranuloma (NXG) is a very rare, progressive variant of non-Langerhans cell histiocytosis. It is known to be associated with multisystem involvement and paraproteinemias.
Shimoni Kadakia   +3 more
doaj   +1 more source

Multiple Myeloma Presenting as Digital Ischaemia Mimicking Rheumatoid Vasculitis: A Diagnostic Challenge [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Multiple myeloma commonly presents with anaemia, bone pain, renal dysfunction, hypercalcaemia, and lytic bone lesions. However, digital ischaemia and gangrenous ulceration as an initial manifestation are exceedingly rare and may mimic rheumatologic or ...
Suryanarayana Reddy Kovvuri   +4 more
doaj   +1 more source

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