Results 41 to 50 of about 13,419 (176)

Renal Biopsy in Patients with Diabetes: Indications, Results, and Clinical Predictors of Diabetic Kidney Disease

open access: yesTurkish Journal of Nephrology, 2021
Objective: Diabetic kidney disease (DKD) is one of the most common etiologies of end-stage kidney disease. Kidney biopsies are performed less frequently in patients with diabetes; however, these patients can have glomerular diseases other than diabetic ...
Ayşe Serra Artan   +4 more
doaj   +1 more source

Presentation_2_Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The “Fil Rouge” of Treg Between IPEX Features and Other Clinical Entities?.ppt

open access: yes, 2022
IntroductionThe Forkhead box protein P3 (FOXP3) is a transcription factor central to the function of regulatory T cells (Treg). Mutations in the FOXP3 gene lead to a systemic disease called immune dysregulation, polyendocrinopathy, and enteropathy, an X ...
Enrico Drago (12395068)   +20 more
core   +1 more source

ST-segment elevation myocardial infarction as the first clue to membranous nephropathy: A case report. [PDF]

open access: yesMedicine (Baltimore)
Rationale: Acute ST-segment elevation myocardial infarction (STEMI) typically results from abrupt coronary occlusion, most often caused by rupture of an atherosclerotic plaque.
Wang D, Deng H, He M, He T.
europepmc   +2 more sources

Pulmonary Aspergillosis in a Patient with Membranous Nephropathy Treated with Rituximab and Cyclophosphamide: A Case Report and Literature Review

open access: yesAnnals of Case Reports, 2023
Over the past decade, the management of membranous nephropathy (MN), a common cause of nephrotic syndrome predominantly affecting adults, has rapidly developed.
Yuting Xue   +5 more
semanticscholar   +1 more source

Table_1_Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The “Fil Rouge” of Treg Between IPEX Features and Other Clinical Entities?.doc

open access: yes, 2022
IntroductionThe Forkhead box protein P3 (FOXP3) is a transcription factor central to the function of regulatory T cells (Treg). Mutations in the FOXP3 gene lead to a systemic disease called immune dysregulation, polyendocrinopathy, and enteropathy, an X ...
Enrico Drago (12395068)   +20 more
core   +1 more source

Presentation_1_Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The “Fil Rouge” of Treg Between IPEX Features and Other Clinical Entities?.ppt

open access: yes, 2022
IntroductionThe Forkhead box protein P3 (FOXP3) is a transcription factor central to the function of regulatory T cells (Treg). Mutations in the FOXP3 gene lead to a systemic disease called immune dysregulation, polyendocrinopathy, and enteropathy, an X ...
Enrico Drago (12395068)   +20 more
core   +1 more source

Complement Inhibitors in Clinical Trials for Glomerular Diseases

open access: yesFrontiers in Immunology, 2019
Defective complement action is a cause of several human glomerular diseases including atypical hemolytic uremic syndrome (aHUS), anti-neutrophil cytoplasmic antibody mediated vasculitis (ANCA), C3 glomerulopathy, IgA nephropathy, immune complex ...
Peter F. Zipfel   +6 more
doaj   +1 more source

Podocyte Infolding Glomerulopathy, First Case Report From North America

open access: yesCanadian Journal of Kidney Health and Disease, 2021
Rationale: Podocyte infolding glomerulopathy (PIG) is a newly described condition with only 37 cases reported worldwide. Due to its rarity, the pathogenesis and evolution of this disease is unclear.
Julie Anne Ting   +5 more
doaj   +1 more source

Clinical and pathological features of anti-glomerular basement membrane disease associated with membranous nephropathy: an observational study

open access: yesRenal Failure, 2022
To investigate the clinical manifestations, pathological features, pathogenesis, treatment, and prognosis of anti-glomerular basement membrane (anti-GBM) disease with membranous nephropathy (MN).
Shasha Zhang   +7 more
doaj   +1 more source

MO252: Complement 3 Deposits on Renal Tubule and Glomeruli in Phospholipase A2 Receptor-Related Idiopathic Membranous Nephropathy

open access: yesNephrology, Dialysis and Transplantation, 2022
Evidence shows galactose-deficient IgG4 is able to act complement system via lectin pathway in phospholipase A2 receptor (PLA2R) related idiopathic membranous nephropathy (IMN).
Haoyuan Cui   +4 more
semanticscholar   +1 more source

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