Results 101 to 110 of about 149,546 (225)

Galactose‐Deficient Immunoglobulin A1 Predicts Immunoglobulin A Nephropathy Recurrence After Kidney Transplantation: A Single‐Center Retrospective Study

open access: yesOrgan Medicine, Volume 3, Issue 3, Page 139-147, September 2026.
Serum galactose‐deficient IgA1 levels at 3 and 6 months predicted recurrent IgA nephropathy after kidney transplantation. Recipients without recurrence showed a rapid decline in galactose‐deficient IgA1 after transplantation. Early identification of recurrence risk provided a potential window for targeted post‐transplant intervention.
Ronghai Deng   +10 more
wiley   +1 more source

A case of rapidly progressive IgA nephropathy in a patient with exacerbation of Crohn’s disease

open access: yesBMC Nephrology, 2012
Background IgA nephropathy has been reported as a renal involvement in Crohn’s disease. Crescentic IgA nephropathy, which accounts for fewer than 5% of cases of IgA nephropathy, has a poorer prognosis than other forms of crescentic glomerulonephritis. We
Choi Ji-Young   +8 more
doaj   +1 more source

BAFF and APRIL Receptors in B Cell Immunity and Autoimmunity

open access: yesImmunological Reviews, Volume 342, Issue 1, September 2026.
ABSTRACT BAFF and APRIL are TNF superfamily proteins that bind to BAFFR, TACI and BCMA, members of the TNF receptor superfamily. These proteins have both unique and overlapping roles in B cell development and survival and are major therapeutic targets for antibody‐ and B‐cell‐driven pathologies.
Daisy H. Luff   +2 more
wiley   +1 more source

Emerging Modes of Treatment of IgA Nephropathy

open access: yes, 2020
IgA nephropathy is the most common primary glomerulonephritis with potentially serious outcome leading to end stage renal disease in 30 to 50% of patients within 20 to 30 years.
Vladimir Tesar, Dita Maixnerova
core   +1 more source

Charge and size of mesangial IgA in IgA nephropathy [PDF]

open access: yes, 1985
Charge and size of mesangial IgA in IgA nephropathy. To characterize the physicochemical properties of the mesangial IgA in primary IgA nephropathy, acid-eluates from percutaneous renal biopsies of 20 patients were examined.
Noel, Laure-Hélène   +5 more
core   +1 more source

Exploration of Artemisinin Against IgA Nephropathy via AKT/Nrf2 Pathway by Bioinformatics and Experimental Validation

open access: yesDrug Design, Development and Therapy, 2023
Wei-guang Yang,* Ao Sun,* Rong Zhu, Nan Liu, Wei-jie He, Lin-lin Liu Department of Nephrology, The First Affiliated Hospital of China Medical University, Shen Yang, Liao Ning, People’s Republic of China*These authors contributed equally to ...
Yang WG   +5 more
doaj  

Office Blood Pressure and Arteriolosclerosis in Biopsy‐Proven Glomerulonephritis: Association With Renal Function Decline and Clinical Outcomes

open access: yesThe Journal of Clinical Hypertension, Volume 28, Issue 9, September 2026.
ABSTRACT Hypertension is a major determinant of chronic kidney disease progression, yet the relationship between standardized office blood pressure measurements (OBPM), chronic vascular lesions, and prognosis in biopsy‐proven glomerulonephritis (GN) remains poorly defined. We investigated the association between OBPM and renal histopathological lesions,
Antonietta Gigante   +8 more
wiley   +1 more source

CD44 expression in IgA nephropathy

open access: yes, 2002
Immunoglobulin A (IgA) nephropathy is a frequent, chronic renal disease characterized by a broad spectrum of clinical presentations and pathologic findings.
Nunziata, Raffaele   +5 more
core   +1 more source

IgA Nephropathy in North West Frontier Province of Pakistan

open access: yesGomal Journal of Medical Sciences, 2004
Background: IgA nephropathy is the most common form of glomerulonephritis in the world. The extent to which IgA nephropathy is diagnosed depends upon the local attitude towards urine testing and renal biopsy.
Mohammad Noor   +4 more
doaj  

A case of renal hypouricemia due to T217M mutation in SLC22A12 incidentally associated with IgA nephropathy

open access: yesClinical Case Reports
Key Clinical Message A T217M heterozygous mutation in the SLC22A12 gene caused renal hypouricemia; this patient with IgA nephropathy had no findings other than IgA nephropathy on renal biopsy.
Yoshimasa Sakurabu   +15 more
doaj   +1 more source

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