Results 81 to 90 of about 17,718 (219)

Acute kidney injury and post-reperfusion syndrome in liver transplantation [PDF]

open access: yes, 2016
In the past decades liver transplantation (LT) has become the treatment of choice for patients with end stage liver disease (ESLD). The chronic shortage of cadaveric organs for transplantation led to the utilization of a greater number of marginal donors
Evison, Felicity   +8 more
core   +3 more sources

Clinical and pathological characteristics of patients with glomerular diseases at a university teaching hospital: 5-year prospective review [PDF]

open access: yes, 1999
OBJECTIVE. To examine the prevalence of glomerular disease in Hong Kong. DESIGN. Prospective review. SETTING. University teaching hospital, Hong Kong. PATIENTS. All patients who presented with suspected glomerular disease from 1993 through 1997. MAIN
Chan, DTM, Chan, KW, Cheng, IKP
core  

Anti-glomerular basement membrane disease superimposed on membranous nephropathy: a case report and review of the literature [PDF]

open access: yes, 2010
Introduction Anti-glomerular basement membrane disease is a rare autoimmune disorder characterized by pulmonary hemorrhage, crescentic glomerulonephritis and the presence of circulating anti-glomerular basement membrane antibodies.
Dhruval Patel   +2 more
core   +1 more source

Diagnosis of membranous nephropathy with Anti-GBM glomerulonephritis: a case series report

open access: yesBMC Nephrology
Background The concomitant occurrence of membranous nephropathy and anti-glomerular basement (anti-GBM) disease has been previously described but is extremely rare.
Ge Liu   +5 more
doaj   +1 more source

Association of extraintestinal manifestations of inflammatory bowel disease in a province of western Hungary with disease phenotype: Results of a 25-year follow-up study [PDF]

open access: yes, 2003
AIM: IBD is a systemic disease associated with a large number of extraintestinal manifestations (EIMs). Our aim was to determine the prevalence of EIMs in a large IBD cohort in Veszprem Province in a 25-year follow-up study.
Balogh, Zsuzsanna   +6 more
core   +1 more source

The continual presence of C3d but not IgG glomerular capillary deposition in stage I idiopathic membranous nephropathy in patients receiving corticosteroid treatment [PDF]

open access: yes, 2012
BACKGROUND: Pathologic diagnosis of stage I idiopathic membranous nephropathy (MN-I) requires electron microscopy or immunohistochemistry that shows a glomerular capillary staining pattern of IgG and C3.
Feng Zheng   +4 more
core   +1 more source

Membranous nephropathy in a child with crescentic glomerulonephritis: Coincidence or comorbidity?

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2019
Rapidly progressive glomerulonephritis (RPGN) is rare syndrome in children, characterized by clinical features of glomerulonephritis and rapid loss of renal function, and is associated with crescentic glomerulonephritis.
Ilknur Girisgen   +4 more
doaj   +1 more source

Pathological analysis and disease spectrum changes of renal biopsy at a single center in northern Guangxi:a report of 1703 cases

open access: yesLinchuang shenzangbing zazhi, 2022
ObjectiveTo explore the distribution characteristics and disease spectrum changes of pathological types in patients with renal puncture biopsy.MethodsFrom January,2005 to December,2019,clinicopathological data were retrospectively reviewed for 1703 renal
Huang Chun-lin   +7 more
doaj  

Pauci Immune crescentic glomerulonephritis in a patient with T-cell lymphoma and argyria [PDF]

open access: yes, 2016
Background Silver is a transition metal, toxic when ingested in significant amounts, causing argyria (skin deposition) and argyrosis (eye deposition).
Cunningham, J   +6 more
core  

Mercury-Induced Nephrotic Syndrome: A Correlation between Pathological Changes and Serum and Urine Biochemistry Parameters in Rats [PDF]

open access: yes, 1998
Nephrotic syndrome (NS) is a renal disease featured mainly by proteinuria, hypoalbuminemia, oedema, and ascites. The etiologies could be diverse while the signs and symptoms are detected only at late stages ofthe disease.
Ibrahim, Suhaidah
core  

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