Disease | nephrotic syndrome |
Symptom | |proteinuria |
Sentences | 54 |
PubMedID- 22661128 | Because of a lack of ultrastructural detail (the electron microscopy was not invented until 50 years later) and limited by only a superficial insight in renal inflammatory processes, the authors failed to recognize the glomerulus as the origin of proteinuria in patients with the nephrotic syndrome and placed too much emphasis on tubular reabsorption patterns coined lipoid nephrosis. |
PubMedID- 23162265 | The limited evidence suggested that dfz appeared to be equally effective in inducing remission or decreasing proteinuria in patients with nephrotic syndrome. |
PubMedID- 23559294 | Background: collapsing glomerulopathy is a cause of nephrotic syndrome with massive proteinuria secondary to podocyte proliferation and glomerular collapse. |
PubMedID- 21132650 | A 47-year-old woman was referred to our unit for evaluation of proteinuria associated with nephrotic syndrome. |
PubMedID- 25834748 | At the age of 35, he had proteinuria and was diagnosed with nephrotic syndrome and kidney injury. |
PubMedID- 24860853 | Although sirolimus is not generally thought to be nephrotoxic, it can be associated with proteinuria, which can lead to nephrotic syndrome and subsequent kidney injury (25). |
PubMedID- 25558821 | Immunosuppressive agents should be used for patients who suffer from refractory proteinuria or complications associated with nephrotic syndrome. |
PubMedID- 23434736 | The proband presented at 3 weeks of age with generalised oedema and was found to have severe hypoalbuminaemia and proteinuria and was diagnosed with congenital nephrotic syndrome. |
PubMedID- 26511325 | Furthermore, a systemic hyperosmolar state from proteinuria and hypoalbuminemia associated with nephrotic syndrome contributes to the leakage of fluid into the suprachoroidal space 6. |
PubMedID- PMC4044283 | Subsequently, the patient developed proteinuria with nephrotic syndrome. |
PubMedID- 26054711 | Conclusions: serum half-life of rtx can be extremely short, partly due to excessive urinary losses in therapy-resistant nephrotic syndrome with non-selective proteinuria, as seen in our patient. |
PubMedID- 24798567 | Rituximab, a chimeric monoclonal antibody against the cd20 antigen on b cells, safely reduced proteinuria in patients with nephrotic syndrome secondary to membranous nephropathy, minimal change disease, or focal segmental glomerulosclerosis. |
PubMedID- 24611049 | In the systemic loop, it binds to glomerular endothelial αvβ5 integrin and reduces proteinuria, the principal driver of nephrotic syndrome. |
PubMedID- 20483511 | Diagnostic strategy relies on the clinical presentation: acute renal failure, chronic kidney disease, glomerular proteinuria with or without nephrotic syndrome, tubular proteinuria, hydroelectrolytic disorders. |
PubMedID- 23275781 | In february 2011, the patient was referred to the department of nephrology for the appearance of edema, increase of the serum creatinine up to 1.5 mg/dl (egfr 45.0 ml/min/1.73 m2), weight gain (weight was 67.5 kg), nephrotic syndrome with proteinuria of 12 g/24 h, dyslipidemia, and hypoalbuminemia. |
PubMedID- 23670304 | Podocyte loss correlated with lower selectivity of proteinuria in patients with minimal change nephrotic syndrome and focal segmental glomerulosclerosis (r = -0.90; p < 0.001). |
PubMedID- 24282415 | Due to persistent activation of the chronic inflammatory process, whether clinically manifested orsubclinically, excess saa is deposited in the form of fibrils in various organs, particularly the kidneys, with the consequent progressive development of severe proteinuria, leading to nephrotic syndrome and kidney failure. |
PubMedID- 20649959 | As previously reported , a single injection of pan (150 mg/kg body wt) to rats induced a marked nephrotic syndrome with severe proteinuria (~10 g/mmol creatinine) and decreased sodium excretion (< 5 mmol/mmol creatinine) (figure 4a). |
PubMedID- 24527245 | These cytokine and inflammatory mediators are thought to damage the glomerular foot processes, leading to proteinuria and other sequelae of nephrotic syndrome 8. |
PubMedID- 23878704 | They further described a glomerulopathy, which was characterised by heavy proteinuria, biochemical features of nephrotic syndrome, renal impairment that rapidly progressed to end stage renal disease (rao et al., 1984). |
PubMedID- 22078716 | Hypo-albuminemia accompanied by significant proteinuria is a component of the nephrotic syndrome that may accompany active lupus renal disease. |
PubMedID- 21403411 | Although a moderate degree of proteinuria is common in patients with igan, nephrotic syndrome is considered uncommon in these patients.3 the course of igan is variable, and 15% to 40% of patients progress to end-stage renal disease over a period of 10 to 20 years.4 the pathogenesis of igan is complex and not completely understood. |
PubMedID- 25874088 | Here we report an association between collapsing glomerulopathy and an acute ebv syndrome, manifesting itself clinically as nephrotic syndrome with massive proteinuria, hypoalbuminemia, anasarca and hypercholesterolemia. |
PubMedID- 22909024 | They are characterized by heavy proteinuria, with nephrotic syndrome and impaired renal function in half of the patients. |
PubMedID- 21497573 | Renal manifestations are frequent, mostly characterized by heavy proteinuria, with nephrotic syndrome and renal failure in more than half of the patients at diagnosis. |
PubMedID- 24886259 | Mutations in the podocin gene cause severe structural podocyte alterations and massive proteinuria leading to nephrotic syndrome . |
PubMedID- 23782479 | Haematuria and proteinuria and subsequent development of nephrotic syndrome and chronic kidney disease (ckd) represent the commonest manifestations of hiv-related glomerular disease (table 1) . |
PubMedID- 23006339 | In september 2010, her nephrotic syndrome returned with proteinuria (9.5 g/d), anasarca (11.3 kg weight gain), hyperlipidemia (total cholesterol 332 mg/dl, ldl 229 mg/dl, triglycerides 270 mg/dl), and a cr of 1.9 mg/dl. |
PubMedID- 23569546 | Gemcitabine treatment may be associated with proteinuria to the extent of nephrotic syndrome. |
PubMedID- 24749114 | A year after the beginning of the symptoms she sought medical attention: a diagnosis of nephrotic syndrome with proteinuria >10 g/l was made. |
PubMedID- 24404368 | During the follow-up period on allopurinole and anti-proteinuirc treatment, the patient had normal renal function with mild to moderate proteinuria and no recurrence of nephrotic syndrome. |
PubMedID- 23197960 | In conclusion, bilateral rae is an alternative, effective, rapid, and safe procedure for the treatment of heavy proteinuria with nephrotic syndrome. |
PubMedID- 23759297 | Results: all patients presented with proteinuria, associated with nephrotic syndrome (41%), hematuria (73%), and hypertension (70%). |
PubMedID- 22534961 | In 129x1/svj mice, proteinuria, chemical indices of nephrotic syndrome and glomerular and tubulointerstitial accumulation of type-i collagen and fibronectin occur sequentially after adr administration. |
PubMedID- 25886386 | Studies also showed that as-iv can attenuate podocyte injury and ameliorate proteinuria in adults with idiopathic nephrotic syndrome . |
PubMedID- 23295293 | Nephropathy in fs consists in nephrotic syndrome (ns) with proteinuria that begins early in childhood and progressively increases with age, mainly due to nonspecific focal and segmental glomerular sclerosis (fsgs). |
PubMedID- 19773419 | Recurrence of nephrotic-range proteinuria in patients with idiopathic nephrotic syndrome (ins) and focal and segmental glomerulosclerosis (fsgs) on native kidneys is associated with poor graft survival. |
PubMedID- 21534236 | Clinically, lg is characterized by proteinuria generally associated with nephrotic syndrome and progressive renal insufficiency. |
PubMedID- 21904677 | The development of nephrotic-range proteinuria, without full nephrotic syndrome, is consistent with the role of b4 as a minor podocyte integrin. |
PubMedID- 26395882 | In the first year of life, 66 % of the patients suffering from hypoalbuminemia and severe proteinuria are diagnosed with genetic nephrotic syndrome (gns) 1. |
PubMedID- 24294005 | At the time of biopsy, six (75%) of them had nephrotic syndrome with mean proteinuria of 3.8 ± 2.24 g/day. |
PubMedID- 23476687 | Mutations in the podocin gene cause severe structural podocyte alterations and massive proteinuria leading to nephrotic syndrome . |
PubMedID- 21502717 | Renal amyloidosis is typically characterized by nephrotic syndrome, often with massive proteinuria and refractory peripheral edema. |
PubMedID- 21335185 | Post-olt 3 patients developed proteinuria, 2 of whom showed increasing nephrotic syndrome. |
PubMedID- 26447100 | Background: proteinuria leading to nephrotic syndrome is a rare adverse event arising from treatment with bevacizumab. |
PubMedID- 24317117 | Circulating angiopoietin-like 4 links proteinuria with hypertriglyceridemia in nephrotic syndrome. |
PubMedID- 21151138 | Therefore, treatment with sialic acid precursors constitute a potential therapeutic tool to reduce proteinuria in some forms of nephrotic syndrome. |
PubMedID- 23479095 | Presenting features comprise any of the following: proteinuria (sometimes with the nephrotic syndrome), haematuria, hypertension and renal failure. |
PubMedID- 26551740 | Focal segmental glomerulosclerosis (fsgs) is a pathologic entity that is a common cause of nephrotic syndrome with severe proteinuria in both adults and children. |
PubMedID- 22461531 | Results: initially, 95% of patients had nephrotic syndrome with proteinuria of 3-12 g per 24 hours, creatinine levels of 0.6-9.6 mg/dl, positive lupus serologies, and normal complement levels in 63%. |
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