Disease | c syndrome |
Comorbidity | C0033687|proteinuria |
Sentences | 52 |
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- 25886386 | Studies also showed that as-iv can attenuate podocyte injury and ameliorate proteinuria in adults with idiopathic nephrotic syndrome [16]. |
PubMedID- 23759297 | Results: all patients presented with proteinuria, associated with nephrotic syndrome (41%), hematuria (73%), and hypertension (70%). |
PubMedID- 21151138 | Therefore, treatment with sialic acid precursors constitute a potential therapeutic tool to reduce proteinuria in some forms of nephrotic syndrome. |
PubMedID- 22543358 | Similarly, podocyte-specific (p)rr knock-out mice are born at mendelian rates, but, early in life, develop nephritic syndrome, with severe proteinuria and albuminuria due to progressive glomerular sclerosis, and die within 2–4 weeks of renal failure [68, 79, 84]. |
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- 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- 21844386 | Mice developed a nephrotic syndrome with severe edema, proteinuria, hypoalbuminemia, and elevated cholesterol and triglycerides. |
PubMedID- 20419132 | Mutations of the nephrin gene lead to congenital nephrotic syndrome with proteinuria and renal failure [12]. |
PubMedID- 24508002 | Presenting features comprise proteinuria (sometimes with nephritic syndrome), haematuria, hypertension and renal failure. |
PubMedID- 21132650 | A 47-year-old woman was referred to our unit for evaluation of proteinuria associated with nephrotic syndrome. |
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- 24151517 | In addition, metabolic syndrome has been associated with proteinuria and reduced gfr, suggesting a link to chronic kidney disease [93, 94]. |
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- 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- 24317117 | Circulating angiopoietin-like 4 links proteinuria with hypertriglyceridemia in nephrotic syndrome. |
PubMedID- 24701044 | Because of the complex clinical syndrome (hypertensive encephalopathy syndrome coupled with proteinuria and active urine sediments), a percutaneous renal biopsy was performed. |
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- 21534236 | Clinically, lg is characterized by proteinuria generally associated with nephrotic syndrome and progressive renal insufficiency. |
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- 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%. |
PubMedID- 21335185 | Post-olt 3 patients developed proteinuria, 2 of whom showed increasing nephrotic syndrome. |
PubMedID- 23559294 | Background: collapsing glomerulopathy is a cause of nephrotic syndrome with massive proteinuria secondary to podocyte proliferation and glomerular collapse. |
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- 25834748 | At the age of 35, he had proteinuria and was diagnosed with nephrotic syndrome and kidney injury. |
PubMedID- 25558821 | Immunosuppressive agents should be used for patients who suffer from refractory proteinuria or complications associated with nephrotic syndrome. |
PubMedID- 21688191 | In contrast, the much rarer homozygous or compound heterozygous of such mutations in the col4a3/col4a4 genes develop the classical autosomal recessive alport syndrome course with early proteinuria and hypertension, reaching eskd by late adolescence and the early 20s. |
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- 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- 20649959 | As previously reported [3,9], 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- 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- 21462608 | The nephritic syndrome is associated with hematuria and proteinuria and abnormal kidney function and carries poorer prognosis and is typically associated with hypertension. |
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- 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- 23433013 | High pulse pressure and metabolic syndrome are associated with proteinuria in young adult women. |
PubMedID- 22909024 | They are characterized by heavy proteinuria, with nephrotic syndrome and impaired renal function in half of the patients. |
PubMedID- 26447100 | Background: proteinuria leading to nephrotic syndrome is a rare adverse event arising from treatment with bevacizumab. |
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- 23197960 | In conclusion, bilateral rae is an alternative, effective, rapid, and safe procedure for the treatment of heavy proteinuria with 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- 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- 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- 25688242 | Lupus nephritis is a frequent and potentially serious complication among patient with systemic lupus erythematosus whose clinical manifestations are varied being the most common manifestations proteinuria (commonly leading to nephrotic syndrome), microscopic hematuria, and reduced gfr. |
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- 24886259 | Mutations in the podocin gene cause severe structural podocyte alterations and massive proteinuria leading to nephrotic syndrome [22]. |
PubMedID- PMC4044283 | Subsequently, the patient developed proteinuria with nephrotic syndrome. |
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- 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. |
Page: 1 2