PedAM
Pediatric Disease Annotations & Medicines
| Disease | focal segmental glomerulosclerosis |
| Phenotype | C0027726|nephrotic syndrome |
| Sentences | 20 |
| PubMedID- 20590696 | At the age of three yr, a male patient had surgical treatment for bilateral vesicoureteral reflux (vur), and at the age of 19 yr, he developed nephrotic syndrome because of focal segmental glomerulosclerosis (fsgs). |
| PubMedID- 26220221 | Risk factors of venous thromboembolism in focal segmental glomerulosclerosis with nephrotic syndrome. |
| PubMedID- 25883898 | His medical history revealed nephrotic syndrome due to focal segmental glomerulosclerosis, which was diagnosed 24 years previously and had progressed to chronic renal failure requiring dialysis therapy. |
| PubMedID- 20567873 | A 74-year-old man was diagnosed with nephrotic syndrome due to focal segmental glomerulosclerosis, and steroid therapy was initiated. |
| PubMedID- 24719498 | Mmp-9/ngal ratio is considered an important marker of the differentiation of minimal change disease and focal segmental glomerulosclerosis in children with nephrotic syndrome [120]. |
| PubMedID- 24771498 | Tacrolimus therapy in adult-onset steroid-resistant nephrotic syndrome due to a focal segmental glomerulosclerosis single-center experience. |
| PubMedID- 26275234 | Background: we investigated the efficacy of rituximab and low-dose cyclosporine combination therapy for focal segmental glomerulosclerosis (fsgs) children with steroid-resistant nephrotic syndrome (srns). |
| PubMedID- 23461215 | [a case of focal segmental glomerulosclerosis with nephrotic syndrome after hematopoietic stem cell transplantatation for aplastic anemia]. |
| PubMedID- 24701046 | We present a case of kin in a child, who was also found to have nephrotic syndrome because of focal segmental glomerulosclerosis on renal biopsy. |
| PubMedID- 24093110 | Urinary igg and alpha2-macroglobulin are powerful predictors of outcome and responsiveness to steroids and cyclophosphamide in idiopathic focal segmental glomerulosclerosis with nephrotic syndrome. |
| PubMedID- 23901340 | Subgroup 1 included 40 patients with steroid resistant nephrotic syndrome (histopathology of focal segmental glomerulosclerosis, fsgs) and subgroup 2 contained 39 kidney transplant recipients. |
| PubMedID- 24429405 | Serum-soluble urokinase receptor levels do not distinguish focal segmental glomerulosclerosis from other causes of nephrotic syndrome in children. |
| PubMedID- 24856380 | Genomic dna samples from polish children (n=33) with steroid-resistant nephrotic syndrome (srns) due to focal segmental glomerulosclerosis (fsgs), manifesting before the age of 13 years old, underwent retrospective analysis of nphs1, nphs2, wt1 (exons 8, 9 and adjacent exon/intron boundaries) and lamb2. |
| PubMedID- 24535024 | In japan, ldl-a to control hyperlipidemia in patients with refractory nephrotic syndrome associated with focal segmental glomerulosclerosis is covered by national health insurance. |
| PubMedID- 23168861 | An 18-year-old man presented with severe nephrotic syndrome due to focal segmental glomerulosclerosis. |
| PubMedID- 26005937 | The first one is a disseminated strongyloidiasis occurred in an ecuadorian male on corticosteroid therapy for nephrotic syndrome due to focal segmental glomerulosclerosis, successfully treated with ivermectin; the second one involves another ecuadorian male affected by acute kidney failure and nephrotic syndrome in iga nephropathy with a diagnosis of chronic strongyloidiasis performed before starting the immunosuppressive treatment. |
| PubMedID- 23602193 | Motivated by a patient with subacute-onset nephrotic syndrome, histologic features of secondary focal segmental glomerulosclerosis, and concurrent mercury toxicity, we conducted a systematic review to explore renal histologic changes in patients with toxic mercury exposures and nephrotic syndrome. |
| PubMedID- 24059478 | We report a case of focal segmental glomerulosclerosis with nephrotic syndrome secondary to high-altitude polycythemia (hapc). |
| PubMedID- 20191367 | We describe the novel association in a girl of nephrotic syndrome due to focal segmental glomerulosclerosis, bilateral sensorineural deafness, basal ganglia calcification, bilateral retinopathy similar to that seen in coats' disease, with de novo duplication of a subtelomeric region of chromosome 4q35. |
| PubMedID- 24381395 | We present a patient with steroid-resistant nephrotic syndrome due to focal segmental glomerulosclerosis along with smoldering multiple myeloma. |
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