PedAM
Pediatric Disease Annotations & Medicines
| Disease | glomerulonephritis |
| Phenotype | C0022658|nephropathy |
| Sentences | 19 |
| PubMedID- 21450108 | Although iga nephropathy associated with mpo-anca positive glomerulonephritis has also been reported previously [17,18], renal biopsy of this case did not show any finding of necrotizing or crescentic glomerulonephritis. |
| PubMedID- 20461128 | The impact of viral genetics was recently investigated in a study that included two pediatric and four adult japanese patients, five of whom had membranous nephropathy, and one with membranoproliferative glomerulonephritis [11]. |
| PubMedID- 24330222 | In japan, iga nephropathy accounts for ≥30% of cases of chronic glomerulonephritis in adults and ≥20% of cases in children [6]. |
| PubMedID- 25647400 | Immunoglobulin a (iga) nephropathy (igan) is one of the most common glomerulonephritis in the world [1]. |
| PubMedID- 22826141 | Fibrillary glomerulonephritis complicated by membranous nephropathy in a patient with tuberculosis. |
| PubMedID- 21755057 | Nonspecific kidney disease and in one adult case iga nephropathy with anca-positive glomerulonephritis have previously been reported in patients with hermansky-pudlak syndrome. |
| PubMedID- 25839741 | Of the glomerulonephritis associated with sarcoidosis, membranous nephropathy (mn) is the most prevalent. |
| PubMedID- 26266064 | The patient received a diagnosis of severe iga nephropathy with crescentic glomerulonephritis and was initially treated with high dose corticosteroids and hemodialysis. |
| PubMedID- 21292302 | We examined the glomerular localization of myeloperoxidase by double immunofluorescence and immunoelectron microscopy in cases of anti-neutrophil cytoplasmic antibody-associated glomerulonephritis with membranous nephropathy-like immunoglobulin g deposition to investigate the immune complex antigens in these cases. |
| PubMedID- 20427882 | However, glomerulonephritis associated with iga nephropathy in dengue virus infection has not been reported previously. |
| PubMedID- 26579219 | Iga nephropathy, a leading cause of primary glomerulonephritis, is also considered an autoimmune disease [68]. |
| PubMedID- 23461642 | Historical presentations include acute progressive protein-losing nephropathy with membranoproliferative glomerulonephritis, tubular necrosis/regeneration, and interstitial nephritis, but possibly milder forms exist. |
| PubMedID- 24327929 | In glomerulonephritis patients (diagnosed with iga nephropathy, henoch-schönlein purpura nephritis, or lupus nephritis) and patients with a diagnosis of nephrotic syndrome, urinary sedimentary podocalyxin (which ppgs was a constituent) was greater than in healthy controls, and podocalyxin concentration was significantly greater in the urinary sediment of glomerulonephritis patients than that of the nephrotic patients [103]. |
| PubMedID- 23190752 | Iga nephropathy is one of the most common glomerulonephritis throughout the world, which is thought to be the multifactorial complex diseases, with genetic and environmental factors contributing to this disease. |
| PubMedID- 26380197 | Immunoglobulin a (iga) nephropathy is one of the most common glomerulonephritis and its frequency is probably underestimated because in most patients the disease has an indolent course and the kidney biopsy is essential for the diagnosis. |
| PubMedID- 22310778 | Patients infected with human immunodeficiency virus (hiv) can present, in addition to hiv-associated nephropathy, different types of immune complex glomerulonephritis, including mpgn, iga nephropathy, non-collapsing focal segmental glomerulosclerosis, membranous nephropathy and lupus-like glomerulonephritis. |
| PubMedID- 24707281 | Iga nephropathy with pathologic features of membranoproliferative glomerulonephritis following burn injury. |
| PubMedID- 25604236 | A case of immunoglobulin-a nephropathy with crescentic glomerulonephritis was described in a ptm coinfected with sivmac and mycobacterium tuberculosis [92]. |
| PubMedID- 24172683 | In cfhr5 nephropathy, familial c3 glomerulopathy of the c3 glomerulonephritis subtype, there is an internal duplication within the cfhr5 gene.3 this specific mutation can be screened by pcr using genomic dna.3 in another familial c3 glomerulopathy (originally described as mpgn type iii subtype), another rearrangement within the cfhr locus was detected in affected individuals. |
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