Renal-limited lupus-like glomerulonephritis

Autor:	Santiago Suria González, Noemí Esparza Martín, Ernesto Fernández Tagarro, Rita Guerra Rodríguez, César García Cantón
Rok vydání:	2017
Předmět:	Pathology medicine.medical_specialty Systemic lupus erythematosus business.industry Lupus nephritis Autosomal dominant polycystic kidney disease Glomerulonephritis Analgesic nephropathy medicine.disease Renal tubular acidosis Immune system Automotive Engineering medicine Alport syndrome business
Zdroj:	Archives of Renal Diseases and Management. :048-048
ISSN:	2455-5495
DOI:	10.17352/2455-5495.000029
Popis:	In the setting of an IgG-dominant immune complexmediated glomerulonephritis, there are multiple pathological fi ndings that strongly suggest the diagnosis of lupus nephritis (LN) including “full-house” immunofl uorescence staining for IgG, IgM, IgA, C3 and C1
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f4486826df5df6e8d852d0badcbc5790 https://doi.org/10.17352/2455-5495.000029 Zobrazit plný text záznamu