Is it possible to predict parameters of the Oxford classification of primary IgA Nephropathy from clinical laboratory data? Focus on the role of segmental glomerulosclerosis subtypes

Author:

Monteiro Maria Luiza Gonçalves dos Reis,Vieira Matheus Rodrigues,Pereira Lívia Helena Morais,Araújo Liliane Silvano,Silva Crislaine Aparecida,Araújo Lúcio Borges,Rocha Laura Penna,Reis Marlene Antônia dos,Machado Juliana Reis

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado de Minas Gerais

Fundação de Ensino e Pesquisa de Uberaba

Publisher

Elsevier BV

Subject

Cell Biology,Pathology and Forensic Medicine

Reference25 articles.

1. Intercapillary deposits of IgA-IgG;Berger;J. Urol. Nephrol.,1968

2. IgA nephropathy in blacks and Indians of Natal;Seedat;Nephron,1988

3. Natural history of idiopathic IgA nephropathy: role of clinical and histological prognostic factors;D’Amico;Am. J. Kidney Dis.,2000

4. Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity;Suzuki;J. Clin. Invest.,2009

5. Idiopathic IgA mesangial nephropathy;D’Amico;Nephron,1985

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