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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 31, 1998
Polymorphisms in angiotensin-converting enzyme gene and severity of renal disease in Henoch-Schoenlein patients. Italian Group of Renal ImmunopathologyA Amoroso, G Danek, S Vatta, et al.
Genetics and Molecular Research : GMR|January 20, 2016
Meta-analysis of STAT4 and IFIH1 polymorphisms in type 1 diabetes mellitus patients with autoimmune polyglandular syndrome type IIIJ de Azevêdo Silva, N A C Tavares, M M S Santos, et al.
Journal of Nephrology|December 4, 2001
Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12D Pirulli, D Puzzer, M De Fusco, et al.
Journal of Toxicology and Environmental Health. Part A|December 22, 2017
A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesotheliomaS Crovella, R R Moura, S Cappellani, et al.
Lupus|February 11, 2012
Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern BraziliansP Sandrin-Garcia, L A C Brandão, R L Guimarães, et al.
Genetics and Molecular Research : GMR|November 25, 2015
Trace samples of human blood in mosquitoes as a forensic investigation toolK C N Rabêlo, C M R Albuquerque, V B Tavares, et al.
International Journal of Immunogenetics|February 25, 2012
Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patientsC B Filho, F F Rodrigues, L Segat, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 29, 2001
Polymorphisms in the promoter region and at codon 54 of the MBL2 gene are not associated with IgA nephropathyD Pirulli, M Boniotto, L Vatta, et al.
Clinical and Experimental Medicine|November 9, 2001
Detection of AGXT bgene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1D Pirulli, M Giordano, M Lessi, et al.
International Journal of Immunogenetics|September 17, 2013
DEFB1 gene 5' untranslated region (UTR) polymorphisms are marginally involved in inflammatory bowel disease in south BraziliansT J Wilson, M Jobim, L Segat, et al.
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