Miroslav Merta
Prague, PR 12800, Czech Republic
Last Updated: 09/26/2026
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Found 11 publications
Molecular profiling in IgA nephropathy and focal and segmental glomerulosclerosis.
Journal: Physiological research
Published: November 16, 2017
Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.
Journal: BMC nephrology
Published: May 22, 2017
IgA nephropathy in Czech patients--are we able reliably predict the outcome?
Journal: Kidney & blood pressure research
Published: November 14, 2014
Nationwide biopsy survey of renal diseases in the Czech Republic during the years 1994-2011.
Journal: Journal of nephrology
Published: October 09, 2013
Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease.
Journal: BMC medical genetics
Published: August 13, 2013
Does KDIGO (Clinical Practice Guideline for Glomerulonephritis) represent a change in the diagnosis and treatment of glomerulonephritis?--editorial
Journal: Vnitrni lekarstvi
Published: April 20, 2013
Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.
Journal: BMC nephrology
Published: October 10, 2012
The coincidence of IgA nephropathy and Fabry disease.
Journal: BMC nephrology
Published: August 07, 2012
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
Journal: Folia biologica
Published: May 15, 2012
Can adequate treatment influence the postembolization syndrome and cytokine release in patients undergoing iatrogenic renal artery embolization?
Journal: Prague medical report
Published: December 07, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026