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M Merta

Showing results (51-60 of 99) with videos related to

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Prague Medical Report|October 28, 2006
The pathogenetic aspects and gene polymorphisms of IgA nephropathyD Maixnerová, M Merta, J Reiterová, et al.
Physiological Research|August 6, 2003
Role of endothelin and nitric oxide in the pathogenesis of arterial hypertension in autosomal dominant polycystic kidney diseaseM Merta, J Reiterová, R Rysavá, et al.
Sbornik Lekarsky|January 1, 1994
[Plasma volume in polycystic kidney disease]M Merta, V Chábová, V Tesar, et al.
Prague Medical Report|June 7, 2006
Genetic basis of nephrotic syndrome--reviewH Obeidová, M Merta, J Reiterová, et al.
Folia Biologica|May 15, 2012
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndromeJ Reiterová, H Safránková, L Obeidová, et al.
Casopis Lekaru Ceskych|April 9, 1998
[Laboratory findings and serum levels of amyloid A and soluble interleukin-2 receptors in patients with renal amyloidosis]R Rysavá, M Merta, V Tesar, et al.
Vnitrni Lekarstvi|October 1, 1993
[DNA diagnosis in families with autosomal dominant hereditary polycystic kidney disease]J Kapras, J Stekrovä, J Zidovská, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 14, 1997
Long-term treatment of IgA nephropathy with cyclosporin A--a preliminary reportV Chábová, V Tesar, J Zabka, et al.
Renal Failure|March 16, 2000
Long term treatment of IgA nephropathy with cyclosporine AV Chábová, V Tesar, J Zabka, et al.
Casopis Lekaru Ceskych|February 14, 1996
[Renal failure caused by rhabdomyolysis induced by hypokalemia in Conn's syndrome]K Malícková, M Merta, J Zabka, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Prague Medical Report|October 28, 2006
The pathogenetic aspects and gene polymorphisms of IgA nephropathyD Maixnerová, M Merta, J Reiterová, et al.
Physiological Research|August 6, 2003
Role of endothelin and nitric oxide in the pathogenesis of arterial hypertension in autosomal dominant polycystic kidney diseaseM Merta, J Reiterová, R Rysavá, et al.
Sbornik Lekarsky|January 1, 1994
[Plasma volume in polycystic kidney disease]M Merta, V Chábová, V Tesar, et al.
Prague Medical Report|June 7, 2006
Genetic basis of nephrotic syndrome--reviewH Obeidová, M Merta, J Reiterová, et al.
Folia Biologica|May 15, 2012
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndromeJ Reiterová, H Safránková, L Obeidová, et al.
Casopis Lekaru Ceskych|April 9, 1998
[Laboratory findings and serum levels of amyloid A and soluble interleukin-2 receptors in patients with renal amyloidosis]R Rysavá, M Merta, V Tesar, et al.
Vnitrni Lekarstvi|October 1, 1993
[DNA diagnosis in families with autosomal dominant hereditary polycystic kidney disease]J Kapras, J Stekrovä, J Zidovská, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 14, 1997
Long-term treatment of IgA nephropathy with cyclosporin A--a preliminary reportV Chábová, V Tesar, J Zabka, et al.
Renal Failure|March 16, 2000
Long term treatment of IgA nephropathy with cyclosporine AV Chábová, V Tesar, J Zabka, et al.
Casopis Lekaru Ceskych|February 14, 1996
[Renal failure caused by rhabdomyolysis induced by hypokalemia in Conn's syndrome]K Malícková, M Merta, J Zabka, et al.
Pageof 10