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Items: 1 to 20 of 48

1.

[Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia].

Ryšavá R, Reiterová J, Urbanová M, Štekrová J, Lněnička P, Tesař V.

Vnitr Lek. 2016 Winter;62(Supplementum 6):78-83. Czech.

PMID:
28124936
2.

Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease.

Obeidova L, Seeman T, Elisakova V, Reiterova J, Puchmajerova A, Stekrova J.

BMC Med Genet. 2015 Dec 22;16:116. doi: 10.1186/s12881-015-0261-3.

3.

IgA nephropathy in Czech patients--are we able reliably predict the outcome?

Maixnerova D, Neprasova M, Skibova J, Mokrisova J, Rysava R, Reiterova J, Jancova E, Merta M, Zadrazil J, Honsova E, Tesar V.

Kidney Blood Press Res. 2014;39(6):555-62. doi: 10.1159/000368467. Epub 2014 Dec 14.

4.

Nationwide biopsy survey of renal diseases in the Czech Republic during the years 1994-2011.

Maixnerova D, Jancova E, Skibova J, Rysava R, Rychlik I, Viklicky O, Merta M, Kolsky A, Reiterova J, Neprasova M, Kidorova J, Honsova E, Tesar V.

J Nephrol. 2015 Feb;28(1):39-49. doi: 10.1007/s40620-014-0090-z. Epub 2014 Apr 23.

PMID:
24756969
5.

Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease.

Obeidova L, Elisakova V, Stekrova J, Reiterova J, Merta M, Tesar V, Losan F, Kohoutova M.

BMC Med Genet. 2014 Apr 3;15:41. doi: 10.1186/1471-2350-15-41.

6.

Mutational analysis of ACTN4, encoding α-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method.

Safaříková M, Reiterová J, Safránková H, Stekrová J, Zidková A, Obeidová L, Kohoutová M, Tesař V.

Folia Biol (Praha). 2013;59(3):110-5.

7.

[Hypertension in patients with polycystic kidney disease -  incidence, pathogenesis, prognosis, therapy].

Tesař V, Reiterová J.

Vnitr Lek. 2013 Jun;59(6):496-500. Review. Czech.

PMID:
23808746
8.

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.

Reiterová J, Štekrová J, Merta M, Kotlas J, Elišáková V, Lněnička P, Korabečná M, Kohoutová M, Tesař V.

BMC Nephrol. 2013 Mar 15;14:59. doi: 10.1186/1471-2369-14-59.

9.

The coincidence of IgA nephropathy and Fabry disease.

Maixnerová D, Tesař V, Ryšavá R, Reiterová J, Poupětová H, Dvořáková L, Goláň L, Neprašová M, Kidorová J, Merta M, Honsová E.

BMC Nephrol. 2013 Jan 11;14:6. doi: 10.1186/1471-2369-14-6.

10.

TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease.

Obeidová L, Reiterová J, Lněnička P, Štekrová J, Šafránková H, Kohoutová M, Tesař V.

Folia Biol (Praha). 2012;58(4):173-6.

11.

Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.

Reiterová J, Safránková H, Obeidová L, Stěkrová J, Maixnerová D, Merta M, Tesař V.

Folia Biol (Praha). 2012;58(2):64-8.

12.

The influence of vascular endothelial growth factor (VEGF) polymorphism on the progression of chronic glomerulonephritides.

Safránková H, Merta M, Reiterová J, Stekrová J, Maixnerová D, Ryšavá R, Skibová J, Tesař V.

Folia Biol (Praha). 2011;57(4):145-50.

13.

The retrospective analysis of 343 Czech patients with IgA nephropathy--one centre experience.

Maixnerova D, Bauerova L, Skibova J, Rysava R, Reiterova J, Merta M, Honsova E, Tesar V.

Nephrol Dial Transplant. 2012 Apr;27(4):1492-8. doi: 10.1093/ndt/gfr482. Epub 2011 Sep 2.

PMID:
21891776
14.

DNA analysis of renal electrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes: summary of mutation screening.

Urbanová M, Reiterová J, Stěkrová J, Lněnička P, Ryšavá R.

Folia Biol (Praha). 2011;57(2):65-73.

15.

New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease.

Stekrova J, Reiterova J, Svobodova S, Kebrdlova V, Lnenicka P, Merta M, Viklicky O, Kohoutova M.

BMC Med Genet. 2009 Aug 17;10:78. doi: 10.1186/1471-2350-10-78.

16.

Influence of VEGF polymorphism on progression of autosomal dominant polycystic kidney disease.

Reiterová J, Obeidová H, Lenícek M, Stekrová J, Merta M, Maixnerová D, Vítek L, Viklický O, Tesar V.

Kidney Blood Press Res. 2008;31(6):398-403. doi: 10.1159/000180269. Epub 2008 Dec 8.

17.

The influence of two megsin polymorphisms on the progression of IgA nephropathy.

Maixnerová D, Merta M, Reiterová J, Stekrová J, Rysavá R, Viklický O, Obeidová H, Tesar V.

Folia Biol (Praha). 2008;54(2):40-5.

18.

The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy.

Reiterová J, Merta M, Stekrová J, Maixnerová D, Obeidová H, Kebrdlová V, Viklický O, Tesar V.

Folia Biol (Praha). 2007;53(4):134-7.

19.

Analysis of published PKD1 gene sequence variants.

Gout AM; ADPKD Gene Variant Consortium, Ravine D, Harris PC, Rossetti S, Peters D, Breuning M, Henske EP, Koizumi A, Inoue S, Shimizu Y, Thongnoppakhun W, Yenchitsomanus PT, Deltas C, Sandford R, Torra R, Turco AE, Jeffery S, Fontes M, Somlo S, Furu LM, Smulders YM, Mercier B, Ferec C, Burtey S, Pei Y, Kalaydjieva L, Bogdanova N, McCluskey M, Geon LJ, Wouters CH, Reiterova J, Stekrová J, San Millan JL, Aguiari G, Del Senno L.

Nat Genet. 2007 Apr;39(4):427-8. Review. No abstract available.

PMID:
17392796
20.

The influence of three endothelin-1 polymorphisms on the progression of IgA nephropathy.

Maixnerová D, Merta M, Reiterová J, Stekrová J, Rysavá R, Obeidová H, Viklický O, Potmĕsil P, Tesar V.

Folia Biol (Praha). 2007;53(1):27-32.

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