Zieg J - Search Results

1

Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.

Fencl F, Malina M, Stará V, Zieg J, Mixová D, Seeman T, Bláhová K. Fencl F, et al. Among authors: zieg j. Eur J Pediatr. 2012 Jan;171(1):121-4. doi: 10.1007/s00431-011-1497-3. Epub 2011 May 26. Eur J Pediatr. 2012. PMID: 21614510

2

Urinary transforming growth factor-β1 in children with obstructive uropathy.

Zieg J, Blahova K, Seeman T, Bronsky J, Dvorakova H, Pechova M, Janda J, Matousovic K. Zieg J, et al. Nephrology (Carlton). 2011 Aug;16(6):595-8. doi: 10.1111/j.1440-1797.2011.01459.x. Nephrology (Carlton). 2011. PMID: 21382126

3

Rituximab resistant evans syndrome and autoimmunity in Schimke immuno-osseous dysplasia.

Zieg J, Krepelova A, Baradaran-Heravi A, Levtchenko E, Guillén-Navarro E, Balascakova M, Sukova M, Seeman T, Dusek J, Simankova N, Rosik T, Skalova S, Lebl J, Boerkoel CF. Zieg J, et al. Pediatr Rheumatol Online J. 2011 Sep 13;9(1):27. doi: 10.1186/1546-0096-9-27. Pediatr Rheumatol Online J. 2011. PMID: 21914180 Free PMC article.

4

Determinants of premature atherosclerosis in children with end-stage renal disease.

Dvořáková HM, Szitányi P, Dvořák P, Janda J, Seeman T, Zieg J, Lánská V, Kotaška K, Piťha J. Dvořáková HM, et al. Among authors: zieg j. Physiol Res. 2012;61(1):53-61. doi: 10.33549/physiolres.932127. Epub 2011 Dec 20. Physiol Res. 2012. PMID: 22188103 Free article.

5

Fatal case of diarrhea-associated hemolytic uremic syndrome with severe neurologic involvement.

Zieg J, Dusek J, Marejkova M, Limrova P, Blazek D, Pavlicek P, Grega M, Janda J, Blahova K. Zieg J, et al. Pediatr Int. 2012 Feb;54(1):166-7. doi: 10.1111/j.1442-200X.2011.03533.x. Pediatr Int. 2012. PMID: 22335333 No abstract available.

6

Proteinuria 1 year after renal transplantation is associated with impaired graft survival in children.

Rosík T, Chadimová M, Dušek J, Háček J, Šimánková N, Vondrák K, Zieg J, Seeman T. Rosík T, et al. Among authors: zieg j. Pediatr Nephrol. 2015 Oct;30(10):1853-60. doi: 10.1007/s00467-015-3114-6. Epub 2015 Apr 30. Pediatr Nephrol. 2015. PMID: 25925040

7

Recurrence of nephrotic proteinuria in children with focal segmental glomerulosclerosis: early treatment with plasmapheresis and immunoadsorption should be associated with better prognosis.

Fencl F, Vondrák K, Rosík T, Zieg J, Chadimová M, Háček J, Dušek J, Seeman T. Fencl F, et al. Among authors: zieg j. Minerva Pediatr. 2016 Oct;68(5):348-54. Epub 2015 Jun 4. Minerva Pediatr. 2016. PMID: 26041001

8

Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93.

Bezdíčka M, Štolbová Š, Seeman T, Cinek O, Malina M, Šimánková N, Průhová Š, Zieg J. Bezdíčka M, et al. Among authors: zieg j. Pediatr Nephrol. 2018 Aug;33(8):1347-1363. doi: 10.1007/s00467-018-3950-2. Epub 2018 Jun 4. Pediatr Nephrol. 2018. PMID: 29869118

9

Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study.

Karnisova L, Hradsky O, Blahova K, Fencl F, Dolezel Z, Zaoral T, Zieg J. Karnisova L, et al. Among authors: zieg j. Eur J Pediatr. 2018 Dec;177(12):1837-1844. doi: 10.1007/s00431-018-3255-2. Epub 2018 Sep 24. Eur J Pediatr. 2018. PMID: 30251107

10

Various phenotypes of disease associated with mutated DGKE gene.

Bezdíčka M, Pavlíček P, Bláhová K, Háček J, Zieg J. Bezdíčka M, et al. Among authors: zieg j. Eur J Med Genet. 2020 Aug;63(8):103953. doi: 10.1016/j.ejmg.2020.103953. Epub 2020 May 13. Eur J Med Genet. 2020. PMID: 32413569

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