Bláhová K - 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: blahova k. 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

Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene.

Fencl F, Bláhová K, Schlingmann KP, Konrad M, Seeman T. Fencl F, et al. Among authors: blahova k. Eur J Pediatr. 2013 Jan;172(1):45-9. doi: 10.1007/s00431-012-1818-1. Epub 2012 Sep 22. Eur J Pediatr. 2013. PMID: 23001465

3

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: blahova k. 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

4

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: blahova k. 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

5

Blood pressure in children with renal cysts and diabetes syndrome.

Seeman T, Weigel F, Blahova K, Fencl F, Pruhova S, Hermes K, Klaus R, Lange-Sperandio B, Grote V, John-Kroegel U. Seeman T, et al. Among authors: blahova k. Eur J Pediatr. 2021 Dec;180(12):3599-3603. doi: 10.1007/s00431-021-04165-1. Epub 2021 Jun 26. Eur J Pediatr. 2021. PMID: 34176013

6

Polycystic kidney and hepatic disease with mental retardation and hand anomalies in three siblings.

Seeman T, Malíková M, Bláhová K, Seemanová E. Seeman T, et al. Among authors: blahova k. Pediatr Nephrol. 2009 Jul;24(7):1409-12. doi: 10.1007/s00467-008-1049-x. Epub 2008 Nov 15. Pediatr Nephrol. 2009. PMID: 19011905

7

Ambulatory blood pressure monitoring in children with unilateral multicystic dysplastic kidney.

Seeman T, John U, Bláhová K, Vondrichová H, Janda J, Misselwitz J. Seeman T, et al. Among authors: blahova k. Eur J Pediatr. 2001 Feb;160(2):78-83. doi: 10.1007/s004310000579. Eur J Pediatr. 2001. PMID: 11271394

8

Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis.

Obeidova L, Seeman T, Fencl F, Blahova K, Hojny J, Elisakova V, Reiterova J, Stekrova J. Obeidova L, et al. Among authors: blahova k. PLoS One. 2020 Jun 23;15(6):e0235071. doi: 10.1371/journal.pone.0235071. eCollection 2020. PLoS One. 2020. PMID: 32574212 Free PMC article.

9

Genotype-phenotype correlation in children with autosomal dominant polycystic kidney disease.

Fencl F, Janda J, Bláhová K, Hríbal Z, Stekrová J, Puchmajerová A, Seeman T. Fencl F, et al. Among authors: blahova k. Pediatr Nephrol. 2009 May;24(5):983-9. doi: 10.1007/s00467-008-1090-9. Epub 2009 Feb 5. Pediatr Nephrol. 2009. PMID: 19194729

10

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. Among authors: blahova k. Nephrology (Carlton). 2011 Aug;16(6):595-8. doi: 10.1111/j.1440-1797.2011.01459.x. Nephrology (Carlton). 2011. PMID: 21382126

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