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» Authors » Kveta Blahova

Kveta Blahova

Explore the profile of Kveta Blahova including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 20
Citations 266
Followers 0
Related Specialties
Pediatrics
Nephrology
General Medicine
Top 10 Co-Authors
Tomas Seeman
Filip Fencl
Jan Janda
Jakub Zieg
Monika Marejkova
Stepanka Pruhova
Jitka Stekrova
Lenka Elblova
Margaret Barrow
Aleksandra Zurowska
Published In
Pediatr Nephrol
Eur J Pediatr
PLoS One
Nephrology (Carlton)
Pediatr Endocrinol Rev
Affiliations
Soon will be listed here.
Recent Articles
1.
Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension
Seeman T, Blahova K, Fencl F, Klaus R, Lange-Sperandio B, Hrckova G, et al.
Pediatr Nephrol . 2022 Dec; 38(7):2093-2100. PMID: 36538056
Background: Impaired kidney concentration capacity is present in half of the patients with autosomal dominant polycystic kidney disease (ADPKD). The kidney concentrating capacity was further impaired within the animal model...
2.
Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres
Seeman T, Blazik R, Fencl F, Blahova K, Obeidova L, Stekrova J, et al.
J Hypertens . 2022 Jan; 40(3):425-431. PMID: 35081580
Objective: : Arterial hypertension is a common complication in patients with autosomal recessive polycystic kidney disease (ARPKD), occurring in 33-75% of children when measured by office blood pressure (OBP). Ambulatory...
3.
Blood pressure in children with renal cysts and diabetes syndrome
Seeman T, Weigel F, Blahova K, Fencl F, Pruhova S, Hermes K, et al.
Eur J Pediatr . 2021 Jun; 180(12):3599-3603. PMID: 34176013
Cystic kidney diseases such as autosomal recessive or dominant polycystic kidney disease (ARPKD and ADPKD) are associated with high prevalence of arterial hypertension. On the contrary, studies on hypertension in...
4.
Increasing prevalence of hypertension during long-term follow-up in children with autosomal dominant polycystic kidney disease
Seeman T, Jansky P, Filip F, Blahova K, Jaros A
Pediatr Nephrol . 2021 May; 36(11):3717-3723. PMID: 34008126
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease. Kidney cysts form over the course of the disease and kidney function slowly declines, usually leading...
5.
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, et al.
PLoS One . 2020 Jun; 15(6):e0235071. PMID: 32574212
Cystic kidney diseases are a very heterogeneous group of chronic kidney diseases. The diagnosis is usually based on clinical and ultrasound characteristics and the final diagnosis is often difficult to...
6.
Various phenotypes of disease associated with mutated DGKE gene
Bezdicka M, Pavlicek P, Blahova K, Hacek J, Zieg J
Eur J Med Genet . 2020 May; 63(8):103953. PMID: 32413569
Atypical haemolytic uraemic syndrome and steroid-resistant nephrotic syndrome are highly rare kidney diseases that can occur in childhood. In some cases, genetic variants may trigger these conditions, although in atypical...
7.
For Debate: The Significance of Etiologic Diagnosis in Neonates with Overgrowth Syndromes. Lesson Learned from the Simpson-Golabi-Behmel Syndrome
Plachy L, Elblova L, Neuman V, Fencl F, Blahova K, Stranak Z, et al.
Pediatr Endocrinol Rev . 2018 Oct; 16(1):171-177. PMID: 30371035
Overgrowth syndromes are rare genetic disorders characterized by excessive pre- and postnatal growth accompanied by dysmorphic features and developmental disorders. In addition to other health hazards, the life expectancy of...
8.
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, et al.
Eur J Pediatr . 2018 Sep; 177(12):1837-1844. PMID: 30251107
Diarrhea-associated hemolytic uremic syndrome is characterized by hemolytic anemia, thrombocytopenia, and acute kidney injury secondary to enteric infection, typically Shiga toxin-producing Escherichia coli. Shiga toxin 2 is able to activate...
9.
Attack of the clones: whole genome-based characterization of two closely related enterohemorrhagic Escherichia coli O26 epidemic lineages
Karnisova L, Marejkova M, Hrbackova H, Mellmann A, Karch H, Fruth A, et al.
BMC Genomics . 2018 Sep; 19(1):647. PMID: 30170539
Background: Enterohemorrhagic Escherichia coli (EHEC) O26:H11/H, the most common non-O157 serotype causing hemolytic uremic syndrome worldwide, are evolutionarily highly dynamic with new pathogenic clones emerging rapidly. Here, we investigated the...
10.
[Overgrowth in children and in adults: novel clinical view, novel genes, novel phenotypes]
Lebl J, Plachy L, Blahova K, Elblova L, Fencl F, Kolouskova S, et al.
Cas Lek Cesk . 2017 Oct; 156(5):233-240. PMID: 28992707
Novel genetic findings allow to more reliably elucidate the aetiology and pathogenesis of overgrowth syndromes in children and in adults. The relatively prevalent overgrowth syndromes in foetuses and neonates include...