Aller au contenu principal
Profil bibliographique

Květa Bláhová

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

65Publications signalées
1070Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Escherichia coli research studiesGenetic and Kidney Cyst DiseasesComplement system in diseasesRenal Diseases and GlomerulopathiesViral gastroenteritis research and epidemiology

Les publications récentes

Accès ouvert 2026 article OpenAlex

Macroscopic hematuria in children with autosomal dominant polycystic kidney disease — report from four European tertiary centers

Tomáš Seeman, Květa Bláhová, Filip Fencl, Ulrike John-Kroegel et autres

In adults with autosomal dominant polycystic kidney disease (ADPKD), episodes of macroscopic hematuria are relatively common and are predictors of hypertension. We hypothesized that a history of macroscopic hematuria will be associated with hypertension also in children with ADPKD. We retrospectively analyzed …

cz, de, sk, ca (code pays fourni par la source)

0 citations European Journal of Pediatrics
Accès ouvert 2025 article OpenAlex

Recommended procedures of the Pediatric nephrology section of the Czech pediatric society for the diagnosis and treatment of thrombotic microangiopathies in children

Terezie Šuláková, Květa Bláhová, Jan Papež, Jiří Štarha et autres

TrombotickĂŠ mikroangiopatie (TMA) jsou skupinou onemocněnĂ­, kterĂĄ je spuĹĄtěna poĹĄkozenĂ­m nebo funkčnĂ­ poruchou endotelu. CharakteristickĂ˝mi znaky TMA jsou mikroangio­patickĂĄ hemolytickĂĄ anĂŠmie, trombocytopenie a ischemickĂŠ poĹĄkozenĂ­ orgĂĄnĹŻ na podkladě mikrotrombotizace v kapilĂĄrnĂ­m řečiĹĄti. Nejčastěji poĹĄkozenĂ˝m orgĂĄnem jsou ledviny. V dětskĂŠm věku se TMA …

cz (code pays fourni par la source)

0 citations Pediatrie pro praxi
Accès ouvert 2022 article OpenAlex

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Tomáš Seeman, Květa Bláhová, Filip Fencl, Richard Klaus et autres

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 of autosomal recessive polycystic kidney disease (ARPKD). To date, only one small …

cz, de, sk (code pays fourni par la source)

6 citations Pediatric Nephrology
Accès ouvert 2021 preprint OpenAlex

Low prevalence of hypertension in children with renal cysts and diabetes syndrome is the hallmark of the disease

Tomáš Seeman, Friederike Weigel, Květa Bláhová, Filip Fencle et autres

Abstract 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 children with renal cysts and diabetes (RCAD) syndrome caused by abnormalities …

de, cz (code pays fourni par la source)

0 citations Research Square
Accès ouvert 2020 article OpenAlex

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

Lena Obeidová, Tomáš Seeman, Filip Fencl, Květa Bláhová et autres

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 be made. Next-generation sequencing (NGS) may help the clinicians to find the …

cz (code pays fourni par la source)

24 citations PLoS ONE
2020 article OpenAlex

Coincidence of giant uterine myomatosis and detection of two advanced malignancies in 77-year-old female patient.

Květa Bláhová, J Presl, Denis Berezovskiy, Pavel Vlasák et autres

OBJECTIVE: Our aim is to emphasize the importance of patient participation in screening programs available in the Czech Republic and in preventive gynaecological examinations. As an example, we present a case report of a 77-year-old female patient with the accumulation of serious …

0 citations PubMed
2019 article OpenAlex

[Overgrowth in children and in adults: novel clinical view, novel genes, novel phenotypes].

Jan Lebl, Lukáš Plachý, Květa Bláhová, Lenka Elblová et autres

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 Beckwith-Wiedemann (BWS) and Sotos syndromes; in addition, several rare conditions may occur …

2 citations PubMed

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.