Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Eva Klaskova"'
Publikováno v:
Life, Vol 14, Iss 3, p 300 (2024)
Arterial stiffness represents an independent predictor of the risk of subsequent cardiovascular events. Early identification of high-risk individuals is necessary for effective prevention and targeted interventions. Carotid wall echo-tracking is a mo
Externí odkaz:
https://doaj.org/article/a3447a7378f44c3186a1d95645343969
Autor:
Andrea Stefekova, Pavlina Capkova, Zuzana Capkova, Vaclava Curtisova, Josef Srovnal, Enkhjargalan Mracka, Eva Klaskova, Martin Prochazka
Publikováno v:
Biomedical Papers, Vol 166, Iss 2, Pp 187-194 (2022)
Aims. The aim of this retrospective study was to determine the detection rate of the pathogenic copy number variants (CNVs) in a cohort of 33 foetuses - 32 with CHD (congenital heart defects) and 1 with kidney defect, after exclusion of common aneupl
Externí odkaz:
https://doaj.org/article/d7895605c7434adb8be9ddb11e1edc9d
Autor:
Petr Vrtel, Radek Vrtel, Eva Klaskova, Dita Vrbicka, Katerina Adamova, Jan Pavlicek, Vaclav Hana, Ondrej Soucek, Veronika Stara, Jan Lebl, Marta Snajdrova, Jirina Zapletalova, Tomas Furst, Sabina Kapralova, Zdenek Tauber, Eva Krejcirikova, Marketa Routilova, Julia Stellmachova, Radek Vodicka, Martin Prochazka
Publikováno v:
Biomedical Papers, Vol 166, Iss 1, Pp 63-67 (2022)
Aims. Turner syndrome is the only chromosome monosomy that is postnatally compatible with life. The reported incidence of TS is 1 in 2500 liveborn girls. The phenotype of these girls is highly variable, with cardiac abnormalities being life-threateni
Externí odkaz:
https://doaj.org/article/25b523ce827d4ec6b9611619f2e11f93
Autor:
Jan Pavlicek, Eva Klaskova, Sabina Kapralova, Alzbeta Moravova Palatova, Alicja Piegzova, Richard Spacek, Tomas Gruszka
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Severe or critical congenital heart defects (CHDs) constitute one third of the heart defect cases detected only after birth. These prenatally unrecognised defects usually manifest as cyanotic or acyanotic lesions and are diagnosed
Externí odkaz:
https://doaj.org/article/fa7d19dfe08542b4b169998aa35c5ee1
Autor:
David Krahulik, Lumir Hrabalek, Filip Blazek, Matej Halaj, Marek Slachta, Eva Klaskova, Klara Maresova
Publikováno v:
Children, Vol 10, Iss 4, p 723 (2023)
Our study evaluates the sensitivity of papilledema as a sign of high intracranial pressure in children. Patients younger than 18 years old, diagnosed with increased ICP, and who had received dilated fundus examination between 2019 and 2021 were retro
Externí odkaz:
https://doaj.org/article/66c0d994d67c4a8d82fd32216d6c9f26
Autor:
Jan Pavlicek, Zdenek Tauber, Eva Klaskova, Katerina Cizkova, Martin Prochazka, Patricie Delongova, Beata Stefunko, Iveta Szotkovska, Jana Dvorackova, Tomas Gruszka
Publikováno v:
Biomedical Papers, Vol 164, Iss 1, Pp 92-99 (2020)
Aims: To determine the frequency of pregnancy terminations due to prenatal congenital heart defect (CHD) and assess the agreement fetal echocardiography (FECHO) and autopsy findings. Methods: The data were retrospectively assessed between 2008 and 20
Externí odkaz:
https://doaj.org/article/1eae8a71cce648d489ca7789254a1e9f
Autor:
Jan Pavlicek, Tomas Gruszka, Sabina Kapralova, Martin Prochazka, Eva Silhanova, Romana Kaniova, Slavka Polanska, Renata Cernickova, Eva Klaskova
Publikováno v:
Biomedical Papers, Vol 163, Iss 1, Pp 67-74 (2019)
Aim: To study congenital heart defects (CHDs), evaluate their relation to extra-cardiac pathologies, and assess the significance of prenatal diagnostics for heart diseases. Methods: Data from 1999-2017 were analyzed for the incidence of significant C
Externí odkaz:
https://doaj.org/article/9097af77262f4248b247d9784cdf379e
Autor:
Jana Volejnikova, Jirina Zapletalova, Marie Jarosova, Helena Urbankova, Petr Vojta, Eva Klaskova, Marshall S. Horwitz, Marian Hajduch, Vladimir Mihal
Publikováno v:
Biomedical Papers, Vol 162, Iss 1, Pp 65-70 (2018)
Background: Leri-Weill syndrome (LWS) ranks among conditions with short stature homeobox gene (SHOX) haploinsufficiency. Data on possible association of SHOX aberrations with malignant diseases are scarce. Methods and Results: We report a unique case
Externí odkaz:
https://doaj.org/article/587fce9b91bd4cf8b81ee17a06ff42b2
Autor:
David Krahulik, Darina Aleksijevic, Vratislav Smolka, Eva Klaskova, Petra Venhacova, Miroslav Vaverka, Vladimir Mihal, Jirina Zapletalova
Publikováno v:
Biomedical Papers, Vol 161, Iss 1, Pp 80-85 (2017)
Background and Aims: Retrospective studies of TBI have found a neuroendocrine dysfunction following traumatic brain injury in 23 to 60% of adults and 15 to 21% of children. Our aims were to determine the prevalence of hypothalamo-hypophyseal dysfunct
Externí odkaz:
https://doaj.org/article/2e31a946847b482f8ca76a95f0d1b01f
Autor:
Eva Klaskova, Jiri Drabek, Milada Hobzova, Vratislav Smolka, Miroslav Seda, Jiri Hyjanek, Rastislav Slavkovsky, Jana Stranska, Martin Prochazka
Publikováno v:
Biomedical Papers, Vol 160, Iss 4, Pp 495-498 (2016)
Background: Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder resulting from mutations in the PHOX2B gene located on chromosome 4p12.3, characterized by hypoventilation secondary to missing responses to both hypercapnia an
Externí odkaz:
https://doaj.org/article/02e24507bce042a6865dd03e28732e7c