Srovnání monitorace srdečního výdeje metodou „Pulse wave transit time" a analýzou arteriální křivky.

Autor: M., Chobola¹, J., Hruda¹, M., Lukeš¹, J., Klimeš¹, V., Šrámek¹, P., Suk¹ pavel.suk@fnusa.cz

Publikováno v: Anaesthesiology & Intensive Medicine / Anesteziologie a Intenzivní Medicína. 2017, Vol. 28 Issue 6, p339-345. 7p.

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Prenatal detection of congenital heart diseaseresults of a national screening programme

Autor: Caroline J. Bax, C. L. van Velzen, Martijn W. Heymans, Eva Pajkrt, Meb Rijlaarsdam, Cjm de Groot, Monique C. Haak, Nico A. Blom, SA Clur, J. Hruda, Mireille N. Bekker

Publikováno v: BJOG, 123(3), 400-407. Wiley-Blackwell
BJOG: An International Journal of Obstetrics and Gynaecology, 123(3), 400-407
BJOG-An International Journal of Obstetrics and Gynaecology, 123(3), 400. Wiley-Blackwell
van Velzen, C L, Clur, S A, Rijlaarsdam, M E B, Bax, C J, Pajkrt, E, Heymans, M W, Bekker, M N, Hruda, J, de Groot, C J M, Blom, N A & Haak, M C 2016, ' Prenatal detection of congenital heart diseaseresults of a national screening programme ', BJOG: An International Journal of Obstetrics & Gynaecology, vol. 123, no. 3, pp. 400-407 . https://doi.org/10.1111/1471-0528.13274
BJOG: An International Journal of Obstetrics & Gynaecology, 123(3), 400-407. Wiley Online Library

Objective Congenital heart disease (CHD) is the most common congenital malformation and causes major morbidity and mortality. Prenatal detection improves the neonatal condition before surgery, resulting in less morbidity and mortality. In the Netherl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1658677659698fdf4b5fa795437d53f9
https://pure.amc.nl/en/publications/prenatal-detection-of-congenital-heart-diseaseresults-of-a-national-screening-programme(f61b1f60-fe02-452e-8695-ebe6b3b6b882).html

OC13.07: * The impact of additional anomalies on head growth in fetuses with congenital heart defects

Autor: J. Hruda, Eva Pajkrt, A. van Nisselrooij, Monique C. Haak, N. van Geloven, F.A. Jansen, Nico A. Blom, I. Linskens, J. Van Lith, Sally-Ann B. Clur

Publikováno v: Ultrasound in Obstetrics & Gynecology. 52:32-32

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::163ba80ce6ff3000f46c7614a5d482bc
https://doi.org/10.1002/uog.19295

Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene

Autor: R. H. Lekanne Deprez, J Hruda, J M van Hagen, J J Muurling-Vlietman, Irene Stolte-Dijkstra, Marielle Alders, Marieke J.H. Baars, Liliane C. D. Wijnaendts

Publikováno v: Journal of medical genetics, 43(10), 829-832. BMJ Publishing Group
JOURNAL OF MEDICAL GENETICS, 43(10), 829-832. BMJ PUBLISHING GROUP

Background: Idiopathic ( primary) hypertrophic cardiomyopathy (HCM) is mainly caused by mutations in genes encoding sarcomeric proteins. One of the most commonly mutated HCM genes is the myosin binding protein C (MYBPC3) gene. Mutations in this gene

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b1528f654af1fdc85fcd31ae6275704
https://doi.org/10.1136/jmg.2005.040329