Zobrazeno 1 - 8
of 8
pro vyhledávání: '"M. E. B. Rijlaarsdam"'
Publikováno v:
Case Reports in Pediatrics, Vol 2012 (2012)
Monochorionic twin pregnancies are at increased risk of perinatal mortality and morbidity due to twin-twin transfusion syndrome (TTTS), selective intrauterine growth restriction (sIUGR), and higher incidence of congenital heart malformations. The inc
Externí odkaz:
https://doaj.org/article/bce1418dbea747d9bcdde303edb635a1
Autor:
J C, van den Bergen, H B, Ginjaar, A J, van Essen, R, Pangalila, I J M, de Groot, P J, Wijkstra, M P, Zijnen, N A M, Cobben, M J, Kampelmacher, B H A, Wokke, I F M, de Coo, J M, Fock, A M C, Horemans, M, van Tol, E, Vroom, M E B, Rijlaarsdam, C S M, Straathof, E H, Niks, J J G M, Verschuuren
Publikováno v:
Journal of neuromuscular diseases. 1(1)
Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy is currently available, but in recent decades standards of care have improved. These improvements include the use of corticosteroids and mechanical ventilation.To
Autor:
F A R, Jansen, E W, van Zwet, M E B, Rijlaarsdam, E, Pajkrt, C L, van Velzen, H R, Zuurveen, A, Kragt, C L, Bax, S-A B, Clur, J M M, van Lith, N A, Blom, M C, Haak
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 48(3)
Congenital heart defects (CHDs) are reported to be associated with a smaller fetal head circumference (HC) and neurodevelopmental delay. Recent studies suggest that altered intrauterine brain hemodynamics may explain these findings. Our objectives we
Autor:
C L, van Velzen, S A, Clur, M E B, Rijlaarsdam, E, Pajkrt, C J, Bax, J, Hruda, C J M, de Groot, N A, Blom, M C, Haak
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 47(5)
To examine the accuracy of fetal echocardiography in diagnosing congenital heart disease (CHD) at the fetal medicine units of three tertiary care centers.This was a multicenter cohort study of tertiary echocardiography referrals between 2002 and 2012
Publikováno v:
Tijdschrift voor kindergeneeskunde. 72:153-158
In Nederland worden per jaar ongeveer 1600 kinderen geboren met een aangeboren hartafwijking. Omdat het aantal verschillende diagnosen groot is, zal de presentatie van deze kinderen divers zijn en soms ook misleidend. Bovendien zal niet elk kind met
Autor:
Y, Hilhorst-Hofstee, A J H A, Scholte, M E B, Rijlaarsdam, A, van Haeringen, L J, Kroft, M, Reijnierse, C A L, Ruivenkamp, M I M, Versteegh, G, Pals, M H, Breuning
Publikováno v:
Clinical genetics. 83(4)
Several genes involved in the familial appearance of thoracic aortic aneurysms and dissections (FTAAD) have been characterized recently, one of which is SMAD3. Mutations of SMAD3 cause a new syndromic form of aortic aneurysms and dissections associat
Autor:
A A W, Roest, F P H A, Vandenbussche, F J C M, Klumper, D, Oepkes, M E B, Rijlaarsdam, N A, Blom
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 152(7)
Foetal supraventricular tachycardia (SVT) with hydrops foetalis is associated with a high morbidity and mortality rate. If SVT with hydrops foetalis persists despite transplacental therapy, direct foetal treatment can be initiated. One foetus was fou
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 146(8)
Evaluation of the first results in the Netherlands of percutaneous and transvenous closure of an ASD II in children with an Amplatzer Septal Occluder (ASO).Prospective.Data were collected from children with an ASD II prior to, during and up to 24 mon