Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

124 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Audit of 10 years of referrals for fetal echocardiography.
Clur SA, Van Brussel PM, Mathijssen IB, Pajkrt E, Ottenkamp J, Bilardo CM. Clur SA, et al. Prenat Diagn. 2011 Dec;31(12):1134-40. doi: 10.1002/pd.2847. Epub 2011 Sep 14. Prenat Diagn. 2011. PMID: 21915886
Cardiac function in trisomy 21 fetuses.
Clur SA, Oude Rengerink K, Ottenkamp J, Bilardo CM. Clur SA, et al. Ultrasound Obstet Gynecol. 2011 Feb;37(2):163-71. doi: 10.1002/uog.8819. Ultrasound Obstet Gynecol. 2011. PMID: 20814928 Free article.
Is fetal cardiac function gender dependent?
Clur SA, Oude Rengerink K, Mol BW, Ottenkamp J, Bilardo CM. Clur SA, et al. Prenat Diagn. 2011 Jun;31(6):536-42. doi: 10.1002/pd.2738. Epub 2011 Mar 17. Prenat Diagn. 2011. PMID: 21413043
Head growth in fetuses with isolated congenital heart defects: lack of influence of aortic arch flow and ascending aorta oxygen saturation.
Jansen FA, van Zwet EW, Rijlaarsdam ME, Pajkrt E, van Velzen CL, Zuurveen HR, Kragt A, Bax CL, Clur SA, van Lith JM, Blom NA, Haak MC. Jansen FA, et al. Among authors: clur sa. Ultrasound Obstet Gynecol. 2016 Sep;48(3):357-64. doi: 10.1002/uog.15980. Epub 2016 Aug 2. Ultrasound Obstet Gynecol. 2016. PMID: 27256792 Free article.
Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.
Nicastro M, Vermeer AMC, Postema PG, Tadros R, Bowling FZ, Aegisdottir HM, Tragante V, Mach L, Postma AV, Lodder EM, van Duijvenboden K, Zwart R, Beekman L, Wu L, van der Zwaag PA, Alders M, Allouba M, Aguib Y, Santomel JL, de Una D, Monserrat L, Miranda AMA, Kanemaru K, Cranley J, van Zeggeren IE, Aronica EMA, Ripolone M, Zanotti S, Sveinbjornsson G, Ivarsdottir EV, Hólm H, Guðbjartsson DF, Skúladóttir ÁT, Stefánsson K, Nadauld L, Knowlton KU, Ostrowski SR, Sørensen E, Vesterager Pedersen OB, Ghouse J, Rand S, Bundgaard H, Ullum H, Erikstrup C, Aagaard B, Bruun MT, Christiansen M, Jensen HK, Carere DA, Cummings CT, Fishler K, Tøring PM, Brusgaard K, Juul TM, Saaby L, Winkel BG, Mogensen J, Fortunato F, Comi GP, Ronchi D, van Tintelen JP, Noseda M, Airola MV, Christiaans I, Wilde AAM, Wilders R, Clur SA, Verkerk AO, Bezzina CR, Lahrouchi N. Nicastro M, et al. Among authors: clur sa. medRxiv [Preprint]. 2024 Jul 5:2024.07.04.24309755. doi: 10.1101/2024.07.04.24309755. medRxiv. 2024. PMID: 39006410 Free PMC article. Preprint.
124 results