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Quoted phrase not found in phrase index: "Congenital heart defects, multiple types, 5"
Page 1
Congenital heart defects in twin gestations.
Campbell KH, Copel JA, Ozan Bahtiyar M. Campbell KH, et al. Minerva Ginecol. 2009 Jun;61(3):239-44. Minerva Ginecol. 2009. PMID: 19415067 Review.
As ultrasound technology advances, diagnosis of fetal malformations, particularly congenital heart defects (CHD) is becoming standard practice. Currently, a key element of obstetrical care is the use of ultrasound to diagnose chorionicity in multiple g …
As ultrasound technology advances, diagnosis of fetal malformations, particularly congenital heart defects (CHD) is bec …
Twinning and major birth defects, National Birth Defects Prevention Study, 1997-2007.
Dawson AL, Tinker SC, Jamieson DJ, Hobbs CA, Berry RJ, Rasmussen SA, Anderka M, Keppler-Noreuil KM, Lin AE, Reefhuis J; National Birth Defects Prevention Study. Dawson AL, et al. J Epidemiol Community Health. 2016 Nov;70(11):1114-1121. doi: 10.1136/jech-2015-206302. Epub 2016 Jun 20. J Epidemiol Community Health. 2016. PMID: 27325867 Free PMC article.
The largest effect estimates were observed for multiple ventricular septal defects and cloacal exstrophy. Among mothers reporting any use of fertility treatments, we observed a significant association with twinning for 5 of 25 defect groups, wit …
The largest effect estimates were observed for multiple ventricular septal defects and cloacal exstrophy. Among mothers …
Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children.
Song Y, Higgins H, Guo J, Harrison K, Schultz EN, Hales BJ, Moses EK, Goldblatt J, Pachter N, Zhang G. Song Y, et al. J Transl Med. 2018 Feb 27;16(1):42. doi: 10.1186/s12967-018-1411-0. J Transl Med. 2018. PMID: 29482591 Free PMC article.
In this study, we aimed to investigate the usefulness of miRNAs as biomarkers in diagnosing and predicting children with congenital heart defects (CHD), particularly in the context of multiple subtypes of CHD. ...Firstly, we screened 84 circulat …
In this study, we aimed to investigate the usefulness of miRNAs as biomarkers in diagnosing and predicting children with congenita …
Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology--a position statement of the development, anatomy, and pathology ESC Working Group.
Pérez-Pomares JM, de la Pompa JL, Franco D, Henderson D, Ho SY, Houyel L, Kelly RG, Sedmera D, Sheppard M, Sperling S, Thiene G, van den Hoff M, Basso C. Pérez-Pomares JM, et al. Cardiovasc Res. 2016 Feb 1;109(2):204-16. doi: 10.1093/cvr/cvv251. Epub 2016 Jan 11. Cardiovasc Res. 2016. PMID: 26811390 Free article. Review.
Congenital coronary artery anomalies are of major significance in clinical cardiology and cardiac surgery due to their association with myocardial ischaemia and sudden death. ...This document identifies the mosaic-like embryonic development of the coronary vascular system, …
Congenital coronary artery anomalies are of major significance in clinical cardiology and cardiac surgery due to their association wi …
Procedural Risk in Congenital Cardiac Catheterization (PREDIC(3)T).
Quinn BP, Yeh M, Gauvreau K, Ali F, Balzer D, Barry O, Batlivala S, Berman D, Foerster S, Goldstein B, Hainstock M, Holzer R, Janssen D, O'Byrne ML, Shirley L, Trucco S, Whiteside W, Bergersen L. Quinn BP, et al. J Am Heart Assoc. 2022 Jan 4;11(1):e022832. doi: 10.1161/JAHA.121.022832. Epub 2021 Dec 22. J Am Heart Assoc. 2022. PMID: 34935425 Free PMC article.
In a multivariable model, case-type risk category (odds ratios for category: 0=0.46, 1=1.00, 2=1.40, 3=2.68, 4=3.64, and 5=5.25; all P0.005) and hemodynamic vulnerability score (odds ratio for score: 0=1.00, 1=1.27, 2=1.89, and 3=2.03; all P0.006) rema …
In a multivariable model, case-type risk category (odds ratios for category: 0=0.46, 1=1.00, 2=1.40, 3=2.68, 4=3.64, and 5=5.2 …
Common Variation in Cytoskeletal Genes is Associated with Conotruncal Heart Defects.
Musfee FI, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Taylor DM, Tristani-Firouzi M, Watkins WS, Yandell M, Mitchell LE. Musfee FI, et al. Genes (Basel). 2021 Apr 27;12(5):655. doi: 10.3390/genes12050655. Genes (Basel). 2021. PMID: 33925651 Free PMC article.
There is strong evidence for a genetic contribution to non-syndromic congenital heart defects (CHDs). However, exome- and genome-wide studies conducted at the variant and gene-level have identified few genome-wide significant CHD-related genes. ...Consequentl …
There is strong evidence for a genetic contribution to non-syndromic congenital heart defects (CHDs). However, exome- a …
Updating an Empirically Based Tool for Analyzing Congenital Heart Surgery Mortality.
Jacobs ML, Jacobs JP, Thibault D, Hill KD, Anderson BR, Eghtesady P, Karamlou T, Kumar SR, Mayer JE, Mery CM, Nathan M, Overman DM, Pasquali SK, St Louis JD, Shahian D, O'Brien SM. Jacobs ML, et al. World J Pediatr Congenit Heart Surg. 2021 Mar;12(2):246-281. doi: 10.1177/2150135121991528. World J Pediatr Congenit Heart Surg. 2021. PMID: 33683997
OBJECTIVES: STAT Mortality Categories (developed 2009) stratify congenital heart surgery procedures into groups of increasing mortality risk to characterize case mix of congenital heart surgery providers. ...RESULTS: Among 161,351 operations at 110 cen …
OBJECTIVES: STAT Mortality Categories (developed 2009) stratify congenital heart surgery procedures into groups of increasing …
RASopathies and hemostatic abnormalities: key role of platelet dysfunction.
Di Candia F, Marchetti V, Cirillo F, Di Minno A, Rosano C, Pagano S, Siano MA, Falco M, Assunto A, Boccia G, Magliacane G, Pinna V, De Luca A, Tartaglia M, Di Minno G, Strisciuglio P, Melis D. Di Candia F, et al. Orphanet J Rare Dis. 2021 Dec 2;16(1):499. doi: 10.1186/s13023-021-02122-7. Orphanet J Rare Dis. 2021. PMID: 34857025 Free PMC article.
RESULTS: Regardless of the gene involved, pathological paediatric bleeding scores were recorded in 14/49 (28.5%) patients. Indeed, 7 were mutated in PTPN11, 3 in SOS1, 2 in RIT1, 1 in BRAF, and 1 in MEK1. ...CONCLUSIONS: Patients with RASopathies and a bleeding tend …
RESULTS: Regardless of the gene involved, pathological paediatric bleeding scores were recorded in 14/49 (28.5%) patients. Ind …
Quality analysis of publicly available information about hypoplastic left heart syndrome.
Brennan Z, Sharaf OM, Treffalls JA, Roa-Vidal N, Weinstein DJ, Bassuk JS, Stukov Y, Peek GJ, Bleiweis MS, Jacobs JP. Brennan Z, et al. Cardiol Young. 2023 Jul;33(7):1079-1085. doi: 10.1017/S1047951123001294. Epub 2023 Aug 22. Cardiol Young. 2023. PMID: 37605817
Forty-two percent (n = 22) of websites were available in Spanish. Total score varied by website type (p = 0.03), with open access sites scoring highest (median = 26.5; interquartile range = 20.5-28.6) and hospital/healthcare organisation websites scoring lowe …
Forty-two percent (n = 22) of websites were available in Spanish. Total score varied by website type (p = 0.03), with open access sit …
Frontal lobe growth is impaired in fetuses with congenital heart disease.
Paladini D, Finarelli A, Donarini G, Parodi S, Lombardo V, Tuo G, Birnbaum R. Paladini D, et al. Ultrasound Obstet Gynecol. 2021 May;57(5):776-782. doi: 10.1002/uog.22127. Epub 2021 Apr 13. Ultrasound Obstet Gynecol. 2021. PMID: 32573836 Free article.
OBJECTIVES: The primary objective of this study was to assess whether fetuses with congenital heart disease (CHD) have smaller frontal brain areas compared with normal controls. ...The study group was subdivided, according to the CHD hemodynamics, as follows: (1) hy …
OBJECTIVES: The primary objective of this study was to assess whether fetuses with congenital heart disease (CHD) have smaller …
46 results