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Surgical outcome of partial Shone complex.
Interact Cardiovasc Thorac Surg. 2012 Apr;14(4):440-4. doi: 10.1093/icvts/ivr169. Epub 2012 Jan 25.
Interact Cardiovasc Thorac Surg. 2012.
PMID: 22279117
Free PMC article.
Partial forms of Shone complex are rare. Surgical outcomes of the complete forms have generally been poor, whereas there is a lack of data on long-term follow-up of surgically treated adult partial complex. ...Data were confirmed by intra-operative findings and repo …
Partial forms of Shone complex are rare. Surgical outcomes of the complete forms have generally been poor, whereas there is a …
Right Ventricular Enlargement In Utero: Is It Coarctation?
Sivanandam S, Nyholm J, Wey A, Bass JL.
Sivanandam S, et al.
Pediatr Cardiol. 2015 Oct;36(7):1376-81. doi: 10.1007/s00246-015-1168-7. Epub 2015 Apr 8.
Pediatr Cardiol. 2015.
PMID: 25851170
We excluded fetuses with TAPVR, Shone complex, interrupted aortic arch, Ebstein anomaly or HLHS. ...The mean fetal carotid-subclavian index (CS Index) was 0.7 mm with coarctation compared with 1.1 mm without coarctation (p < 0.0001). The mean difference in diamet
…
We excluded fetuses with TAPVR, Shone complex, interrupted aortic arch, Ebstein anomaly or HLHS. ...The mean fetal carotid-sub …
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Ross procedure in neonates and infants: A valuable operation with defined limits.
Cleveland JD, Bansal N, Wells WJ, Wiggins LM, Kumar SR, Starnes VA.
Cleveland JD, et al.
J Thorac Cardiovasc Surg. 2023 Jan;165(1):262-272.e3. doi: 10.1016/j.jtcvs.2022.04.015. Epub 2022 Apr 25.
J Thorac Cardiovasc Surg. 2023.
PMID: 35599209
Multiple regression analysis of the entire cohort identified young age (hazard ratio [HR], 1.037; P = .0045), Shone complex (HR, 17.637; P = .009), and interrupted aortic arch with ventricular septal defect (HR, 16.01; P = .031) as independent predictors of i …
Multiple regression analysis of the entire cohort identified young age (hazard ratio [HR], 1.037; P = .0045), Shone complex (H …
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Congenital heart defects in molecularly proven Kabuki syndrome patients.
Digilio MC, Gnazzo M, Lepri F, Dentici ML, Pisaneschi E, Baban A, Passarelli C, Capolino R, Angioni A, Novelli A, Marino B, Dallapiccola B.
Digilio MC, et al.
Am J Med Genet A. 2017 Nov;173(11):2912-2922. doi: 10.1002/ajmg.a.38417. Epub 2017 Sep 8.
Am J Med Genet A. 2017.
PMID: 28884922
In conclusion, a CHD is detected in 70% of patients with KMT2D (MLL2) pathogenic variants, most commonly left-sided obstructive lesions, including multiple left-sided obstructions similar to those observed in the spectrum of the Shone complex, and septal defe …
In conclusion, a CHD is detected in 70% of patients with KMT2D (MLL2) pathogenic variants, most commonly left-sided obstructive lesions, inc …
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