Results 21 to 30 of about 3,161 (171)

Functional Status After Operation for Ebstein Anomaly The Mayo Clinic Experience [PDF]

, 2008
ObjectivesThe objective of this study was to review the long-term functional outcome of patients with Ebstein anomaly who had cardiac operation at our institution.BackgroundEbstein anomaly is a spectrum of tricuspid valvular and right ventricular ...
Brown, Morgan L., Dearani, Joseph A., Danielson, Gordon K., Cetta, Frank, Connolly, Heidi M., Warnes, Carole A., Li, Zhuo, Hodge, David O., Driscoll, David J.   +8 more
core   +1 more source

Anesthetic management for patient with severe cyanosis following bioprosthetic valve stenosis [PDF]

Revista Brasileira de Anestesiologia, 2019
We presented a 39-year-old female patient with life-threatening hypoxemia after tricuspid valve replacement because of Ebstein's anomaly. And the severe cyanosis is due to bioprosthetic valve stenosis and atrial septal defect.
Jun Zeng, Wei Wei
doaj   +5 more sources

Lithium Prescribing during Pregnancy: A UK Primary Care Database Study [PDF]

, 2015
Women taking lithium must decide whether to continue the medication if they conceive or plan to conceive.
Cowen, PJ, Evans, SJ, McCrea, RL, Nazareth, I, Osborn, DP, Petersen, I, Pinfold, V   +6 more
core   +2 more sources

Postpartum Deterioration of Hemodynamics in a Case of Uncorrected Ebstein's Anomaly

Case Reports in Cardiology, 2012
Ebstein's anomaly is a rare congenital cardiac malformation that is characterized by abnormalities of the tricuspid valve and right ventricle. Pregnancy is usually well tolerated unless cyanosis or arrhythmia develops.
Masato Kimura, Shuhei Kakizaki, Seiichi Tazawa, Osamu Adachi, Yoshikatsu Saiki, Shigeo Kure   +5 more
doaj   +1 more source

Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7 [PDF]

, 2011
Ebstein's anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium.
A. F. M. Moorman, A. T. J. M. Helderman-van den Enden, A. V. Postma, B. J. M. Mulder, B. Keavney, H. W. Vliegen, J-W Sels, J. B. A. van de Meerakker, J. Goodship, J. W. Roos-Hesselink, K. van Engelen, M. J. H. Baars, S. Klaassen, S. R. Sperling, T. Pickardt, T. Rahman, U. Bauer   +16 more
core   +1 more source

Successful ablation of coexistent Mahaim tachycardia and right posterior accessory pathway in a patient with Ebstein's anomaly

Türk Kardiyoloji Derneği Arşivi, 2016
Summary– The atriofascicular accessory pathway (AP), known as the Mahaim pathway, is a rare form of pre-excitation, comprising less than 3% of all APs.
Enes Elvin Gül, Celal Akdeniz, Volkan Tuzcu   +2 more
doaj   +1 more source

Cone reconstruction in Ebstein's anomaly repair: early and long-term results [PDF]

, 2011
FUNDAMENTO: As principais correções da anomalia de Ebstein (AE) baseiam-se na reconstrução monocúspide da valva tricúspide e são limitadas pela frequente necessidade de substituição ou pela alta reincidência de insuficiência valvar.
BAUMGRATZ, José Francisco, FRANCHI, Sônia Meiken, LIANZA, Alessandro Cavalcante, LOPEZ, Lilian Maria, MOREIRA, Luiz Felipe P., SILVA, José Pedro da, SILVA, Luciana da Fonseca da, TAVARES, Glaucia Maria P.   +7 more
core   +4 more sources

Operação de um ventrículo e meio como uma alternativa para o ventrículo direito hipoplásico [PDF]

, 2010
Objective: Patients with complex congenital heart disease, characterized by right ventricle hypoplasia, had a palliative surgical option with one and a half ventricular repair.Methods: From July 2001 to March 2009, nine patients (mean age 5.2 years ...
Carvalho, Antonio Carlos, Carvalho, Werther Brunow, Maluf, Miguel Angel   +2 more
core   +4 more sources

Incidental Finding of Ebstein's Anomaly in an Adolescent with an Upper Respiratory Infection: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2016
Ebstein’s anomaly is a rare congenital heart disorder and has a varied clinical course, with detection as late as the seventh decade. We hereby describe an 11-year-old child in whom Ebstein’s anomaly was diagnosed.
Rohit Kapoor, Premila Paul, Premchand Anne   +2 more
doaj   +1 more source

A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects [PDF]

, 2017
Background Mutations in the myosin heavy chain 7 (MYH7) gene commonly cause cardiomyopathy but are less frequently associated with congenital heart defects.
Barge-Schaapveld, D.Q.C.M. (Daniela), Bootsma, M. (Marianne), Boven, L.G. (Ludolf), Breuning, M.H. (Martijn), Bökenkamp, A. (Arend), Herkert, J.C. (Johanna), Hiemstra, Y.L. (Y. L.), Jongbloed, J.D.H. (Jan), Lekanne Deprez, R.H., Mil, A.M. (Anneke) van, Ruivenkamp, C.A. (Claudia), Slegtenhorst, M.A. (Marjon) van, Spaendonck-Zwarts, K.Y. (Karin) van, Ten Broeke, S.W. (Sanne W.), van der Linde, I.H.M. (I. H.M.), Veldkamp, R.F. (Rolf), Waning, J. (Jaap) van, Zwaag, P.A. (Paul) van der   +17 more
core   +1 more source