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Retrospective analysis of prenatal echcardiography findings in cases of congenital heart defects: comparison with postnatal pulmonary hypertension revealed by lungs histopathology (2010-2015)

circulation in the distribution of human fetal cardiac output during the second half of pregnancy. Circulation. 1996;94:1068 -1073 20. Nagata H, Yamamura K, Ikeda K, Ihara K. Preoperative management with nitrogen inhalation therapy for a low-birth weight infant with tetralogy of Fallot and absent pulmonary valve. Pediatr Cardiol. 2011;32:685-8 21. Humbert M, Sitbon O, Simonneau G: Treatment of pulmonary arterial hypertension. N. Engl. J. Med 2004: 351: 1425-1436 22. Machado RD, Eickelberg O, Elliott CG et al.: Genetics and

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Lower costs of hospital stay for newborns with HLHS after prenatal diagnoses comparing with postnatal diagnoses

- aktualne problemy. Prenat Cardio. 2012; Apr 2(2) supl:34-37 5. Peterson AL , Quartermain MD , Ades A , Khalek N , Johnson MP , Rychik J: Impact of mode of delivery on markers of perinatal hemodynamics in infants with hypoplastic left heart syndrome. The Journal Of Pediatrics 2011; 159 (1): 64-69 6. Kipps AK , Feuille C , Azakie A , Hoffman JI , Tabbutt S , Brook MM ,Moon-Grady AJ: Prenatal diagnosis of hypoplastic left heart syndrome in current era. The American Journal Of Cardiology 2011; 108 (3): 421-427 7. Attar MA

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Comparison of the clinical status and the effects of treatment of newborns with interrupted aortic arch diagnosed prenatally and postnatally in the "Polish Mother's Memorial" Institute in Lodz in the years 2003-2012

. Pulse oximetry as a screening test for congenital heart defects in newborn infants. A test accuracy study with evaluation of acceptability and cost-effectiveness. Health Technology Assessment 2012;2(16) 22. Nowy podział wad serca płodu na 4 grupy, wg 23. Respondek-Liberska M. Nowy Podział wad serca u płodu (z punktu widzenia kardiologii prenatalnej) 24. Respondek-Liberska M. Atlas wad serca u płodu. Wybór patologii pod kątem ich

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Fetal Triploidy; Two Case Reports with Particular Emphasis on Echocardiographic Assessment and Literature Review

haploid set. Am J Med Genet 1991;38:535-538 4. Doshi N, Surti U, Szulman AE. Morphologic anomalies in triploid liveborn fetuses. Hum Pathol 1983;14:716-723 5. Jacobs PA, Angell RR, Buchanan IM, Hassold TJ, Matsuyama AM, Manuel B. The origin of human triploids. Ann Hum Genet. 1978;42:49-57 6. McFadden DE, Robinson WP. Phenotype of triploid embryos. J Med Genet. 2006;43:609-612 7. Rosenbusch BE. Mechanisms giving rise to triploid zygotes during assisted reproduction. Fertil Steril. 2008

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Can Inflammatory Markers Diagnosed Upon Ultrasound Examination During Pregnancy Regress After Administration of Vaginal Treatment? – A Pilot Study

labour. BJOG 2005, 1: 48-50 8. Hamza A, Herr M, Solomayer M, Meyberg-Solomayer G.: Polyhydramnios: Causes, Diagnosis and Therapy. Geburtshilfe und Frauenhei/kunde 2013, 12: 1241-1246 9. Golan A, Wolman I, Sagi J.: Persistence of polyhydramnios during pregnancy - its significance and correlation with maternal and fetal complications. Gynecol Obstet Invest 1994, 37: 18 10. Pri-paz S, Khalek N, Fuchs K.M, Simpson LL.: Maximal amniotic fluid index as a prognostic factor in pregnancies complicated by polyhydramnios. Ultrasound

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Review Paper. Transplacental Digoxin Treatment In Prenatal Cardiac Problems In Singleton Pregnancies - Meta Analysis (Based On Literature: 1992–2015)

-277 41. Strizek B, Berg C, Gottschalk I, Herberg U, Geipel A, Gembruch U. High-dose flecainide is the most effective treatment of fetal supraventricular tachycardia. Heart Rhythm. 2016, 13(6), 1283-1289 42. Itoh S, Tanaka C, Nakamura Y,Yoshida K, Mitsuhashi N, Takeuchi H, Kuwabara Y. Prenatal management of fetal cardiac tumors. Two case reports. Fetal Diagn Ther.1996, 11(5), 361-365 43. Hoeschen RJ, Proveda V. Serum digoxin by radioimmunoassay. Can Med Assoc J. 1971,105(2), 170-173 44. Bodem G. Radioimmunological

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Isolated Double Aortic Arch (Daa) – Prenatal Detection with Postnatal Follow-Up, Case Report and Literature Review

References 1. Hunter L., Callaghan N., Patel K., Prenatal echocardiographic diagnosis of double aortic arch, Ultrasound Obstet Gynecol. 2015; 45: 483-485 2. Gou Z., He Y., Zhang Y., et al., Prenatal diagnosis of fetal double aortic arch: report of a case, Int J Clin Exp Pathol 2015; 8 (10): 13565-13567 3. Wójtowicz A., Respondek- Liberska M., et al., The significance of a prenatal diagnosis of right aortic arch, Prenatal diagnosis 2017; 37 (4): 365-374 4. Slodki M, Moszura T, Janiak K, Sysa A

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DORV in fetuses: how to consult future parents at a prenatal cardiology center? Retrospective analysis of 39 cases

detection and postnatal management of double outlet rightventricle (DORV) in 21 singleton pregnancies;J Matern Fetal Neonatal Med;2012; 25(1): 58-63 14. Kim N, Friedberg M, Silverman N H: Diagnosis and prognosis of fetuses with double outlet right ventricle;Prenat Diagn;2006; 26: 740-745 15. Gedikbasi A, Oztarhan K , Gul A, Sargin A, Ceylan Y: Diagnosis and prognosis in double-outlet right ventricle; Am J Perinatol;2008;25:427-434 16. Harris JA, Francannet C, Pradat P, Robert E: The epidemiology of cardiovascular defects

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Duodenal obstruction in prenatal ultrasound examinations - duodenal atresia versus annular pancreas - reports on two cases and literature review

References 1. Pariente G, Landau D, Aviram M, Hershkovitz R. PrenPariente G, Landau D, Aviram M, Hershkovitz R. Prenatal Diagnosis of a Rare Sonographic Appearance of Duodenal Atresia. Report of 2 cases and literature review. J Ultrasound Med 2012;31:1829-1833 2. Jeng Hsiu Hung, Shu Huei Shen, Tai Wai Chin, Chi Yi Selena Hung. Letters to the editor . Prenatal diagnosis of double duodenal atresia by ultrasound and magnetic resonance image. Prenat Diagn 2000; 27: 380-387. 3. Choudhry MS, Rahman N, Boyd P, Lakhoo K

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Jacobsen Syndrome - Prenatal and Postnatal Phenotypic Changes - Case Report and Review

References 1. Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.: An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Hum Hered 1973, 23: 568-585 2. Grossfeld PD, Mattina T, Lai Z, Favier R, Jones KL, Cotter F, Jones C.: The 11q terminal deletion disorder: a prospective study of 110 cases. Am J Med Genet 2004; 129A: 51-61 3. Pivnick EK, Velagaleti GV, Wilroy RS, Smith ME, Rose ME, Tipton RE, Tharapel

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