Doğumsal Kalp Anomalileri
Özet
Referanslar
Human Embryology and Developmental Biology.
Yun SW. Congenital heart disease in the newborn requiring early intervention. Vol. 54, Korean Journal of Pediatrics. Korean Pediatric Society; 2011. p. 183–91.
Keith L. Moore, T.V.N.Persaud, Mark G. Torchia: The Developing Human. Clinically Oriented Embryology. 11th edition.
Azhar M, Ware SM. Genetic and Developmental Basis of Cardiovascular Malformations. Vol. 43, Clinics in Perinatology. W.B. Saunders; 2016. p. 39–53.
Karunamuni GH, Ma P, Gu S, Rollins AM, Jenkins MW, Watanabe M. Connecting teratogen-induced congenital heart defects to neural crest cells and their effect on cardiac function. Birth Defects Res C Embryo Today. 2014 Sep 1;102(3):227–50.
10.1016/b978-1-4557-0684-6.01001-8. CrossRef Listing of Deleted DOIs. 2000;
Yasuhara J, Garg V. Genetics of congenital heart disease: A narrative review of recent advances and clinical implications. Vol. 10, Translational Pediatrics. AME Publishing Company; 2021. p. 2366–86.
Bruce Carlson - Human Embryology and Developmental Biology.
Romeo FJ, Mavropoulos SA, Ishikawa K. Progress in Clinical Gene Therapy for Cardiac Disorders. Vol. 27, Molecular Diagnosis and Therapy. Adis; 2023. p. 179–91.
Kim Y, Landstrom AP, Shah SH, Wu JC, Seidman CE. Gene Therapy in Cardiovascular Disease: Recent Advances and Future Directions in Science: A Science Advisory From the American Heart Association. Vol. 150, Circulation. Lippincott Williams and Wilkins; 2024. p. e471–80.
Barnes RM, Black BL. Nodal signaling and congenital heart defects. In: Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology. Springer Japan; 2016. p. 183–92.
Shad J, Budhwani K, Biswas R. Thoracic ectopia cordis. BMJ Case Rep. 2012;
Smith BJ, Flyer JN, Edwards EM, Soll RF, Horbar JD, Yeager SB. Outcomes for Ectopia Cordis. Journal of Pediatrics. 2020 Jan 1;216:67–72.
Nashat H, Montanaro C, Li W, Kempny A, Wort SJ, Dimopoulos K, et al. Atrial septal defects and pulmonary arterial hypertension. Vol. 10, Journal of Thoracic Disease. AME Publishing Company; 2018. p. S2953–65.
Meng X, Song M, Zhang K, Lu W, Li Y, Zhang C, et al. Congenital heart disease: types, pathophysiology, diagnosis, and treatment options. Vol. 5, MedComm. John Wiley and Sons Inc; 2024.
Kheiwa A, Hari P, Madabhushi P, Varadarajan P. Patent foramen ovale and atrial septal defect. Echocardiography. 2020 Dec 1;37(12):2172–84.
Granados-Riveron JT, Pope M, Bu’lock FA, Thornborough C, Eason J, Setchfield K, et al. Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutationsc hd_573 151..159 [Internet]. 2011. Available from: http://wileyonlinelibrary.
Eyileten Z, Uysalel A. Isolated ventricular septal defect in infants. E Journal of Cardiovascular Medicine. 2017 Jun 15;5(2):27–33.
Sadler_T_W_--_Langman_39_s_medical_embryology.
Larsen’s Human Embryology. 10.1016/b978-1-4557-0684-6.01001-8. CrossRef Listing of Deleted DOIs. 2000;