Search Results - "congenital heart defect"

Helsmoortel-van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report by Li-juan Chen, Zhong-min You, Wen-hong Chen, Si Yang, Chun-chen Feng, Hai-yong Wang, Ting Wang, Yuan-yuan Zhu

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Challenges in Pediatric Cardiac Anesthesia in Developing Countries by Mirjana Cvetkovic

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Complete Colonic Duplication and Perineal Fistula: Transanal Mucosectomy of the Ectopic Rectum by Johannes W. Duess, Peter Zimmermann, Franz W. Hirsch, Daniel Graefe, Martin Lacher, Jan-Hendrik Gosemann

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Long-Term Effects of Child Early Surgical Ventricular Septal Defect Repair on Maternal Stress by Jennifer Gerlach, Elena S. Decker, Anne-Christine Plank, Stefan Mestermann, Ariawan Purbojo, Robert A. Cesnjevar, Oliver Kratz, Anna Eichler

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Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay by Go Hun Seo, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo

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Diagnosis and management of aorto-left ventricular tunnel by Pallavi Kathare, Rama G Subramanyam, Tapan Kumar Dash, Kalyana Sundaram Muthuswamy, K Raghu, Nageswara Rao Koneti

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Prenatal arsenic exposure alters the placental expression of multiple epigenetic regulators in a sex-dependent manner by Emily F. Winterbottom, Yuka Moroishi, Yuliya Halchenko, David A. Armstrong, Paul J. Beach, Quang P. Nguyen, Anthony J. Capobianco, Nagi G. Ayad, Carmen J. Marsit, Zhigang Li, Margaret R. Karagas, David J. Robbins

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Acquired von Willebrand syndrome is common in infants with systemic-to-pulmonary shunts: Retrospective case-series by Vanya Icheva, Ulrich Budde, Harry Magunia, Karl Jaschonek, Clemens Hinterleitner, Felix Neunhoeffer, Christian Schlensak, Michael Hofbeck, Gesa Wiegand

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Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family by Peng Tu, Hairui Sun, Xiaohang Zhang, Qian Ran, Yihua He, Suzhen Ran

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The yield of SNP microarray analysis for fetal ultrasound cardiac abnormalities by Fenglei Ye, Xiayuan Xu, Yi Wang, Lifang Chen, Qunda Shan, Qijing Wang, Fan Jin

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Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women by Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong

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ECHO-CARDIOGRAPHIC STUDY OF VENTRICULAR SEPTAL DEFECT IN 1-12 YEARS OF CHILDREN VISITING TERTIARY CARE CENTER. by Amish Kumar, Pankaj Kumar, Nirav Kumar, Avanish Kumar

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Feasibility of neurosonography in CHD-fetuses and controls in a clinical tertiary setting by Sheila M. Everwijn, Jiska F. van Bohemen, Fenna A. Jansen, Sylke J. Steggerda, Aalbertine K. Teunissen, Monique C. Haak

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Part II. Comparison of Neurodevelopmental Outcomes Between Normothermic and Hypothermic Pediatric Cardiopulmonary Bypass by Claire E. Hannon, Zachary Osman, Cathy Grant, Emma M. L. Chung, Emma M. L. Chung, Emma M. L. Chung, Antonio F. Corno, Antonio F. Corno

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Long-term Associations of an Early Corrected Ventricular Septal Defect and Stress Systems of Child and Mother at Primary School Age by Valeska Stonawski, Valeska Stonawski, Laura Vollmer, Nicola Köhler-Jonas, Nicolas Rohleder, Yulia Golub, Ariawan Purbojo, Gunther H. Moll, Hartmut Heinrich, Hartmut Heinrich, Robert A. Cesnjevar, Oliver Kratz, Anna Eichler

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Arrhythmia during diagnostic cardiac catheterization in pediatric patients with congenital heart disease by Taner Kasar, Ibrahim Cansaran Tanıdır, Erkut Öztürk, Selman Gökalp, Gülhan Tunca Şahin, Mehmet Akın Topkarcı, Yakup Ergül, Alper Güzeltaş

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Anesthetic management of caesarean section in a patient with double outlet right ventricle by Rohith Krishna, Umesh Goneppanavar

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Major heart defects: the diagnostic evaluations of first-year-olds by Jan Pavlicek, Eva Klaskova, Sabina Kapralova, Alzbeta Moravova Palatova, Alicja Piegzova, Richard Spacek, Tomas Gruszka

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Etiology and Morphogenesis of Congenital Heart Disease From Gene Function and Cellular Interaction to Morphology /

Table of Contents: “…Current Genetics in Congenital Heart Diseases -- Genetic discovery for congenital heart defects -- Evidence that deletion of ETS-1, a gene in the Jacobsen syndrome (11q-) cardiac critical region, causes congenital heart defects through impaired cardiac neural crest cell function -- Notch signaling in aortic valve development and disease -- To detect and explore mechanism of CITED2 mutation and methylation in children with congenital heart disease.…”
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Peculiarities of psychoemotional condition of pregnant women before foetus echocardiography and parents' reaction to the prenatal diagnosis by A. Yu. Sydorenko, A. K. Kurkevych, M. V. Markova

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