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Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 2, 2006
Changes in cerebral saturation profile in response to mechanical ventilation alterations in infants with bidirectional superior cavopulmonary connectionAntonio R Mott, Ahmed Alomrani, Tia A Tortoriello, et al.The Journal of Pediatrics|July 25, 2006
N-terminal pro-B-type natriuretic peptide levels in acute versus chronic left ventricular dysfunctionIris Fried, Benjamin Bar-Oz, Zeev Perles, et al.Fetal Diagnosis and Therapy|July 2, 2003
Absent ductus venosus in the fetus: review of the literature and first report of direct umbilical venous drainage to the coronary sinusZeev Perles, Amiram Nir, Michael Nadjari, et al.Pediatrics|May 4, 2005
Amino-terminal pro-brain-type natriuretic peptide: heart or lung disease in pediatric respiratory distress?Shlomo Cohen, Chaim Springer, Avraham Avital, et al.The American Journal of Cardiology|July 30, 2013
Prevalence of persistent superior vena cava and association with congenital heart anomaliesZeev Perles, Amiram Nir, Sagui Gavri, et al.European Journal of Human Genetics : EJHG|December 4, 2014
A human laterality disorder associated with a homozygous WDR16 deletionAsaf Ta-Shma, Zeev Perles, Barak Yaacov, et al.Journal of Medical Genetics|May 12, 2012
A human laterality disorder associated with recessive CCDC11 mutationZeev Perles, Yuval Cinnamon, Asaf Ta-Shma, et al.Journal of Pediatric Hematology/Oncology|July 5, 2007
N-terminal-proB-type natriuretic peptide as a marker for acute anthracycline cardiotoxicity in childrenSivan Ekstein, Amiram Nir, Azaria J J T Rein, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 14, 2007
Analysis of segmental and global function of the fetal heart using novel automatic functional imagingAsaf Ta-Shma, Zeev Perles, Sagui Gavri, et al.Journal of Medical Genetics|October 3, 2015
A human laterality disorder caused by a homozygous deleterious mutation in MMP21Zeev Perles, Sungjin Moon, Asaf Ta-Shma, et al.Pageof 3