Zeev Perles
Jerusalem, JM, Israel
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications
Immune-Mediated Fetal Complete Atrioventricular Block: Can Dexamethasone Therapy Revert the Process?
Immune-Mediated Fetal Complete Atrioventricular Block: Can Dexamethasone Therapy Revert the Process?
Journal: The Israel Medical Association journal : IMAJ
Published: November 29, 2020
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy.
Journal: The Journal of clinical investigation
Published: July 09, 2020
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
Journal: Nature communications
Published: November 03, 2019
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.
Journal: PLoS genetics
Published: March 23, 2018
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy.
Journal: American journal of human genetics
Published: December 11, 2017
Postmortem Computer Tomography Appearance of the Aortic Arch in Children: What Is Considered Normal?
Postmortem Computer Tomography Appearance of the Aortic Arch in Children: What Is Considered Normal?
Journal: The Israel Medical Association journal : IMAJ
Published: November 06, 2017
Roles of the cilium-associated gene CCDC11 in left-right patterning and in laterality disorders in humans.
Journal: The International journal of developmental biology
Published: June 17, 2017
Congenital valvular defects associated with deleterious mutations in the PLD1 gene.
Journal: Journal of medical genetics
Published: August 20, 2016
Hepatopulmonary Syndrome in Patients With Cystic Fibrosis and Liver Disease.
Journal: Chest
Published: February 13, 2016
Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family.
Journal: Pediatric pulmonology
Published: November 11, 2015
A human laterality disorder caused by a homozygous deleterious mutation in MMP21.
Journal: Journal of medical genetics
Published: June 24, 2015
A human laterality disorder associated with a homozygous WDR16 deletion.
Journal: European journal of human genetics : EJHG
Published: July 20, 2014
Last Updated: 09/26/2026