Publications by authors named "Stephanie Libzon"

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Blood Pressure Profile in Pediatric Moyamoya: Longitudinal Analysis and Revascularization Impact.
Nour Suliman, Roxana Cleper, Shelly I Shiran, Stéphanie Libzon, Bar Nishry

Pediatr Neurol· December 2025

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Neurodevelopmental outcome of perinatal intracranial haemorrhage in patients born at term: A prospective study.
Stephanie Libzon, Shelly I Shiran, Aviva Fattal-Valevski, Nira Schneebaum-Sender, Jonathan Roth

Dev Med Child Neurol· October 2025

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Antenatal subpial hemorrhage diagnosed by fetal magnetic resonance imaging: imaging spectrum and autopsy findings.
Stephanie Libzon, Debora Kidron, Uri Erlik, Karina Krajden-Haratz, Moran Hausman-Kedem

Pediatr Radiol· August 2025

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Parental counselling and autopsy results: A retrospective diagnostic cohort study at a multidisciplinary fetal neurology clinic.
Avi Shariv, Michal Gafner, Zvi Leibovitz, Letizia Schreiber, Dvora Kidron, Stephanie Libzon

Dev Med Child Neurol· August 2025

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A Novel Pathogenic Variant Identified in HIKESHI-Related Hypomyelinating Leukodystrophy Disrupts Heat Shock Response in iPSCs.
Mahmood Ali Saleh, Maria Boichuck, Aner Ottolenghi, Tatiana Rabinski, Omri Goldenthal, Stephanie Libzon

Int J Mol Sci· June 2025

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Parental magnetic resonance imaging for the evaluation of fetuses with brain anomalies.
Stephanie Libzon, Michal Gafner, Dorit Lev, Nilly Waiserberg, Liat Gindes

Dev Med Child Neurol· April 2025

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Clinical and neuroimaging patterns of perinatal intracranial haemorrhage in fetuses and term-born neonates: a prospective observational cohort study.
Moran Hausman-Kedem, Stephanie Libzon, Aviva Fattal Valevski, Gustavo Malinger, Nina Krajden Haratz

Arch Dis Child Fetal Neonatal Ed· April 2025

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Heterozygous de novo variants in cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisation.
Marina Eskin-Schwartz, Shaikah Seraidy, Eyal Paz, Maism Molhem, Emmanuelle Ranza, Stephanie Libzon

J Med Genet· December 2024

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Hydrocephalus associated with a molar tooth sign: A distinct subtype of Joubert syndrome.
Michal Gafner, Leila Haddad, Rachna Gupta, Zvi Leibovitz, Itamar Zilberman Ron, Stephanie Libzon

Dev Med Child Neurol· July 2024

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Utility of genetic testing in children with leukodystrophy.
Ayelet Zerem, Stephanie Libzon, Liat Ben Sira, Hadas Meirson, Moran Hausman-Kedem

Eur J Paediatr Neurol· July 2023

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Clinical phenotypes of infantile onset CACNA1A-related disorder.
Tamar Gur-Hartman, Oren Berkowitz, Keren Yosovich, Agathe Roubertie, Ginevra Zanni, Stephanie Libzon

Eur J Paediatr Neurol· January 2021

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Metabolic stroke in a patient with bi-allelic OPA1 mutations.
Ayelet Zerem, Keren Yosovich, Yael Cohen Rappaport, Stephanie Libzon, Lubov Blumkin

Metab Brain Dis· August 2019

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Medical Cannabis for Pediatric Moderate to Severe Complex Motor Disorders.
Stephanie Libzon, Lihi Bar-Lev Schleider, Naama Saban, Luda Levit, Yulia Tamari

J Child Neurol· August 2018

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