Reham Nazzal-Khalaf
Janin, WBK, Palestine
Last Updated: 09/26/2026
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Found 14 publications
Clinical Profiles, Genetic Variants, and Neurodevelopmental Outcomes Following Liver Transplantation in Maple Syrup Urine Disease: A Study From Palestine.
Journal: JIMD reports
Published: November 23, 2025
TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from Palestine.
Journal: American journal of medical genetics. Part A
Published: October 11, 2023
Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder.
Journal: American journal of human genetics
Published: August 04, 2022
Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene.
Journal: Frontiers in genetics
Published: July 27, 2022
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission.
Journal: Brain : a journal of neurology
Published: April 08, 2022
Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families.
Journal: Brain & development
Published: December 28, 2021
Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells.
Journal: Neurobiology of disease
Published: October 11, 2021
Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency.
Journal: European journal of human genetics : EJHG
Published: October 17, 2020
Early born neurons are abnormally positioned in the doublecortin knockout hippocampus.
Journal: Human molecular genetics
Published: July 11, 2016
Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse.
Journal: Neurobiology of disease
Published: January 21, 2014
Last Updated: 09/26/2026