Dr. Reham Nazal Articles

Date	Title
2024	TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from Palestine
2023	SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission
2022	Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene
2022	Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder
2022	ORIGINAL ARTICLE\|ARTICLES IN PRESS Purchase Subscribe Save Share Reprints Request Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families
2022	ORIGINAL ARTICLE\|ARTICLES IN PRESS Purchase Subscribe Save Share Reprints Request Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families
2022	Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families
2022	Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells
2021	Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency
2021	Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia
2017	Structural Basis of the Oncogenic Interaction of Phosphatase PRL-1 with the Magnesium Transporter CNNM2.
2017	Early born neurons are abnormally positioned in the doublecortin knockout hippocampus
2013	Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice
2013	Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse
2013	Hippocampal development - Old and new findings.
2013	New insights into genotype-phenotype correlations for the DCX-related lissencephaly spectrum.