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Home
Dr. Reham Nazal
Dr. Reham Nazal Publications
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Dr. Reham Nazal Publications
Article
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
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
ORIGINAL ARTICLE|ARTICLES IN PRESS Purchase Subscribe Save Share Reprints Request 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.