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