Area of research
Psychiatry and Mental health · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Epilepsy research and treatment, Pharmacological Effects and Toxicity Studies, Neuroscience and Neuropharmacology Research, and Hereditary Neurological Disorders.
Pediatric functional seizures: Demographics, clinical and psychological characteristics and risk factors.
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.
Epilepsy secondary to intracranial calcification cause by hypothyroidism and chronic hypocalcaemia: a case report
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.
SLK is mutated in individuals with a neurodevelopmental disorder
From Expert Judgment to Structured Guidelines: A Brief History and Bright Future of DNA Variant Interpretation.
Case-based genomics education and training of neurologists: an Egyptian initiative.
The HUGO Clinical Genomics & Genomic Medicine Education Survey: clinicians globally need and want genomic medicine training.
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy
The effect of anticholinergic drugs on cognition of patients with Parkinson's disease: a cohort study from the Egyptian population.
The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson's disease.
The effect of epilepsy and antiseizure medications on cardiac autonomic functions in children with epilepsy.
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
Restless leg syndrome in patients with chronic kidney disease: a hospital-based study from Upper Egypt.
The effectiveness of cerebrolysin, a multi-modal neurotrophic factor, for treatment of post-covid-19 persistent olfactory, gustatory and trigeminal chemosensory dysfunctions: a randomized clinical trial.
Evaluation of chronic idiopathic tinnitus and its psychosocial triggers.
Idiopathic steno-occlusive disease with bilateral internal carotid artery occlusion: A Case Report.
Peripartum depression and its predictors: A longitudinal observational hospital-based study.
Vestibular function in children with generalized epilepsy and treated with valproate.
Biallelic variants in <i>HPDL</i> cause pure and complicated hereditary spastic paraplegia
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Behavioral assessment of children and adolescents with Graves' disease: A prospective study.
Behavioral problems in children with primary monosymptomatic nocturnal enuresis.
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome.
Behavioral assessment of females with congenital adrenal hyperplasia.
Vestibular Function in Children with Type 1 Diabetes: Videonystagmography Testing.
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.