All Stories

  1. Bridging the gap: associations between gut microbiota and psychiatric disorders

    Article • Middle East Current Psychiatry, January 2024, Springer Science + Business Media

    Nourelhoda Haridy

  2. Long-term outcomes of plasma exchange versus intravenous immunoglobulin for the treatment of Guillain-Barré Syndrome: A double-blind, randomized clinical trial

    Article • Restorative Neurology and Neuroscience, January 2024, IOS Press

    eman khedr, Nourelhoda Haridy

  3. Predictors of long-term health-related quality of life in Guillain-Barré syndrome: A hospital-based study

    Article • Clinical Neurology and Neurosurgery, December 2023, Elsevier

    Nourelhoda Haridy

  4. Myasthenia gravis with achalasia secondary to thymoma: a case report and literature review

    Article • The Egyptian Journal of Neurology Psychiatry and Neurosurgery, March 2023, Springer Science + Business Media

    Nourelhoda Haridy

  5. Relationship Between Disability and Psychiatric Outcome in Multiple Sclerosis Patients and Its Determinants

    Article • Multiple Sclerosis and Related Disorders, March 2023, Elsevier

    Nourelhoda Haridy

  6. Effects of transcranial direct current stimulation in pain and opioid consumption after spine surgery

    Article • European Journal of Pain, June 2022, Wiley

    Nourelhoda Haridy

  7. Relationship between Attention Deficit Hyperactivity Disorder and epilepsy: a literature review

    Article • The Egyptian Journal of Neurology Psychiatry and Neurosurgery, May 2022, Springer Science + Business Media

    Nourelhoda Haridy

  8. Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

    Article • Nature Genetics, May 2020, Springer Science + Business Media

    Nourelhoda Haridy

  9. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

    Article • Nature Genetics, May 2020, Springer Science + Business Media

    Nourelhoda Haridy

  10. Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination

    Article • European Journal of Neurology, October 2019, Wiley

    Nourelhoda Haridy

  11. PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

    Article • Annals of Neurology, July 2019, Wiley

    Prof Maria Rosaria Conte, Professor Kyproula Christodoulou, Nourelhoda Haridy

  12. An update on advances in magnetic resonance imaging of multiple system atrophy

    Article • Journal of Neurology, November 2018, Springer Science + Business Media

    Nourelhoda Haridy

  13. Clinical and Genetic analysis of Egyptian hereditary spastic paraplegia using next generation sequencing

    Article • Neuromuscular Disorders, April 2018, Elsevier

    Nourelhoda Haridy

  14. Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14

    Article • Movement Disorders, March 2018, Wiley

    Nourelhoda Haridy

  15. Sequencing analysis of the SCA6 CAG expansion excludes an influence of repeat interruptions on disease onset

    Article • Journal of Neurology Neurosurgery & Psychiatry, January 2018, BMJ

    Nourelhoda Haridy

  16. Severe axonal neuropathy is a late manifestation of SPG11

    Article • Deutsche Zeitschrift für Nervenheilkunde, August 2016, Springer Science + Business Media

    Nourelhoda Haridy