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  1. Article

    Open Access

    Two ischemic stroke events within 48 h: a case report of an unusual presentation of thrombotic thrombocytopenic purpura

    Thrombotic thrombocytopenic purpura (TTP) considers a rare cause of ischemic stroke (IS). We reported a case of a newly diagnosed patient with acquired immune-mediated TTP (iTTP), in whom two IS events develop...

    Melika Jameie, Sanaz Heydari, Mojdeh Ghabaee, Hamed Amirifard in BMC Neurology (2023)

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  2. No Access

    Article

    Advanced weight-bearing mat exercises combined with functional electrical stimulation to improve the ability of wheelchair-dependent people with spinal cord injury to transfer and attain independence in activities of daily living: a randomized controlled trial

    Randomized controlled trial.

    Mostafa Rahimi, Giti Torkaman, Mojdeh Ghabaee, Ali Ghasem-Zadeh in Spinal Cord (2020)

  3. No Access

    Article

    Immunomodulatory function of Treg-derived exosomes is impaired in patients with relapsing-remitting multiple sclerosis

    Multiple sclerosis (MS) is an autoimmune disease which is characterized by neuroaxonal degeneration in the central nervous system. Impaired function of regulatory T cells (Tregs) is believed to be an underlyin...

    Maryam Azimi, Mojdeh Ghabaee, Abdorreza Naser Moghadasi… in Immunologic Research (2018)

  4. No Access

    Article

    Predictive ability of C-reactive protein for early mortality after ischemic stroke: comparison with NIHSS score

    We aimed to compare the association of high-sensitivity C-reactive protein (CRP) and National Institutes of Health Stroke Scale (NIHSS) score with mortality risk and to determine the optimal threshold of CRP f...

    Mojdeh Ghabaee, Ali Zandieh, Shahrzad Mohebbi, Mohammad Fakhri… in Acta Neurologica Belgica (2014)

  5. No Access

    Article

    Mitochondrial Mutation in Iranian Patients with Multiple Sclerosis, Correlation Between Haplogroups H, A and Clinical Manifestations

    As multiple sclerosis (MS) has long been known to be associated with Leber, hereditary optic neuropathy (LHON), a disease caused by mitochondrial (mtDNA) mutations, in this study we assessed possible involveme...

    Mojdeh Ghabaee, Motahar Omranisikaroudi… in Cellular and Molecular Neurobiology (2009)

  6. No Access

    Article

    Analysis of HLA DR2&DQ6 (DRB1*1501, DQA1*0102, DQB1*0602) Haplotypes in Iranian Patients with Multiple Sclerosis

    Multiple sclerosis (MS) is prototype of inflammatory demyelinating disease of the central nervous system .The etiology of MS remains unclear, but according to current data the disease develops in genetically s...

    Mojdeh Ghabaee, Asghar Bayati… in Cellular and Molecular Neurobiology (2009)

  7. No Access

    Article

    Mitochondrial D-Loop Variation in Persian Multiple Sclerosis Patients: K and A Haplogroups as a Risk Factor!!

    Multiple Sclerosis (MS) is a multifocal demyelinating central nervous system disorder in which interplay between genes and the environment are supposed to be involved. Mitochondrial DNA (mtDNA) has the only no...

    Hassan Hassani- Kumleh, Massoud Houshmand… in Cellular and Molecular Neurobiology (2006)