Labib DM - Search Results

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Cognitive and physical disability in Egyptian patients with multiple sclerosis: genetic and optical coherence tomography study.

Abdel Naseer M, Fathi S, Roshdy NK, Labib DM, Khalil DH, Ibrahim W, Magdy R. Abdel Naseer M, et al. Among authors: labib dm. Neurol Res. 2019 Jul;41(7):644-651. doi: 10.1080/01616412.2019.1609203. Epub 2019 Apr 26. Neurol Res. 2019. PMID: 31025605

Evaluating sex hormones and cytokine profile in Egyptian females with relapsing-remitting multiple sclerosis.

Talaat FM, Abokrysha NT, Labib DM, El Khateeb E, El Aziz GHA. Talaat FM, et al. Among authors: labib dm. Egypt J Neurol Psychiatr Neurosurg. 2018;54(1):30. doi: 10.1186/s41983-018-0030-2. Epub 2018 Nov 3. Egypt J Neurol Psychiatr Neurosurg. 2018. PMID: 30459503 Free PMC article.

Vascular endothelial growth factor G1612A (rs10434) gene polymorphism and neuropsychiatric manifestations in systemic lupus erythematosus patients.

Taha S, Gamal SM, Nabil M, Naeem N, Labib D, Siam I, Gheita TA. Taha S, et al. Rev Bras Reumatol Engl Ed. 2017 Mar-Apr;57(2):149-153. doi: 10.1016/j.rbre.2016.11.007. Epub 2016 Dec 14. Rev Bras Reumatol Engl Ed. 2017. PMID: 28343620 Free article. English, Portuguese.

Focal interictal epileptiform discharges in idiopathic generalized epilepsy.

Esmail EH, Nawito AM, Labib DM, Basheer MA. Esmail EH, et al. Among authors: labib dm. Neurol Sci. 2016 Jul;37(7):1071-7. doi: 10.1007/s10072-016-2538-5. Epub 2016 Mar 8. Neurol Sci. 2016. PMID: 26956566

Association of serotonin transporter gene (5HTT) polymorphism and juvenile myoclonic epilepsy: a case-control study.

Esmail EH, Labib DM, Rabie WA. Esmail EH, et al. Among authors: labib dm. Acta Neurol Belg. 2015 Sep;115(3):247-51. doi: 10.1007/s13760-014-0400-1. Epub 2014 Dec 7. Acta Neurol Belg. 2015. PMID: 25481722

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