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65 results

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Page 1
Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.
Elsayed LEO, AlHarbi NA, Alqarni AM, Eltayeb HHE, Mostafa NMM, Abdulrahim MM, Zaid HIB, Alanzi LM, Ababtain SA, Aldulaijan K, Aloyouni SY, Othman MAK, Alkheilewi MA, Binduraihem AM, Alrukban HA, Ahmed HY, AlRadini FA, Alahdal HM, Mushiba AM, Alzaher OA. Elsayed LEO, et al. Hum Genomics. 2024 Sep 4;18(1):95. doi: 10.1186/s40246-024-00662-0. Hum Genomics. 2024. PMID: 39232803 Free PMC article.
Met/HGFR triggers detrimental reactive microglia in TBI.
Rehman R, Miller M, Krishnamurthy SS, Kjell J, Elsayed L, Hauck SM, Olde Heuvel F, Conquest A, Chandrasekar A, Ludolph A, Boeckers T, Mulaw MA, Goetz M, Morganti-Kossmann MC, Takeoka A, Roselli F. Rehman R, et al. Among authors: elsayed l. Cell Rep. 2022 Dec 27;41(13):111867. doi: 10.1016/j.celrep.2022.111867. Cell Rep. 2022. PMID: 36577378 Free article.
Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism.
Dahawi M, de Sainte Agathe JM, Elmagzoub MS, Ahmed EA, Buratti J, Courtin T, Noé E, Bogoin J, Copin B, Elmugadam FA, Abdelgadir WA, Ahmed AKMA, Daldoum MA, Altayeb RMI, Bashir M, Khalid LM, Gamil S, Baldassari S, Elsayed L, Keren B, Nuel G, Ahmed AE, Leguern E. Dahawi M, et al. Among authors: elsayed l. Hum Genomics. 2024 Nov 21;18(1):130. doi: 10.1186/s40246-024-00659-9. Hum Genomics. 2024. PMID: 39574152 Free PMC article.
Methylation of alpha-synuclein in a Sudanese cohort.
Bakhit Y, Schmitt I, Hamed A, Ibrahim EAA, Mohamed IN, El-Sadig SM, Elseed MA, Alebeed MA, Shaheen MT, Ibrahim MO, Elhassan AA, Eltom K, Ali HA, Ibrahim YA, Almak ME, Abubaker R, Ahmed MA, Abugrain AA, Elrasheed SM, Omar MA, Almahal MA, MohamedSharif AA, Tahir MY, Malik SM, Eldirdiri HS, Khidir RJ, Mohamed MT, Abdalla A, Omer FY, Elsayed LEO, Babikir HEH, Bukhari EA, Seidi O, Wüllner U. Bakhit Y, et al. Among authors: elsayed leo. Parkinsonism Relat Disord. 2022 Aug;101:6-8. doi: 10.1016/j.parkreldis.2022.05.009. Epub 2022 Jun 4. Parkinsonism Relat Disord. 2022. PMID: 35728367
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes.
Flannery KP, Safwat S, Matsell E, Battula N, Hamed AAA, Mohamed IN, Elseed MA, Koko M, Abubaker R, Abozar F, Elsayed LEO, Bhise V, Molday RS, Salih MA, Yahia A, Manzini MC. Flannery KP, et al. Among authors: elsayed leo. Neurogenetics. 2024 Oct;25(4):425-433. doi: 10.1007/s10048-024-00773-9. Epub 2024 Jul 27. Neurogenetics. 2024. PMID: 39066872 Free PMC article.
PLA2G6-associated late-onset parkinsonism in a Sudanese family.
Bakhit Y, Tesson C, Ibrahim MO, Eltom K, Eltazi I, Elsayed LEO, Lesage S, Seidi O, Corvol JC, Wüllner U; Sudanese Parkinson's Disease Study Group. Bakhit Y, et al. Among authors: elsayed leo. Ann Clin Transl Neurol. 2023 Jun;10(6):983-989. doi: 10.1002/acn3.51781. Epub 2023 May 3. Ann Clin Transl Neurol. 2023. PMID: 37139542 Free PMC article.
Intrafamilial and interfamilial heterogeneity of PINK1-associated Parkinson's disease in Sudan.
Bakhit Y, Ibrahim MO, Tesson C, Elhassan AA, Ahmed MA, Alebeed MA, Elrasheed SM, Omar MA, Abubaker R, Eltom K, Shaheen MT, Ibrahim YA, Almak ME, Ali HA, Abugrain AA, Almahal MA, MohamedSharif AA, Tahir MY, Malik SM, Eldirdiri Abdelrahman H, Khidir RJ, Mohamed MT, Abdalla A, Elsayed LEO, Lesage S, Corvol JC, Seidi O, Wüllner U. Bakhit Y, et al. Among authors: elsayed leo. Parkinsonism Relat Disord. 2023 Jun;111:105401. doi: 10.1016/j.parkreldis.2023.105401. Epub 2023 Apr 25. Parkinsonism Relat Disord. 2023. PMID: 37150071
65 results