Search Results - "Ibrahim, Yousuf A."

Intrafamilial and interfamilial heterogeneity of PINK1-associated Parkinson's disease in Sudan by Bakhit, Yousuf, Ibrahim, Mohamed O., Tesson, Christelle, Elhassan, Ali A., Ahmed, Mohamed Anwer, Alebeed, Mohamed A., Elrasheed, Salma M., Omar, Mawia A., Abubaker, Rayan, Eltom, Khalid, Shaheen, Mutaz T., Ibrahim, Yousuf A., Almak, Murad E., Ali, Hiba A., Abugrain, Ahmed A., Almahal, Mohamed A., MohamedSharif, Abubaker A., Tahir, Mohamed Y., Malik, Sawazen M., Eldirdiri Abdelrahman, Hazim, Khidir, Reem J., Mohamed, Malaz T., Abdalla, Abdelmohaymin, Elsayed, Liena E.O., Lesage, Suzanne, Corvol, Jean-Christophe, Seidi, Osheik, Wüllner, Ullrich

“…PINK1 is the second most predominant gene associated with autosomal recessive Parkinson's disease. Homozygous mutations in this gene are associated with an…”
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Methylation of alpha-synuclein in a Sudanese cohort by Bakhit, Yousuf, Schmitt, Ina, Hamed, Ahlam, Ibrahim, Etedal Ahmed A., Mohamed, Inaam N., El-Sadig, Sarah M., Elseed, Maha A., Alebeed, Mohamed A., Shaheen, Mutaz T., Ibrahim, Mohamed O., Elhassan, Ali A., Eltom, Khalid, Ali, Hiba A., Ibrahim, Yousuf A., Almak, Murad E., Abubaker, Rayan, Ahmed, Mohamed Anwer, Abugrain, Ahmed A., Elrasheed, Salma M., Omar, Mawia A., Almahal, Mohamed A., MohamedSharif, Abubaker A., Tahir, Mohamed Y., Malik, Sawazen M., Eldirdiri, Hazim S., Khidir, Reem J., Mohamed, Malaz T., Abdalla, Abdelmohaymin, Omer, Farouk Yassen, Elsayed, Liena E.O., Babikir, Haydar El Hadi, Bukhari, Elfateh Abd-Allah, Seidi, Osheik, Wüllner, Ullrich

“…Several studies suggested a significant role of epigenetic changes, including alterations in miRNA, histone modifications, and DNA methylation of α-synuclein…”
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