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Year Number of Results
2013 3
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2015 2
2016 2
2017 1
2018 1
2020 1
2024 0

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13 results

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Page 1
Parkinson's Disease in Saudi Patients: A Genetic Study.
Al-Mubarak BR, Bohlega SA, Alkhairallah TS, Magrashi AI, AlTurki MI, Khalil DS, AlAbdulaziz BS, Abou Al-Shaar H, Mustafa AE, Alyemni EA, Alsaffar BA, Tahir AI, Al Tassan NA. Al-Mubarak BR, et al. Among authors: tahir ai. PLoS One. 2015 Aug 14;10(8):e0135950. doi: 10.1371/journal.pone.0135950. eCollection 2015. PLoS One. 2015. PMID: 26274610 Free PMC article. Clinical Trial.
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.
Bohlega SA, Al-Mubarak BR, Alyemni EA, Abouelhoda M, Monies D, Mustafa AE, Khalil DS, Al Haibi S, Abou Al-Shaar H, Faquih T, El-Kalioby M, Tahir AI, Al Tassan NA. Bohlega SA, et al. Among authors: tahir ai. BMC Res Notes. 2016 Jun 7;9:295. doi: 10.1186/s13104-016-2102-7. BMC Res Notes. 2016. PMID: 27268037 Free PMC article.
Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection.
Mustafa AE, Faquih T, Baz B, Kattan R, Al-Issa A, Tahir AI, Imtiaz F, Ramzan K, Al-Sayed M, Alowain M, Al-Hassnan Z, Al-Zaidan H, Abouelhoda M, Al-Mubarak BR, Al Tassan NA. Mustafa AE, et al. Among authors: tahir ai. Genes (Basel). 2018 May 22;9(5):267. doi: 10.3390/genes9050267. Genes (Basel). 2018. PMID: 29789446 Free PMC article.
Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease.
Imtiaz F, Al-Mostafa A, Allam R, Ramzan K, Al-Tassan N, Tahir AI, Al-Numair NS, Al-Hamed MH, Al-Hassnan Z, Al-Owain M, Al-Zaidan H, Al-Amoudi M, Qari A, Balobaid A, Al-Sayed M. Imtiaz F, et al. Among authors: tahir ai. Mol Genet Metab Rep. 2017 Apr 7;11:17-23. doi: 10.1016/j.ymgmr.2017.03.006. eCollection 2017 Jun. Mol Genet Metab Rep. 2017. PMID: 28417071 Free PMC article.
13 results