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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.
Hum Genet. 2017 Aug;136(8):921-939. doi: 10.1007/s00439-017-1821-8. Epub 2017 Jun 9.
Hum Genet. 2017.
PMID: 28600779
Free PMC article.
Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update.
Maddirevula S, Shamseldin HE, Sirr A, AlAbdi L, Lo RS, Ewida N, Al-Qahtani M, Hashem M, Abdulwahab F, Aboyousef O, Kaya N, Monies D, Salem MH, Al Harbi N, Aldhalaan HM, Alzaidan H, Almanea HM, Alsalamah AK, Al Mutairi F, Ismail S, Abdel-Salam GMH, Alhashem A, Asery A, Faqeih E, AlQassmi A, Al-Hamoudi W, Algoufi T, Shagrani M, Dudley AM, Alkuraya FS.
Maddirevula S, et al. Among authors: alqassmi a.
Front Genet. 2020 Dec 31;11:580484. doi: 10.3389/fgene.2020.580484. eCollection 2020.
Front Genet. 2020.
PMID: 33456446
Free PMC article.
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The challenge of diagnosing and successfully treating anti-NMDA receptor encephalitis in a toddler.
Alqassmi AA, Alaklabi F, Alzomor OA, Salih MA.
Alqassmi AA, et al.
Sudan J Paediatr. 2021;21(1):76-81. doi: 10.24911/SJP.106-1601560207.
Sudan J Paediatr. 2021.
PMID: 33879947
Free PMC article.
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Benign mesial temporal lobe epilepsy: A clinical cohort and literature review.
AlQassmi A, Burneo JG, McLachlan RS, Mirsattari SM.
AlQassmi A, et al.
Epilepsy Behav. 2016 Dec;65:60-64. doi: 10.1016/j.yebeh.2016.09.017. Epub 2016 Nov 23.
Epilepsy Behav. 2016.
PMID: 27889242
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