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A multicenter clinical exome study in unselected cohorts from a consanguineous population of Saudi Arabia demonstrated a high diagnostic yield.
Alfares A, Alfadhel M, Wani T, Alsahli S, Alluhaydan I, Al Mutairi F, Alothaim A, Albalwi M, Al Subaie L, Alturki S, Al-Twaijri W, Alrifai M, Al-Rumayya A, Alameer S, Faqeeh E, Alasmari A, Alsamman A, Tashkandia S, Alghamdi A, Alhashem A, Tabarki B, AlShahwan S, Hundallah K, Wali S, Al-Hebbi H, Babiker A, Mohamed S, Eyaid W, Zada AAP. Alfares A, et al. Among authors: alghamdi a. Mol Genet Metab. 2017 Jun;121(2):91-95. doi: 10.1016/j.ymgme.2017.04.002. Epub 2017 Apr 7. Mol Genet Metab. 2017. PMID: 28454995 No abstract available.
A novel variant of RBCK1 gene causes mild polyglucosan myopathy.
AlAnzi T, Al Harbi F, AlGhamdi A, Mohamed S. AlAnzi T, et al. Among authors: alghamdi a. Neurosciences (Riyadh). 2022 Jan;27(1):45-49. doi: 10.17712/nsj.2022.1.20210681. Neurosciences (Riyadh). 2022. PMID: 35017290 Free PMC article.
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease.
Marais A, Bertoli-Avella AM, Beetz C, Altunoglu U, Alhashem A, Mohamed S, Alghamdi A, Willems P, Tsoutsou E, Fryssira H, Pons R, Almarzooq R, Karatoprak EY, Ayaz A, Ünverengil G, Calvo M, Yüksel Z, Bauer P. Marais A, et al. Among authors: alghamdi a. Eur J Med Genet. 2022 Aug;65(8):104537. doi: 10.1016/j.ejmg.2022.104537. Epub 2022 Jun 9. Eur J Med Genet. 2022. PMID: 35690317
Hereditary Hyperekplexia in Saudi Arabia.
Aldhilan A, Alhakeem A, Al Hajjaj S, Abukhalid M, Aldhalaan H, Salah E, Saeed M, Tabassum S, El Khashab HY, Aljabri M, Ali ES, Alwadei A, Hundallah K, Alghamdi A, Hakami W, AlShafi S, Alkuraya FS, Alanazy N, Seidahmed MZ, Alfadhel M, Tabarki B. Aldhilan A, et al. Among authors: alghamdi a. Pediatr Neurol. 2022 Sep;134:78-82. doi: 10.1016/j.pediatrneurol.2022.06.015. Epub 2022 Jun 24. Pediatr Neurol. 2022. PMID: 35841715
Bi-allelic variants in HCRT cause autosomal recessive narcolepsy.
Hakami W, Thabet F, Alhashem A, Alghamdi A, Alshahwan S, Alkuraya FS, Tabarki B. Hakami W, et al. Among authors: alghamdi a. Neurogenetics. 2024 Apr;25(2):79-83. doi: 10.1007/s10048-024-00744-0. Epub 2024 Jan 19. Neurogenetics. 2024. PMID: 38240911
Scholarly Activity of Radiation Oncologists in High-Income Developing Countries: Saudi Arabia as an Example.
Alghamdi MA, Alghamdi SM, Bahadur YA, Asiri MA, AlHussain HA, Alhebshi AS, Alothman MO, Al-Omair AS, Alghamdi AA, Qanat AS, Aqeeli MO, Alsuhaibani AA, Alshehri SM, Alotain IM, Mail NK, Alhashemi HH, Alassaf HA. Alghamdi MA, et al. Among authors: alghamdi aa, alghamdi sm. JCO Glob Oncol. 2021 Mar;7:378-383. doi: 10.1200/GO.20.00449. JCO Glob Oncol. 2021. PMID: 33720748 Free PMC article.
Oncology research in Saudi Arabia over a 10-year period. A synopsis.
Alghamdi MA, Alzahrani RA, Alhashemi HH, Obaid AA, Alghamdi AG, Aldokhi MA, Alghamdi AM, Alghamdi AA, Qanat AS, Jastaniah WA, Alghamdi SM. Alghamdi MA, et al. Among authors: alghamdi aa, alghamdi sm, alghamdi am, alghamdi ag. Saudi Med J. 2020 Mar;41(3):261-266. doi: 10.15537/smj.2020.3.24912. Saudi Med J. 2020. PMID: 32114598 Free PMC article.
Echocardiographic and Clinical Correlates of Ejection Fraction Among 2000 Patients with Heart Failure in Western Saudi Arabia.
Subki AH, Almalki MA, Butt NS, Alsallum MS, Almutairi HM, Khatib HA, Alzahrani AM, Babaker AS, Addas FA, Mashat AA, Jad AY, Zafar ZA, Nogali BW, Alghamdi AA, Alghamdi NA, Dakhakhni MF, Asaad OT, Alghalayini KW. Subki AH, et al. Int J Gen Med. 2020 Jun 9;13:281-288. doi: 10.2147/IJGM.S251924. eCollection 2020. Int J Gen Med. 2020. PMID: 32606892 Free PMC article.
1,553 results