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2020 1
2021 1
2022 3
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Page 1
Childhood Asthma Awareness in Saudi Arabia: Five-Year Follow-Up Study.
Alharbi SA, Kobeisy SAN, AlKhater SA, Alharbi AS, Alqwaiee MM, Alotaibi FN, Alawam KA, Alahmadi TS, Al-Somali FM, Almaghamsi TM, Yousef AA. Alharbi SA, et al. Among authors: almaghamsi tm. J Asthma Allergy. 2020 Oct 2;13:399-407. doi: 10.2147/JAA.S272850. eCollection 2020. J Asthma Allergy. 2020. PMID: 33061466 Free PMC article.
Severe asthma in children: An official statement from Saudi Pediatric Pulmonology Association.
Alharbi AS, Yousef AA, Alharbi SA, Almaghamsi TM, Al Qwaiee MM, Al-Somali FM, Alahmadi TS, Alhaider SA, Alotaibi WH, Albalawi MA, Alotaibi FN, Alenizi AS, Alsaadi MM, Said YS. Alharbi AS, et al. Among authors: almaghamsi tm. Saudi Med J. 2022 Apr;43(4):329-340. doi: 10.15537/smj.2022.4.43.20210756. Saudi Med J. 2022. PMID: 35414610 Free article.
Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients.
Mabrouk I, Al-Harthi N, Mani R, Montantin G, Tissier S, Lagha R, Ben Abdallah F, Hassan MM, Alhomrani M, Gaber A, Alsanie WF, Ouali H, Jambi FA, Almaghamsi TM, Alqarni NA, Alfarsi NA, Kashgari K, Al-Zahrani HJ, Al-Shamary ZA, Al-Harbi A, Amselem S, Escudier E, Legendre M. Mabrouk I, et al. Among authors: almaghamsi tm. J Hum Genet. 2022 Jan 20. doi: 10.1038/s10038-021-01006-9. Online ahead of print. J Hum Genet. 2022. PMID: 35046476
A single-centre study of genetic mutations, audiology, echocardiogram and pulmonary function in Saudi children with osteogenesis imperfecta.
Ahmad N, Aleysae NA, Sobaihi M, Naitah N, Rasol MA, Al-Kouatli AA, Almaghamsi TM, Heaphy ELG, Attiyah MH, Hrays M, Alghamdi B, Alzahrani AS. Ahmad N, et al. Among authors: almaghamsi tm. J Pediatr Endocrinol Metab. 2021 Dec 23;35(3):355-362. doi: 10.1515/jpem-2021-0587. Print 2022 Mar 28. J Pediatr Endocrinol Metab. 2021. PMID: 34954934