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Page 1
Genetic mutations associated with neonatal diabetes mellitus in Omani patients.
Al Senani A, Hamza N, Al Azkawi H, Al Kharusi M, Al Sukaiti N, Al Badi M, Al Yahyai M, Johnson M, De Franco E, Flanagan S, Hattersley A, Ellard S, Mula-Abed WA. Al Senani A, et al. Among authors: al sukaiti n, al badi m, al yahyai m, al kharusi m, al azkawi h. J Pediatr Endocrinol Metab. 2018 Jan 26;31(2):195-204. doi: 10.1515/jpem-2017-0284. J Pediatr Endocrinol Metab. 2018. PMID: 29329106 Free PMC article.
Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder.
Mohammed M, Al-Hashmi N, Al-Rashdi S, Al-Sukaiti N, Al-Adawi K, Al-Riyami M, Al-Maawali A. Mohammed M, et al. Among authors: al sukaiti n, al adawi k, al maawali a, al riyami m, al rashdi s, al hashmi n. Eur J Med Genet. 2019 Nov;62(11):103583. doi: 10.1016/j.ejmg.2018.11.017. Epub 2018 Nov 22. Eur J Med Genet. 2019. PMID: 30472485
Chronic Q Fever Endocarditis in an Omani Child: The First Pediatric Case Report from Oman.
Al-Araimi HA, Al-Alawi K, Al-Jardani AK, Paul G, Al-Sukaiti N, Al-Farqani A, Al-Maani AS. Al-Araimi HA, et al. Among authors: al alawi k, al sukaiti n, al jardani ak, al farqani a, al maani as. Oman Med J. 2020 Sep 30;35(5):e180. doi: 10.5001/omj.2020.121. eCollection 2020 Sep. Oman Med J. 2020. PMID: 33083038 Free PMC article.
Hermansky-Pudlak Syndrome: Spectrum in Oman.
Nazir HF, Al Sukaiti N, Khater D, Elbeshlawy I, Hassanein N. Nazir HF, et al. Among authors: al sukaiti n. J Pediatr Hematol Oncol. 2023 Apr 1;45(3):e389-e394. doi: 10.1097/MPH.0000000000002552. Epub 2022 Sep 21. J Pediatr Hematol Oncol. 2023. PMID: 36162005
Bacillus Calmette-Guérin vaccine-related complications in children in Oman.
Al Waili B, Al Mufarajii N, Al Hashmi S, Al Ajmi A, Al Sukaiti N. Al Waili B, et al. Among authors: al sukaiti n, al hashmi s, al ajmi a, al mufarajii n. Ann Saudi Med. 2021 Jan-Feb;41(1):24-30. doi: 10.5144/0256-4947.2021.24. Epub 2021 Feb 4. Ann Saudi Med. 2021. PMID: 33550906 Free PMC article.
Biallelic ZNFX1 variants are associated with a spectrum of immuno-hematological abnormalities.
Alawbathani S, Westenberger A, Ordonez-Herrera N, Al-Hilali M, Al Hebby H, Alabbas F, Alhashem AM, Elyamany G, Megarbane A, Kose M, Alhashmi N, Al Sukaiti N, Al-Raqad M, Al-Tawalbeh S, Abu Adas Blanco O, Alkhattabi F, Sng D, Al-Ali R, Khan S, Tawamie H, Tripolszki K, Karageorgou V, Trunzo R, Al Mutairi F, Reversade B, Bauer P, Bertoli-Avella AM. Alawbathani S, et al. Among authors: al sukaiti n, al hebby h, al tawalbeh s, al raqad m, al mutairi f, al hilali m, al ali r. Clin Genet. 2022 Feb;101(2):247-254. doi: 10.1111/cge.14081. Epub 2021 Nov 6. Clin Genet. 2022. PMID: 34708404
The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity.
Baris S, Abolhassani H, Massaad MJ, Al-Nesf M, Chavoshzadeh Z, Keles S, Reisli I, Tahiat A, Shendi HM, Elaziz DA, Belaid B, Al Dhaheri F, Haskologlu S, Dogu F, Ben-Mustapha I, Sobh A, Galal N, Meshaal S, Elhawary R, El-Marsafy A, Alroqi FJ, Al-Saud B, Al-Ahmad M, Al Farsi T, Al Sukaiti N, Al-Tamemi S, Mehawej C, Dbaibo G, ElGhazali G, Kilic SS, Genel F, Kiykim A, Musabak U, Artac H, Guner SN, Boukari R, Djidjik R, Kechout N, Cagdas D, El-Sayed ZA, Karakoc-Aydiner E, Alzyoud R, Barbouche MR, Adeli M, Wakim RH, Reda SM, Ikinciogullari A, Ozen A, Bousfiha A, Al-Mousa H, Rezaei N, Al-Herz W, Geha RS. Baris S, et al. Among authors: al sukaiti n. J Allergy Clin Immunol Pract. 2023 Jan;11(1):158-180.e11. doi: 10.1016/j.jaip.2022.10.003. Epub 2022 Oct 17. J Allergy Clin Immunol Pract. 2023. PMID: 36265766 Review.
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