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Meningoencephalitis in a novel mutation in MNGIE (mitochondrial neurogastrointestinal encephalomyopathy) ending a familial diagnostic odyssey: A case series report.
J Cent Nerv Syst Dis. 2024 Mar 27;16:11795735241241423. doi: 10.1177/11795735241241423. eCollection 2024.
J Cent Nerv Syst Dis. 2024.
PMID: 38550250
Free PMC article.
The Impact of the COVID-19 Pandemic on Educational and Academic Activities of Healthcare Professionals in Bahrain.
Ali K, Isa HM, Ali MF, Ali FA, Alsahlawi Z, Alsaffar H.
Ali K, et al. Among authors: alsahlawi z.
Cureus. 2023 Dec 19;15(12):e50779. doi: 10.7759/cureus.50779. eCollection 2023 Dec.
Cureus. 2023.
PMID: 38239538
Free PMC article.
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Clinical spectrum and outcome of nine patients with a novel genetic variant of galactosialidosis in the Kingdom of Bahrain.
Alsahlawi Z, Aljishi E, Kheyami A, Alekri A, Alwedaie SMJ.
Alsahlawi Z, et al.
JIMD Rep. 2022 Sep 4;63(6):614-620. doi: 10.1002/jmd2.12330. eCollection 2022 Nov.
JIMD Rep. 2022.
PMID: 36341164
Free PMC article.
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HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H-TM protein.
Kraatari-Tiri M, Soikkonen L, Myllykoski M, Jamshidi Y, Karimiani EG, Komulainen-Ebrahim J, Kallankari H, Mignot C, Depienne C, Keren B, Nougues MC, Alsahlawi Z, Romito A, Martini J, Toosi MB, Carroll CJ, Tripolszki K, Bauer P, Uusimaa J, Bertoli-Avella AM, Koivunen P, Rahikkala E.
Kraatari-Tiri M, et al. Among authors: alsahlawi z.
Clin Genet. 2022 Nov;102(5):444-450. doi: 10.1111/cge.14203. Epub 2022 Aug 19.
Clin Genet. 2022.
PMID: 35908151
Free PMC article.
Review.
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A Case of Carnitine Palmitoyltransferase II Deficiency in Bahrain With a Novel Mutation.
Alsahlawi Z, Fadhul Z, Mahmood A, Mohamed A, Khalil M, Aljishi E.
Alsahlawi Z, et al.
Cureus. 2022 Jun 17;14(6):e26043. doi: 10.7759/cureus.26043. eCollection 2022 Jun.
Cureus. 2022.
PMID: 35859960
Free PMC article.
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A Case of DeSanto-Shinawi Syndrome in Bahrain with a Novel Mutation.
Alsahlawi Z, Jailani M, Alaradi H, AlAbbad A.
Alsahlawi Z, et al.
Case Rep Pediatr. 2020 Oct 16;2020:8820966. doi: 10.1155/2020/8820966. eCollection 2020.
Case Rep Pediatr. 2020.
PMID: 33123400
Free PMC article.
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Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature.
Khalifa O, Al-Sahlawi Z, Imtiaz F, Ramzan K, Allam R, Al-Mostafa A, Abdel-Fattah M, Abuharb G, Nester M, Verloes A, Al-Zaidan H.
Khalifa O, et al.
Eur J Med Genet. 2015 May;58(5):293-9. doi: 10.1016/j.ejmg.2014.12.008. Epub 2015 Feb 13.
Eur J Med Genet. 2015.
PMID: 25682901
Review.
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