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Serum levels of BAFF, but not APRIL, are increased after rituximab treatment in patients with primary Sjogren's syndrome: data from a placebo-controlled clinical trial.
Pollard RP, Abdulahad WH, Vissink A, Hamza N, Burgerhof JG, Meijer JM, Visser A, Huitema MG, Spijkervet FK, Kallenberg CG, Bootsma H, Kroese FG. Pollard RP, et al. Among authors: hamza n. Ann Rheum Dis. 2013 Jan;72(1):146-8. doi: 10.1136/annrheumdis-2012-202071. Epub 2012 Jul 31. Ann Rheum Dis. 2013. PMID: 22851468 Clinical Trial. No abstract available.
A first case report of hypohidrotic ectodermal dysplasia from Oman.
Al-Araimi M, Hamza N, Al Hosni A, Al Mazrooey H. Al-Araimi M, et al. Among authors: hamza n. Clin Case Rep. 2020 Feb 29;8(4):716-718. doi: 10.1002/ccr3.2723. eCollection 2020 Apr. Clin Case Rep. 2020. PMID: 32274043 Free PMC article.
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: hamza n. 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.
Rare NF1 microdeletion syndrome in an Omani patient.
Al-Araimi M, Hamza N, Al Yahmadi A, Al Mazrooey H, Elsheikh A, Al Amri A, Al Harrasi S, Hausdorf L, Mula-Abed WA. Al-Araimi M, et al. Among authors: hamza n. Clin Case Rep. 2018 Oct 26;6(12):2424-2426. doi: 10.1002/ccr3.1881. eCollection 2018 Dec. Clin Case Rep. 2018. PMID: 30564341 Free PMC article.
Repository of mutations from Oman: The entry point to a national mutation database.
Rajab A, Hamza N, Al Harasi S, Al Lawati F, Gibbons U, Al Alawi I, Kobus K, Hassan S, Mahir G, Al Salmi Q, Mons B, Robinson P. Rajab A, et al. Among authors: hamza n. F1000Res. 2015 Sep 23;4:891. doi: 10.12688/f1000research.6938.1. eCollection 2015. F1000Res. 2015. PMID: 26594346 Free PMC article.
91 results