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Year | Number of Results |
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2013 | 1 |
2018 | 1 |
2019 | 1 |
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2022 | 4 |
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Page 1
Management of Dactylitis in Patients With Psoriatic Arthritis: An Updated Literature Review Informing the 2021 GRAPPA Treatment Recommendations.
J Rheumatol. 2023 Feb;50(2):265-278. doi: 10.3899/jrheum.220311. Epub 2022 Nov 1.
J Rheumatol. 2023.
PMID: 36319013
Free article.
Review.
Consensus statements for evaluation and nonpharmacological Management of Psoriatic Arthritis in UAE.
Alnaqbi KA, Hannawi S, Namas R, Alshehhi W, Badsha H, Al-Saleh J.
Alnaqbi KA, et al. Among authors: alshehhi w.
Int J Rheum Dis. 2022 Jul;25(7):725-732. doi: 10.1111/1756-185X.14357. Epub 2022 Jun 9.
Int J Rheum Dis. 2022.
PMID: 35678066
Free PMC article.
Review.
Item in Clipboard
Treatment with High-Dose Prednisolone in Vigabatrin-Refractory Infantile Spasms.
Al-Shehhi W, Chau V, Boyd J, Snead C, Sharma R, Donner E, Go C, Jain P.
Al-Shehhi W, et al.
Can J Neurol Sci. 2022 Jul;49(4):532-539. doi: 10.1017/cjn.2021.156. Epub 2021 Jul 2.
Can J Neurol Sci. 2022.
PMID: 34212837
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Consensus statements for pharmacological management, monitoring of therapies, and comorbidity management of psoriatic arthritis in the United Arab Emirates.
Alnaqbi KA, Hannawi S, Namas R, Alshehhi W, Badsha H, Al-Saleh J.
Alnaqbi KA, et al. Among authors: alshehhi w.
Int J Rheum Dis. 2022 Oct;25(10):1107-1122. doi: 10.1111/1756-185X.14406. Epub 2022 Aug 2.
Int J Rheum Dis. 2022.
PMID: 35916205
Free PMC article.
Review.
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Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants.
Al-Murshedi F, Mirza H, Al-Saegh A, Al-Nabhani M, Al-Shabibi S, Baawain S, Al-Futaisi A, Al-Shehhi W, Al-Maawali A.
Al-Murshedi F, et al.
Clin Genet. 2020 Nov;98(5):520-521. doi: 10.1111/cge.13838. Epub 2020 Sep 9.
Clin Genet. 2020.
PMID: 32901920
No abstract available.
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Mucolipidosis II: first report from Saudi Arabia.
Alfadhel M, AlShehhi W, Alshaalan H, Al Balwi M, Eyaid W.
Alfadhel M, et al. Among authors: alshehhi w.
Ann Saudi Med. 2013 Jul-Aug;33(4):382-6. doi: 10.5144/0256-4947.2013.382.
Ann Saudi Med. 2013.
PMID: 24060719
Free PMC article.
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A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients.
Musa S, Eyaid W, Kamer K, Ali R, Al-Mureikhi M, Shahbeck N, Al Mesaifri F, Makhseed N, Mohamed Z, AlShehhi WA, Mootha VK, Juusola J, Ben-Omran T.
Musa S, et al. Among authors: alshehhi wa.
JIMD Rep. 2019;43:79-83. doi: 10.1007/8904_2018_107. Epub 2018 May 3.
JIMD Rep. 2019.
PMID: 29721912
Free PMC article.
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