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Year Number of Results
2002 1
2003 1
2005 1
2010 2
2011 1
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2013 2
2014 1
2015 2
2016 1
2017 3
2018 3
2019 3
2020 3
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33 results

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Page 1
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: al ajmi a. Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder.
Aughey GN, Cali E, Maroofian R, Zaki MS, Pagnamenta AT, Ali Z, Abdulllah U, Rahman F, Menzies L, Shafique A, Suri M, Roze E, Aguennouz M, Ghizlane Z, Saadi SM, Fatima A, Cheema HA, Anjum MN, Morel G, Robin S, McFarland R, Altunoglu U, Kraus V, Shoukier M, Murphy D, Flemming K, Yttervik H, Rhouda H, Lesca G, Chatron N, Rossi M, Murtaza BN, Ur Rehman M, Lord J, Giacopuzzi E, Hayat A, Siraj M; SYNAPS Study Group; Badv RS, Seo GH, Beetz C, Kayserili H, Krioulie Y, Chung WK, Naz S, Maqbool S, Chandler K, Kershaw C, Wright T, Banka S, Gleeson JG, Taylor JC, Efthymiou S, Baig SM, Severino M, Jepson JEC, Houlden H. Aughey GN, et al. Brain. 2024 Dec 18:awae363. doi: 10.1093/brain/awae363. Online ahead of print. Brain. 2024. PMID: 39692517
Exclusive Breastfeeding: Barrier analysis amongst Omani mothers.
Al-Ghannami S, Al-Mamari S, Chekaraou D, Abla C, Al-Ghmmari I, Al-Ajmi A, Al-Shammkhi S, Al-Balushi RM, Al-Mamari F, Mabry RM. Al-Ghannami S, et al. Among authors: al ajmi a. Sultan Qaboos Univ Med J. 2023 May;23(2):158-167. doi: 10.18295/squmj.5.2022.038. Epub 2023 May 31. Sultan Qaboos Univ Med J. 2023. PMID: 37377837 Free PMC article.
The role of BRCA1/2 in hereditary and familial breast and ovarian cancers.
Hawsawi YM, Al-Numair NS, Sobahy TM, Al-Ajmi AM, Al-Harbi RM, Baghdadi MA, Oyouni AA, Alamer OM. Hawsawi YM, et al. Among authors: al ajmi am. Mol Genet Genomic Med. 2019 Sep;7(9):e879. doi: 10.1002/mgg3.879. Epub 2019 Jul 17. Mol Genet Genomic Med. 2019. PMID: 31317679 Free PMC article. Review.
Prevalence of joint hypermobility in Kuwait.
Al-Jarallah K, Shehab D, Al-Jaser MT, Al-Azemi KM, Wais FF, Al-Saleh AM, Al-Ajmi AS, Al-Omairah HA, Abraham M, Sharma PN. Al-Jarallah K, et al. Among authors: al ajmi as. Int J Rheum Dis. 2017 Aug;20(8):935-940. doi: 10.1111/1756-185X.12556. Epub 2014 Dec 20. Int J Rheum Dis. 2017. PMID: 25529052
Reversible Ethyl Chloride Neurotoxicity: A Case Report.
Al-Ajmi AM, Morad MA, Cooper PE, Hassino LH, Siddeiq MA. Al-Ajmi AM, et al. Can J Neurol Sci. 2018 Jan;45(1):119-120. doi: 10.1017/cjn.2017.262. Epub 2017 Nov 21. Can J Neurol Sci. 2018. PMID: 29157319 No abstract available.
33 results