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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1995 1
1997 1
1999 1
2003 1
2006 1
2008 1
2009 1
2011 1
2012 3
2013 2
2017 1
2018 1
2019 1
2023 1
2024 0

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17 results

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Page 1
Efficacy of topical cysteamine in nephropathic cystinosis.
Al-Hemidan A, Shoughy SS, Kozak I, Tabbara KF. Al-Hemidan A, et al. Br J Ophthalmol. 2017 Sep;101(9):1234-1237. doi: 10.1136/bjophthalmol-2016-309278. Epub 2017 Jan 5. Br J Ophthalmol. 2017. PMID: 28057644
Mutation in MPDZ causes severe congenital hydrocephalus.
Al-Dosari MS, Al-Owain M, Tulbah M, Kurdi W, Adly N, Al-Hemidan A, Masoodi TA, Albash B, Alkuraya FS. Al-Dosari MS, et al. J Med Genet. 2013 Jan;50(1):54-8. doi: 10.1136/jmedgenet-2012-101294. J Med Genet. 2013. PMID: 23240096
Novel mutation in GLRB in a large family with hereditary hyperekplexia.
Al-Owain M, Colak D, Al-Bakheet A, Al-Hashmi N, Shuaib T, Al-Hemidan A, Aldhalaan H, Rahbeeni Z, Al-Sayed M, Al-Younes B, Ozand PT, Kaya N. Al-Owain M, et al. Clin Genet. 2012 May;81(5):479-84. doi: 10.1111/j.1399-0004.2011.01661.x. Epub 2011 Apr 7. Clin Genet. 2012. PMID: 21391991
Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies.
Patel N, Alkuraya H, Alzahrani SS, Nowailaty SR, Seidahmed MZ, Alhemidan A, Ben-Omran T, Ghazi NG, Al-Aqeel A, Al-Owain M, Alzaidan HI, Faqeih E, Kurdi W, Rahbeeni Z, Ibrahim N, Abdulwahab F, Hashem M, Shaheen R, Abouelhoda M, Monies D, Khan AO, Aldahmesh MA, Alkuraya FS. Patel N, et al. Among authors: alhemidan a. Clin Genet. 2018 Dec;94(6):554-563. doi: 10.1111/cge.13426. Epub 2018 Sep 3. Clin Genet. 2018. PMID: 30054919
Ocular manifestations in chronic granulomatous disease in Saudi Arabia.
Al-Muhsen S, Al-Hemidan A, Al-Shehri A, Al-Harbi A, Al-Ghonaium A, Al-Saud B, Al-Mousa H, Al-Dhekri H, Arnaout R, Al-Mohsen I, Alsmadi O. Al-Muhsen S, et al. J AAPOS. 2009 Aug;13(4):396-9. doi: 10.1016/j.jaapos.2009.05.011. J AAPOS. 2009. PMID: 19683193
17 results