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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 3
2008 1
2009 1
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2012 3
2013 2
2017 1
2024 0

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16 results

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Page 1
Ophthalmic manifestations of Sanjad-Sakati syndrome.
Al Dhoyan N, Al Hemidan AI, Ozand PT. Al Dhoyan N, et al. Among authors: al hemidan ai. Ophthalmic Genet. 2006 Sep;27(3):83-7. doi: 10.1080/13816810600862568. Ophthalmic Genet. 2006. PMID: 17050283
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. Among authors: al hemidan a. 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. Among authors: al hemidan a. 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
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. Among authors: al hemidan a. J AAPOS. 2009 Aug;13(4):396-9. doi: 10.1016/j.jaapos.2009.05.011. J AAPOS. 2009. PMID: 19683193
A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene.
Khalifa O, Imtiaz F, Allam R, Al-Hassnan Z, Al-Hemidan A, Al-Mane K, Abuharb G, Balobaid A, Sakati N, Hyland J, Al-Owain M. Khalifa O, et al. Among authors: al hemidan a. J Med Genet. 2012 Apr;49(4):246-8. doi: 10.1136/jmedgenet-2012-100783. J Med Genet. 2012. PMID: 22499343 No abstract available.
Novel splice (IVS18+1G>C) mutation in COL2A1 causing Kniest dysplasia.
Al-Hashmi N, Imtiaz F, Ramzan K, Faden M, Shuaib T, Al-Otaibi L, Al-Hemidan A, Al-Owain M. Al-Hashmi N, et al. Among authors: al hemidan a. Clin Dysmorphol. 2013 Jan;22(1):39-41. doi: 10.1097/MCD.0b013e32835c297e. Clin Dysmorphol. 2013. PMID: 23188137 No abstract available.
Optic disc elevation in Down syndrome.
Al-Hemidan AI, Al-Hazzaa SA, Chavis P, Al-Hussein H. Al-Hemidan AI, et al. Ophthalmic Genet. 1999 Mar;20(1):45-51. doi: 10.1076/opge.20.1.45.2297. Ophthalmic Genet. 1999. PMID: 10415465
16 results