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Year Number of Results
2005 1
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2007 2
2008 1
2009 1
2010 2
2011 1
2012 1
2013 5
2014 3
2015 8
2016 6
2018 4
2019 3
2020 8
2021 8
2022 5
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2025 0

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49 results

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Page 1
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.
Patel N, Aldahmesh MA, Alkuraya H, Anazi S, Alsharif H, Khan AO, Sunker A, Al-Mohsen S, Abboud EB, Nowilaty SR, Alowain M, Al-Zaidan H, Al-Saud B, Alasmari A, Abdel-Salam GM, Abouelhoda M, Abdulwahab FM, Ibrahim N, Naim E, Al-Younes B, E AlMostafa A, AlIssa A, Hashem M, Buzovetsky O, Xiong Y, Monies D, Altassan N, Shaheen R, Al-Hazzaa SA, Alkuraya FS. Patel N, et al. Among authors: nowilaty sr. Genet Med. 2016 Jun;18(6):554-62. doi: 10.1038/gim.2015.127. Epub 2015 Sep 10. Genet Med. 2016. PMID: 26355662 Free article.
The morbid genome of ciliopathies: an update.
Shamseldin HE, Shaheen R, Ewida N, Bubshait DK, Alkuraya H, Almardawi E, Howaidi A, Sabr Y, Abdalla EM, Alfaifi AY, Alghamdi JM, Alsagheir A, Alfares A, Morsy H, Hussein MH, Al-Muhaizea MA, Shagrani M, Al Sabban E, Salih MA, Meriki N, Khan R, Almugbel M, Qari A, Tulba M, Mahnashi M, Alhazmi K, Alsalamah AK, Nowilaty SR, Alhashem A, Hashem M, Abdulwahab F, Ibrahim N, Alshidi T, AlObeid E, Alenazi MM, Alzaidan H, Rahbeeni Z, Al-Owain M, Sogaty S, Seidahmed MZ, Alkuraya FS. Shamseldin HE, et al. Among authors: nowilaty sr. Genet Med. 2020 Jun;22(6):1051-1060. doi: 10.1038/s41436-020-0761-1. Epub 2020 Feb 14. Genet Med. 2020. PMID: 32055034 Free article.
Evolution of macular hole in enhanced S-cone syndrome.
Magliyah MS, AlSulaiman SM, Schatz P, Nowilaty SR. Magliyah MS, et al. Among authors: nowilaty sr. Doc Ophthalmol. 2021 Apr;142(2):239-245. doi: 10.1007/s10633-020-09787-8. Epub 2020 Aug 19. Doc Ophthalmol. 2021. PMID: 32815098
The morbid genome of ciliopathies: an update.
Shamseldin HE, Shaheen R, Ewida N, Bubshait DK, Alkuraya H, Almardawi E, Howaidi A, Sabr Y, Abdalla EM, Alfaifi AY, Mohammed Alghamdi J, Alsagheir A, Alfares A, Morsy H, Hussein MH, Al-Muhaizea MA, Shagrani M, Al Sabban E, Salih MA, Meriki N, Khan R, Almugbel M, Qari A, Tulba M, Mahnashi M, Alhazmi K, Alsalamah AK, Nowilaty SR, Alhashem A, Hashem M, Abdulwahab F, Ibrahim N, Alshidi T, AlObeid E, Alenazi MM, Alzaidan H, Rahbeeni Z, Al-Owain M, Sogaty S, Zain Seidahmed M, Alkuraya FS. Shamseldin HE, et al. Among authors: nowilaty sr. Genet Med. 2022 Apr;24(4):966. doi: 10.1016/j.gim.2022.01.019. Genet Med. 2022. PMID: 35394428 Free article. No abstract available.
Reply: To PMID 25892126.
Alsulaiman SM, Almasaud J, Alkharashi AS, Alzahrani Y, Abboud EB, Nowilaty SR, Al-Amry M, Alrashaed S, Alrushood AA, Arevalo JF, Ghazi NG. Alsulaiman SM, et al. Among authors: nowilaty sr. Am J Ophthalmol. 2015 Nov;160(5):1085. doi: 10.1016/j.ajo.2015.08.003. Epub 2015 Aug 28. Am J Ophthalmol. 2015. PMID: 26318771 No abstract available.
Macular hole in juvenile X-linked retinoschisis.
Al-Swaina N, Nowilaty SR. Al-Swaina N, et al. Among authors: nowilaty sr. Saudi J Ophthalmol. 2013 Oct;27(4):283-6. doi: 10.1016/j.sjopt.2013.05.001. Epub 2013 May 30. Saudi J Ophthalmol. 2013. PMID: 24409088 Free PMC article.
Novel causative variants in patients with achromatopsia.
Abdelkader E, Brandau O, Bergmann C, AlSalamah N, Nowilaty S, Schatz P. Abdelkader E, et al. Among authors: nowilaty s. Ophthalmic Genet. 2018 Dec;39(6):678-683. doi: 10.1080/13816810.2018.1522653. Epub 2018 Oct 5. Ophthalmic Genet. 2018. PMID: 30289319
49 results