Cataract Surgery Audit at a Private Hospital in Saudi Arabia

Por Alasbali, Tariq, Lofty, Nancy Maher, Al-Gehaban, Saeed, Alkuraya, Hisham S., Alsharif, Abdulrahman M., Khandekar, Rajiv
Publicado no Middle East Afr J Ophthalmol (2015)

Lack of Correlation Between Diabetic Macular Edema and Thickness of the Peripapillary Retinal Nerve Fibre Layer

Por Alkuraya, Hisham S., Al-Gehedan, Saeed M., Alsharif, Abdulrahman M., Alasbali, Tariq, Lotfy, Nancy M., Khandekar, Rajiv
Publicado no Middle East Afr J Ophthalmol (2016)

Argon Laser Photoablation for Treating Benign Pigmented Conjunctival Nevi

Por Alsharif, Abdulrahman M., Al-Gehedan, Saeed M., Alasbali, Tariq, Alkuraya, Hisham S., Lotfy, Nancy M., Khandekar, Rajiv
Publicado no Middle East Afr J Ophthalmol (2016)

Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia

Por Aldahmesh, Mohammed A., Mohamed, Jawahir Y., Alkuraya, Hisham S., Verma, Ishwar C., Puri, Ratna D., Alaiya, Ayodele A., Rizzo, William B., Alkuraya, Fowzan S.
Publicado em 2011

A Calcineurin-Independent Mechanism of Angiogenesis Inhibition by a Nonimmunosuppressive Cyclosporin A Analog

Por Nacev, Benjamin A., Low, Woon-Kai, Huang, Zhennian, Su, Tina T., Su, Zhuang, Alkuraya, Hisham, Kasuga, Dan, Sun, Woong, Träger, Mario, Braun, Manfred, Fischer, Gunter, Zhang, Kang, Liu, Jun O.
Publicado em 2011

Ocular manifestations of branchio-oculo-facial syndrome: Report of a novel mutation and review of the literature

Por Al-Dosari, M.S., Almazyad, M., Al-Ebdi, L., Mohamed, J.Y., Al-Dahmash, Saad, Al-Dhibi, Hassan, Al-Kahtani, Eman, Al-Turkmani, Shahira, Alkuraya, Hisham, Hall, B.D., Alkuraya, F.S.
Publicado em 2010

Mutation of IGFBP7 Causes Upregulation of BRAF/MEK/ERK Pathway and Familial Retinal Arterial Macroaneurysms

Por Abu-Safieh, Leen, Abboud, Emad B., Alkuraya, Hisham, Shamseldin, Hanan, Al-Enzi, Shamsa, Al-Abdi, Lama, Hashem, Mais, Colak, Dilek, Jarallah, Abdullah, Ahmad, Hala, Bobis, Steve, Nemer, Georges, Bitar, Fadi, Alkuraya, Fowzan S.
Publicado em 2011

IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet–Biedl syndrome

Por Aldahmesh, Mohammed A., Li, Yuanyuan, Alhashem, Amal, Anazi, Shams, Alkuraya, Hisham, Hashem, Mais, Awaji, Ali A., Sogaty, Sameera, Alkharashi, Abdullah, Alzahrani, Saeed, Al Hazzaa, Selwa A., Xiong, Yong, Kong, Shanshan, Sun, Zhaoxia, Alkuraya, Fowzan S.
Publicado em 2014

Molecular characterization of retinitis pigmentosa in Saudi Arabia

Por Aldahmesh, Mohammed A., Abu Safieh, Leen, Alkuraya, Hisham, Al-Rajhi, Ali, Shamseldin, Hanan, Hashem, Mais, Alzahrani, Fatemah, Khan, Arif O., Alqahtani, Faisal, Rahbeeni, Zuhair, Alowain, Mohammed, Khalak, Hanif, Al-Hazzaa, Salwa, Meyer, Brian F., Alkuraya, Fowzan S.
Publicado em 2009

Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

Por Aldahmesh, Mohammed A., Khan, Arif O., Alkuraya, Hisham, Adly, Nouran, Anazi, Shamsa, Al-Saleh, Ahmed A., Mohamed, Jawahir Y., Hijazi, Hadia, Prabakaran, Sarita, Tacke, Marlene, Al-Khrashi, Abdullah, Hashem, Mais, Reinheckel, Thomas, Assiri, Abdullah, Alkuraya, Fowzan S.
Publicado em 2013

Essential Role of ELOVL4 Protein in Very Long Chain Fatty Acid Synthesis and Retinal Function

Por Harkewicz, Richard, Du, Hongjun, Tong, Zongzhong, Alkuraya, Hisham, Bedell, Matthew, Sun, Woong, Wang, Xiaolei, Hsu, Yuan-Hao, Esteve-Rudd, Julian, Hughes, Guy, Su, Zhiguang, Zhang, Ming, Lopes, Vanda S., Molday, Robert S., Williams, David S., Dennis, Edward A., Zhang, Kang
Publicado em 2012

In search of triallelism in Bardet–Biedl syndrome

Por Abu-Safieh, Leen, Al-Anazi, Shamsa, Al-Abdi, Lama, Hashem, Mais, Alkuraya, Hisham, Alamr, Mushari, Sirelkhatim, Mugtaba O, Al-Hassnan, Zuhair, Alkuraya, Basim, Mohamed, Jawahir Y, Al-Salem, Ahmad, Alrashed, May, Faqeih, Eissa, Softah, Ameen, Al-Hashem, Amal, Wali, Sami, Rahbeeni, Zuhair, Alsayed, Moeen, Khan, Arif O, Al-Gazali, Lihadh, Taschner, Peter EM, Al-Hazzaa, Selwa, Alkuraya, Fowzan S
Publicado em 2012

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

Por Abu-Safieh, Leen, Alrashed, May, Anazi, Shamsa, Alkuraya, Hisham, Khan, Arif O., Al-Owain, Mohammed, Al-Zahrani, Jawahir, Al-Abdi, Lama, Hashem, Mais, Al-Tarimi, Salwa, Sebai, Mohammed-Adeeb, Shamia, Ahmed, Ray-zack, Mohamed D., Nassan, Malik, Al-Hassnan, Zuhair N., Rahbeeni, Zuhair, Waheeb, Saad, Alkharashi, Abdullah, Abboud, Emad, Al-Hazzaa, Selwa A.F., Alkuraya, Fowzan S.
Publicado em 2013

Characterizing the morbid genome of ciliopathies

Por Shaheen, Ranad, Szymanska, Katarzyna, Basu, Basudha, Patel, Nisha, Ewida, Nour, Faqeih, Eissa, Al Hashem, Amal, Derar, Nada, Alsharif, Hadeel, Aldahmesh, Mohammed A., Alazami, Anas M., Hashem, Mais, Ibrahim, Niema, Abdulwahab, Firdous M., Sonbul, Rawda, Alkuraya, Hisham, Alnemer, Maha, Al Tala, Saeed, Al-Husain, Muneera, Morsy, Heba, Seidahmed, Mohammed Zain, Meriki, Neama, Al-Owain, Mohammed, AlShahwan, Saad, Tabarki, Brahim, Salih, Mustafa A., Faquih, Tariq, El-Kalioby, Mohamed, Ueffing, Marius, Boldt, Karsten, Logan, Clare V., Parry, David A., Al Tassan, Nada, Monies, Dorota, Megarbane, Andre, Abouelhoda, Mohamed, Halees, Anason, Johnson, Colin A., Alkuraya, Fowzan S.
Publicado no Genome Biol (2016)