Resultados da pesquisa - Al‐Zuhaibi, Sana
- A mostrar 1 - 17 resultados de 17
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Am I going blind? Por Al-Farsi, Ammar Hamad, Al-Zuhaibi, Sana, Ganesh, Anuradha
Publicado em 2020Text -
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Visual Rehabilitation by Scleral Fixation of Posterior Chamber Intraocular Lenses in Amblyopic Aphakic Children Por Ganesh, Anuradha, Bialasiewicz, Alexander A., Al-Zuhaibi, Sana M., Sabt, Buthaina I., Ganguly, Shyam S.
Publicado em 2008Text -
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Normal electro-oculography in a young Omani male with genetically confirmed best disease complicated by choroidal neovascularization Por Al-Abri, Mohamed, Al-Hinai, Ahmed, Al Zuhaibi, Sana, Ganesh, Anuradha, Al Ghafri, Alyaqdhan, Al-Thihli, Khalid
Publicado em 2019Text -
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Molecular analysis of CYP1B1 in Omani patients with primary congenital glaucoma: a pilot study Por El-Gayar, Stefan, Ganesh, Anuradha, Chavarria-Soley, Gabriela, Al-Zuhaibi, Sana, Al-Mjeni, Rayhanah, Raeburn, Sandy, Bialasiewicz, Alexander A.
Publicado em 2009Text -
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Septo-optic dysplasia complex: Clinical and radiological manifestations in Omani children Por Al-Senawi, Rana, Al-Jabri, Bushra, Al-Zuhaibi, Sana, Al-Azri, Faisal, Al-Yarubi, Saif, Harikrishna, Beena, Al-Futaisi, Amna, Ganesh, Anuradha
Publicado em 2013Text -
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Mitochondrial RNA processing defect caused by a SUPV3L1 mutation in two siblings with a novel neurodegenerative syndrome Por van Esveld, Selma L., Rodenburg, Richard J., Al‐Murshedi, Fathiya, Al‐Ajmi, Eiman, Al‐Zuhaibi, Sana, Huynen, Martijn A., Spelbrink, Johannes N.
Publicado em 2022Text -
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Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects Por Janecke, Andreas R., Liu, Xiaoqin, Adam, Rüdiger, Punuru, Sumanth, Viestenz, Arne, Strauß, Valeria, Laass, Martin, Sanchez, Elizabeth, Adachi, Roberto, Schatz, Martha P., Saboo, Ujwala S., Mittal, Naveen, Rohrschneider, Klaus, Escher, Johanna, Ganesh, Anuradha, Al Zuhaibi, Sana, Al Murshedi, Fathiya, AlSaleem, Badr, Alfadhel, Majid, Al Sinani, Siham, Alkuraya, Fowzan S., Huber, Lukas A., Müller, Thomas, Heidelberger, Ruth, Janz, Roger
Publicado em 2021Text -
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A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis Por Ahmed, Mustafa Y, Al-Khayat, Aisha, Al-Murshedi, Fathiya, Al-Futaisi, Amna, Chioza, Barry A, Pedro Fernandez-Murray, J, Self, Jay E, Salter, Claire G, Harlalka, Gaurav V, Rawlins, Lettie E, Al-Zuhaibi, Sana, Al-Azri, Faisal, Al-Rashdi, Fatma, Cazenave-Gassiot, Amaury, Wenk, Markus R, Al-Salmi, Fatema, Patton, Michael A, Silver, David L, Baple, Emma L, McMaster, Christopher R, Crosby, Andrew H
Publicado em 2017Text