Facing the epidemic of myopia: Exploring the possibilities

por Mameesh, Maha, Ganesh, Anuradha, Al Zuhaibi, Sana
Publicado 2017

A 22-year-old lady with squint

por Harikrishna, Beena, Cooymans, Pascale, Ganesh, Anuradha, -Al-Zuhaibi, Sana
Publicado 2010

Am I going blind?

por Al-Farsi, Ammar Hamad, Al-Zuhaibi, Sana, Ganesh, Anuradha
Publicado 2020

Congenital fibrosis of the extraocular muscles

por Cooymans, Pascale, Al-Zuhaibi, Sana, Al-Senawi, Rana, Ganesh, Anuradha
Publicado 2010

Accommodative esotropia: An outcome analysis from a tertiary center in Oman

por Sreelatha, OK, Al-Marshoudi, Hajar Ali, Mameesh, Maha, Al Zuhaibi, Sana, Ganesh, Anuradha
Publicado 2022

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 2008

Chronic myelogenous leukemia in a child following treatment for bilateral retinoblastoma

por Al-Mahrouqi, Haitham Hilal, Ganesh, Anuradha, Al-Rawas, Abdulhakim, Khetan, Vikas, Al-Zuhaibi, Sana
Publicado 2021

Compliance of amblyopic patients with occlusion therapy: A pilot study

por Al-Zuhaibi, Sana, Al-Harthi, Iman, Cooymans, Pascale, Al-Busaidi, Aisha, Al-Farsi, Yahya, Ganesh, Anuradha
Publicado 2009

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 2019

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 2009

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 2013

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 2022

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 2021

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 2017