Rezultati - Moin Mohamed

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  1. 1
    Paracentral acute middle maculopathy and acute macular neuroretinopathy following SARS-CoV-2 infection

    Paracentral acute middle maculopathy and acute macular neuroretinopathy following SARS-CoV-2 infection od Jonathan Virgo, Moin Mohamed

    Izdano 2020
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    Carta
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  2. 2
    Anti‐vascular endothelial growth factor therapies in ophthalmology: current use, controversies and the future

    Anti‐vascular endothelial growth factor therapies in ophthalmology: current use, controversies and the future od Tsong Qiang Kwong, Moin Mohamed

    Izdano 2014
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  3. 3
    Ethnic Variations in the Prevalence of Diabetic Retinopathy in People with Diabetes Attending Screening in the United Kingdom (DRIVE UK)

    Ethnic Variations in the Prevalence of Diabetic Retinopathy in People with Diabetes Attending Screening in the United Kingdom (DRIVE UK) od Sobha Sivaprasad, Bhaskar Gupta, Martin Gulliford, Hiten Dodhia, Moin Mohamed, Dinesh Nagi, Jennifer Evans

    Izdano 2012
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    Artigo
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  4. 4
    Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes

    Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes od Kamron Khan, Omar A. Mahroo, Rehna Khan, Moin Mohamed, Martin McKibbin, Alan C. Bird, Michel Michaelides, Adnan Tufail, Anthony T. Moore

    Izdano 2016
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  5. 5
    The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies

    The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies od Samantha R. De Silva, Gavin Arno, Anthony G. Robson, Ana Fakin, Nikolas Pontikos, Moin Mohamed, Alan C. Bird, Anthony T. Moore, Michel Michaelides, Andrew R. Webster, Omar A. Mahroo

    Izdano 2020
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  6. 6
    Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease

    Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease od C. Geoffrey Woods, James J. Cox, Kelly Springell, Daniel J. Hampshire, Moin Mohamed, Martin McKibbin, Rowena Stern, F. Lucy Raymond, Richard Sandford, Saghira Malik Sharif, Gulshan Karbani, Mustaq Ahmed, Jacquelyn Bond, David Clayton, Chris F. Inglehearn

    Izdano 2006
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  7. 7
    Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

    Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy od James A. Poulter, Manir Ali, David F. Gilmour, Aine Rice, Hiroyuki Kondo, Kenshi Hayashi, David A. Mackey, Lisa S. Kearns, Jonathan B. Ruddle, Jamie E. Craig, Eric A. Pierce, Louise Downey, Moin Mohamed, Alexander F. Markham, Chris F. Inglehearn, Carmel Toomes

    Izdano 2010
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    Errata/Corrigenda
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  8. 8
    Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

    Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects od Kamron Khan, Clare V. Logan, Martin McKibbin, Eamonn Sheridan, Nursel Elçioğlu, Özlem Yenice, David Parry, Narcís Fernández‐Fuentes, Zakia Abdelhamed, Ahmed Al-Maskari, James A. Poulter, Moin Mohamed, Ian Carr, Joanne Morgan, Hussain Jafri, Yasmin Raashid, Graham R. Taylor, Colin A. Johnson, Chris F. Inglehearn, Carmel Toomes, Manir Ali

    Izdano 2011
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  9. 9
    Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism

    Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism od James A. Poulter, Musallam Al‐Araimi, Iván Conte, Maria M. van Genderen, Eamonn Sheridan, Ian Carr, David Parry, Mike Shires, Sabrina Carrella, John Bradbury, Kamron Khan, Phillis Lakeman, Panagiotis I. Sergouniotis, Andrew R. Webster, Anthony T. Moore, Bishwanath Pal, Moin Mohamed, Venkataramana Anandula, Vedam L. Ramprasad, Rohit Shetty, Saktivel Murugan, Govindasamy Kumaramanickavel, Alex Tan, David A. Mackey, Alex W. Hewitt, Sandro Banfi, Manir Ali, Chris F. Inglehearn, Carmel Toomes

    Izdano 2013
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  10. 10
    Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

    Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma od Kamron Khan, Adam K Rudkin, David Parry, Kathryn P. Burdon, Martin McKibbin, Clare V. Logan, Zakia Abdelhamed, James Muecke, Narcís Fernández‐Fuentes, Kate J. Laurie, Mike Shires, Rhys A Fogarty, Ian Carr, James A. Poulter, Joanne Morgan, Moin Mohamed, Hussain Jafri, Yasmin Raashid, Ngy Meng, Horm Piseth, Carmel Toomes, Robert J. Casson, Graham R. Taylor, Michael Hammerton, Eamonn Sheridan, Colin A. Johnson, Chris F. Inglehearn, Jamie E. Craig, Manir Ali

    Izdano 2011
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  11. 11
    Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

    Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration od Robert K. Koenekoop, Hui Wang, Jacek Majewski, Xia Wang, Irma López, Huanan Ren, Yiyun Chen, Yumei Li, Gerald A. Fishman, Mohammed Genead, Jeremy Schwartzentruber, Naimesh Solanki, Elias I. Traboulsi, Jingliang Cheng, Clare V. Logan, Martin McKibbin, Bruce E. Hayward, David Parry, Colin A. Johnson, Mohammed Nageeb, James A. Poulter, Moin Mohamed, Hussain Jafri, Yasmin Abdul Rashid, Graham R. Taylor, Vafa Keser, Graeme Mardon, Huidan Xu, Chris F. Inglehearn, Qing Fu, Carmel Toomes, Rui Chen

    Izdano 2012
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