Showing 1 - 17 results of 17 for search 'Patrick Yu-Wai-Man', query time: 0.20s Refine Results
  1. 1
    OPA1 Modulates Mitochondrial Ca2+ Uptake Through ER-Mitochondria Coupling
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  2. 2
    Retinal Ganglion Cells—Diversity of Cell Types and Clinical Relevance
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  3. 3
    Optical Coherence Tomography Angiography Reveals Distinct Retinal Structural and Microvascular Abnormalities in Cerebrovascular Disease
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  4. 4
    Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals
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  5. 5
    Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
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  6. 6
    From Transcriptomics to Treatment in Inherited Optic Neuropathies
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  7. 7
    Angiopoietins in Diabetic Retinopathy: Current Understanding and Therapeutic Potential
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  8. 8
    Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy.
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  9. 9
    Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison
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  10. 10
    Neuroimaging in Leber Hereditary Optic Neuropathy: State-of-the-art and future prospects
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  11. 11
    High‐throughput screening identifies suppressors of mitochondrial fragmentation in OPA1 fibroblasts
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  12. 12
    Monoamine oxidase-A promotes protective autophagy in human SH-SY5Y neuroblastoma cells through Bcl-2 phosphorylation
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  13. 13
    CRISPR-Cas9 correction of OPA1 c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCs
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  14. 14
    Biodistribution of intravitreal lenadogene nolparvovec gene therapy in nonhuman primates
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  15. 15
    Absence of lenadogene nolparvovec DNA in a brain tumor biopsy from a patient in the REVERSE clinical study, a case report
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  16. 16
    Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia.
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  17. 17
    Study design and baseline characteristics for the reflect gene therapy trial ofm.11778g>A/ND4-LHON
    by Nancy J Newman, Valérie Biousse, José-Alain Sahel, Patrick Yu-Wai-Man, Sean Donahue, Gema Rebolleda, Prem S Subramanian, Bart P Leroy, Alfredo A Sadun, Robert C Sergott, Catherine Vignal-Clermont, Bart K Chwalisz, Mark Moster, An-Guor Wang, Valerio Carelli, Rudrani Banik, Fabienne Bazin, Eric Cox, Michel Roux, Magali Taiel, Amore Giulia, Anand Shweta, Banik Rudrani, Barboni Piero, Biousse Valérie, Boston Hayley, Burale Asma, Carbonelli Michele, Carelli Valerio, Chen Celia, Cheng Hui-Chen, Cho Steve, K Chwalisz Bart, Contin Manuela, D’Agati Pietro, A DeBusk Adam, De Zaeytijd Julie, Dobbs Jannah, P Donahue Sean, DuBois Lindreth, Esposti Simona, Fernandes Filho Alcides, Fortin Elizabeth, Gangaputra Sapna, Gibbs Deborah, Girmens Jean François, Hage Rabih, A Haller Julia, Heilweil Gad, Hubbard III GeorgeBaker, Hwang Jeong-Min, Jaumendreu Urquijo Laia, Jurkute Neringa, Karanjia Rustum, Khemliche Wahiba, La Morgia Chiara, P Leroy Bart, Massini Maria, Mathias Marc, A Memon Muhammad, Mohamed Susan, L Moster Mark, J Muñoz NegreteFrancisco, J Newman Nancy, O’Keefe Ghazala, Patel Shriji, Pecen Paula, H Peragallo Jason, Plaine Lise, Preston Mary, Rebolleda Fernández Gema, Romagnoli Martina, A Sadun Alfredo, A Sahel José, SantaMaria Melissa, C Sergott Robert, S Subramanian Prem, Sun Chuanbin, Tai Katy, Tollis Heather, Tsui Irena, R Tucker William, Vignal-Clermont Catherine, Wang An-Guor, Wilkins Saige, Yu-Wai-Man Patrick
    Published 2022-10-01
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