Ngā hua rapu - Yu‐Wai‐Man, Patrick

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  1. 1
    Traumatic optic neuropathy—Clinical features and management issues

    Traumatic optic neuropathy—Clinical features and management issues mā Yu-Wai-Man, Patrick

    I whakaputaina 2015
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  2. 2
    Genetic manipulation for inherited neurodegenerative diseases: myth or reality?

    Genetic manipulation for inherited neurodegenerative diseases: myth or reality? mā Yu-Wai-Man, Patrick

    I whakaputaina 2016
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  3. 3
    Delayed Optochiasmal Arachnoiditis following Intervention for a Subarachnoid Haemorrhage

    Delayed Optochiasmal Arachnoiditis following Intervention for a Subarachnoid Haemorrhage mā Yu-Wai-Man, Patrick, Neoh, Christopher

    I whakaputaina 2013
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  4. 4
    Leber hereditary optic neuropathy: bridging the translational gap

    Leber hereditary optic neuropathy: bridging the translational gap mā Jurkute, Neringa, Yu-Wai-Man, Patrick

    I whakaputaina 2017
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  5. 5
    From Bench to Bedside—Delivering Gene Therapy for Leber Hereditary Optic Neuropathy

    From Bench to Bedside—Delivering Gene Therapy for Leber Hereditary Optic Neuropathy mā Chen, Benson S., Yu-Wai-Man, Patrick

    I whakaputaina 2022
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  6. 6
    Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation

    Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation mā Yu-Wai-Man, Patrick, Chinnery, Patrick F.

    I whakaputaina 2011
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  7. 7
    Reply: Sensorineural hearing loss in OPA1-linked disorders

    Reply: Sensorineural hearing loss in OPA1-linked disorders mā Yu-Wai-Man, Patrick, Chinnery, Patrick F.

    I whakaputaina 2013
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  8. 8
    Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

    Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1 mā Yu-Wai-Man, Patrick, Chinnery, Patrick F.

    I whakaputaina 2014
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  9. 9
    Reply: ‘Behr syndrome’ with OPA1 compound heterozygote mutations

    Reply: ‘Behr syndrome’ with OPA1 compound heterozygote mutations mā Yu-Wai-Man, Patrick, Chinnery, Patrick F.

    I whakaputaina 2015
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  10. 10
    Leber Hereditary Optic Neuropathy – Therapeutic Challenges and Early Promise

    Leber Hereditary Optic Neuropathy – Therapeutic Challenges and Early Promise mā Yu-Wai-Man, Patrick, Chinnery, Patrick F.

    I whakaputaina 2011
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  11. 11
    Inherited eye-related disorders due to mitochondrial dysfunction

    Inherited eye-related disorders due to mitochondrial dysfunction mā Yu-Wai-Man, Patrick, Newman, Nancy J.

    I whakaputaina 2017
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  12. 12
    Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates

    Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates mā Yu-Wai-Man, Patrick, Chinnery, Patrick F.

    I whakaputaina 2013
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  13. 13
    Surgery for traumatic optic neuropathy

    Surgery for traumatic optic neuropathy mā Yu‐Wai‐Man, Patrick, Griffiths, Philip G

    I whakaputaina 2013
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  14. 14
    Steroids for traumatic optic neuropathy

    Steroids for traumatic optic neuropathy mā Yu‐Wai‐Man, Patrick, Griffiths, Philip G

    I whakaputaina 2013
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  15. 15
    Disorders of the Optic Nerve in Mitochondrial Cytopathies: New Ideas on Pathogenesis and Therapeutic Targets

    Disorders of the Optic Nerve in Mitochondrial Cytopathies: New Ideas on Pathogenesis and Therapeutic Targets mā Sitarz, Kamil S., Chinnery, Patrick F., Yu-Wai-Man, Patrick

    I whakaputaina 2012
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  16. 16
    Mitochondrial optic neuropathies – Disease mechanisms and therapeutic strategies

    Mitochondrial optic neuropathies – Disease mechanisms and therapeutic strategies mā Yu-Wai-Man, Patrick, Griffiths, Philip G., Chinnery, Patrick F.

    I whakaputaina 2011
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  17. 17
    The clinical spectrum of mitochondrial genetic disorders

    The clinical spectrum of mitochondrial genetic disorders mā Kirkman, Matthew A, Yu-Wai-Man, Patrick, Chinnery, Patrick F

    I whakaputaina 2008
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  18. 18
    Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

    Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction mā Harvey, Joshua Paul, Yu-Wai-Man, Patrick, Cheetham, Michael Edward

    I whakaputaina 2022
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    Genetic variation in the methylenetetrahydrofolate reductase gene, MTHFR, does not alter the risk of visual failure in Leber’s hereditary optic neuropathy

    Genetic variation in the methylenetetrahydrofolate reductase gene, MTHFR, does not alter the risk of visual failure in Leber’s hereditary optic neuropathy mā Hudson, Gavin, Yu-Wai-Man, Patrick, Zeviani, Massimo, Chinnery, Patrick F.

    I whakaputaina 2009
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  20. 20
    Reply: Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion

    Reply: Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion mā Yu-Wai-Man, Patrick, Hudson, Gavin, Klopstock, Thomas, Chinnery, Patrick F.

    I whakaputaina 2016
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