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Eloise Watson on Muck Rack

Eloise Watson

Lima
As seen in: The American Journal of Human Genetics, Neurology Journal, The Medical Republic

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Articles

Author Response: Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis

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By Ryan Davis Verified, Kishore Kumar, Eloise Watson, Carolyn M. Sue
| Neurology Journal Verified
REQUIREMENTS If you are uploading a letter concerning an article: You must have updated your disclosures within six months: http://submit.neurology.org Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
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Low disease risk and penetrance in Leber hereditary optic neuropathy

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By Eloise Watson, Reserve Rd, Ryan Davis
| The American Journal of Human Genetics Verified
Main text We read with interest the article by Lopez Sanchez and colleagues, examining the epidemiology and risk of vision loss in Leber hereditary optic neuropathy (LHON) in Australia through review of a national clinical register. 1 Lopez Sanchez M.I.G. Kearns L.S. Staffieri S.E. Clarke L. McGuinness M.B. Meteoukki W. Samuel S. Ruddle J.B. Chen C. Fraser C.L. et al. Establishing risk of vision loss in Leber hereditary optic neuropathy.
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The challenges of recognising mitochondrial diseases • The Medical Republic

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By Eloise Watson, Kate Ahmad, Ryan Davis, byDr Eloise Watson
| The Medical Republic Verified
The presentations for mitochondrial diseases is highly variable and diagnosis can be challenging, even for specialist clinicians. With limited teaching and awareness of mitochondrial diseases, it is important that mitochondrial diseases can be recognised on the frontline. CLINICAL VIGNETTE A 48-year-old lady presents to you describing “missing” parts of her vision with preserved central acuity, which has been gradually getting worse over several months.
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