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2. Comorbid Medical Conditions in Friedreich Ataxia: Association With Inflammatory Bowel Disease and Growth Hormone Deficiency. (August 2016)

3. Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss. (August 2015)

4. Compound heterozygous FXN mutations and clinical outcome in friedreich ataxia. Issue 3 (March 2016)

5. Dejerine–Sottas disease in childhood—Genetic and sonographic heterogeneity. Issue 4 (21st February 2018)

6. Delivering multidisciplinary neuromuscular care for children via telehealth. Issue 1 (29th April 2022)

8. Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy. Issue 5 (26th April 2017)

9. Geographic Expansion of Japanese Encephalitis Virus to Australia: Neuroinflammatory Sequelae and Consideration of Immunomodulation. Issue 5 (16th February 2023)

10. HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia. Issue 7 (3rd January 2014)