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1. A novel ex vivo immunoproteomic approach characterising Fasciola hepatica tegumental antigens identified using immune antibody from resistant sheep. Issue 9 (August 2017)

2. Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis. Issue 1 (January 2019)

4. Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA. Issue 2 (February 2022)

5. Immunotherapy-responsive childhood neurodegeneration with systemic and central nervous system inflammation. (September 2018)

6. Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities. Issue 5 (21st September 2020)

7. Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Issue 3 (2nd March 2017)

8. SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20. (9th April 2018)

9. The ARSACS phenotype can include supranuclear gaze palsy and skin lipofuscin deposits. Issue 1 (3rd November 2012)