Reduced bioavailable manganese causes striatal urea cycle pathology in Huntington's disease mouse model
2017 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 43 citations
https://doi.org/10.1016/j.bbadis.2017.02.013
T
Terry Jo Bichell
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Terry Jo Bichell is an academic researcher from Brentwood Hospital. The author has contributed to research in topics: Genetic Syndromes and Imprinting & Genetic Neurodegenerative Diseases & Genetics and Neurodevelopmental Disorders. The author has an h-index of 16, co-authored 37 publications.
ORCID: 0000-0002-1055-4993Papers by this author
worksEnabling endpoint development for interventional clinical trials in individuals with Angelman syndrome: a prospective, longitudinal, observational clinical study (FREESIAS)
2023 · Journal of Neurodevelopmental Disorders · 23 citations
https://doi.org/10.1186/s11689-023-09494-w
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndrome
2019 · Orphanet Journal of Rare Diseases · 5 citations
https://doi.org/10.1186/s13023-019-1216-0
ZTTK-iPSC: A Framework for the rapid generation of patient-specific rare disease cell models
2025 · Cytotherapy · 0 citations
https://doi.org/10.1016/j.jcyt.2025.03.485
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