Bryony Ryder

A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy

Bryony Ryder, Maria Tolomeo, Zahra Nochi et al. · JIMD Reports · 2018 · 37 citations · Full text

New insights into carnitine‐acylcarnitine translocase deficiency from 23 cases: Management challenges and potential therapeutic approaches

Bryony Ryder, Michal Inbar‐Feigenberg, Emma Glamuzina et al. · Journal of Inherited Metabolic Disease · 2021 · 21 citations · Full text

Fumarase Deficiency: A Safe and Potentially Disease Modifying Effect of High Fat/Low Carbohydrate Diet

Bryony Ryder, Francesca Moore, A. Mitchell et al. · JIMD Reports · 2017 · 15 citations · Full text

The natural history of elevated tetradecenoyl‐L‐carnitine detected by newborn screening in New Zealand: implications for very long chain acyl‐CoA dehydrogenase deficiency screening and treatment

Bryony Ryder, Detlef Knoll, Donald R. Love et al. · Journal of Inherited Metabolic Disease · 2016 · 13 citations

Plasma ammonia concentrations in extremely low birthweight infants in the first week after birth: secondary analysis from the ProVIDe randomized clinical trial

Barbara E. Cormack, Yannan Jiang, Jane E. Harding et al. · Pediatric Research · 2020 · 10 citations · Full text