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Author/Creator Ryder, Bryony

1. New insights into carnitine‐acylcarnitine translocase deficiency from 23 cases: Management challenges and potential therapeutic approaches. Issue 4 (29th March 2021)

Authors:
Ryder, Bryony; Inbar‐Feigenberg, Michal; Glamuzina, Emma; Halligan, Rebecca; Vara, Roshni; Elliot, Aoife; Coman, David; Minto, Tahlee; Lewis, Katherine; Schiff, Manuel; Vijay, Suresh; Akroyd, Rhonda; Thompson, Sue; MacDonald, Anita; Woodward, Abigail J. M.; Gribben, Joanne. E. L.; Grunewald, Step...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 44:Issue 4(2021)
Page Start:
903
Record Type:
Journal Article
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2. Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2. (3rd August 2022)

Authors:
Tolomeo, Maria; Chimienti, Guglielmina; Lanza, Martina; Barbaro, Roberto; Nisco, Alessia; Latronico, Tiziana; Leone, Piero; Petrosillo, Giuseppe; Liuzzi, Grazia Maria; Ryder, Bryony; Inbar-Feigenberg, Michal; Colella, Matilde; Lezza, Angela M. S.; Olsen, Rikke K. J.; Barile, Maria
Journal:
Free radical research
Issue:
Volume 56:Number 7/8(2022)
Page Start:
511
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. 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. Issue 3 (7th January 2016)

Authors:
Ryder, Bryony; Knoll, Detlef; Love, Donald R.; Shepherd, Phillip; Love, Jennifer M.; Reed, Peter W.; de Hora, Mark; Webster, Dianne; Glamuzina, Emma; Wilson, Callum
Journal:
Journal of inherited metabolic disease
Issue:
Volume 39:Issue 3(2016)
Page Start:
409
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗