1. Brain dopamine‐serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorder. Issue 2 (26th October 2015) Authors: Jacobsen, Jessie C.; Wilson, Callum; Cunningham, Vicki; Glamuzina, Emma; Prosser, Debra O.; Love, Donald R.; Burgess, Trent; Taylor, Juliet; Swan, Brendan; Hill, Rosamund; Robertson, Stephen P.; Snell, Russell G.; Lehnert, Klaus Journal: Journal of inherited metabolic disease Issue: Volume 39:Issue 2(2016) Page Start: 305 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cellulose Microfibrils as a Pore Former in Electroless Co-Deposited Anodes for Solid Oxide Fuel Cells. (30th May 2017) Authors: Turnbull, Rob James; Shearer, Neil; Wilson, Callum Journal: ECS transactions Issue: Volume 78:Number 1(2017) Page Start: 1447 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2. Issue 1 (9th March 2021) Authors: Antonarakis, Stylianos E; Holoubek, Aleš; Rapti, Melivoia; Rademaker, Jesse; Meylan, Jenny; Iwaszkiewicz, Justyna; Zoete, Vincent; Wilson, Callum; Taylor, Juliet; Ansar, Muhammad; Borel, Christelle; Menzel, Olivier; Kuželová, Kateřina; Santoni, Federico A Journal: Human molecular genetics Issue: Volume 31:Issue 1(2022) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Enabling intelligent onboard guidance, navigation, and control using reinforcement learning on near-term flight hardware. (October 2022) Authors: Wilson, Callum; Riccardi, Annalisa Journal: Acta astronautica Issue: Volume 199(2022) Page Start: 374 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genotype–phenotype correlations in CPT1A deficiency detected by newborn screening in Pacific populations. Issue 4 (26th March 2022) Authors: Bernhardt, Isaac; Glamuzina, Emma; Dowsett, Leah K.; Webster, Dianne; Knoll, Detlef; Carpenter, Kevin; Bennett, Michael J.; Maeda, Michelle; Wilson, Callum Journal: JIMD reports Issue: Volume 63:Issue 4(2022) Page Start: 322 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Intellectual functioning in alpha‐mannosidosis. Issue 1 (21st September 2019) Authors: Cathey, Sara S.; Sarasua, Sara M.; Simensen, Richard; Pietris, Katie; Kimbrell, Gordon; Sillence, David; Wilson, Callum; Horowitz, Lucia Journal: JIMD reports Issue: Volume 50:Issue 1(2019) Page Start: 44 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Manufacture of Solid Oxide Fuel Cells Using Electroless Co-Deposition: A Review of Work Carried out at Edinburgh Napier University. (2nd June 2015) Authors: Davidson, Alan; Wilson, Callum; Shearer, Neil Journal: ECS transactions Issue: Volume 68:Number 1(2015) Page Start: 1735 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Metabolic disease in the Pacific: Lessons for indigenous populations. Issue 5 (17th March 2022) Authors: Wilson, Callum Other Names: Bhattacharya Kaustuv guestEditor. Journal: Journal of inherited metabolic disease Issue: Volume 45:Issue 5(2022) Page Start: 919 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 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 View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The decision to discontinue screening for carnitine uptake disorder in New Zealand. Issue 1 (11th February 2019) Authors: Wilson, Callum; Knoll, Detlef; de Hora, Mark; Kyle, Campbell; Glamuzina, Emma; Webster, Dianne Journal: Journal of inherited metabolic disease Issue: Volume 42:Issue 1(2019) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗