1. Acute presentations of inherited metabolic disorders: investigation and initial management. Issue 3 (March 2019) Authors: Ghosh, Arunabha; Morris, Andrew A M Journal: Paediatrics and child health Issue: Volume 29:Issue 3(2019) Page Start: 99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Asymmetric Supercapacitors Based on Graphene/MnO2 Nanospheres and Graphene/MoO3 Nanosheets with High Energy Density. (30th August 2013) Authors: Chang, Jian; Jin, Meihua; Yao, Fei; Kim, Tae Hyung; Le, Viet Thong; Yue, Hongyan; Gunes, Fethullah; Li, Bing; Ghosh, Arunabha; Xie, Sishen; Lee, Young Hee Journal: Advanced functional materials Issue: Volume 23:Number 40(2013) Page Start: 5074 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Continuous glucose monitoring for hypoglycaemia in children: Perspectives in 2020. Issue 5 (4th May 2020) Authors: Worth, Chris; Dunne, Mark; Ghosh, Arunabha; Harper, Simon; Banerjee, Indraneel Journal: Pediatric diabetes Issue: Volume 21:Issue 5(2020) Page Start: 697 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Determining the Fermi level by absorption quenching of monolayer graphene by charge transfer doping. Issue 44 (27th October 2016) Authors: Adhikari, Subash; Perello, David J.; Biswas, Chandan; Ghosh, Arunabha; Luan, Nguyen Van; Park, Jihoon; Yao, Fei; Rotkin, Slava V.; Lee, Young Hee Journal: Nanoscale Issue: Volume 8:Issue 44(2016) Page Start: 18710 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing. Issue 11 (3rd May 2017) Authors: Ghosh, Arunabha; Schlecht, Helene; Heptinstall, Lesley E; Bassett, John K; Cartwright, Eleanor; Bhaskar, Sanjeev S; Urquhart, Jill; Broomfield, Alexander; Morris, Andrew AM; Jameson, Elisabeth; Schwahn, Bernd C; Walter, John H; Douzgou, Sofia; Murphy, Helen; Hendriksz, Chris; Sharma, Reena; Wilco... Journal: Archives of disease in childhood Issue: Volume 102:Issue 11(2017) Page Start: 1019 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Haematopoietic stem cell gene therapy with IL‐1Ra rescues cognitive loss in mucopolysaccharidosis IIIA. Issue 3 (14th February 2020) Authors: Parker, Helen; Ellison, Stuart M; Holley, Rebecca J; O'Leary, Claire; Liao, Aiyin; Asadi, Jalal; Glover, Emily; Ghosh, Arunabha; Jones, Simon; Wilkinson, Fiona L; Brough, David; Pinteaux, Emmanuel; Boutin, Hervé; Bigger, Brian W Journal: EMBO molecular medicine Issue: Volume 12:Issue 3(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. High dose genistein in Sanfilippo syndrome: A randomised controlled trial. Issue 5 (13th June 2021) Authors: Ghosh, Arunabha; Rust, Stewart; Langford‐Smith, Kia; Weisberg, Daniel; Canal, Maria; Breen, Catherine; Hepburn, Michelle; Tylee, Karen; Vaz, Frédéric M.; Vail, Andy; Wijburg, Frits; O'Leary, Claire; Parker, Helen; Wraith, J. Ed; Bigger, Brian W.; Jones, Simon A. Journal: Journal of inherited metabolic disease Issue: Volume 44:Issue 5(2021) Page Start: 1248 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Long term survival and cardiopulmonary outcome in children with Hurler syndrome after haematopoietic stem cell transplantation. Issue 3 (10th March 2017) Authors: Lum, Su Han; Stepien, Karolina M.; Ghosh, Arunabha; Broomfield, Alexander; Church, Heather; Mercer, Jean; Jones, Simon; Wynn, Robert Journal: Journal of inherited metabolic disease Issue: Volume 40:Issue 3(2017) Page Start: 455 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Phenotypic Heterogeneity in a Congenital Disorder of Glycosylation Caused by Mutations in STT3A. (May 2017) Authors: Ghosh, Arunabha; Urquhart, Jill; Daly, Sarah; Ferguson, Anne; Scotcher, Diana; Morris, Andrew A. M.; Clayton-Smith, Jill Journal: Journal of child neurology Issue: Volume 32:Number 6(2017:Jun.) Page Start: 560 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Prolidase deficiency in an infant with an incidental finding of methaemoglobinaemia. Issue 11 (18th November 2021) Authors: Tan, Chern Yan; Kothandaraman, Easwari; Ghosh, Arunabha Journal: BMJ case reports Issue: Volume 14:Issue 11(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗