1. Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease. Issue 10 (19th September 2011) Authors: Uusimaa, J; Jungbluth, H; Fratter, C; Crisponi, G; Feng, L; Zeviani, M; Hughes, I; Treacy, E P; Birks, J; Brown, G K; Sewry, C A; McDermott, M; Muntoni, F; Poulton, J Journal: Journal of medical genetics Issue: Volume 48:Issue 10(2011) Page Start: 660 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Confusing terminology attempts to define the undefinable. Issue 2 (30th January 2007) Authors: Hughes, I Journal: Archives of disease in childhood Issue: Volume 92:Issue 2(2007) Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. O-010 Five-year australian experience with pipeline™ flex embolization devices with shield technology™: real world evidence (SCOPE-AUS). (22nd July 2019) Authors: Rice, H; de Villiers, L; Owusu, M; Wenderoth, J; Chiu, A; Manning, N; Cheung, A; Phillips, T; Rapier, C; Gatty, S; Ninnes, L; Hughes, I; Green, T Journal: Journal of neurointerventional surgery Issue: Volume 11(2019)Supplement 1 Page Start: A7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evaluation of prognostic risk models for postoperative pulmonary complications in adult patients undergoing major abdominal surgery: a systematic review and international external validation cohort study. Issue 7 (July 2022) Authors: Kouli, O; Murray, V; Bhatia, S; Cambridge, WA; Kawka, M; Shafi, S; Knight, SR; Kamarajah, SK; McLean, KA; Glasbey, JC; Khaw, RA; Ahmed, W; Akhbari, M; Baker, D; Borakati, A; Mills, E; Thavayogan, R; Yasin, I; Raubenheimer, K; Ridley, W Journal: Lancet Issue: Volume 4:Issue 7(2022) Page Start: e520 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Congenital adrenal hyperplasia--a clinical and genetic survey. Are we detecting male salt-losers?. Issue 8 (August 1980) Authors: Murtaza, L; Sibert, J R; Hughes, I; Balfour, I C Journal: Archives of disease in childhood Issue: Volume 55:Issue 8(1980) Page Start: 622 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Pregnanediols and breast milk jaundice. Issue 6 (June 1981) Authors: Murphy, J F; Hughes, I; Verrier Jones, E R; Gaskell, S; Pike, A W Journal: Archives of disease in childhood Issue: Volume 56:Issue 6(1981) Page Start: 474 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Congenital anomalies associated with hypothyroidism. Issue 6 (June 1986) Authors: Bamforth, J S; Hughes, I; Lazarus, J; John, R Journal: Archives of disease in childhood Issue: Volume 61:Issue 6(1986) Page Start: 608 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita. Issue 9 (1st September 2008) Authors: Shaikh, M G; Boyes, L; Kingston, H; Collins, R; Besley, G T N; Padmakumar, B; Ismayl, O; Hughes, I; Hall, C M; Hellerud, C; Achermann, J C; Clayton, P E Journal: Journal of medical genetics Issue: Volume 45:Issue 9(2008) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Recurrent severe hyperandrogenism during pregnancy: a case report. Issue 4 (24th March 2005) Authors: Holt, H B; Medbak, S; Kirk, D; Guirgis, R; Hughes, I; Cummings, M H; Meeking, D R Journal: Journal of clinical pathology Issue: Volume 58:Issue 4(2005) Page Start: 439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects. Issue 6 (June 1996) Authors: Kwok, C; Tyler-Smith, C; Mendonca, B B; Hughes, I; Berkovitz, G D; Goodfellow, P N; Hawkins, J R Journal: Journal of medical genetics Issue: Volume 33:Issue 6(1996) Page Start: 465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗