1. "Pseudonormonatraemia". Issue 6198 (3rd November 1979) Authors: Burn, J; Gill, G V Journal: BMJ Issue: Volume 2:Issue 6198(1979) Page Start: 1110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 018 Neuroferritinopathy: a new finding in a novel disease. Issue 3 (9th February 2012) Authors: Keogh, M; Jones, P; Coulthard, A; Chinnery, P F; Burn, J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 3(2012) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 46Stroke and bleed events in patients with non-valvular atrial fibrillation on direct oral anticoagulants: a retrospective study across 200 clinical commissioning groups in NHS England from 2013 to 2016. (10th October 2018) Authors: Sheth, H; McNally, D; Santibanez-Koref, M; Burn, J Journal: Europace Issue: Volume 20(2018)Supplement 4 Page Start: iv22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male. Issue 10 (October 1990) Authors: Martin, F; Platt, J; Tawn, E J; Burn, J Journal: Journal of medical genetics Issue: Volume 27:Issue 10(1990) Page Start: 637 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome. Issue 9 (September 1991) Authors: Ireland, M; English, C; Cross, I; Houlsby, W T; Burn, J Journal: Journal of medical genetics Issue: Volume 28:Issue 9(1991) Page Start: 639 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A female infant with features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity?. Issue 1 (February 1983) Authors: Baraitser, M; Burn, J; Fixsen, J Journal: Journal of medical genetics Issue: Volume 20:Issue 1(1983) Page Start: 65 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A male with type I orofaciodigital syndrome. Issue 10 (October 1991) Authors: Goodship, J; Platt, J; Smith, R; Burn, J Journal: Journal of medical genetics Issue: Volume 28:Issue 10(1991) Page Start: 691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A novel FTL insertion causing neuroferritinopathy. Issue 1 (11th January 2010) Authors: Batey, S; Vuillaume, I; Devos, D; Destée, A; Curtis, A J; Lombes, A; Curtis, A; Burn, J; Chinnery, P F Journal: Journal of medical genetics Issue: Volume 47:Issue 1(2010) Page Start: 71 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project--1981-86. 2. Incidence, case fatality rates and overall outcome at one year of cerebral infarction, primary intracerebral and subarachnoid haemorrhage. Issue 1 (January 1990) Authors: Bamford, J; Sandercock, P; Dennis, M; Burn, J; Warlow, C Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 53:Issue 1(1990) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A recessively inherited windmill-vane camptodactyly/ichthyosis syndrome. Issue 2 (April 1983) Authors: Baraitser, M; Burn, J; Fixsen, J Journal: Journal of medical genetics Issue: Volume 20:Issue 2(1983) Page Start: 125 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗