1. Cerebral venous sinus thrombosis: a case series including thrombolysis. Issue 10 (24th June 2009) Authors: Mallick, A A; Sharples, P M; Calvert, S E; Jones, R W A; Leary, M; Lux, A L; O'Callaghan, F J; Osborne, J P; Patel, J S; Prendiville, A T; Renowden, S; Jardine, P E Journal: Archives of disease in childhood Issue: Volume 94:Issue 10(2009) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). Issue 3 (September 1994) Authors: Jardine, P E; Koch, M C; Lunt, P W; Maynard, J; Bathke, K D; Harper, P S; Upadhyaya, M Journal: Archives of disease in childhood Issue: Volume 71:Issue 3(1994) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Familial bilateral periventricular nodular heterotopia mimics tuberous sclerosis. Issue 3 (March 1996) Authors: Jardine, P E; Clarke, M A; Super, M Journal: Archives of disease in childhood Issue: Volume 74:Issue 3(1996) Page Start: 244 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Optic disc drusen masquerading as papilloedema. Issue 8 (3rd June 2010) Authors: Fong, C Y; Williams, C; Pople, I K; Jardine, P E Journal: Archives of disease in childhood Issue: Volume 95:Issue 8(2010) Page Start: 629 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis. Issue 3 (March 1994) Authors: Jardine, P E; Cotter, P D; Johnson, S A; Fitzsimons, E J; Tyfield, L; Lunt, P W; Bishop, D F Journal: Journal of medical genetics Issue: Volume 31:Issue 3(1994) Page Start: 213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The importance of testing for adrenoleucodystrophy in males with idiopathic Addison's disease. Issue 3 (1st March 2002) Authors: Ronghe, M D; Barton, J; Jardine, P E; Crowne, E C; Webster, M H; Armitage, M; Allen, J T; Steward, C G Journal: Archives of disease in childhood Issue: Volume 86:Issue 3(2002) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗