1. A profile of lipid dysregulation in harlequin ichthyosis. (19th October 2017) Authors: Ip, S.C.I.; Cottle, D.L.; Jones, L.K.; Weir, J.M.; Kelsell, D.P.; O'Toole, E.A.; Meikle, P.J.; Smyth, I.M. Journal: British journal of dermatology Issue: Volume 177:Number 5(2017) Page Start: e217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A profile of lipid dysregulation in harlequin ichthyosis. (1st November 2017) Authors: Ip, S.C.I.; Cottle, D.L.; Jones, L.K.; Weir, J.M.; Kelsell, D.P.; O'Toole, E.A.; Meikle, P.J.; Smyth, I.M. Journal: British journal of dermatology Issue: Volume 177:Number 5(2017) Page Start: e217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B. (18th May 2015) Authors: Bland, P.J.; Chronnell, C.; Plagnol, V.; Kayserili, H.; Kelsell, D.P. Journal: British journal of dermatology Issue: Volume 173:Number 1(2015:Jul.) Page Start: 285 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B. (1st July 2015) Authors: Bland, P.J.; Chronnell, C.; Plagnol, V.; Kayserili, H.; Kelsell, D.P. Journal: British journal of dermatology Issue: Volume 173:Number 1(2015:Jul.) Page Start: 285 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cardiomyopathy diagnosed in the eldest child harbouring p.S24X mutation in JUP. (1st September 2016) Authors: Boente, M. del C.; Nanda, A.; Baselaga, P.A.; Kelsell, D.P.; McGrath, J.A.; South, A.P. Journal: British journal of dermatology Issue: Volume 175:Number 3(2016) Page Start: 644 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cardiomyopathy diagnosed in the eldest child harbouring p.S24X mutation in JUP. (25th July 2016) Authors: Boente, M. del C.; Nanda, A.; Baselaga, P.A.; Kelsell, D.P.; McGrath, J.A.; South, A.P. Journal: British journal of dermatology Issue: Volume 175:Number 3(2016) Page Start: 644 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Cover image: Unpeeling the layers of harlequin ichthyosis. (1st May 2016) Authors: Harris, A.G.; Choy, C.; Pigors, M.; Kelsell, D.P.; Murrell, D.F. Journal: British journal of dermatology Issue: Volume 174:Number 5(2016) Page Start: 1160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Cover image: Unpeeling the layers of harlequin ichthyosis. (May 2016) Authors: Harris, A.G.; Choy, C.; Pigors, M.; Kelsell, D.P.; Murrell, D.F. Journal: British journal of dermatology Issue: Volume 174:Number 5(2016) Page Start: 1160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DSP mutations and arrhythmogenic cardiomyopathy. (1st May 2019) Authors: Maruthappu, T.; Posafalvi, A.; Castelletti, S.; Delaney, P.J.; Syrris, P.; O'Toole, E.A.; Green, K.J.; Elliott, P.M.; Lambiase, P.D.; Tinker, A.; McKenna, W.J.; Kelsell, D.P. Journal: British journal of dermatology Issue: Volume 180:Number 5(2019) Page Start: e157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. DSP mutations and arrhythmogenic cardiomyopathy. (26th April 2019) Authors: Maruthappu, T.; Posafalvi, A.; Castelletti, S.; Delaney, P.J.; Syrris, P.; O'Toole, E.A.; Green, K.J.; Elliott, P.M.; Lambiase, P.D.; Tinker, A.; McKenna, W.J.; Kelsell, D.P. Journal: British journal of dermatology Issue: Volume 180:Number 5(2019) Page Start: e157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗