1. Chronic pain in pachyonychia congenita: evidence for neuropathic origin. (1st July 2018) Authors: Brill, S.; Sprecher, E.; Smith, F.J.D.; Geva, N.; Gruener, H.; Nahman‐Averbuch, H.; Defrin, R. Journal: British journal of dermatology Issue: Volume 179:Number 1(2018) Page Start: 154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chronic pain in pachyonychia congenita: evidence for neuropathic origin. (25th April 2018) Authors: Brill, S.; Sprecher, E.; Smith, F.J.D.; Geva, N.; Gruener, H.; Nahman‐Averbuch, H.; Defrin, R. Journal: British journal of dermatology Issue: Volume 179:Number 1(2018) Page Start: 154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Focal PPK secondary to a novel KRT6C mutation (Pachyonychia congenita‐K6c). (24th August 2015) Authors: Wee, J.S.; Smith, F.J.D.; Wilson, N.J.; O'Toole, E.A. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 30:Number 8(2016:Aug.) Page Start: 1415 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Heterozygous frameshift mutation in keratin 5 in a family with Galli–Galli disease. (1st June 2014) Authors: Reisenauer, A.K.; Wordingham, S.V.; York, J.; Kokkonen, E.W.J.; Mclean, W.H.I.; Wilson, N.J.; Smith, F.J.D. Journal: British journal of dermatology Issue: Volume 170:Number 6(2014:Jun.) Page Start: 1362 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Heterozygous frameshift mutation in keratin 5 in a family with Galli–Galli disease. (June 2014) Authors: Reisenauer, A.K.; Wordingham, S.V.; York, J.; Kokkonen, E.W.J.; Mclean, W.H.I.; Wilson, N.J.; Smith, F.J.D. Journal: British journal of dermatology Issue: Volume 170:Number 6(2014:Jun.) Page Start: 1362 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening. (1st May 2017) Authors: Lovgren, M.‐L.; McAleer, M.A.; Irvine, A.D.; Wilson, N.J.; Tavadia, S.; Schwartz, M.E.; Cole, C.; Sandilands, A.; Smith, F.J.D.; Zamiri, M. Journal: British journal of dermatology Issue: Volume 176:Number 5(2017) Page Start: 1345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening. (2nd April 2017) Authors: Lovgren, M.‐L.; McAleer, M.A.; Irvine, A.D.; Wilson, N.J.; Tavadia, S.; Schwartz, M.E.; Cole, C.; Sandilands, A.; Smith, F.J.D.; Zamiri, M. Journal: British journal of dermatology Issue: Volume 176:Number 5(2017) Page Start: 1345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutations in GJB6 causing phenotype resembling pachyonychia congenita. (13th March 2015) Authors: Hale, G.I.; Wilson, N.J.; Smith, F.J.D.; Wylie, G.; Schwartz, M.E.; Zamiri, M. Journal: British journal of dermatology Issue: Volume 172:Number 5(2015:May) Page Start: 1447 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mutations in GJB6 causing phenotype resembling pachyonychia congenita. (1st May 2015) Authors: Hale, G.I.; Wilson, N.J.; Smith, F.J.D.; Wylie, G.; Schwartz, M.E.; Zamiri, M. Journal: British journal of dermatology Issue: Volume 172:Number 5(2015:May) Page Start: 1447 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutations in POGLUT1 in Galli–Galli/Dowling–Degos disease. (1st January 2017) Authors: Wilson, N.J.; Cole, C.; Kroboth, K.; Hunter, W.N.; Mann, J.A.; McLean, W.H.I.; Kernland Lang, K.; Beltraminelli, H.; Sabroe, R.A.; Tiffin, N.; Sobey, G.J.; Borradori, L.; Simpson, E.; Smith, F.J.D. Journal: British journal of dermatology Issue: Volume 176:Number 1(2017) Page Start: 270 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗