1. A study of gene mutations and how they relate to the different types of ichthyosis. (1st March 2020) Authors: Simpson, J.K.; Martinez‐Queipo, M.; Onoufriadis, A.; Tso, S.; Glass, E.; Liu, L.; Higashino, T.; Scott, W.; Tierney, C.; Simpson, M.A.; Desomchoke, R.; Youssefian, L.; SaeIdian, A.H.; Vahidnezhad, H.; Bisquera, A.; Ravenscroft, J.; Moss, C.; O'Toole, E.A.; Burrows, N.; Leech, S. Journal: British journal of dermatology Issue: Volume 182:Number 3(2020) Page Start: e101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A study of gene mutations and how they relate to the different types of ichthyosis. (28th February 2020) Authors: Simpson, J.K.; Martinez‐Queipo, M.; Onoufriadis, A.; Tso, S.; Glass, E.; Liu, L.; Higashino, T.; Scott, W.; Tierney, C.; Simpson, M.A.; Desomchoke, R.; Youssefian, L.; SaeIdian, A.H.; Vahidnezhad, H.; Bisquera, A.; Ravenscroft, J.; Moss, C.; O'Toole, E.A.; Burrows, N.; Leech, S. Journal: British journal of dermatology Issue: Volume 182:Number 3(2020) Page Start: e101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Autosomal dominant diffuse nonepidermolytic palmoplantar keratoderma due to a recurrent mutation in aquaporin‐5. (12th November 2015) Authors: Abdul‐Wahab, A.; Takeichi, T.; Liu, L.; Lomas, D.; Hughes, B.; Akiyama, M.; McGrath, J.A.; Mellerio, J.E. Journal: British journal of dermatology Issue: Volume 174:Number 2(2016) Page Start: 430 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal dominant diffuse nonepidermolytic palmoplantar keratoderma due to a recurrent mutation in aquaporin‐5. (1st February 2016) Authors: Abdul‐Wahab, A.; Takeichi, T.; Liu, L.; Lomas, D.; Hughes, B.; Akiyama, M.; McGrath, J.A.; Mellerio, J.E. Journal: British journal of dermatology Issue: Volume 174:Number 2(2016) Page Start: 430 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Characteristics of children with Netherton syndrome: a review of 21 patients. (29th March 2021) Authors: Prodinger, C.; Yerlett, N.; MacDonald, C.; Subhanitthaya, C.; Laimer, M.; Goh, L.; Du Toit, G.; Mellerio, J.E.; Petrof, G.; Martinez, A.E. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 35:Number 7(2021) Page Start: e466 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical features and WNT10A mutations in seven unrelated cases of Schöpf–Schulz–Passarge syndrome. (15th October 2014) Authors: Tziotzios, C.; Petrof, G.; Liu, L.; Verma, A.; Wedgeworth, E.K.; Mellerio, J.E.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 171:Number 5(2014:Nov.) Page Start: 1211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Clinical features and WNT10A mutations in seven unrelated cases of Schöpf–Schulz–Passarge syndrome. (15th October 2014) Authors: Tziotzios, C.; Petrof, G.; Liu, L.; Verma, A.; Wedgeworth, E.K.; Mellerio, J.E.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 171:Number 5(2014:Nov.) Page Start: 1211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical features and WNT10A mutations in seven unrelated cases of Schöpf–Schulz–Passarge syndrome. (1st November 2014) Authors: Tziotzios, C.; Petrof, G.; Liu, L.; Verma, A.; Wedgeworth, E.K.; Mellerio, J.E.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 171:Number 5(2014:Nov.) Page Start: 1211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility. (11th March 2020) Authors: Has, C.; Bauer, J.W.; Bodemer, C.; Bolling, M.C.; Bruckner‐Tuderman, L.; Diem, A.; Fine, J.‐D.; Heagerty, A.; Hovnanian, A.; Marinkovich, M.P.; Martinez, A.E.; McGrath, J.A.; Moss, C.; Murrell, D.F.; Palisson, F.; Schwieger‐Briel, A.; Sprecher, E.; Tamai, K.; Uitto, J.; Woodley, D.T. Journal: British journal of dermatology Issue: Volume 183:Number 4(2020) Page Start: 614 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility. (1st October 2020) Authors: Has, C.; Bauer, J.W.; Bodemer, C.; Bolling, M.C.; Bruckner‐Tuderman, L.; Diem, A.; Fine, J.‐D.; Heagerty, A.; Hovnanian, A.; Marinkovich, M.P.; Martinez, A.E.; McGrath, J.A.; Moss, C.; Murrell, D.F.; Palisson, F.; Schwieger‐Briel, A.; Sprecher, E.; Tamai, K.; Uitto, J.; Woodley, D.T. Journal: British journal of dermatology Issue: Volume 183:Number 4(2020) Page Start: 614 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗