1. A unique LAMB3 splice‐site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countries. (1st October 2016) Authors: Mayer, B.; Silló, P.; Mazán, M.; Pintér, D.; Medvecz, M.; Has, C.; Castiglia, D.; Petit, F.; Charlesworth, A.; Hatvani, Zs.; Pamjav, H.; Kárpáti, S. Journal: British journal of dermatology Issue: Volume 175:Number 4(2016) Page Start: 721 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A unique LAMB3 splice‐site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countries. (8th August 2016) Authors: Mayer, B.; Silló, P.; Mazán, M.; Pintér, D.; Medvecz, M.; Has, C.; Castiglia, D.; Petit, F.; Charlesworth, A.; Hatvani, Zs.; Pamjav, H.; Kárpáti, S. Journal: British journal of dermatology Issue: Volume 175:Number 4(2016) Page Start: 721 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational study. (1st April 2014) Authors: Chiaverini, C.; Charlesworth, A.; Fernandez, A.; Barbarot, S.; Bessis, D.; Bodemer, C.; Bursztejn, A.‐C.; Cobo, A.‐M.; Del Rio, M.; D'Incan, M.; Labrèze, C.; Langlet, C.; Mazereeuw, J.; Miquel, J.; Vabres, P.; Meneguzzi, G.; Lacour, J.‐P. Journal: British journal of dermatology Issue: Volume 170:Number 4(2014:Apr.) Page Start: 901 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational study. (April 2014) Authors: Chiaverini, C.; Charlesworth, A.; Fernandez, A.; Barbarot, S.; Bessis, D.; Bodemer, C.; Bursztejn, A.‐C.; Cobo, A.‐M.; Del Rio, M.; D'Incan, M.; Labrèze, C.; Langlet, C.; Mazereeuw, J.; Miquel, J.; Vabres, P.; Meneguzzi, G.; Lacour, J.‐P. Journal: British journal of dermatology Issue: Volume 170:Number 4(2014:Apr.) Page Start: 901 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Epidermolysis bullosa simplex with PLEC mutations: new phenotypes and new mutations. (25th March 2013) Authors: Charlesworth, A.; Chiaverini, C.; Chevrant‐Breton, J.; DelRio, M.; Diociaiuti, A.; Dupuis, R.P.; El Hachem, M.; Le Fiblec, B.; Sankari‐Ho, A.M.; Valhquist, A.; Wierzbicka, E.; Lacour, J.P.; Meneguzzi, G. Journal: British journal of dermatology Issue: Volume 168:Number 4(2013:Apr.) Page Start: 808 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations. (1st March 2021) Authors: Hérissé, A.L.; Charlesworth, A.; Bellon, N.; Leclerc‐Mercier, S.; Bourrat, E.; Hadj‐Rabia, S.; Bodemer, C.; Lacour, J.P.; Chiaverini, C. Journal: British journal of dermatology Issue: Volume 184:Number 5(2021) Page Start: 960 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations. (1st May 2021) Authors: Hérissé, A.L.; Charlesworth, A.; Bellon, N.; Leclerc‐Mercier, S.; Bourrat, E.; Hadj‐Rabia, S.; Bodemer, C.; Lacour, J.P.; Chiaverini, C. Journal: British journal of dermatology Issue: Volume 184:Number 5(2021) Page Start: 960 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases. Issue 1 (December 2016) Authors: Montaudié, H.; Chiaverini, C.; Sbidian, E.; Charlesworth, A.; Lacour, J-P. Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Late‐onset skin fragility in childhood: a case of junctional epidermolysis bullosa of late onset caused by a missense mutation in COL17A1. (30th August 2013) Authors: Vanotti, S.; Chiaverini, C.; Charlesworth, A.; Bonnet, N.; Berbis, P.; Meneguzzi, G.; Lacour, J.‐P. Journal: British journal of dermatology Issue: Volume 169:Number 3(2013:Sep.) Page Start: 714 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Oral erythromycin therapy in epidermolysis bullosa simplex generalized severe. (10th June 2015) Authors: Chiaverini, C.; Fontas, E.; Vabres, P.; Bessis, D.; Mazereeuw, J.; Charlesworth, A.; Meneguzzi, G.; Lacour, J.‐P. Journal: British journal of dermatology Issue: Volume 173:Number 2(2015:Aug.) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗