1. A case for diagnosis. (1st August 2015) Authors: Samuelov, L.; Sarig, O.; Goldsmith, T.; Pavlovsky, M.; Goldberg, I.; Sagie, S.; Selig, S.; Sprecher, E. Journal: Clinical and experimental dermatology Issue: Volume 40:Number 6(2015) Page Start: 697 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A case for diagnosis. (22nd February 2015) Authors: Samuelov, L.; Sarig, O.; Goldsmith, T.; Pavlovsky, M.; Goldberg, I.; Sagie, S.; Selig, S.; Sprecher, E. Journal: Clinical and experimental dermatology Issue: Volume 40:Number 6(2015) Page Start: 697 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel homozygous deletion in EXPH5 causes a skin fragility phenotype. (11th October 2016) Authors: Malchin, N.; Sarig, O.; Grafi‐Cohen, M.; Geller, S.; Goldberg, I.; Shani, A.; Gat, A; Sprecher, E.; Mashiah, J. Journal: Clinical and experimental dermatology Issue: Volume 41:Number 8(2016) Page Start: 915 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A novel homozygous deletion in EXPH5 causes a skin fragility phenotype. (1st December 2016) Authors: Malchin, N.; Sarig, O.; Grafi‐Cohen, M.; Geller, S.; Goldberg, I.; Shani, A.; Gat, A; Sprecher, E.; Mashiah, J. Journal: Clinical and experimental dermatology Issue: Volume 41:Number 8(2016) Page Start: 915 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A novel splice‐site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large family. (1st March 2014) Authors: Eytan, O.; Sarig, O.; Israeli, S.; Mevorah, B.; Basel‐Vanagaite, L.; Sprecher, E. Journal: Clinical and experimental dermatology Issue: Volume 39:Number 2(2014) Page Start: 182 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A novel splice‐site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large family. (2nd December 2013) Authors: Eytan, O.; Sarig, O.; Israeli, S.; Mevorah, B.; Basel‐Vanagaite, L.; Sprecher, E. Journal: Clinical and experimental dermatology Issue: Volume 39:Number 2(2014) Page Start: 182 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in PSENEN. (14th February 2018) Authors: Pavlovsky, M.; Sarig, O.; Eskin‐Schwartz, M.; Malchin, N.; Bochner, R.; Mohamad, J.; Gat, A.; Peled, A.; Hafner, A.; Sprecher, E. Journal: British journal of dermatology Issue: Volume 178:Number 2(2018) Page Start: e160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in PSENEN. (18th December 2017) Authors: Pavlovsky, M.; Sarig, O.; Eskin‐Schwartz, M.; Malchin, N.; Bochner, R.; Mohamad, J.; Gat, A.; Peled, A.; Hafner, A.; Sprecher, E. Journal: British journal of dermatology Issue: Volume 178:Number 2(2018) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in PSENEN. (1st February 2018) Authors: Pavlovsky, M.; Sarig, O.; Eskin‐Schwartz, M.; Malchin, N.; Bochner, R.; Mohamad, J.; Gat, A.; Peled, A.; Hafner, A.; Sprecher, E. Journal: British journal of dermatology Issue: Volume 178:Number 2(2018) Page Start: e160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in PSENEN. (1st February 2018) Authors: Pavlovsky, M.; Sarig, O.; Eskin‐Schwartz, M.; Malchin, N.; Bochner, R.; Mohamad, J.; Gat, A.; Peled, A.; Hafner, A.; Sprecher, E. Journal: British journal of dermatology Issue: Volume 178:Number 2(2018) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗