1. Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1. Issue 10 (3rd August 2022) Authors: Mohamad, Janan; Samuelov, Liat; Assaf, Sari; Malki, Liron; Malovitski, Kiril; Meijers, Odile; Adir, Noam; Granot, Ester; Pavlovsky, Mor; Sarig, Ofer; Sprecher, Eli Journal: American journal of medical genetics Issue: Volume 188:Issue 10(2022) Page Start: 2879 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence. (17th June 2022) Authors: Pavlovsky, Mor; Peled, Alon; Sarig, Ofer; Astman, Nadav; Malki, Liron; Meijers, Odile; Assaf, Sari; Schwartz, Janice; Malovitski, Kiril; Hansen, David; Sprecher, Eli; Samuelov, Liat Journal: British journal of dermatology Issue: Volume 187:Number 3(2022) Page Start: 392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence. (1st September 2022) Authors: Pavlovsky, Mor; Peled, Alon; Sarig, Ofer; Astman, Nadav; Malki, Liron; Meijers, Odile; Assaf, Sari; Schwartz, Janice; Malovitski, Kiril; Hansen, David; Sprecher, Eli; Samuelov, Liat Journal: British journal of dermatology Issue: Volume 187:Number 3(2022) Page Start: 392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy. (1st November 2022) Authors: Malovitski, Kiril; Meijers, Odile; Cohen‐Barak, Eran; Bergman, James; Adir, Noam; Giladi, Moshe; Shalev, Stavit; Sarig, Ofer; Schwartz, Janice; Evans, Holly; Sprecher, Eli; Samuelov, Liat Journal: British journal of dermatology Issue: Volume 187:Number 5(2022) Page Start: 826 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy. (9th August 2022) Authors: Malovitski, Kiril; Meijers, Odile; Cohen‐Barak, Eran; Bergman, James; Adir, Noam; Giladi, Moshe; Shalev, Stavit; Sarig, Ofer; Schwartz, Janice; Evans, Holly; Sprecher, Eli; Samuelov, Liat Journal: British journal of dermatology Issue: Volume 187:Number 5(2022) Page Start: 826 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti‐tumour necrosis factor‐α and interleukin‐12/23 blockade. (19th April 2022) Authors: Samuelov, Liat; Sarig, Ofer; Malovitski, Kiril; Bergson, Shir; Meijers, Odile; Shouval, Dror S.; Sprecher, Eli Journal: British journal of dermatology Issue: Volume 186:Number 6(2022) Page Start: 1026 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti‐tumour necrosis factor‐α and interleukin‐12/23 blockade. (1st June 2022) Authors: Samuelov, Liat; Sarig, Ofer; Malovitski, Kiril; Bergson, Shir; Meijers, Odile; Shouval, Dror S.; Sprecher, Eli Journal: British journal of dermatology Issue: Volume 186:Number 6(2022) Page Start: 1026 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗