1. A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes. (1st November 2022) Authors: Mohamad, Janan; Sarig, Ofer; Beattie, Paula; Malovitski, Kiril; Assaf, Sari; O'Toole, Edel; Schwartz, Janice; Evans, Holly; Samuelov, Liat; Sprecher, Eli Journal: British journal of dermatology Issue: Volume 187:Number 5(2022) Page Start: 773 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes. (8th August 2022) Authors: Mohamad, Janan; Sarig, Ofer; Beattie, Paula; Malovitski, Kiril; Assaf, Sari; O'Toole, Edel; Schwartz, Janice; Evans, Holly; Samuelov, Liat; Sprecher, Eli Journal: British journal of dermatology Issue: Volume 187:Number 5(2022) Page Start: 773 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. (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) ↗
4. 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) ↗
5. 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) ↗
6. 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) ↗
7. Influence of age on the relationship between apixaban concentration and anti-factor Xa activity in older patients with non-valvular atrial fibrillation. (15th May 2021) Authors: Kalaria, Shamir N.; Zhu, Hao; Liu, Qi; Florian, Jeffrey; Wang, Yaning; Schwartz, Janice Journal: International journal of cardiology Issue: Volume 331(2021) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. P2‐079: Neuronal origin plasma exosomes provide novel biomarkers for lysosomal dysfunction in Alzheimer's disease. (1st July 2015) Authors: Kapogiannis, Dimitrios; Mustapic, Maja; Eitan, Erez; Boxer, Adam L.; Schwartz, Janice; Abner, Erin; Petersen, Ronald C.; Miller, Bruce L.; Goetzl, Edward J. Journal: Alzheimer's & dementia Issue: Volume 11(2015)Supplement 7S:Part 11 Page Start: P513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗