1. A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts. Issue 1 (1st January 2002) Authors: Shinar, Y; Ben-Zeev, B; Brand, N; Lahat, H; Gross-Zur, V; MacGregor, D; Bahan, T; Kastner, D L; Pras, E Journal: Journal of medical genetics Issue: Volume 39:Issue 1(2002) Page Start: 54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22-23. Issue 10 (17th October 2006) Authors: Pras, E; Mahler, O; Kumar, V; Frydman, M; Gefen, N; Pras, E; Hejtmancik, J F Journal: Journal of medical genetics Issue: Volume 43:Issue 10(2006) Page Start: e50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Issue 9 (September 2019) Authors: de Boer, Stephanie M; Powell, Melanie E; Mileshkin, Linda; Katsaros, Dionyssios; Bessette, Paul; Haie-Meder, Christine; Ottevanger, Petronella B; Ledermann, Jonathan A; Khaw, Pearly; D'Amico, Romerai; Fyles, Anthony; Baron, Marie-Helene; Jürgenliemk-Schulz, Ina M; Kitchener, Henry C; Nijman, Hans... Journal: Lancet oncology Issue: Volume 20:Issue 9(2019) Page Start: 1273 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Close association of HLA-B51 and B52 in Israeli patients with Behçet's syndrome. Issue 6 (June 1991) Authors: Arber, N; Klein, T; Meiner, Z; Pras, E; Weinberger, A Journal: Annals of the rheumatic diseases Issue: Volume 50:Issue 6(1991) Page Start: 351 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Over representation of the A allele in the IL23R rs1004819 polymorphism in M694V homozygote non-responsive FMF patients. Issue 1 (December 2015) Authors: Pras, E; Dahan, S; Epstein, A; Zvi, I; Marek-Yagel, D; Shinar, Y; Lidar, M; Livneh, A Journal: Pediatric rheumatology online journal Issue: Volume 13:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗