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La Tunisie Medicale|June 3, 2010
[Obstetric vesicovaginal fistulas, about 131 cases]Dalenda Chelli, Hela Chelli, Abdelaziz Falfoul, et al.Journal of Pediatric Orthopedics|December 25, 2009
Magnetic resonance evaluation of acetabular residual dysplasia in developmental dysplasia of the hip: a preliminary study of 27 patientsWièm Douira-Khomsi, Mahmoud Smida, Hela Louati, et al.Cancer Genetics|March 10, 2025
HSP110 T17 marker matches the pentaplex panel and outperforms CAT-25 for detecting microsatellite instability in sporadic colorectal cancerNasreddine Rajoua, Antoine Daunay, Wissem Triki, et al.African Journal of Paediatric Surgery : AJPS|August 3, 2021
Infantile systemic hyalinosis: Variable grades of severityAli Al Kaissi, Marwa Hilmi, Zulfiya Betadolova, et al.Frontiers in Pediatrics|May 7, 2020
Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 CasesSami Bouchoucha, Asma Chikhaoui, Dorra Najjar, et al.Diagnostics (Basel, Switzerland)|October 27, 2022
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic EntitiesAli Al Kaissi, Sergey Ryabykh, Nabil Nassib, et al.Orphanet Journal of Rare Diseases|March 6, 2022
Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutationsAsma Chikhaoui, Ichraf Kraoua, Nadège Calmels, et al.Genes|December 24, 2021
Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome BKhouloud Zayoud, Ichraf Kraoua, Asma Chikhaoui, et al.Plos One|October 6, 2021
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairmentRahma Mkaouar, Zied Riahi, Cherine Charfeddine, et al.Pageof 5