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Clinical Medicine (London, England)|December 3, 2017
An approach to familial lymphoedemaGabriela E Jones, Sahar MansourAmerican Journal of Medical Genetics. Part A|May 26, 2017
Renal anomalies and lymphedema distichiasis syndrome. A rare association?Gabriela E Jones, Anna K Richmond, Osric Navti, et al.European Journal of Endocrinology|January 31, 2008
The association of primary hyperparathyroidism and primary ovarian failure: a de novo t(X; 2) (q22p13) reciprocal translocationGul Bano, Sahar Mansour, Stephen NusseyThe British Journal of Radiology|February 10, 2022
Spectrum of Ovarian Incidentalomas: Diagnosis and ManagementSahar Mansour, Soha Hamed, Rasha KamalCardiology in the Young|February 9, 2026
An adult patient with pulmonary atresia with ventricular septal defect and chromosome 17p13.3 microdeletion including YWHAE geneElla McDonnell, Ioannis Kasouridis, Sahar MansourEuropean Journal of Medical Genetics|April 19, 2023
Consensus recommendations on lymphedema in Phelan-McDermid syndromeRobert J Damstra, Stéphane Vignes, , et al.The Journal of Physiology|January 14, 2018
Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes?Silvia Martin-Almedina, Sahar Mansour, Pia OstergaardThe Journal of Hand Surgery, European Volume|September 27, 2018
A clinical review and introduction of the diagnostic algorithm for thalidomide embryopathy (DATE)Sahar Mansour, Emma Baple, Christine M HallEuropean Journal of Medical Genetics|November 12, 2025
Pathogenic variant in GATA4 associated with atrioventricular septal defect and congenital diaphragmatic hernia: A case reportJohn Howat, Trisha Vigneswaran, Aris Papageorghiou, et al.The Breast Journal|December 9, 2020
The role of automated breast ultrasound in the assessment of the local extent of breast cancerMaha Helal, Sahar Mansour, Rana Khaled, et al.Pageof 16