1. Can myocardial remodeling be a useful surrogate predictor of myocardial iron load? A 3D echocardiographic multicentric study. Issue 10 (6th June 2018) Authors: Agha, Hala Mounir; AbdelMassih, Antoine Fakhry; AbdelRahman, Mohamed Youssef; Milanesi, Ornella; Castaldi, Biagio; Geranio, Giulia; Putti, Maria Caterina; Kharabish, Ahmed; Esmail, Reem; El‐Kamah, Ghada; Hamdy, Mona; El‐Baz, Heba; Behairy, Noha; Hanna, Carol; El‐Tagy, Hassan; Mishriky, Mary Atef;... Journal: Pediatric blood & cancer Issue: Volume 65:Issue 10(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Concise Review: Getting to the Core of Inherited Bone Marrow Failures. (4th December 2016) Authors: Adam, Soheir; Melguizo Sanchis, Dario; El‐Kamah, Ghada; Samarasinghe, Sujith; Alharthi, Sameer; Armstrong, Lyle; Lako, Majlinda Journal: Stem cells Issue: Volume 35:Number 2(2017:Feb.) Page Start: 284 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Lenz–Majewski syndrome in a patient from Egypt. Issue 10 (12th August 2019) Authors: Afifi, Hanan H.; Abdel‐Hamid, Mohamed S.; Mehrez, Mennat I.; El‐Kamah, Ghada; Abdel‐Salam, Ghada M. H. Journal: American journal of medical genetics Issue: Volume 179:Issue 10(2019) Page Start: 2039 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. Issue 6 (8th April 2020) Authors: Abdel‐Salam, Ghada M. H.; Sayed, Inas S. M.; Afifi, Hanan H.; Abdel‐Ghafar, Sherif F.; Abouzaid, Maha R.; Ismail, Samira I.; Aglan, Mona S.; Issa, Mahmoud Y.; EL‐Bassyouni, Hala T.; El‐Kamah, Ghada; Effat, Laila K.; Eid, Maha; Zaki, Maha S.; Temtamy, Samia A.; Abdel‐Hamid, Mohamed S. Journal: American journal of medical genetics Issue: Volume 182:Issue 6(2020) Page Start: 1407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine‐responsive megaloblastic anemia in an Egyptian family. Issue 7 (29th May 2019) Authors: Amr, Khalda; Pawlikowska, Patrycja; Aoufouchi, Said; Rosselli, Filippo; El‐Kamah, Ghada Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 7(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗