Search Results - "Hadi, Dina"

Goal-Directed Haemodynamic Therapy Improves Patient Outcomes in Kidney Transplantation by Fabes, Jez, Al Midani, Ammar, Sarna, Aman S, Hadi, Dina H, Naji, Saqib A, Banga, Neal R, Jones, Gareth L, Berry, Peter D, Wittenberg, Marc D

“…Introduction: Kidney transplant graft function depends on optimised haemodynamics. However, high fluid volumes risk hypervolaemic complications. The Edwards…”
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Scaling up of safety and quality improvement interventions in perioperative care: a systematic scoping review of implementation strategies and effectiveness by White, Michelle C, Ahuja, Shalini, Peven, Kimberly, McLean, Susanna Ritchie, Hadi, Dina, Okonkwo, Ijeoma, Clancy, Olivia, Turner, Maryann, Henry, Jaymie Claire Ang, Sevdalis, Nick

“…BackgroundGlobally, 5 billion people lack access to safe surgical care with more deaths due to lack of quality care rather than lack of access. While many…”
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A novel fibrillin-1 mutation in an Egyptian marfan family : a proband showing nephrotic syndrome due to focal segmental glomerulosclerosis by al-Rifai, Ahmad, Abd al-Hadi, Dina, al-Hajjar, Muhammad, Yahya, Suhayr, Hammad, Ayman, Shaltout, Ali, Sarhan, Amr, Id, Abd al-Rahman, Id, Riham, Hafiz, Muna, al-Husayni, Fatimah, Coucke, Paul J., Bakr, Ashraf, Wahba, Yahya

“…Marfan syndrome (MFS), the founding member of connective tissue disorder, is an autosomal dominant disease; it is caused by a deficiency of the microfibrillar…”
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Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi–Bickel syndrome: revisited gene atlas for renumbering by Al-Haggar, Mohammad, Sakamoto, Osamu, Shaltout, Ali, Al-Hawari, Amani, Wahba, Yahya, Abdel-Hadi, Dina

“…Background Fanconi–Bickel syndrome (FBS) is an autosomal recessive disorder caused by defects in the facilitative glucose transporter 2 (GLUT2 or SLC2A2 ) gene…”
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Fanconi Bickel Syndrome : Novel Mutations in GLUT 2 Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families by al-Haggar, Mohammad, Sakamoto, Osamu, Shaltout, Ali, El-Hawary, Amany, Wahba, Yahya, Abdel-Hady, Dina

“…Background. Fanconi-Bickel syndrome (FBS) is an autosomal recessive disorder caused by defects in facilitative glucose transporter 2 (GLUT2 or SLC2A2) gene…”
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A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome by AL-HAGGAR, Mohammad, MADEJ-PILARCZYK, Agnieszka, KOZLOWSKI, Lukasz, BUJNICKI, Janusz M, YAHIA, Sohier, ABDEL-HADI, Dina, SHAMS, Amany, AHMAD, Nermin, HAMED, Sahar, PUZIANOWSKA-KUZNICKA, Monika

“…Mandibuloacral dysplasia (MAD) is a rare disease resulting from a mutation of LMNA gene encoding lamins A and C. The most common mutation associated with this…”
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The Artemis project: Picosatellites and the feasibility of the smaller, faster, cheaper approach by Valdez, A., Hu, C., Kitts, C., Breiling, M., Slaughterbeck, A., Ota, J., Hadi, D., Kuhlman, T., Lyons, S.

“…The Santa Clara Remote Extreme Environment Mechanism (SCREEM) Laboratory is developing small satellites as part of its educational program. The cost…”
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