Search Results - Ali Alsafi

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  1. 1

    Cerebral Venous Sinus Thrombosis, a Nonenhanced CT Diagnosis? by Ali Alsafi, Amish Lakhani, Lalani Carlton Jones, Kyriakos Lobotesis

    Published in Radiology Research and Practice (2015-01-01)
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  2. 2

    Changes in Renal Function in Elderly Patients Following Intravenous Iodinated Contrast Administration: A Retrospective Study by Ali Alsafi, Zaid Alsafi, Amish Lakhani, Nicola H. Strickland

    Published in Radiology Research and Practice (2014-01-01)
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  3. 3

    Foundation Doctors’ Exposure to Interventional Radiology in Two Large Teaching Hospitals in the United Kingdom by Zaid Alsafi, Sanjeev Ramachandran, Vamsee Bhrugubanda, Alison Graham, Ali Alsafi

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  4. 4

    Splenic Artery Embolisation for the Emergency Treatment of Sinistral Portal Hypertension: A Systematic Review by Harriet Grout-Smith, Ozbil Dumenci, N. Paul Tait, Ali Alsafi

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  5. 5

    Elective Thoracic Surgical Resections for Pulmonary Arteriovenous Malformations ‐ A 16 Year Single‐Center Experience by May Al‐Sahaf, Jon Anderson, Jayanta Nandi, Ali Alsafi, Claire L. Shovlin

    Published in Pulmonary Circulation (2025-01-01)
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  6. 6

    Adrenal Vein Sampling: Radiation Dose Reduction on New Angiography Platform by Ali Alsafi, Florian Wernig, Jeannie Todd, Tricia Tan, F. Fausto Palazzo, Karim Meeran, James E. Jackson

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  7. 7

    A rare cause of severe Cushing’s syndrome by Shamaila Zaman, Bijal Patel, Paul Glynne, Mark Vanderpump, Ali Alsafi, Sairah Khan, Rashpal Flora, Fausto Palazzo, Florian Wernig

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  8. 8

    Case selection of adrenal vein sampling in young patients with primary aldosteronism: a retrospective analysis of imaging and AVS concordance, and histopathological outcomes by Zin Htut, Namir Asmar, Joshua Agilinko, Rashpal Flora, Fausto Palazzo, Aimee Di Marco, Jeannie Todd, Karim Meeran, Florian Wernig, Ali Alsafi

    Published in Endocrine Connections (2025-09-01)
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  9. 9

    European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) by Omer F. Eker, Edoardo Boccardi, Ulrich Sure, Maneesh C. Patel, Saverio Alicante, Ali Alsafi, Nicola Coote, Freya Droege, Olivier Dupuis, Annette Dam Fialla, Bryony Jones, Ujwal Kariholu, Anette D. Kjeldsen, David Lefroy, Gennaro M. Lenato, Hans Jurgen Mager, Guido Manfredi, Troels H. Nielsen, Fabio Pagella, Marco C. Post, Catherine Rennie, Carlo Sabbà, Patrizia Suppressa, Pernille M. Toerring, Sara Ugolini, Elisabetta Buscarini, Sophie Dupuis-Girod, Claire L. Shovlin

    Published in Orphanet Journal of Rare Diseases (2020-06-01)
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