Search Results - "TAHER, Ali"

Thalassaemia by Taher, Ali T, Weatherall, David J, Cappellini, Maria Domenica

“…Inherited haemoglobin disorders, including thalassaemia and sickle-cell disease, are the most common monogenic diseases worldwide. Several clinical forms of…”
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How I manage medical complications of β-thalassemia in adults by Taher, Ali T., Cappellini, Maria Domenica

“…The complex pathophysiology in β-thalassemia can translate to multiple morbidities that affect every organ system. Improved survival due to advances in…”
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β-Thalassemias by Taher, Ali T, Musallam, Khaled M, Cappellini, M. Domenica

“…Defective synthesis of the β-globin chain causes recessively inherited disorders characterized by inadequate hemoglobin production and chronic anemia…”
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Iron overload in thalassemia: different organs at different rates by Taher, Ali T, Saliba, Antoine N

“…Thalassemic disorders lie on a phenotypic spectrum of clinical severity that depends on the severity of the globin gene mutation and coinheritance of other…”
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Beta Thalassemia: New Therapeutic Options Beyond Transfusion and Iron Chelation by Motta, Irene, Bou-Fakhredin, Rayan, Taher, Ali T., Cappellini, Maria Domenica

“…Hemoglobinopathies are among the most common monogenic diseases worldwide. Approximately 1–5% of the global population are carriers for a genetic thalassemia…”
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Non-Transfusion-Dependent Thalassemia: An Update on Complications and Management by Sleiman, Joseph, Tarhini, Ali, Bou-Fakhredin, Rayan, Saliba, Antoine N, Cappellini, Maria Domenica, Taher, Ali T

“…Patients with non-transfusion-dependent thalassemia (NTDT) experience many clinical complications despite their independence from frequent transfusions…”
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Assessment of X-ray films and image quality in diagnostic radiology departments of teaching hospitals in Iraq by Taher Ali, Ronak

“…Background: Patients undergo repeated X-ray examinations after their initial X-ray radiographs are rejected due to poor image quality. Reject analysis in…”
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Iron deficiency beyond erythropoiesis: should we be concerned? by Musallam, Khaled M., Taher, Ali T.

“…Objective: To consider the key implications of iron deficiency for biochemical and physiological functions beyond erythropoiesis. Methods: PubMed was searched…”
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A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies? by Cappellini, Maria Domenica, Porter, John B., Viprakasit, Vip, Taher, Ali T.

“…Beta-thalassaemia causes defective haemoglobin synthesis leading to ineffective erythropoiesis, chronic haemolytic anaemia, and subsequent clinical…”
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Luspatercept for β-thalassemia: beyond red blood cell transfusions by Taher, Ali T, Cappellini, Maria Domenica

“…Red blood cell transfusions and iron chelation therapy are the cornerstone of treatment for β-thalassemia, with allogeneic hematopoietic stem cell…”
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Iron deficiency across chronic inflammatory conditions: International expert opinion on definition, diagnosis, and management by Cappellini, Maria Domenica, Comin-Colet, Josep, de Francisco, Angel, Dignass, Axel, Doehner, Wolfram, Lam, Carolyn S, Macdougall, Iain C, Rogler, Gerhard, Camaschella, Clara, Kadir, Rezan, Kassebaum, Nicholas J, Spahn, Donat R, Taher, Ali T, Musallam, Khaled M

“…Iron deficiency, even in the absence of anemia, can be debilitating, and exacerbate any underlying chronic disease, leading to increased morbidity and…”
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Paraspinal extramedullary hematopoiesis in patients with thalassemia intermedia by Haidar, Rachid, Mhaidli, Hani, Taher, Ali T.

“…Ineffective erythropoiesis in patients with thalassemia intermedia drives extramedullary hematopoietic tumor formation in several parts of the body. Paraspinal…”
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Thalassaemia—A global view by Hokland, Peter, Daar, Shahina, Khair, Wael, Sheth, Sujit, Taher, Ali T., Torti, Lorenza, Hantaweepant, Chattree, Rund, Deborah

“…Summary The thalassaemias are a group of genetic disorders of haemoglobin which are endemic in the tropics but are now found worldwide due to migration. Basic…”
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Preoperative anaemia and postoperative outcomes in non-cardiac surgery: a retrospective cohort study by Musallam, Khaled M, MD, Tamim, Hani M, PhD, Richards, Toby, MD, Spahn, Donat R, Prof, Rosendaal, Frits R, Prof, Habbal, Aida, BSN, Khreiss, Mohammad, MD, Dahdaleh, Fadi S, MD, Khavandi, Kaivan, MD, Sfeir, Pierre M, MD, Soweid, Assaad, MD, Hoballah, Jamal J, Prof, Taher, Ali T, Prof, Jamali, Faek R, Dr

“…Summary Background Preoperative anaemia is associated with adverse outcomes after cardiac surgery but outcomes after non-cardiac surgery are not well…”
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How I treat non-transfusion-dependent β-thalassemia by Saliba, Antoine N., Musallam, Khaled M., Taher, Ali T.

“…[Display omitted] The intricate interplay of anemia and iron overload under the pathophysiological umbrella of ineffective erythropoiesis in…”
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Hepatocellular carcinoma as an emerging morbidity in the thalassemia syndromes: A comprehensive review by Moukhadder, Hassan M., Halawi, Racha, Cappellini, Maria Domenica, Taher, Ali T.

“…The incidence of hepatocellular carcinoma (HCC) in patients with thalassemia is on the rise. The 2 well recognized HCC risk factors in thalassemia are iron…”
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Variations in hemoglobin level and morbidity burden in non-transfusion-dependent β-thalassemia by Musallam, Khaled M., Cappellini, Maria Domenica, Taher, Ali T.

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2021 update on clinical trials in β‐thalassemia by Musallam, Khaled M., Bou‐Fakhredin, Rayan, Cappellini, Maria Domenica, Taher, Ali T.

“…The treatment landscape for patients with β‐thalassemia is witnessing a swift evolution, yet several unmet needs continue to persist. Patients with…”
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Ineffective Erythropoiesis: Anemia and Iron Overload by Gupta, Ritama, PhD, Musallam, Khaled M., MD, PhD, Taher, Ali T., MD, PhD, FRCP, Rivella, Stefano, PhD

“…Stress erythropoiesis (SE) is characterized by an imbalance in erythroid proliferation and differentiation under increased demands of erythrocyte generation…”
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Management of luspatercept therapy in patients with transfusion‐dependent β‐thalassaemia by Sheth, Sujit, Taher, Ali T., Coates, Thomas D., Kattamis, Antonis, Cappellini, Maria Domenica

“…Summary Patients with transfusion‐dependent β‐thalassaemia require lifelong, regular red blood cell transfusions for survival; however, frequent blood…”
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