المؤلفون: Musallam KM; Center for Research on Rare Blood Disorders (CR-RBD), Burjeel Medical City, Abu Dhabi, United Arab Emirates., Cappellini MD; Department of Clinical Sciences and Community, University of Milan, Ca' Granda Foundation IRCCS Maggiore Policlinico Hospital, Milan, Italy., Coates TD; Hematology Section, Cancer and Blood Disease Institute, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, CA, USA., Kuo KHM; Division of Hematology, Department of Medicine, University of Toronto, Toronto, ON, Canada., Al-Samkari H; Center for Hematology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA., Sheth S; Division of Pediatric Hematology and Oncology, Department of Pediatrics, Weill Cornell Medicine, New York, NY, USA., Viprakasit V; Department of Pediatrics & Thalassemia Center, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand., Taher AT; Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon. Electronic address: ataher@aub.edu.lb.

المصدر: Blood reviews [Blood Rev] 2024 Mar; Vol. 64, pp. 101165. Date of Electronic Publication: 2024 Jan 03.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Elsevier Country of Publication: England NLM ID: 8708558 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-1681 (Electronic) Linking ISSN: 0268960X NLM ISO Abbreviation: Blood Rev Subsets: MEDLINE

مواضيع طبية MeSH: beta-Thalassemia*/therapy , alpha-Thalassemia*/diagnosis , alpha-Thalassemia*/genetics , alpha-Thalassemia*/therapy , Hematologic Diseases* , Iron Overload*/diagnosis , Iron Overload*/etiology , Iron Overload*/therapy, Humans ; Erythropoiesis ; Erythrocyte Transfusion

المؤلفون: Musallam KM; Thalassemia Center, Burjeel Medical City, Abu Dhabi, United Arab Emirates., Lombard L; Agios Pharmaceuticals, Cambridge, Massachusetts, USA., Kistler KD; Xcenda LLC, Carrollton, Texas, USA., Arregui M; Xcenda LLC, Carrollton, Texas, USA., Gilroy KS; Agios Pharmaceuticals, Cambridge, Massachusetts, USA., Chamberlain C; Agios Pharmaceuticals, Cambridge, Massachusetts, USA., Zagadailov E; Agios Pharmaceuticals, Cambridge, Massachusetts, USA., Ruiz K; Xcenda LLC, Carrollton, Texas, USA., Taher AT; Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

المصدر: American journal of hematology [Am J Hematol] 2023 Sep; Vol. 98 (9), pp. 1436-1451. Date of Electronic Publication: 2023 Jun 26.

نوع المنشور: Systematic Review; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-8652 (Electronic) Linking ISSN: 03618609 NLM ISO Abbreviation: Am J Hematol Subsets: MEDLINE

مواضيع طبية MeSH: alpha-Thalassemia*/epidemiology , beta-Thalassemia*/epidemiology , Hemoglobins, Abnormal*, Pregnancy ; Female ; Humans ; Prenatal Diagnosis/methods ; Hydrops Fetalis/diagnosis ; Asia

المؤلفون: Taher AT; American University of Beirut Medical Center, Beirut, Lebanon ataher@aub.edu.lb., Musallam KM; International Network of Hematology, London, United Kingdom., Cappellini MD; University of Milan, Milan, Italy.

المصدر: The New England journal of medicine [N Engl J Med] 2021 Jun 03; Vol. 384 (22), pp. 2166.

نوع المنشور: Letter; Comment

بيانات الدورية: Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print Cited Medium: Internet ISSN: 1533-4406 (Electronic) Linking ISSN: 00284793 NLM ISO Abbreviation: N Engl J Med Subsets: MEDLINE

مواضيع طبية MeSH: alpha-Thalassemia* , beta-Thalassemia*/therapy, Humans

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