Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review
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Published in | Pediatric blood & cancer Vol. 69; no. 9; pp. e29629 - n/a |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.09.2022
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Author | Baharin, Mohd Farid Abdul Hamid, Faidatul Syazlin Hashim, Hafizah Ahmad, Rahimah Nadarajaw, Thiyagar Aziz, Aisyah Fauzi, Muhammad Yusri |
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Cites_doi | 10.3109/03630269.2012.747441 10.1016/j.bcmd.2011.12.002 10.1177/0267659107084143 10.5555/URI:PII:0022214375904862 10.1002/PRCA.200900073 10.1089/109065701753617471 10.1101/cshperspect.a011734 10.1007/BF01698489 10.3109/03630267809005343 10.3109/03630269.2012.703980 10.1373/49.10.1679 10.1016/0005‐2795(75)90034‐3 10.3109/03630269209005679 10.1182/asheducation‐2007.1.79 10.1182/BLOOD.V69.1.1.1 10.1080/00313020600922538 10.1016/j.blre.2018.02.001 10.1016/0022‐2836(74)90337‐4 10.1371/journal.pone.0081820 10.1177/003591577306600607 10.1016/0005‐2795(77)90115‐5 |
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References | e_1_2_1_4_10_1 e_1_2_1_4_4_1 e_1_2_1_4_26_1 e_1_2_1_4_5_1 e_1_2_1_4_27_1 e_1_2_1_4_6_1 e_1_2_1_4_7_1 e_1_2_1_4_9_1 e_1_2_1_4_22_1 e_1_2_1_4_8_1 e_1_2_1_4_23_1 Thein SL (e_1_2_1_4_18_1) 2005; 90 e_1_2_1_4_24_1 e_1_2_1_4_25_1 e_1_2_1_4_2_1 e_1_2_1_4_3_1 e_1_2_1_4_20_1 e_1_2_1_4_21_1 e_1_2_1_4_14_1 e_1_2_1_4_12_1 e_1_2_1_4_11_1 e_1_2_1_4_17_1 e_1_2_1_4_16_1 e_1_2_1_4_15_1 Hassan S (e_1_2_1_4_13_1) 2013; 20 e_1_2_1_4_19_1 |
References_xml | – ident: e_1_2_1_4_16_1 doi: 10.3109/03630269.2012.747441 – ident: e_1_2_1_4_21_1 doi: 10.1016/j.bcmd.2011.12.002 – ident: e_1_2_1_4_11_1 doi: 10.1177/0267659107084143 – ident: e_1_2_1_4_19_1 doi: 10.5555/URI:PII:0022214375904862 – ident: e_1_2_1_4_23_1 doi: 10.1002/PRCA.200900073 – ident: e_1_2_1_4_15_1 doi: 10.1089/109065701753617471 – ident: e_1_2_1_4_6_1 – ident: e_1_2_1_4_3_1 doi: 10.1101/cshperspect.a011734 – volume: 90 start-page: 649 issue: 5 year: 2005 ident: e_1_2_1_4_18_1 article-title: Genetic modifiers of β‐thalassemia publication-title: Haematologica contributor: fullname: Thein SL – ident: e_1_2_1_4_10_1 doi: 10.1007/BF01698489 – ident: e_1_2_1_4_8_1 doi: 10.3109/03630267809005343 – ident: e_1_2_1_4_12_1 doi: 10.3109/03630269.2012.703980 – ident: e_1_2_1_4_14_1 doi: 10.1373/49.10.1679 – ident: e_1_2_1_4_25_1 doi: 10.1016/0005‐2795(75)90034‐3 – ident: e_1_2_1_4_27_1 – ident: e_1_2_1_4_5_1 – ident: e_1_2_1_4_9_1 doi: 10.3109/03630269209005679 – volume: 20 start-page: 13 issue: 1 year: 2013 ident: e_1_2_1_4_13_1 article-title: Detection of β‐globin gene mutations among β‐thalassaemia carriers and patients in malaysia: application of multiplex amplification refractory mutation system‐polymerase chain reaction publication-title: Malays J Med Sci contributor: fullname: Hassan S – ident: e_1_2_1_4_2_1 doi: 10.1182/asheducation‐2007.1.79 – ident: e_1_2_1_4_20_1 doi: 10.1182/BLOOD.V69.1.1.1 – ident: e_1_2_1_4_17_1 doi: 10.1080/00313020600922538 – ident: e_1_2_1_4_4_1 doi: 10.1016/j.blre.2018.02.001 – ident: e_1_2_1_4_26_1 doi: 10.1016/0022‐2836(74)90337‐4 – ident: e_1_2_1_4_22_1 doi: 10.1371/journal.pone.0081820 – ident: e_1_2_1_4_7_1 doi: 10.1177/003591577306600607 – ident: e_1_2_1_4_24_1 doi: 10.1016/0005‐2795(77)90115‐5 |
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Title | Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review |
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