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For: Badawy SM, Liem RI, Rigsby CK, Labotka RJ, Defreitas RA, Thompson AA. Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease. Br J Haematol 2016;175:705-13. [DOI: 10.1111/bjh.14277] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Hsu CC, Senussi NH, Fertrin KY, Kowdley KV. Iron overload disorders. Hepatol Commun 2022. [PMID: 35699322 DOI: 10.1002/hep4.2012] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Stępniak J, Rynkowska A, Karbownik-lewińska M. Membrane Lipids in the Thyroid Comparing to Those in Non-Endocrine Tissues Are Less Sensitive to Pro-Oxidative Effects of Fenton Reaction Substrates. Front Mol Biosci 2022;9:901062. [DOI: 10.3389/fmolb.2022.901062] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Won S, Kim J. The detection of Fe (III) and ascorbic acid by fluorescence quenching and recovery of carbon dots prepared from coffee waste. Korean J Chem Eng . [DOI: 10.1007/s11814-022-1138-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Shin H, Jannah F, Yoo EJ, Kim J. A colorimetric and fluorescence “turn-on” sensor for Fe(III) ion based on imidazole-functionalized polydiacetylene. Sensors and Actuators B: Chemical 2022;350:130885. [DOI: 10.1016/j.snb.2021.130885] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 10.0] [Reference Citation Analysis]
5 Badawy SM, Cronin RM, Liem RI, Palermo TM. Digital behavioural interventions for people with sickle cell disease. Cochrane Libr 2021;2021. [PMID: 34650329 DOI: 10.1002/14651858.CD014669] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Badawy SM, Payne AB, Hulihan MM, Coates TD, Majumdar S, Smith D, Thompson AA. Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiving chronic transfusions: an analysis from the Centers for Disease Control haemoglobinopathy blood safety project. Br J Haematol 2021. [PMID: 34431082 DOI: 10.1111/bjh.17798] [Reference Citation Analysis]
7 Allali S, Taylor M, Brice J, Montalembert M. Chronic organ injuries in children with sickle cell disease. Haematologica 2021;106:1535-44. [PMID: 33626864 DOI: 10.3324/haematol.2020.271353] [Reference Citation Analysis]
8 Friedman D, Dozor AJ, Milner J, D'Souza M, Talano JA, Moore TB, Shenoy S, Shi Q, Walters MC, Vichinsky E, Parsons SK, Braniecki S, Moorthy CR, Ayello J, Flower A, Morris E, Mahanti H, Fabricatore S, Klejmont L, van de Ven C, Baxter-Lowe LA, Cairo MS. Stable to improved cardiac and pulmonary function in children with high-risk sickle cell disease following haploidentical stem cell transplantation. Bone Marrow Transplant 2021;56:2221-30. [PMID: 33958740 DOI: 10.1038/s41409-021-01298-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
9 Jhaveri S, Choueiter N, Manwani D, Ranabothu S, Morrone K, Hafeman M, Reidy K, Kaskel F, Mahgerefteh J. Association of Anemia and Blood Pressure With Novel Markers of Diastolic Function in Pediatric Sickle Cell Disease. J Pediatr Hematol Oncol 2021;43:e486-93. [PMID: 33625076 DOI: 10.1097/MPH.0000000000002104] [Reference Citation Analysis]
10 Ryan TD, Moore RA, Lang SM, Khoury P, Dandoy CE, Davies SM, Taylor MD. Rapid cardiac MRI protocol for cardiac assessment in paediatric and young adult patients undergoing haematopoietic stem cell transplant: a feasibility study. Cardiol Young 2021;31:973-8. [DOI: 10.1017/s1047951120004990] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Praharaj DL, Anand AC. Sickle Hepatopathy. J Clin Exp Hepatol 2021;11:82-96. [PMID: 33679049 DOI: 10.1016/j.jceh.2020.08.003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
12 Le TH, Lee HJ, Kim JH, Park SJ. Detection of Ferric Ions and Catecholamine Neurotransmitters via Highly Fluorescent Heteroatom Co-Doped Carbon Dots. Sensors (Basel) 2020;20:E3470. [PMID: 32575578 DOI: 10.3390/s20123470] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
13 Mangaonkar AA, Thawer F, Son J, Ajebo G, Xu H, Barrett NJ, Wells LG, Bowman L, Clair B, Patel N, Bora P, Jung G, Nemeth E, Kutlar A. Regulation of iron homeostasis through the erythroferrone-hepcidin axis in sickle cell disease. Br J Haematol 2020;189:1204-9. [PMID: 32030737 DOI: 10.1111/bjh.16498] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
14 Puri L, Flanagan JM, Kang G, Ding J, Bi W, McCarville BM, Loeffler RB, Tipirneni-Sajja A, Villavicencio M, Crews KR, Hillenbrand CM, Hankins JS. GSTM1 and Liver Iron Content in Children with Sickle Cell Anemia and Iron Overload. J Clin Med 2019;8:E1878. [PMID: 31694285 DOI: 10.3390/jcm8111878] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
15 Ben Yakov G, Sharma D, Alao H, Surana P, Kapuria D, Etzion O, Hsieh MM, Tisdale JF, Fitzhugh CD, Kleiner DE, Levy EB, Chang R, Rivera E, Huang A, Koh C, Heller T. Vibration Controlled Transient Elastography (Fibroscan®) in sickle cell liver disease - could we strike while the liver is hard? Br J Haematol 2019;187:117-23. [PMID: 31218662 DOI: 10.1111/bjh.16047] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
16 Tavares AHJ, Benites BD, Fertrin KY. Myocardial Iron Overload in Sickle Cell Disease: A Rare But Potentially Fatal Complication of Transfusion. Transfus Med Rev 2019;33:170-5. [PMID: 31153715 DOI: 10.1016/j.tmrv.2019.04.001] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Díez-López C, Comín-Colet J, González-Costello J. Iron overload cardiomyopathy: from diagnosis to management. Curr Opin Cardiol 2018;33:334-40. [PMID: 29543671 DOI: 10.1097/HCO.0000000000000511] [Cited by in Crossref: 12] [Cited by in F6Publishing: 15] [Article Influence: 4.0] [Reference Citation Analysis]
18 Theocharidou E, Suddle AR. The Liver in Sickle Cell Disease. Clinics in Liver Disease 2019;23:177-89. [DOI: 10.1016/j.cld.2018.12.002] [Cited by in Crossref: 13] [Cited by in F6Publishing: 18] [Article Influence: 4.3] [Reference Citation Analysis]
19 Antmen B, Karakaş Z, Yeşilipek MA, Küpesiz OA, Şaşmaz İ, Uygun V, Kurtoğlu E, Oktay G, Aydogan G, Akın M, Salcioglu Z, Vergin C, Kazancı EG, Ünal S, Çalışkan Ü, Aral YZ, Türkkan E, Meral Güneş A, Tunç B, Gümrük F, Ayhan AC, Söker M, Koç A, Oymak Y, Ertem M, Timur Ç, Yıldırmak Y, İrken G, Apak H, Biner B, Eren TG, Işık Balcı Y, Koçak Ü, Karasu G, Akkaynak D, Patıroğlu T. Deferasirox in children with transfusion‐dependent thalassemia or sickle cell anemia: A large cohort real‐life experience from Turkey (REACH‐THEM). Eur J Haematol 2018;102:123-30. [DOI: 10.1111/ejh.13180] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
20 Voskaridou E, Kattamis A, Fragodimitri C, Kourakli A, Chalkia P, Diamantidis M, Vlachaki E, Drosou M, Lafioniatis S, Maragkos K, Petropoulou F, Eftihiadis E, Economou M, Klironomos E, Koutsouka F, Nestora K, Tzoumari I, Papageorgiou O, Basileiadi A, Lafiatis I, Dimitriadou E, Kalpaka A, Kalkana C, Xanthopoulidis G, Adamopoulos I, Kaiafas P, Mpitzioni A, Goula A, Kontonis I, Alepi C, Anastasiadis A, Papadopoulou M, Maili P, Dionisopoulou D, Tsirka A, Makis A, Kostaridou S, Politou M, Papassotiriou I; on behalf of the Greek Haemoglobinopathies Study Group. National registry of hemoglobinopathies in Greece: updated demographics, current trends in affected births, and causes of mortality. Ann Hematol 2019;98:55-66. [DOI: 10.1007/s00277-018-3493-4] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 4.3] [Reference Citation Analysis]
21 Latus H, Voges I. Quantitative Tissue Characterization in Pediatric Cardiology. Curr Cardiovasc Imaging Rep 2017;10. [DOI: 10.1007/s12410-017-9405-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
22 Azar S, Wong TE. Sickle Cell Disease. Medical Clinics of North America 2017;101:375-93. [DOI: 10.1016/j.mcna.2016.09.009] [Cited by in Crossref: 39] [Cited by in F6Publishing: 38] [Article Influence: 7.8] [Reference Citation Analysis]
23 Shenoy S, Angelucci E, Arnold SD, Baker KS, Bhatia M, Bresters D, Dietz AC, De La Fuente J, Duncan C, Gaziev J, King AA, Pulsipher MA, Smith AR, Walters MC. Current Results and Future Research Priorities in Late Effects after Hematopoietic Stem Cell Transplantation for Children with Sickle Cell Disease and Thalassemia: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric Hematopoietic Stem Cell Transplantation. Biol Blood Marrow Transplant 2017;23:552-61. [PMID: 28065838 DOI: 10.1016/j.bbmt.2017.01.009] [Cited by in Crossref: 33] [Cited by in F6Publishing: 48] [Article Influence: 6.6] [Reference Citation Analysis]
24 Oduor H, Minniti CP, Brofferio A, Gharib AM, Abd-Elmoniem KZ, Hsieh MM, Tisdale JF, Fitzhugh CD. Severe cardiac iron toxicity in two adults with sickle cell disease. Transfusion 2017;57:700-4. [PMID: 28019032 DOI: 10.1111/trf.13961] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis]