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Feb 8, 2016 (publication date) through May 5, 2024
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Publication Name
World Journal of Clinical Pediatrics
ISSN
2219-2808
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Iughetti L, Bigi E, Venturelli D. Novel insights in the management of sickle cell disease in childhood. World J Clin Pediatr 2016; 5(1): 25-34 [PMID: 26862499 DOI: 10.5409/wjcp.v5.i1.25] |
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| URL: | https://www.wjgnet.com/2219-2808/full/v5/i1/25.htm |
| Number | Citing Articles |
| 1 |
Sawsan M. Moeen, Ahmad F. Thabet, Hosam A. Hasan, Medhat A. Saleh. Lower Transcranial Doppler Flow Velocities in Sickle Cell Anemia Patients on Hydroxyurea: Myth or Fact. Indian Journal of Hematology and Blood Transfusion 2018; 34(1): 97 doi: 10.1007/s12288-017-0814-z
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| 2 |
HayfaaMohammed Mones, MeaadKadhum Hassan, BahaaAbd Al Hussein Ahmed. Health-related quality of life of adolescents with sickle cell disease on hydroxyurea: A case-control study. Journal of Applied Hematology 2022; 13(1): 13 doi: 10.4103/joah.joah_7_21
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| 3 |
Larissa C. Rocha, Magda O. S. Carvalho, Valma M. L. Nascimento, Milena S. dos Santos, Tânia F. Barros, Elisângela V. Adorno, Joice N. Reis, Caroline C. da Guarda, Rayra P. Santiago, Marilda de Souza Gonçalves. Nasopharyngeal and Oropharyngeal Colonization by Staphylococcus aureus and Streptococcus pneumoniae and Prognostic Markers in Children with Sickle Cell Disease from the Northeast of Brazil. Frontiers in Microbiology 2017; 8 doi: 10.3389/fmicb.2017.00217
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| 4 |
V. Mandese, E. Bigi, P. Bruzzi, G. Palazzi, B. Predieri, L. Lucaccioni, M. Cellini, L. Iughetti. Endocrine and metabolic complications in children and adolescents with Sickle Cell Disease: an Italian cohort study. BMC Pediatrics 2019; 19(1) doi: 10.1186/s12887-019-1423-9
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| 5 |
Fellipe Bondança Pereira, Glaura César Pedroso, Rosa Miranda Resegue, Marcos Vinicius Vieira Ribeiro, Mary Hokazono, Josefina Aparecida Pellegrini Braga. BEHAVIORAL CHARACTERISTICS OF CHILDREN WITH SICKLE CELL DISEASE. Revista Paulista de Pediatria 2021; 39 doi: 10.1590/1984-0462/2021/39/2019341
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| 6 |
Sarah L. Reeves, Hannah K. Peng, Jeffrey J. Wing, Lindsay W. Cogan, Alka Goel, David Anders, Nancy S. Green, Lynda D. Lisabeth, Kevin J. Dombkowski. Changes in Hydroxyurea Use Among Youths Enrolled in Medicaid With Sickle Cell Anemia After 2014 Revision of Clinical Guidelines. JAMA Network Open 2023; 6(3): e234584 doi: 10.1001/jamanetworkopen.2023.4584
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| 7 |
Elaine Cristina Rodrigues Gesteira, Regina Szylit, Maiara Rodrigues dos Santos, Carolliny Rossi de FariaIchikawa, Patricia Peres de Oliveira, Edilene Aparecida Araújo Silveira. Family management ofchildren who experience sickle cell disease: a qualitative study. Revista Brasileira de Enfermagem 2020; 73( suppl 4) doi: 10.1590/0034-7167-2019-0521
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| 8 |
Emmanuel Ifeanyi Obeagu, Getrude Uzoma Obeagu. Management of diabetes mellitus patients with sickle cell anemia: Challenges and therapeutic approaches. Medicine 2024; 103(17): e37941 doi: 10.1097/MD.0000000000037941
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| 9 |
Narjeet Khurmi, Andrew Gorlin, Lopa Misra. Perioperative considerations for patients with sickle cell disease: a narrative review. Canadian Journal of Anesthesia/Journal canadien d'anesthésie 2017; 64(8): 860 doi: 10.1007/s12630-017-0883-3
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| 10 |
Milena Magalhães Aleluia, Caroline Conceição da Guarda, Rayra Pereira Santiago, Teresa Cristina Cardoso Fonseca, Fábia Idalina Neves, Regiana Quinto de Souza, Larissa Alves Farias, Felipe Araújo Pimenta, Luciana Magalhães Fiuza, Thassila Nogueira Pitanga, Júnia Raquel Dutra Ferreira, Elisângela Vitória Adorno, Bruno Antônio Veloso Cerqueira, Marilda de Souza Gonçalves. Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia. Lipids in Health and Disease 2017; 16(1) doi: 10.1186/s12944-017-0454-1
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| 11 |
Faramarz Naeim, P. Nagesh Rao, Sophie X. Song, Ryan T. Phan. Atlas of Hematopathology. 2008; : 885 doi: 10.1016/B978-0-12-809843-1.00064-4
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| 12 |
Sarah L. Reeves, Hannah K. Jary, Jennifer P. Gondhi, Jean L. Raphael, Lynda D. Lisabeth, Kevin J. Dombkowski. Hydroxyurea Initiation Among Children With Sickle Cell Anemia. Clinical Pediatrics 2019; 58(13): 1394 doi: 10.1177/0009922819850476
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| 13 |
Aimé Lukusa Kazadi, René Makuala Ngiyulu, Jean Lambert Gini-Ehungu, Jean Marie Mbuyi-Muamba, Michel Ntetani Aloni. Factors Associated with Growth Retardation in Children Suffering from Sickle Cell Anemia: First Report from Central Africa. Anemia 2017; 2017: 1 doi: 10.1155/2017/7916348
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| 14 |
Talal Qadah. The Effect of Fetal Hemoglobin on RBC Parameters among Sickle Cell Anemia Patients: A Cross Sectional Study from Makkah City; Western Saudi Arabia. Hematology & Transfusion International Journal 2016; 3(1) doi: 10.15406/htij.2016.03.00059
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| 15 |
Bertin Tshimanga Kadima, Jean Lambert Gini‐Ehungu, Fiston Ikwa Ndol Mbutiwi, John Tunda Bahati, Michel Ntetani Aloni. Validity of simple clinical and biological parameters as screening tool for sickle cell anemia for referral to tertiary center in highly resource constraints. Journal of Clinical Laboratory Analysis 2017; 31(6) doi: 10.1002/jcla.22145
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| 16 |
Sherif M. Badawy. Fetal hemoglobin level and nutritional status in patients with sickle cell disease. Nutrition Journal 2015; 15(1) doi: 10.1186/s12937-016-0181-x
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| 17 |
Sahar Alrayyes, Anne-Ashley Compton, Nadia Kawar. Oral health considerations for pediatric patients with sickle cell disease. Disease-a-Month 2018; 64(6): 302 doi: 10.1016/j.disamonth.2017.12.006
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| 18 |
Stephen Otieno Gwer, Kennedy Odoyo Onyango. Prevalence and incidence of congenital anomalies amongst babies born to women with sickle cell disease and exposed to hydroxyurea during pregnancy: a systematic review protocol. JBI Database of Systematic Reviews and Implementation Reports 2018; 16(5): 1135 doi: 10.11124/JBISRIR-2017-003548
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| 19 |
Baba Psalm Duniya Inusa, Wale Atoyebi, Abdul Aziz Hassan, Tushar Idhate, Livingstone Dogara, Ifeoma Ijei, Yewen Qin, Kofi Anie, Juliana Olufunke Lawson, Lewis Hsu. Low-dose hydroxycarbamide therapy may offer similar benefit as maximum tolerated dose for children and young adults with sickle cell disease in low-middle-income settings. F1000Research 2018; 7: 1407 doi: 10.12688/f1000research.14589.1
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| 20 |
Liliane K. Siransy, Romuald S. Dasse, Honoré Adou, Patricia Kouacou, Sidonie Kouamenan, Yassongui Sekongo, Richard Yeboah, Charlene Memel, Aniella Assi-Sahoin, Salimata Y. Moussa, Doris Oura, Jocelyne Seri. Are IL-1 family cytokines important in management of sickle cell disease in Sub-Saharan Africa patients?. Frontiers in Immunology 2023; 14 doi: 10.3389/fimmu.2023.954054
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| 21 |
Sylvia Thurn, Katharina Kleinschmidt, Irena Kovacic, Christina Wendl, Ralf A. Linker, Selim Corbacioglu, Felix Schlachetzki. Transcranial Doppler sonography and the effect of haematopoietic stem cell transplantation in sickle cell disease. Neurological Research and Practice 2022; 4(1) doi: 10.1186/s42466-022-00175-y
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| 22 |
Clark Brown, Modupe Idowu, Richard Drachtman, Anne Beaubrun, Irene Agodoa, Andy Nguyen, Kelly Lipman, Olga Moshkovich, Ryan Murphy, M. Alex Bellenger, Wally Smith, Krzysztof Siemianowicz. Patient-Reported Experiences in Voxelotor-Treated Children and Adults with Sickle Cell Disease: A Semistructured Interview Study. BioMed Research International 2023; 2023: 1 doi: 10.1155/2023/7533111
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