"Anemia, Sickle Cell" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.
| Descriptor ID |
D000755
|
| MeSH Number(s) |
C15.378.071.141.150.150 C15.378.420.155 C16.320.070.150 C16.320.365.155
|
| Concept/Terms |
Anemia, Sickle Cell- Anemia, Sickle Cell
- Anemias, Sickle Cell
- Sickle Cell Anemias
- Hemoglobin S Disease
- Disease, Hemoglobin S
- Hemoglobin S Diseases
- Sickle Cell Anemia
- Sickle Cell Disorders
- Cell Disorder, Sickle
- Cell Disorders, Sickle
- Sickle Cell Disorder
- Sickling Disorder Due to Hemoglobin S
- HbS Disease
- Sickle Cell Disease
- Cell Disease, Sickle
- Cell Diseases, Sickle
- Sickle Cell Diseases
|
Below are MeSH descriptors whose meaning is more general than "Anemia, Sickle Cell".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Anemia, Sickle Cell [C15.378.071.141.150.150]
- Hemoglobinopathies [C15.378.420]
- Anemia, Sickle Cell [C15.378.420.155]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Anemia, Sickle Cell [C16.320.070.150]
- Hemoglobinopathies [C16.320.365]
- Anemia, Sickle Cell [C16.320.365.155]
Below are MeSH descriptors whose meaning is more specific than "Anemia, Sickle Cell".
This graph shows the total number of publications written about "Anemia, Sickle Cell" by people in this website by year, and whether "Anemia, Sickle Cell" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 6 | 0 | 6 |
| 1995 | 4 | 0 | 4 |
| 1996 | 3 | 0 | 3 |
| 1997 | 5 | 0 | 5 |
| 1998 | 4 | 0 | 4 |
| 1999 | 2 | 0 | 2 |
| 2000 | 4 | 1 | 5 |
| 2001 | 8 | 0 | 8 |
| 2002 | 1 | 0 | 1 |
| 2003 | 7 | 0 | 7 |
| 2004 | 10 | 0 | 10 |
| 2005 | 6 | 0 | 6 |
| 2006 | 12 | 0 | 12 |
| 2007 | 5 | 0 | 5 |
| 2008 | 5 | 1 | 6 |
| 2009 | 7 | 1 | 8 |
| 2010 | 16 | 2 | 18 |
| 2011 | 12 | 0 | 12 |
| 2012 | 7 | 0 | 7 |
| 2013 | 6 | 0 | 6 |
| 2014 | 12 | 0 | 12 |
| 2015 | 9 | 1 | 10 |
| 2016 | 7 | 1 | 8 |
| 2017 | 9 | 2 | 11 |
| 2018 | 11 | 0 | 11 |
| 2019 | 10 | 0 | 10 |
| 2020 | 8 | 0 | 8 |
| 2021 | 12 | 0 | 12 |
| 2022 | 9 | 0 | 9 |
| 2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Anemia, Sickle Cell" by people in Profiles.
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Sickle cell disease care in Lebanon: resource-constrained and humanitarian crisis adaptations. Lancet Haematol. 2023 02; 10(2):e91-e92.
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Sleep quality and pain in adolescents and young adults with sickle cell disease. J Clin Sleep Med. 2022 Dec 01; 18(12):2845-2853.
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Characterising the prevalence of overweight and obese status among adults with sickle cell disease. Br J Haematol. 2023 03; 200(5):633-642.
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What does it mean to be affiliated with care?: Delphi consensus on the definition of "unaffiliation" and "specialist" in sickle cell disease. PLoS One. 2022; 17(11):e0272204.
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Hemorrhagic Stroke in Children and Adults With Sickle Cell Anemia: The Post-STOP Cohort. Stroke. 2022 11; 53(11):e463-e466.
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Ticagrelor vs placebo for the reduction of vaso-occlusive crises in pediatric sickle cell disease: the HESTIA3 study. Blood. 2022 09 29; 140(13):1470-1481.
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Voxelotor for the treatment of sickle cell disease in pediatric patients. Expert Rev Hematol. 2022 06; 15(6):485-492.
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Safety and efficacy of voxelotor in pediatric patients with sickle cell disease aged 4 to 11?years. Pediatr Blood Cancer. 2022 08; 69(8):e29716.
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Perspectives of individuals with sickle cell disease on barriers to care. PLoS One. 2022; 17(3):e0265342.
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Barriers and Facilitators to Chronic Red Cell Transfusion Therapy in Pediatric Sickle Cell Anemia. J Pediatr Hematol Oncol Nurs. 2022 Jul-Aug; 39(4):209-220.