"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 |
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1994 | 0 | 1 | 1 |
1997 | 1 | 0 | 1 |
1999 | 1 | 0 | 1 |
2000 | 2 | 0 | 2 |
2001 | 1 | 2 | 3 |
2003 | 1 | 1 | 2 |
2004 | 2 | 1 | 3 |
2005 | 2 | 0 | 2 |
2006 | 1 | 0 | 1 |
2008 | 2 | 0 | 2 |
2009 | 6 | 0 | 6 |
2010 | 6 | 1 | 7 |
2011 | 2 | 1 | 3 |
2012 | 2 | 0 | 2 |
2013 | 1 | 0 | 1 |
2014 | 3 | 1 | 4 |
2015 | 4 | 1 | 5 |
2016 | 6 | 0 | 6 |
2017 | 4 | 1 | 5 |
2018 | 8 | 0 | 8 |
2019 | 2 | 0 | 2 |
2020 | 5 | 0 | 5 |
2021 | 1 | 0 | 1 |
2022 | 5 | 0 | 5 |
2023 | 6 | 0 | 6 |
2024 | 8 | 0 | 8 |
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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A severe case of delayed transfusion reaction in a patient with sickle cell disease while preparing for allogeneic stem cell transplant. Pediatr Blood Cancer. 2024 Aug; 71(8):e31086.
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A Rare Cause of Giant Intrathoracic Mass in a Woman with Sickle Cell Disease: Extramedullary Hematopoiesis Turk J Haematol. 2024 08 28; 41(3):188-189.
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Food insecurity and quality of life in patients with sickle cell disease. Pediatr Blood Cancer. 2024 Jul; 71(7):e31045.
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Sickle Cell Disease: Past, Present, and Future. Pediatr Ann. 2024 02; 53(2):e42.
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Disease-Modifying Therapies for Sickle Cell Disease-An Overview. Pediatr Ann. 2024 Feb; 53(2):e52-e55.
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Curative Therapies for Sickle Cell Disease. Pediatr Ann. 2024 Feb; 53(2):e56-e61.
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Management of Acute Complications of Sickle Cell Disease. Pediatr Ann. 2024 Feb; 53(2):e47-e51.
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Foreword for The Role of Gene Therapy in Sickle Cell Disease and Parkinson's Disease. Dis Mon. 2024 Jul; 70(7):101688.
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An Ethical and Financial Obligation for Sickle Cell Disease Gene Therapy in the United States. Ann Intern Med. 2024 01; 177(1):85-86.
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Relative anemia and perioperative stroke in children with moyamoya. J Stroke Cerebrovasc Dis. 2024 Jan; 33(1):107476.