Economic and Clinical Burden of Managing Sickle Cell Disease with Recurrent Vaso-Occlusive Crises in the United States
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Economic and Clinical Burden of Managing Sickle Cell Disease with Recurrent Vaso-Occlusive Crises in the United States ; volume:40 ; number:8 ; day:18 ; month:6 ; year:2023 ; pages:3543-3558 ; date:8.2023
Advances in therapy ; 40, Heft 8 (18.6.2023), 3543-3558, 8.2023
- Creator
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Udeze, Chuka
Evans, Kristin A.
Yang, Yoojung
Lillehaugen, Timothy
Manjelievskaia, Janna
Mujumdar, Urvi
Li, Nanxin
Andemariam, Biree
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s12325-023-02545-7
- URN
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urn:nbn:de:101:1-2023112416394211466388
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:35 AM CEST
Data provider
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Associated
- Udeze, Chuka
- Evans, Kristin A.
- Yang, Yoojung
- Lillehaugen, Timothy
- Manjelievskaia, Janna
- Mujumdar, Urvi
- Li, Nanxin
- Andemariam, Biree
- SpringerLink (Online service)
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Risk factors for acute chest syndrome among children with sickle cell anemia hospitalized for vaso-occlusive crises
Vaso-occlusive crisis in sickle cell disease: a vicious cycle of secondary events
Association of Circulating Procoagulant Microvesicles with Painful Vaso-Occlusive Crisis in Sickle Cell Disease
Lactate dehydrogenase and hemolysis index to predict vaso-occlusive crisis in sickle cell disease
Sickle Cell Anemia Presenting with Vaso-Occlusive Pain: Should We Screen for COVID-19?
The impact of Hydroxyurea on the rates of Vaso–occlusive crises in patients with sickle cell disease in Saudi Arabia: a single–center study
The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease
Diagnosis of Bone Marrow Necrosis following Severe Vaso-Occlusive Crisis in Patient with Compound Heterozygous Sickle Cell Disease
Increased Circulating Copeptin Levels Are Associated with Vaso-Occlusive Crisis and Right Ventricular Dysfunction in Sickle Cell Anemia
A systematic literature review of frequency of vaso-occlusive crises in sickle cell disease
Correction to: Economic and Clinical Burden of Managing Sickle Cell Disease with Recurrent Vaso-Occlusive Crises in the United States
Sickle cell vaso-occlusive crisis: it’s a gut feeling
Risk factors for acute chest syndrome among children with sickle cell anemia hospitalized for vaso-occlusive crises
Vaso-occlusive crisis in sickle cell disease: a vicious cycle of secondary events
Association of Circulating Procoagulant Microvesicles with Painful Vaso-Occlusive Crisis in Sickle Cell Disease
Lactate dehydrogenase and hemolysis index to predict vaso-occlusive crisis in sickle cell disease
Sickle Cell Anemia Presenting with Vaso-Occlusive Pain: Should We Screen for COVID-19?
The impact of Hydroxyurea on the rates of Vaso–occlusive crises in patients with sickle cell disease in Saudi Arabia: a single–center study
The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease
Diagnosis of Bone Marrow Necrosis following Severe Vaso-Occlusive Crisis in Patient with Compound Heterozygous Sickle Cell Disease
Increased Circulating Copeptin Levels Are Associated with Vaso-Occlusive Crisis and Right Ventricular Dysfunction in Sickle Cell Anemia
A systematic literature review of frequency of vaso-occlusive crises in sickle cell disease
Correction to: Economic and Clinical Burden of Managing Sickle Cell Disease with Recurrent Vaso-Occlusive Crises in the United States
Sickle cell vaso-occlusive crisis: it’s a gut feeling
Risk factors for acute chest syndrome among children with sickle cell anemia hospitalized for vaso-occlusive crises
Vaso-occlusive crisis in sickle cell disease: a vicious cycle of secondary events
Association of Circulating Procoagulant Microvesicles with Painful Vaso-Occlusive Crisis in Sickle Cell Disease
Lactate dehydrogenase and hemolysis index to predict vaso-occlusive crisis in sickle cell disease
Sickle Cell Anemia Presenting with Vaso-Occlusive Pain: Should We Screen for COVID-19?
The impact of Hydroxyurea on the rates of Vaso–occlusive crises in patients with sickle cell disease in Saudi Arabia: a single–center study
The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease
Diagnosis of Bone Marrow Necrosis following Severe Vaso-Occlusive Crisis in Patient with Compound Heterozygous Sickle Cell Disease