Prevalence and Genetic Analysis of α- and β-Thalassemia and Sickle Cell Anemia in Southwest Iran
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Prevalence and Genetic Analysis of α- and β-Thalassemia and Sickle Cell Anemia in Southwest Iran ; volume:8 ; number:3-4 ; day:31 ; month:12 ; year:2018 ; pages:189-195 ; date:12.2018
Journal of epidemiology and global health ; 8, Heft 3-4 (31.12.2018), 189-195, 12.2018
- Creator
-
Nezhad, Forozan H.
Nezhad, Khojasteh H.
Choghakabodi, Parastoo M.
Keikhaei, Bijan
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.2991/j.jegh.2018.04.103
- URN
-
urn:nbn:de:101:1-2024032208581751400518
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Nezhad, Forozan H.
- Nezhad, Khojasteh H.
- Choghakabodi, Parastoo M.
- Keikhaei, Bijan
- SpringerLink (Online service)
Other Objects (12)
A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
Plasminogen activator inhibitor-2 and impaired fibrinolysis in pregnancy and sickle cell anemia
Coexistent sickle-cell anemia and autoimmune disease in eight children: pitfalls and challenges
Biventricular dimensions and function in pediatric sickle-cell disease and thalassemia major patients without cardiac iron
Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Biophysical chemistry behind sickle cell anemia and the mechanism of voxelotor action
Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia
Conventional and advanced brain MR imaging in patients with sickle cell anemia
Parvovirus B19 infection in Tunisian patients with sickle-cell anemia and acute erythroblastopenia
Differential expression of adhesion molecules in sickle cell anemia and gut microbiome effect
A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
Plasminogen activator inhibitor-2 and impaired fibrinolysis in pregnancy and sickle cell anemia
Coexistent sickle-cell anemia and autoimmune disease in eight children: pitfalls and challenges
Biventricular dimensions and function in pediatric sickle-cell disease and thalassemia major patients without cardiac iron
Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Biophysical chemistry behind sickle cell anemia and the mechanism of voxelotor action
Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia
Conventional and advanced brain MR imaging in patients with sickle cell anemia
Parvovirus B19 infection in Tunisian patients with sickle-cell anemia and acute erythroblastopenia
Differential expression of adhesion molecules in sickle cell anemia and gut microbiome effect
A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
Plasminogen activator inhibitor-2 and impaired fibrinolysis in pregnancy and sickle cell anemia
Coexistent sickle-cell anemia and autoimmune disease in eight children: pitfalls and challenges
Biventricular dimensions and function in pediatric sickle-cell disease and thalassemia major patients without cardiac iron
Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Biophysical chemistry behind sickle cell anemia and the mechanism of voxelotor action
Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia
Conventional and advanced brain MR imaging in patients with sickle cell anemia
Parvovirus B19 infection in Tunisian patients with sickle-cell anemia and acute erythroblastopenia