Fetal hemoglobin level and nutritional status in patients with sickle cell disease
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1475-2891
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Fetal hemoglobin level and nutritional status in patients with sickle cell disease ; volume:15 ; number:1 ; day:8 ; month:7 ; year:2016 ; pages:1-2 ; date:12.2015
Nutrition journal ; 15, Heft 1 (8.7.2016), 1-2, 12.2015
- Urheber
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Badawy, Sherif M.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s12937-016-0181-x
- URN
-
urn:nbn:de:1111-2016071122426
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 10:51 MESZ
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Beteiligte
- Badawy, Sherif M.
- SpringerLink (Online service)
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SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon
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The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease
Correlates of Pulmonary Function in Children with Sickle Cell Disease and Elevated Fetal Hemoglobin
Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia
Gum Arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study
SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon
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An α-chain modification rivals the effect of fetal hemoglobin in retarding the rate of sickle cell fiber formation
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