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Hemoglobin

Showing results (301-310 of 3,216) with videos related to

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Hemoglobin|April 1, 2010
Forecasting hemoglobinopathy burden through neonatal screening in Omani neonatesSalam Alkindi, Shoaib Al Zadjali, Ali Al Madhani, et al.
Hemoglobin|April 1, 2010
Misdiagnosis of a beta-thalassemia heterozygote using a reverse dot-blot method may be caused by a polymorphic locus in the wild type sequence of the beta-globin genePing Yi, Jianxin Guo, Zhuqin Chen, et al.
Hemoglobin|April 1, 2010
Extended molecular spectrum of beta- and alpha-thalassemia in OmanSuha M Hassan, Nishat Hamza, Fatma Jaffer Al-Lawatiya, et al.
Hemoglobin|April 18, 2009
Hemoglobin variants in CyprusAndreani R Kyrri, Xenia Felekis, Eleni Kalogerou, et al.
Hemoglobin|April 18, 2009
A new beta-chain variant: Hb stockholm [beta 7(A4)GluAsp] causes falsely low Hb A(1c)Ann-Charlotte Bergman, Soheir Beshara, Irene Byman, et al.
Hemoglobin|April 18, 2009
The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patientImane Agouti, Mohcine Bennani, Nicolas Levy, et al.
Hemoglobin|December 24, 2005
Alpha-thalassemia among tribal populations of Eastern IndiaRinini Sen, Sila Chakrabarti, Bani Sengupta, et al.
Hemoglobin|September 15, 2016
Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct OriginCornelis L Harteveld, Serge Pissard, Anna M H Korver, et al.
Hemoglobin|June 9, 2017
Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's SyndromeFaten Haddad, Nawel Trabelsi, Leila Chaouch, et al.
Hemoglobin|June 10, 2017
Evaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate β-Thalassemia Trait from Iron Deficiency Anemia in the Thai PopulationSakorn Pornprasert, Choosak Thongsat, Uraiporn Panyachadporn
Pageof 322

Showing results (301-310 of 3,216) with videos related to

Sort By:
Pageof 322
Hemoglobin|April 1, 2010
Forecasting hemoglobinopathy burden through neonatal screening in Omani neonatesSalam Alkindi, Shoaib Al Zadjali, Ali Al Madhani, et al.
Hemoglobin|April 1, 2010
Misdiagnosis of a beta-thalassemia heterozygote using a reverse dot-blot method may be caused by a polymorphic locus in the wild type sequence of the beta-globin genePing Yi, Jianxin Guo, Zhuqin Chen, et al.
Hemoglobin|April 1, 2010
Extended molecular spectrum of beta- and alpha-thalassemia in OmanSuha M Hassan, Nishat Hamza, Fatma Jaffer Al-Lawatiya, et al.
Hemoglobin|April 18, 2009
Hemoglobin variants in CyprusAndreani R Kyrri, Xenia Felekis, Eleni Kalogerou, et al.
Hemoglobin|April 18, 2009
A new beta-chain variant: Hb stockholm [beta 7(A4)GluAsp] causes falsely low Hb A(1c)Ann-Charlotte Bergman, Soheir Beshara, Irene Byman, et al.
Hemoglobin|April 18, 2009
The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patientImane Agouti, Mohcine Bennani, Nicolas Levy, et al.
Hemoglobin|December 24, 2005
Alpha-thalassemia among tribal populations of Eastern IndiaRinini Sen, Sila Chakrabarti, Bani Sengupta, et al.
Hemoglobin|September 15, 2016
Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct OriginCornelis L Harteveld, Serge Pissard, Anna M H Korver, et al.
Hemoglobin|June 9, 2017
Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's SyndromeFaten Haddad, Nawel Trabelsi, Leila Chaouch, et al.
Hemoglobin|June 10, 2017
Evaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate β-Thalassemia Trait from Iron Deficiency Anemia in the Thai PopulationSakorn Pornprasert, Choosak Thongsat, Uraiporn Panyachadporn
Pageof 322