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Hemoglobin

Showing results (531-540 of 3,216) with videos related to

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Hemoglobin|August 13, 2025
Sickling Disorder Caused by Co-Inheritance of Hemoglobin Maputo and Hemoglobin S: Case Report and Review of the LiteratureSakina Loonat, Nitien Naran, Narisha Ramparsad, et al.
Hemoglobin|August 19, 2025
Identification of a New δ chain hemoglobin Variant, Hb A2-Malay [δ46(CD5)Gly > Arg, <i>HBD</i>: C.139G > C;316-443A > G]Syahzuwan Hassan, Ezalia Esa, Norafiza Mohd Yasin, et al.
Hemoglobin|July 27, 2025
When Unstable Hemoglobin Lansing Interacts with Alpha Thalassemia Along with <i>HbS</i>: An Interesting Case with Unique Clinical PresentationAdwait Marhatta, Jui Choudhuri, Joseph J Mulvey, et al.
Hemoglobin|July 16, 2014
The effect and side effect of hydroxyurea therapy on patients with β-thalassemia: a systematic review to December 2012Mehrnoush Kosaryan, Mandana Zafari, Abbass Alipur, et al.
Hemoglobin|July 18, 2014
Thalassemias and hemoglobinopathies in TurkeyDuran Canatan
Hemoglobin|April 26, 2013
Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional α(+)-thalassemia mutations: diverse hematological and clinical featuresIta M Nainggolan, Alida Harahap, Debby D Ambarwati, et al.
Hemoglobin|April 19, 2013
The current status of β-thalassemia major in Mainland ChinaLu-Hong Xu, Jian-Pei Fang
Hemoglobin|April 23, 2013
Leg ulcers in sickle cell disease: current patterns and practicesKara-Marie H Delaney, Karen C Axelrod, Ashley Buscetta, et al.
Hemoglobin|April 23, 2013
A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon geneChris Adhiyanto, Yasuhiro Yamashiro, Yukio Hattori, et al.
Hemoglobin|May 9, 2013
Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)John S Waye, Barry Eng, Laurie Hellens, et al.
Pageof 322

Showing results (531-540 of 3,216) with videos related to

Sort By:
Pageof 322
Hemoglobin|August 13, 2025
Sickling Disorder Caused by Co-Inheritance of Hemoglobin Maputo and Hemoglobin S: Case Report and Review of the LiteratureSakina Loonat, Nitien Naran, Narisha Ramparsad, et al.
Hemoglobin|August 19, 2025
Identification of a New δ chain hemoglobin Variant, Hb A2-Malay [δ46(CD5)Gly > Arg, <i>HBD</i>: C.139G > C;316-443A > G]Syahzuwan Hassan, Ezalia Esa, Norafiza Mohd Yasin, et al.
Hemoglobin|July 27, 2025
When Unstable Hemoglobin Lansing Interacts with Alpha Thalassemia Along with <i>HbS</i>: An Interesting Case with Unique Clinical PresentationAdwait Marhatta, Jui Choudhuri, Joseph J Mulvey, et al.
Hemoglobin|July 16, 2014
The effect and side effect of hydroxyurea therapy on patients with β-thalassemia: a systematic review to December 2012Mehrnoush Kosaryan, Mandana Zafari, Abbass Alipur, et al.
Hemoglobin|July 18, 2014
Thalassemias and hemoglobinopathies in TurkeyDuran Canatan
Hemoglobin|April 26, 2013
Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional α(+)-thalassemia mutations: diverse hematological and clinical featuresIta M Nainggolan, Alida Harahap, Debby D Ambarwati, et al.
Hemoglobin|April 19, 2013
The current status of β-thalassemia major in Mainland ChinaLu-Hong Xu, Jian-Pei Fang
Hemoglobin|April 23, 2013
Leg ulcers in sickle cell disease: current patterns and practicesKara-Marie H Delaney, Karen C Axelrod, Ashley Buscetta, et al.
Hemoglobin|April 23, 2013
A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon geneChris Adhiyanto, Yasuhiro Yamashiro, Yukio Hattori, et al.
Hemoglobin|May 9, 2013
Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)John S Waye, Barry Eng, Laurie Hellens, et al.
Pageof 322