Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hemoglobin

Showing results (841-850 of 2,379) with videos related to

Pageof 238
Sort By:
Hemoglobin|November 4, 2024
Analysis of Iron Status in Sickle Cell Disease Patients During Steady State at the Center de Recherche et de Lutte contre la Drépanocytose (CRLD) BamakoAldiouma Guindo, Abdulmalik Koya, Yeya Dit Sadio Sarro, et al.
Hemoglobin|March 4, 2025
Prevalence and Associated Factors of Zinc and Vitamin D Deficiencies in Pediatric and Young Adult Patients with Non-Transfusion-Dependent ThalassemiaPoonyapon Rodchaprom, Kanda Fanhchaksai, Supawadee Maneekesorn, et al.
Hemoglobin|February 7, 2025
Long-Term Survival Rates of a Sickle Cell Disease Cohort in Saudi Arabia: A 2009-2023 Observational StudyTamader A Aloofy, Aamer Aleem, Farjah H Algahtani, et al.
Hemoglobin|August 15, 2024
A Review of Gene Therapies for HemoglobinopathiesBoubini Jones-Wonni, Amar H Kelkar, Maureen O Achebe
Hemoglobin|August 5, 2024
A Novel Frameshift Mutation of <i>HBB</i> Causing Dominant β-Thalassemia in a Chinese IndividualCuili Yao, Long Chen, Jingting Ma, et al.
Hemoglobin|June 27, 2006
A new alpha chain hemoglobin variant: Hb Al-Hammadi Riyadh [alpha75(EF4)Asp-->Val (alpha2)]Nelly Burnichon, Philippe Lacan, Michel Becchi, et al.
Hemoglobin|June 27, 2006
Secretory phospholipase A2 levels in patients with sickle cell disease and acute chest syndromeSamir K Ballas, Beatrice Files, Lori Luchtman-Jones, et al.
Hemoglobin|June 27, 2006
The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese familyDongzhi Li, Can Liao, Jian Li, et al.
Hemoglobin|June 27, 2006
Iron mobilization from transferrin and non-transferrin-bound-iron by deferiprone. Implications in the treatment of thalassemia, anemia of chronic disease, cancer and other conditionsGeorge J Kontoghiorghes
Hemoglobin|June 27, 2006
Radiation protection by deferiprone in animal modelsSatoshi Fukuda, Mizuyo Ikeda, Kazunori Anzai, et al.
Pageof 238

Showing results (841-850 of 2,379) with videos related to

Sort By:
Pageof 238
Hemoglobin|November 4, 2024
Analysis of Iron Status in Sickle Cell Disease Patients During Steady State at the Center de Recherche et de Lutte contre la Drépanocytose (CRLD) BamakoAldiouma Guindo, Abdulmalik Koya, Yeya Dit Sadio Sarro, et al.
Hemoglobin|March 4, 2025
Prevalence and Associated Factors of Zinc and Vitamin D Deficiencies in Pediatric and Young Adult Patients with Non-Transfusion-Dependent ThalassemiaPoonyapon Rodchaprom, Kanda Fanhchaksai, Supawadee Maneekesorn, et al.
Hemoglobin|February 7, 2025
Long-Term Survival Rates of a Sickle Cell Disease Cohort in Saudi Arabia: A 2009-2023 Observational StudyTamader A Aloofy, Aamer Aleem, Farjah H Algahtani, et al.
Hemoglobin|August 15, 2024
A Review of Gene Therapies for HemoglobinopathiesBoubini Jones-Wonni, Amar H Kelkar, Maureen O Achebe
Hemoglobin|August 5, 2024
A Novel Frameshift Mutation of <i>HBB</i> Causing Dominant β-Thalassemia in a Chinese IndividualCuili Yao, Long Chen, Jingting Ma, et al.
Hemoglobin|June 27, 2006
A new alpha chain hemoglobin variant: Hb Al-Hammadi Riyadh [alpha75(EF4)Asp-->Val (alpha2)]Nelly Burnichon, Philippe Lacan, Michel Becchi, et al.
Hemoglobin|June 27, 2006
Secretory phospholipase A2 levels in patients with sickle cell disease and acute chest syndromeSamir K Ballas, Beatrice Files, Lori Luchtman-Jones, et al.
Hemoglobin|June 27, 2006
The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese familyDongzhi Li, Can Liao, Jian Li, et al.
Hemoglobin|June 27, 2006
Iron mobilization from transferrin and non-transferrin-bound-iron by deferiprone. Implications in the treatment of thalassemia, anemia of chronic disease, cancer and other conditionsGeorge J Kontoghiorghes
Hemoglobin|June 27, 2006
Radiation protection by deferiprone in animal modelsSatoshi Fukuda, Mizuyo Ikeda, Kazunori Anzai, et al.
Pageof 238