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Hemoglobin

Showing results (1201-1210 of 2,379) with videos related to

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Hemoglobin|August 16, 2019
A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature reviewMichael K Wang, Ravi Shergill, Matthew Jefkins, et al.
Hemoglobin|March 2, 2019
First Report of a Coincidental Discovery of Hb Shimonoseki [α54(E3)Gln→Arg, HBA2: c.164A > G (or HBA1)] in a Greek FamilyStamatia Theodoridou, Evangelia Delaki, Evangelia Skatharoudi, et al.
Hemoglobin|February 16, 2021
Case Report of Acute Splenic Sequestration Crisis in an Adult Patient with Hb S Disease and Suspected Hereditary Persistence of Fetal HemoglobinIan R Sigal, Christine A Ciunci
Hemoglobin|February 24, 2021
Determinants of the Outcome of the Transition of Children with Sickle Cell Disease to Adult ProgramsSamir K Ballas, Gaye Riddick-Burden, Elisabeth Congdon-Martin
Hemoglobin|August 15, 2019
The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern TurkeySedat Yılmaz
Hemoglobin|March 11, 1998
Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-AmericansJ D Hoyer, M J Wick, S N Thibodeau, et al.
Hemoglobin|March 11, 1998
Persistent iron and folate deficiency in a patient with deletional hereditary persistence of fetal hemoglobin; the effect on the relative levels of Hb F and G gamma chains and the corresponding mRNAsH Landman, T H Huisman
Hemoglobin|October 16, 2004
Hb Suan-Dok [alpha109(G16)Leu-->Arg; CTG-->CGG (alpha2)] described in a patient of African ancestryMarlies E Regtuijt, Cornelis L Harteveld, Peter Van Delft, et al.
Hemoglobin|October 16, 2004
Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversityImen Chouk, Béchir Ben Daoud, Fethi Mellouli, et al.
Hemoglobin|October 16, 2004
Compound heterozygosity for two new mutations in the beta-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA-->AAAAAA)] leads to thalassemia intermedia in a Tunisian patientAurelia Jacquette, Geneviève Le Roux, Chantal Lacombe, et al.
Pageof 238

Showing results (1201-1210 of 2,379) with videos related to

Sort By:
Pageof 238
Hemoglobin|August 16, 2019
A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature reviewMichael K Wang, Ravi Shergill, Matthew Jefkins, et al.
Hemoglobin|March 2, 2019
First Report of a Coincidental Discovery of Hb Shimonoseki [α54(E3)Gln→Arg, HBA2: c.164A > G (or HBA1)] in a Greek FamilyStamatia Theodoridou, Evangelia Delaki, Evangelia Skatharoudi, et al.
Hemoglobin|February 16, 2021
Case Report of Acute Splenic Sequestration Crisis in an Adult Patient with Hb S Disease and Suspected Hereditary Persistence of Fetal HemoglobinIan R Sigal, Christine A Ciunci
Hemoglobin|February 24, 2021
Determinants of the Outcome of the Transition of Children with Sickle Cell Disease to Adult ProgramsSamir K Ballas, Gaye Riddick-Burden, Elisabeth Congdon-Martin
Hemoglobin|August 15, 2019
The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern TurkeySedat Yılmaz
Hemoglobin|March 11, 1998
Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-AmericansJ D Hoyer, M J Wick, S N Thibodeau, et al.
Hemoglobin|March 11, 1998
Persistent iron and folate deficiency in a patient with deletional hereditary persistence of fetal hemoglobin; the effect on the relative levels of Hb F and G gamma chains and the corresponding mRNAsH Landman, T H Huisman
Hemoglobin|October 16, 2004
Hb Suan-Dok [alpha109(G16)Leu-->Arg; CTG-->CGG (alpha2)] described in a patient of African ancestryMarlies E Regtuijt, Cornelis L Harteveld, Peter Van Delft, et al.
Hemoglobin|October 16, 2004
Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversityImen Chouk, Béchir Ben Daoud, Fethi Mellouli, et al.
Hemoglobin|October 16, 2004
Compound heterozygosity for two new mutations in the beta-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA-->AAAAAA)] leads to thalassemia intermedia in a Tunisian patientAurelia Jacquette, Geneviève Le Roux, Chantal Lacombe, et al.
Pageof 238