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Showing results (721-730 of 2,379) with videos related to
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Hemoglobin
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April 12, 2017
Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family
Allan Pernudy-Ubau, Jaslyn Salinas-Molina, Yaneris Requenez, et al.
Hemoglobin
|
March 28, 2014
Challenge of managing sickle cell disease in a pediatric population living in kinshasa, democratic republic of congo: a sickle cell center experience
Michel Ntetani Aloni, Leonard Nkee
Hemoglobin
|
March 28, 2014
Proteasome inhibition induces both antioxidant and hb f responses in sickle cell disease via the nrf2 pathway
Vinod Pullarkat, Zhuo Meng, Stanley M Tahara, et al.
Hemoglobin
|
January 1, 1988
Overview of the beta thalassemias: genetic and clinical aspects
E Schwartz, A Cohen, S Surrey
Hemoglobin
|
March 10, 2017
β-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study
Ayşegül Kurtoğlu, Volkan Karakuş, Özgür Erkal, et al.
Hemoglobin
|
January 1, 1989
Hb Moriguchi or alpha 2 beta 2(97) (FG4)His---Tyr substitution at the alpha 1-beta 2 interface
Y Ohba, K Imai, I Kumada, et al.
Hemoglobin
|
November 11, 2016
A novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C)
Lin Zhao, Jilin Qing, Yue Liang, et al.
Hemoglobin
|
October 1, 2016
Can Neuroimaging Markers of Vascular Pathology Explain Cognitive Performance in Adults With Sickle Cell Anemia? A review of the Literature
Dana R Jorgensen, Caterina Rosano, Enrico M Novelli
Hemoglobin
|
October 1, 2016
Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran
Sima M Derakhshan, Mahmoud S Khaniani, Fateme Afkhami, et al.
Hemoglobin
|
August 12, 2003
Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype
Giuseppina Lacerra, Rosario Testa, Maria De Angioletti, et al.
Page
of 238
Search research articles
Search
Showing results (721-730 of 2,379) with videos related to
Sort By:
Page
of 238
Hemoglobin
|
April 12, 2017
Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family
Allan Pernudy-Ubau, Jaslyn Salinas-Molina, Yaneris Requenez, et al.
Hemoglobin
|
March 28, 2014
Challenge of managing sickle cell disease in a pediatric population living in kinshasa, democratic republic of congo: a sickle cell center experience
Michel Ntetani Aloni, Leonard Nkee
Hemoglobin
|
March 28, 2014
Proteasome inhibition induces both antioxidant and hb f responses in sickle cell disease via the nrf2 pathway
Vinod Pullarkat, Zhuo Meng, Stanley M Tahara, et al.
Hemoglobin
|
January 1, 1988
Overview of the beta thalassemias: genetic and clinical aspects
E Schwartz, A Cohen, S Surrey
Hemoglobin
|
March 10, 2017
β-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study
Ayşegül Kurtoğlu, Volkan Karakuş, Özgür Erkal, et al.
Hemoglobin
|
January 1, 1989
Hb Moriguchi or alpha 2 beta 2(97) (FG4)His---Tyr substitution at the alpha 1-beta 2 interface
Y Ohba, K Imai, I Kumada, et al.
Hemoglobin
|
November 11, 2016
A novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C)
Lin Zhao, Jilin Qing, Yue Liang, et al.
Hemoglobin
|
October 1, 2016
Can Neuroimaging Markers of Vascular Pathology Explain Cognitive Performance in Adults With Sickle Cell Anemia? A review of the Literature
Dana R Jorgensen, Caterina Rosano, Enrico M Novelli
Hemoglobin
|
October 1, 2016
Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran
Sima M Derakhshan, Mahmoud S Khaniani, Fateme Afkhami, et al.
Hemoglobin
|
August 12, 2003
Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype
Giuseppina Lacerra, Rosario Testa, Maria De Angioletti, et al.
Page
of 238