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Hemoglobin
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February 1, 1996
beta S haplotypes, alpha-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.)
L Kéclard, V Ollendorf, C Berchel, et al.
Hemoglobin
|
October 1, 1993
Hb Val de Marne [alpha 133(H16)Ser-->Arg]: a new hemoglobin variant with moderate increase in oxygen affinity
H Wajcman, J Kister, A M'Rad, et al.
Hemoglobin
|
January 1, 1995
The sickle cell painful crisis in adults: phases and objective signs
S K Ballas
Hemoglobin
|
November 9, 2016
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)
John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin
|
April 1, 2017
Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl
Hua Jiang, Jin-Mei Yan, Jian-Ying Zhou, et al.
Hemoglobin
|
April 1, 2017
Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients
Yunli Lai, Yun Chen, Biyan Chen, et al.
Hemoglobin
|
April 4, 2017
Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil
Gisele C S Carrocini, Larissa P R Venancio, Viviani L R Pessoa, et al.
Hemoglobin
|
April 5, 2017
Insulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell Disease
Maria P Yavropoulou, Maria Pikilidou, Despoina Pantelidou, et al.
Hemoglobin
|
January 30, 2014
A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]
Imen Moumni, Amine Zorai, Sonia Mahjoub, et al.
Hemoglobin
|
January 30, 2014
Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A]
Ferdane Kutlar, Yoram Unguru, Natalia Dixon, et al.
Page
of 238
Search research articles
Search
Showing results (711-720 of 2,379) with videos related to
Sort By:
Page
of 238
Hemoglobin
|
February 1, 1996
beta S haplotypes, alpha-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.)
L Kéclard, V Ollendorf, C Berchel, et al.
Hemoglobin
|
October 1, 1993
Hb Val de Marne [alpha 133(H16)Ser-->Arg]: a new hemoglobin variant with moderate increase in oxygen affinity
H Wajcman, J Kister, A M'Rad, et al.
Hemoglobin
|
January 1, 1995
The sickle cell painful crisis in adults: phases and objective signs
S K Ballas
Hemoglobin
|
November 9, 2016
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)
John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin
|
April 1, 2017
Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl
Hua Jiang, Jin-Mei Yan, Jian-Ying Zhou, et al.
Hemoglobin
|
April 1, 2017
Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients
Yunli Lai, Yun Chen, Biyan Chen, et al.
Hemoglobin
|
April 4, 2017
Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil
Gisele C S Carrocini, Larissa P R Venancio, Viviani L R Pessoa, et al.
Hemoglobin
|
April 5, 2017
Insulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell Disease
Maria P Yavropoulou, Maria Pikilidou, Despoina Pantelidou, et al.
Hemoglobin
|
January 30, 2014
A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]
Imen Moumni, Amine Zorai, Sonia Mahjoub, et al.
Hemoglobin
|
January 30, 2014
Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A]
Ferdane Kutlar, Yoram Unguru, Natalia Dixon, et al.
Page
of 238