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Hemoglobin
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June 27, 2006
Low serum ferritin levels are misleading for detecting cardiac iron overload and increase the risk of cardiomyopathy in thalassemia patients. The importance of cardiac iron overload monitoring using magnetic resonance imaging T2 and T2*
Annita Kolnagou, Charalambos Economides, Eleni Eracleous, et al.
Hemoglobin
|
June 27, 2006
Glutathione S-transferase M1 gene polymorphisms are associated with cardiac iron deposition in patients with beta-thalassemia major
Kang-Hsi Wu, Jan-Gowth Chang, Yung-Jen Ho, et al.
Hemoglobin
|
June 27, 2006
Future chelation monotherapy and combination therapy strategies in thalassemia and other conditions. comparison of deferiprone, deferoxamine, ICL670, GT56-252, L1NAll and starch deferoxamine polymers
George J Kontoghiorghes
Hemoglobin
|
September 22, 2006
Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G)
Amina Bibi, Taieb Messaoud, Cherif Beldjord, et al.
Hemoglobin
|
September 22, 2006
Association of the methylenetetrahydrofolate reductase A1298C but not the C677T single nucleotide polymorphism with sickle cell disease in Bahrain
Iman K Al-Absi, Abeer M Al-Subaie, Ghada Ameen, et al.
Hemoglobin
|
September 22, 2006
The JAK2 V617F mutation is absent in patients with erythrocytosis due to high oxygen affinity hemoglobin variants
Rebecca F McClure, James D Hoyer, Ming Mai
Hemoglobin
|
January 1, 1991
Hb F-Cosenza or G gamma 25(B7)Gly----Glu: a new fast-moving fetal hemoglobin variant
A Qualtieri, L Crescibene, A Bagalà, et al.
Hemoglobin
|
January 1, 1991
Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with Msp I
S Liang, X J Wen, W X Lin
Hemoglobin
|
January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia
R Oner, S Agarwal, A J Dimovski, et al.
Hemoglobin
|
June 1, 2005
A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2)
Guillermo Martin, Ana Villegas, Fernando Ataulfo González, et al.
Page
of 238
Search research articles
Search
Showing results (851-860 of 2,379) with videos related to
Sort By:
Page
of 238
Hemoglobin
|
June 27, 2006
Low serum ferritin levels are misleading for detecting cardiac iron overload and increase the risk of cardiomyopathy in thalassemia patients. The importance of cardiac iron overload monitoring using magnetic resonance imaging T2 and T2*
Annita Kolnagou, Charalambos Economides, Eleni Eracleous, et al.
Hemoglobin
|
June 27, 2006
Glutathione S-transferase M1 gene polymorphisms are associated with cardiac iron deposition in patients with beta-thalassemia major
Kang-Hsi Wu, Jan-Gowth Chang, Yung-Jen Ho, et al.
Hemoglobin
|
June 27, 2006
Future chelation monotherapy and combination therapy strategies in thalassemia and other conditions. comparison of deferiprone, deferoxamine, ICL670, GT56-252, L1NAll and starch deferoxamine polymers
George J Kontoghiorghes
Hemoglobin
|
September 22, 2006
Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G)
Amina Bibi, Taieb Messaoud, Cherif Beldjord, et al.
Hemoglobin
|
September 22, 2006
Association of the methylenetetrahydrofolate reductase A1298C but not the C677T single nucleotide polymorphism with sickle cell disease in Bahrain
Iman K Al-Absi, Abeer M Al-Subaie, Ghada Ameen, et al.
Hemoglobin
|
September 22, 2006
The JAK2 V617F mutation is absent in patients with erythrocytosis due to high oxygen affinity hemoglobin variants
Rebecca F McClure, James D Hoyer, Ming Mai
Hemoglobin
|
January 1, 1991
Hb F-Cosenza or G gamma 25(B7)Gly----Glu: a new fast-moving fetal hemoglobin variant
A Qualtieri, L Crescibene, A Bagalà, et al.
Hemoglobin
|
January 1, 1991
Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with Msp I
S Liang, X J Wen, W X Lin
Hemoglobin
|
January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia
R Oner, S Agarwal, A J Dimovski, et al.
Hemoglobin
|
June 1, 2005
A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2)
Guillermo Martin, Ana Villegas, Fernando Ataulfo González, et al.
Page
of 238