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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1951 8
1952 16
1953 24
1954 27
1955 25
1956 20
1957 18
1958 20
1959 25
1960 21
1961 20
1962 16
1964 4
1966 20
1967 26
1968 33
1969 37
1970 44
1971 44
1972 44
1973 53
1974 102
1975 57
1976 77
1977 57
1978 102
1979 97
1980 103
1981 104
1982 106
1983 96
1984 106
1985 99
1986 100
1987 148
1988 81
1989 112
1990 83
1991 76
1992 101
1993 98
1994 76
1995 70
1996 65
1997 73
1998 88
1999 54
2000 62
2001 65
2002 65
2003 61
2004 65
2005 84
2006 104
2007 83
2008 106
2009 96
2010 107
2011 95
2012 112
2013 131
2014 153
2015 149
2016 123
2017 149
2018 136
2019 96
2020 2
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4,658 results
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Page 1
Imbalance of erythropoiesis and iron metabolism in patients with thalassemia
Huang Y, et al. Int J Med Sci 2019. PMID 30745811 Free PMC article.
Hepcidin levels and ratios of hepcidin to erythropoietic activity and to iron biomarker levels were lower in patients with β-thalassemia intermedia or hemoglobin (Hb) E/β-thalassemia than in patients with HbH disease. ...
Hepcidin levels and ratios of hepcidin to erythropoietic activity and to iron biomarker levels were lower in patients with β-thalassemia int …
"Sickling" in vertebrates: Animal studies vs. sickle cell disease
Steinberg MH. Blood Rev 2019 - Review. PMID 31084943
HbS and some deer hemoglobins polymerize because of specific amino acid contacts between hemoglobin beta-globin chains, although different amino acid residues form the contact points of the polymer. ...A similar selective advantage for "sickling" animal hemoglobins is unproven. The mean corpuscular hemoglobin concentration is about 30 to 35 g/dL. ...
HbS and some deer hemoglobins polymerize because of specific amino acid contacts between hemoglobin beta-globin chains, althou …
Advances in detection of hemoglobinopathies.
Greene DN, et al. Clin Chim Acta 2015 - Review. PMID 25314938
Hemoglobin disorders are recognized as one of the most common inherited diseases worldwide. Detecting and characterizing variant hemoglobins and thalassemias depends primarily on clinical laboratory methods. ...Proper characterization of hemoglobin variants is necessary for diagnosis, primary prevention and genetic counseling for underlying disorders. ...
Hemoglobin disorders are recognized as one of the most common inherited diseases worldwide. Detecting and characterizing variant h
Approaches for Analysis of Erythroid Cell Parameters and Hemoglobinopathies in Mouse Models.
Trudel M and Sedzro JC. Methods Mol Biol 2018. PMID 29076086
Over the last decades several mouse models of human hemoglobin disorders have been and continue to be generated. This chapter aims at describing various approaches to evaluate the global red blood cell properties in mouse models of human hemoglobin disorders, in particular thalassemia and sickle cell disease. ...
Over the last decades several mouse models of human hemoglobin disorders have been and continue to be generated. This chapter aims at …
Prothrombotic markers in Thalassemia major patients: A paradigm shift
Sultan S, et al. Med J Malaysia 2018. PMID 30121679 Free article.
Protein C deficiency divulged positive correlation with protein S deficiency (p = 0.035) and antithrombin deficiency with hemoglobin of ≤8gm% (p<0.0025). ...
Protein C deficiency divulged positive correlation with protein S deficiency (p = 0.035) and antithrombin deficiency with hemoglobin
Diagnosis and clinical presentation of hemoglobin Kirksey.
Hitaka D and Arai J. Pediatr Int 2016 - Review. PMID 26678362
More than 1000 hemoglobin (Hb) variants have been identified. Hb Kirksey, a rare Hb variant involving mutation at codon 94 of α2-globin, is associated with low oxygen affinity. ...
More than 1000 hemoglobin (Hb) variants have been identified. Hb Kirksey, a rare Hb variant involving mutation at codon 94 of α2-glob …
Fetal red blood cell parameters in thalassemia and hemoglobinopathies.
Karnpean R, et al. Fetal Diagn Ther 2013. PMID 24051385
Hemoglobin (Hb) and DNA analyses were performed for definite genotyping. RESULTS: No significant difference in RBC parameters was observed between non-thalassemic fetuses and those with β-thalassemia trait, Hb E trait, homozygous Hb E and β-thalassemia/Hb E disease. ...
Hemoglobin (Hb) and DNA analyses were performed for definite genotyping. RESULTS: No significant difference in RBC parameters was obs
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