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

Year Number of Results
1932 1
1942 1
1944 1
1945 2
1950 1
1951 2
1952 6
1953 1
1954 15
1955 15
1956 6
1957 3
1958 6
1959 3
1960 3
1961 42
1962 56
1963 14
1964 21
1965 10
1966 9
1967 14
1968 15
1969 13
1970 17
1971 21
1972 21
1973 9
1974 29
1975 48
1976 29
1977 43
1978 44
1979 48
1980 54
1981 65
1982 57
1983 74
1984 62
1985 79
1986 72
1987 66
1988 84
1989 92
1990 103
1991 82
1992 89
1993 115
1994 76
1995 92
1996 101
1997 95
1998 101
1999 108
2000 95
2001 120
2002 113
2003 126
2004 126
2005 127
2006 152
2007 179
2008 157
2009 154
2010 154
2011 187
2012 205
2013 206
2014 193
2015 206
2016 236
2017 211
2018 219
2019 216
2020 242
2021 260
2022 249
2023 253
2024 127

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6,239 results

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Page 1
Diagnosis and screening of abnormal hemoglobins.
Sani A, Idrees Khan M, Shah S, Tian Y, Zha G, Fan L, Zhang Q, Cao C. Sani A, et al. Clin Chim Acta. 2024 Jan 1;552:117685. doi: 10.1016/j.cca.2023.117685. Epub 2023 Nov 27. Clin Chim Acta. 2024. PMID: 38030031 Review.
Hemoglobin (Hb) abnormalities, such as thalassemia and structural Hb variants, are among the most prevalent inherited diseases and are associated with significant mortality and morbidity worldwide. ...
Hemoglobin (Hb) abnormalities, such as thalassemia and structural Hb variants, are among the most prevalent inherited diseases …
Anemia.
English EC. English EC. J Fam Pract. 1987 May;24(5):521-7. J Fam Pract. 1987. PMID: 3572323
Abnormalities in the routine blood count alert the physician to hematologic problems. The most common of these are red cell abnormalities as reflected in decreased levels of hemoglobin and hematocrit together with changes in mean corpuscular volume and red ce …
Abnormalities in the routine blood count alert the physician to hematologic problems. The most common of these are red cell abnorm …
Homozygous haemoglobin D Punjab.
Politis-Tsegos C, Kynoch P, Lang A, Lehmann H, Lorkin PA, Stathopoulou R, Wakefield G. Politis-Tsegos C, et al. J Med Genet. 1975 Sep;12(3):269-74. doi: 10.1136/jmg.12.3.269. J Med Genet. 1975. PMID: 1177278 Free PMC article.
The diagnosis is supported by the peptide analysis of the haemoglobin and the examination of both parents. There was no anaemia or reticulocytosis and there was balanced synthesis of both the alphaA- and betaD-globin chains in reticulocytes. However, the oxygen affinity of …
The diagnosis is supported by the peptide analysis of the haemoglobin and the examination of both parents. There was no anaemia or re …
[Inherited polycythemia].
Pavic M, Rousset H. Pavic M, et al. Rev Med Interne. 2003 Aug;24(8):514-21. doi: 10.1016/s0248-8663(03)00059-6. Rev Med Interne. 2003. PMID: 12888172 Review. French.
CURRENT KNOWLEDGE AND KEY POINTS: Although polycythemias linked to a anomaly of the haemoglobin affinity for oxygen are well understood (haemoglobin mutants with high oxygen affinity, 2-3 Diphosphoglycerate deficiency and methemoglobinemia), so called primary …
CURRENT KNOWLEDGE AND KEY POINTS: Although polycythemias linked to a anomaly of the haemoglobin affinity for oxygen are well u …
Lipid peroxidation in erythrocytes.
Clemens MR, Waller HD. Clemens MR, et al. Chem Phys Lipids. 1987 Nov-Dec;45(2-4):251-68. doi: 10.1016/0009-3084(87)90068-5. Chem Phys Lipids. 1987. PMID: 3319229 Review.
This review surveys mechanisms which lead to red cell lipid autoxidation and the role of haemoglobin in these processes. The influence of haemoglobinopathies, of lipid composition and of abnormalities in antioxidant mechanisms induced by exogenous oxidant stress is …
This review surveys mechanisms which lead to red cell lipid autoxidation and the role of haemoglobin in these processes. The influenc …
Haemoglobin J-Baltimore can be detected by HbA1c electropherogram but with underestimated HbA1c value.
Brunel V, Lahary A, Chagraoui A, Thuillez C. Brunel V, et al. Biochem Med (Zagreb). 2016;26(2):240-2. doi: 10.11613/BM.2016.026. Biochem Med (Zagreb). 2016. PMID: 27346969 Free PMC article.
Glycated haemoglobin (HbA(1c)) is considered the gold standard for assessing diabetes compensation and treatment. ...A patient followed for gestational diabetes in our laboratory presented unknown haemoglobin on Capillarys 2 Flex Piercing analyser which was identifi …
Glycated haemoglobin (HbA(1c)) is considered the gold standard for assessing diabetes compensation and treatment. ...A patient follow …
[Haemoglobin M-Homburg (author's transl)].
Schneider W, Kirsch W. Schneider W, et al. Dtsch Med Wochenschr. 1976 Mar 12;101(11):405-8. doi: 10.1055/s-0028-1104097. Dtsch Med Wochenschr. 1976. PMID: 1253702 German.
Haemoglobin M is a rare cause of congenital cyanosis and is usually misdiagnosed as being due to congenital heart disease. ...In five members of three generations the characteristic grey-blue cyanosis was due to a haemoglobin M anomaly. In all of them cardiop …
Haemoglobin M is a rare cause of congenital cyanosis and is usually misdiagnosed as being due to congenital heart disease. ...In five …
MEDICAL GENETICS 1962.
MCKUSICK VA. MCKUSICK VA. J Chronic Dis. 1963 Jun;16:457-634. doi: 10.1016/0021-9681(63)90148-6. J Chronic Dis. 1963. PMID: 14042963 Review. No abstract available.
Inherited disorders of hemoglobin: A review of old and new diagnostic methods.
Franco E, Karkoska KA, McGann PT. Franco E, et al. Blood Cells Mol Dis. 2024 Jan;104:102758. doi: 10.1016/j.bcmd.2023.102758. Epub 2023 May 18. Blood Cells Mol Dis. 2024. PMID: 37246072 Review.
The genetic regulation of hemoglobin is complex and there are a number of genetic abnormalities that result in clinically important hemoglobin disorders. ...We discuss the utility and limitations of the various methodologies to fractionate hemoglobin, …
The genetic regulation of hemoglobin is complex and there are a number of genetic abnormalities that result in clinically impo …
Haemoglobin Bristol-Alesha in a child with non-spherocytic severe haemolytic anaemia and marked anisochromic poikilocytosis with basophilic stippling and amorphous intracellular content.
Corrons JV, Bain BJ. Corrons JV, et al. Blood Cells Mol Dis. 2022 May;94:102652. doi: 10.1016/j.bcmd.2022.102652. Epub 2022 Jan 22. Blood Cells Mol Dis. 2022. PMID: 35091138
Targeted next generation sequencing (t-NGS) revealed haemoglobin Bristol-Alesha, a hyper unstable haemoglobinopathy associated with severe haemolytic anaemia. Since unstable haemoglobins do not necessarily have specific red cell morphological abnormalities, o …
Targeted next generation sequencing (t-NGS) revealed haemoglobin Bristol-Alesha, a hyper unstable haemoglobinopathy associated with s …
6,239 results