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Hemoglobin, 1983
A survey of the various hemoglobinopathies in Israel is reported. The information was supplied from 13 hematology services throughout the country and from the Ministry of Health. The common hemoglobinopathies encountered were the thalassemias and sickle cell anemia. In addition, hemoglobin C and O Arab were found in isolated communities. Sporadic cases
R, Eliakim, E A, Rachmilewitz
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A survey of the various hemoglobinopathies in Israel is reported. The information was supplied from 13 hematology services throughout the country and from the Ministry of Health. The common hemoglobinopathies encountered were the thalassemias and sickle cell anemia. In addition, hemoglobin C and O Arab were found in isolated communities. Sporadic cases
R, Eliakim, E A, Rachmilewitz
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Clinica Chimica Acta, 2015
Variations in hemoglobin structure as well as number of globin chains give rise to a wide spectrum of heritable disorders. As such, their detection is significant from epidemiological perspective, especially in India in which there is a large multi-cultural population with distinct geographic distribution.
Sandhya, Iyer +3 more
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Variations in hemoglobin structure as well as number of globin chains give rise to a wide spectrum of heritable disorders. As such, their detection is significant from epidemiological perspective, especially in India in which there is a large multi-cultural population with distinct geographic distribution.
Sandhya, Iyer +3 more
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Hemoglobin, 1983
Hungary is a country in Central Europe where hemoglobinopathies were known to be rather rare. That is the reason why no survey was organized for studying the frequency of the occurrence of certain hemoglobinopathies in the Hungarian population. In spite of this, during our diagnostic work in the last fifteen years, several abnormal hemoglobin variants,
J, Szelényi +4 more
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Hungary is a country in Central Europe where hemoglobinopathies were known to be rather rare. That is the reason why no survey was organized for studying the frequency of the occurrence of certain hemoglobinopathies in the Hungarian population. In spite of this, during our diagnostic work in the last fifteen years, several abnormal hemoglobin variants,
J, Szelényi +4 more
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Current Opinion in Pediatrics, 1993
Neonatal screening for hemoglobinopathies, coupled with comprehensive medical care that includes parental education, prophylactic penicillin, and immunizations, has markedly reduced mortality from sickle hemoglobinopathies during infancy and early childhood.
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Neonatal screening for hemoglobinopathies, coupled with comprehensive medical care that includes parental education, prophylactic penicillin, and immunizations, has markedly reduced mortality from sickle hemoglobinopathies during infancy and early childhood.
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Hemoglobinopathies in the Neonate
NeoReviewsHemoglobinopathies in neonates constitute a group of disorders influenced by genetic mutations in the human globin genes. They are often broadly categorized into quantitative defects or qualitative defects, though they are not mutually exclusive. In quantitative defects, the mutation causes insufficient production of a normal globin chain, which can ...
Katrina, Blankenhorn, Kaitlin, Strumph
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