Results 201 to 210 of about 18,864 (254)
Some of the next articles are maybe not open access.
Hemoglobinopathies in the Sudan
Hemoglobin, 2008In a prospective study, we evaluated hematological parameters in freshly obtained venous blood samples from 632 Sudanese patients attending the outpatient department at Khartoum Teaching Hospital, Khartoum, Sudan, in the period between March and July 2005. The patients were surveyed for full blood count (FBC) and hemoglobin (Hb) electrophoresis using a
Elderdery, A. +5 more
openaire +3 more sources
Hemoglobinopathies in Xinjiang
Hemoglobin, 1986The present report summarizes the results of a search for hemoglobinopathies in 142,171 persons in Xinjiang, the results of structural analyses of abnormal hemoglobins in 134 families, and the incidence and distribution of abnormal hemoglobins and the thalassemias in eight ethnic groups or nationalities.
H. J. Li +30 more
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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.
openaire +2 more sources
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.
openaire +2 more sources
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
openaire +2 more sources
Anesthesia and Hemoglobinopathies
Anesthesiology Clinics, 2009Hemoglobinopathies are diseases involving abnormalities of the structure or production of hemoglobin. Examples include sickle cell disease, the thalassemias, and rare hemoglobin variants producing cyanosis. Recent advances in the understanding of the consequences of hemoglobin dysfunction on nitric oxide signaling have led to a reassessment of the ...
openaire +2 more sources
Hemoglobin, 1981
Hemglobin variants, thalassemia, hereditary persistence of fetal herroglobin and compound disorders reported from India are listed in tabular form by state and population.In India, the heimglobinopathies occur in the midst of a uniqe genetic heterogeneity. The population of nearly 700 millim is divided into thousands of highly endogamus groups, many of
openaire +2 more sources
Hemglobin variants, thalassemia, hereditary persistence of fetal herroglobin and compound disorders reported from India are listed in tabular form by state and population.In India, the heimglobinopathies occur in the midst of a uniqe genetic heterogeneity. The population of nearly 700 millim is divided into thousands of highly endogamus groups, many of
openaire +2 more sources