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Pregnancy outcomes in women with a hemoglobinopathy trait: a multicenter, retrospective study [PDF]
Archives of Gynecology and Obstetrics, 2021 Purpose To determine the risk of adverse maternal and neonatal outcomes in pregnant women with a hemoglobinopathy trait. Materials and methods Retrospective cohort study was conducted to compare adverse maternal and neonatal outcomes between ...
Tilo Burkhardt +1 more
exaly +2 more sources
Tissue Oxygenation in Patients with Hemoglobinopathy H
Pediatric Hematology and Oncology, 1997 To evaluate the degree of tissue hypoxia in patients with hemoglobinopathy H disease, whole blood oxygen affinity was estimated and analyzed in 33 patients.
Emmanuel Kanavakis +2 more
exaly +2 more sources
Diagnostics, 2021 Genetic hemoglobinopathies are the most common single-gene disorder worldwide. Some automated hematology analyzers have the capability of flagging individuals who may have hematological disorders based on complete blood count (CBC) biomarkers.
Kelsey Cochrane +2 more
exaly +2 more sources
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Hematology, 2003
AbstractThe outlook for patients with sickle cell disease has improved steadily during the last two decades. In spite of these improvements, curative therapies are currently available only to a small minority of patients. The main theme of this chapter is to describe new therapeutic options that are at different stages of development that might result ...
George F, Atweh +7 more
openaire +2 more sources
AbstractThe outlook for patients with sickle cell disease has improved steadily during the last two decades. In spite of these improvements, curative therapies are currently available only to a small minority of patients. The main theme of this chapter is to describe new therapeutic options that are at different stages of development that might result ...
George F, Atweh +7 more
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
Hemoglobinopathies in pregnancy
Obstetrics and Gynecology Clinics of North America, 2004Hemoglobinopathies represent a unique set of genetic disorders. Formerly, many affected individuals did not survive to childbearing age. Affected women now commonly reach childbearing age and desire pregnancy. Successful pregnancy is possible in many cases with carefully coordinated obstetric and medical management.
Valerie J, Rappaport +2 more
openaire +2 more sources
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
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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
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
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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
openaire +2 more sources