Results 211 to 220 of about 19,583 (241)
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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
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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
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Hemoglobinopathies in Pregnancy
2012Pregnancies in women with both sickle and thalassemia disorders are seen increasingly worldwide, but outside a small number of specialist centers, most obstetricians and hematologists will see only a few affected pregnancies. Prospective trials addressing the challenges of managing these disorders in pregnancy remain limited so that current management ...
John Porter +3 more
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Hemoglobinopathies and Leg Ulcers
The International Journal of Lower Extremity Wounds, 2015Major hemoglobinopathies, including sickle cell anemia, are becoming a global health issue. Leg ulcers are the most common cutaneous manifestation of sickle cell disease and an important contributor to morbidity burden in this population. Leg ulcers following sickling disorders are extremely painful, and hard to heal.
Robert S. Kirsner, Afsaneh Alavi
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2014
Over 1,000 hemoglobinopathies have been identified. On a routine basis there are about a dozen hemoglobinopathies that we deal with. There are multiple methodologies employed to detect hemoglobinopathies. This chapter will discuss the principles of detection of hemoglobinopathies and highlight the role of gel electrophoresis, HPLC, and capillary ...
Amitava Dasgupta, Amer Wahed
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Over 1,000 hemoglobinopathies have been identified. On a routine basis there are about a dozen hemoglobinopathies that we deal with. There are multiple methodologies employed to detect hemoglobinopathies. This chapter will discuss the principles of detection of hemoglobinopathies and highlight the role of gel electrophoresis, HPLC, and capillary ...
Amitava Dasgupta, Amer Wahed
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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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Thalassemias and Hemoglobinopathies in Turkey
Hemoglobin, 2014Thalassemias and hemoglobinopathies are a serious health problem in Turkey. There is a 70-year history of thalassemia in Turkey. The first patient with β-thalassemia major (β-TM) was reported in 1941. The first clinical and hematological studies were published by Aksoy in 1958.
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2012
Anemia is defined as a hemoglobin (or hematocrit) below the lower limit of the normal range for age and sex of an individual. About 40 years ago, a World Health Organization expert committee suggested 12 g/dL as the lower limit of normal for nonpregnant women and 13 g/dL as the lower limit for adult men, values that have been used in many studies as ...
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Anemia is defined as a hemoglobin (or hematocrit) below the lower limit of the normal range for age and sex of an individual. About 40 years ago, a World Health Organization expert committee suggested 12 g/dL as the lower limit of normal for nonpregnant women and 13 g/dL as the lower limit for adult men, values that have been used in many studies as ...
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2016
This chapter describes the clinical manifestations, diagnosis, complications, and management of sickle cell disease, thalassemia, and other hemoglobinopathies.
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This chapter describes the clinical manifestations, diagnosis, complications, and management of sickle cell disease, thalassemia, and other hemoglobinopathies.
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