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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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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 ...
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Journal of Maternal-Fetal & Neonatal Medicine, 2019
Objectives HBB-related significant hemoglobinopathies have been anecdotally associated with low fetal fraction on noninvasive prenatal screening (NIPS).
M. Putra +10 more
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Objectives HBB-related significant hemoglobinopathies have been anecdotally associated with low fetal fraction on noninvasive prenatal screening (NIPS).
M. Putra +10 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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Gene Therapy for Hemoglobinopathies: Beta-Thalassemia, Sickle Cell Disease.
Hematology/Oncology Clinics of North America, 2022Alexis Leonard, J. Tisdale, M. Bonner
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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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Genome editing approaches to β-hemoglobinopathies.
Progress in Molecular Biology and Translational Science, 2021Mégane Brusson, A. Miccio
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Hemoglobinopathies in Bulgaria
Hemoglobin, 1987E S, Tasheva, S A, Toshkov, A M, Dobreva
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