Results 21 to 30 of about 50,967 (156)
Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency [PDF]
Korean Journal of Pediatrics, 2017 PurposeThis study aimed to determine the prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency among infants with neonatal indirect hyperbilirubinemia (NIH); compare G6PD-deficient and G6PD-normal patients regarding hyperbilirubinemia and ...
Hasan M. Isa +4 more
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Acquired glucose‐6‐phosphate dehydrogenase deficiency after allogeneic stem‐cell transplantation [PDF]
eJHaemQuentin Vô +3 more
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Glucose-6-Phosphate Dehydrogenase Deficiency in Greece [PDF]
Blood, 1961 Abstract The glutathione stability of red cells was estimated in 40 patients during acute hemolysis induced by fava beans. There were wide individual differences but in all cases except one (Case 18) the post-incubation GSH fell to levels below 40 mg. per cent packed RBC which is the lower normal limit.
L, ZANNOS-MARIOLEA, C, KATTAMIS
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Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Oman
Oman Medical Journal, 2023 Objectives: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most encountered abnormality of red blood cell metabolism worldwide and has a high prevalence in Oman.
Ammar Al-Sheryani1, +5 more
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Fulminant hemolysis in glucose‐6‐phosphate dehydrogenase deficiency
Clinical Case Reports, 2018 Key Clinical Message Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is an X‐linked disorder affecting some 400 million people worldwide. Though clinically silent, it may result in hemolysis on oxidative stress induced by drugs or infections.
Bushra Moiz, Sidra Asad Ali
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Glucose-6-phosphate dehydrogenase deficiency in Chinese [PDF]
Journal of Clinical Pathology, 1968 In a Chinese population 1,000 full-term male neonates and a further 117 jaundiced neonates of both sexes were studied in an investigation of the frequency of deficiency of erythrocyte glucose-6-phosphate dehydrogenase (G6PD). This enzyme was found to be deficient in 3·6% of male neonates.
H C, Lai, M P, Lai, K S, Leung
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Journal of Medical Case Reports, 2008 Introduction Glucose-6-phosphate dehydrogenase deficiency is an X-linked recessive disease that causes acute or chronic hemolytic anemia and potentially leads to severe jaundice in response to oxidative agents.
Cossio de Gurrola Gladys +7 more
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G6PD Deficiency in Neonatal Jaundice
Van Tıp Dergisi, 2022 INTRODUCTION: Neonatal jaundice is one of the important problems encountered by the newborn in the first week after birth, the etiology of which is very diverse and sometimes no cause can be detected.
Altay Babacan +2 more
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Glucose‐6‐phosphate dehydrogenase deficiency in northern Vietnam [PDF]
Tropical Medicine & International Health, 2000 Summary Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency was evaluated in 1676 schoolboys in northern Vietnam. The trait was nearly absent in boys of the Kinh (0.5%) and the Mong (0.7%) ethnic groups that traditionally have lived outside malaria transmission areas.
Verlé, P. +7 more
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Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia [PDF]
Iranian Journal of Neonatology, 2015 Background: Jaundice is affecting over 60-80 percent of neonates in the first week of life. Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which is an important cause of pathologic hyperbilirubinemia, can lead to hemolytic anemia, jaundice and ...
Ezzat Khodashenas +4 more
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