Results 121 to 130 of about 50,967 (156)

Glucose-6-phosphate dehydrogenase deficiency

Baillière's Clinical Haematology, 1992
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy. Because its gene locus is on the X-chromosome it is more common in males than females in all populations. Prevalence rates vary from 62% among Kurdish Jews to the very low rates (0.1% or less in Japan, for example), which are compatible with sporadic cases arising
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Glucose-6-phosphate dehydrogenase deficiency in neonates

The Indian Journal of Pediatrics, 2003
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited deficiency that may be the cause of neonatal hyperbilirubinemia, as has been found in several countries and among widely different ethnic groups, especially in Mediterranean region. Our aim was to study the prevalence of G6PD deficiency in relation to neonatal jaundice.From March 1998 ...
R, Iranpour, M R, Akbar, I, Haghshenas
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Glucose-6-Phosphate Dehydrogenase Deficiency and Blood Transfusion

Vox Sanguinis, 1975
Abstract.Seven White American male blood donors with Italian surnames were found to have red cell glucose‐6‐phosphate dehydrogenase (G‐6‐PD) deficiency among 1,285 with Greek or Italian surnames screened. Five different genetic variants were found: G‐6‐PDs Mediterranean (2), ‘Athens‐like’ (2), San Juan, Columbus and ‘Canton‐like’.
P R, McCurdy, E E, Morse
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Malaria and Glucose-6-phosphate Dehydrogenase Deficiency

Nature, 1963
DRS. C. Kidson and J. G. Gorman1 report observations on frequencies of glucose-6-phosphate dehydrogenase (G6PD) deficiency in different parts of New Guinea and New Britain, which make a welcome addition to our knowledge of the population genetics of this area.
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Glucose-6-Phosphate Dehydrogenase Deficiency

Research Journal of Pharmacy and Technology, 2015
Aim: To review the inheritance, manifestation and management of glucose-6-phosphate dehydrogenase deficiency Objective: The article reviews the inheritance, management and manifestation of glucose-6- phosphate dehydrogenase (G6PD) deficiency. Background: Glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency) is an X-linked recessive genetic ...
J. Insira Sarbeen, Gowri Sethu
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Glucose-6-Phosphate Dehydrogenase Deficiency With Psychosis

Archives of General Psychiatry, 1976
Several authors have attempted to establish a correlation between glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and chronic schizophrenia, and the results were contradictory. We propose that the correlation between G-6-PD deficiency and schizophrenia is to be found in the form of an acute delirium.
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Glucose 6-Phosphate Dehydrogenase (G6PD) Deficiency

2001
Deficiency of the enzyme glucose 6-phosphate dehydrogenase (G6PD) in red blood cells is an inherited abnormality due to mutations of the G6PD gene on the X chromosome that renders the cells vulnerable to oxidative damage.
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Unexpected glucose‐6‐phosphate dehydrogenase deficiency

British Journal of Haematology, 2009
Wing-Yan, Au, Jovic, Tse, Jason C C, So, Thomas S K, Wan, Karl, Young   +4 more
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Prevalence of glucose-6-phosphate dehydrogenase deficiency

The Journal of Pediatrics, 1988
A K, Leung, D R, McLeod
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GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY IN LEPROSY

The Lancet, 1969
J H, Pettit, J, Chin
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