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Results of search for 'su:"Glucosephosphate Dehydrogenase Deficiency"', page 131 of 236
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Authors
Bancone, Germana
Beutler, E
Boivin, P
Calabrese, E J
Cutillo, S
De Flora, A
Fiorelli, G
Fujii, H
Hammerman, C
Jacobasch, G
Kahn, A
Kaplan, M
Kaplan, Michael
Luzzatto, L
Meloni, T
Miwa, S
Morelli, A
Saha, N
Yoshida, A
el-Hazmi, M A
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Topics
Adolescent
Adult
Anemia, Hemolytic
Child
Child, Preschool
Erythrocytes
Female
Glucosephosphate Dehydrogenase
Glucosephosphate Dehydrogenase Deficiency
Humans
Infant, Newborn
Male
blood
complications
diagnosis
enzymology
epidemiology
etiology
genetics
metabolism
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2601.
[Hereditary coproporphyria with grand mal epilepsy, glucose-6-phosphate dehydrogenase deficiency and phenobarbital tolerance].
[electronic resource]
by
Grosser, S
Klose, G
Weisner, B
Doss, M
Producer:
19870130
In:
Der Internist
vol. 27
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2602.
The plasma membrane of human erythrocyte with different levels of glucose-6-phosphate dehydrogenase.
[electronic resource]
by
Afolayan, A
Producer:
19790917
In:
The International journal of biochemistry
vol. 10
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2603.
A combined system for the study of glutathione metabolism in erythrocytes.
[electronic resource]
by
Ishida, Y
Nakashima, K
Fujii, H
Miwa, S
Producer:
19790816
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 93
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2604.
Regulation of 5-phosphoribosyl-1-pyrophosphate synthesis in human fibroblasts by the concentration of inorganic phosphate.
[electronic resource]
by
Raivio, K O
Lazar, C S
Becker, M A
Producer:
19820222
In:
Biochimica et biophysica acta
vol. 678
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2605.
New genetic variants of glucose 6-phosphate dehydrogenase (G6PD) in Italy.
[electronic resource]
by
Sansone, G
Perroni, L
Testa, U
Mareni, C
Luzzatto, L
Producer:
19820212
In:
Annals of human genetics
vol. 45
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2606.
[Etiology of hemolytic anemia].
[electronic resource]
by
Schmidt, P M
Producer:
19811122
In:
Schweizerische medizinische Wochenschrift
vol. 111
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2607.
Survey on haemoglobin variants, beta-thalassaemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobin types in Turkish people living in Manavgat, Serik and Boztepe (Antalya).
[electronic resource]
by
Aksoy, M
Dinçol, G
Erdem, S
Producer:
19800425
In:
Human heredity
vol. 30
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2608.
Mosaicism in female hybrid hares heterozygous for glucose-6-phosphate dehydrogenase (G-6-PD). II. Changes in the ratios of G-6-PD types in skin fibroblast cultures carried through multiple passages.
[electronic resource]
by
Janakidevi, K
Lee, K T
Thomas, W A
Reiner, J M
Murray, C D
Producer:
19810528
In:
Experimental and molecular pathology
vol. 34
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2609.
Neonatal hyperbilirubinaemia in heterozygous glucose-6-phosphate dehydrogenase deficient females.
[electronic resource]
by
Meloni, T
Forteleoni, G
Dore, A
Cutillo, S
Producer:
19830324
In:
British journal of haematology
vol. 53
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2610.
Further evidence for heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Papua New Guinea.
[electronic resource]
by
Chockkalingam, K
Board, P G
Producer:
19810327
In:
Human genetics
vol. 56
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2611.
The nonspherocytic congenital haemolytic anaemias.
[electronic resource]
by
de Gruchy, G C
Grimes, A J
Producer:
19730313
In:
British journal of haematology
vol. 23
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2612.
Glucose-6-phosphate dehydrogenase deficiency and intravascular haemolysis.
[electronic resource]
by
Onadeko, B O
Bademosi, O
Producer:
19741108
In:
Irish journal of medical science
vol. 143
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2613.
Childhood anaemias in Melanesia: a haematological survey among children of Papua-New Guinea.
[electronic resource]
by
Kidson, C
Curtain, C C
Gorman, J G
Producer:
19670228
In:
The Medical journal of Australia
vol. 2
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2614.
Glucose-6-phosphate dehydrogenase deficiency, hemoglobin and haptoglobin types in Mexicans and American Negroes.
[electronic resource]
by
Naik, S N
Anderson, D E
Producer:
19711112
In:
Texas reports on biology and medicine
vol. 29
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2615.
Acute haemolysis complicating co-trimoxazole therapy for typhoid fever in a patient with G.-6-P.D. deficiency.
[electronic resource]
by
Owusu, S K
Producer:
19721116
In:
Lancet (London, England)
vol. 2
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2616.
Xg blood-groups and clonal-origin theory of chronic myeloid leukaemia.
[electronic resource]
by
Lawler, S D
Sanger, R
Producer:
19700420
In:
Lancet (London, England)
vol. 1
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2617.
[Unusual causes of neonatal jaundice].
[electronic resource]
by
Cordone, G
Borrone, C
Massimo, L
Famularo, L
Moscatelli, P
Producer:
19690404
In:
Minerva pediatrica
vol. 19
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2618.
Hemolysis and jaundice in the newborn following maternal treatment with sulfamethoxypyridazine (kynex).
[electronic resource]
by
Brown, A K
Cevik, N
Producer:
19660203
In:
Pediatrics
vol. 36
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2619.
Three genetic markers and malaria in upper caste hindus of Kheda District of Gujarat State.
[electronic resource]
by
Pant, C S
Gupta, D K
Bhatt, R M
Gautam, A S
Sharma, R C
Producer:
19940815
In:
Indian journal of malariology
vol. 30
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2620.
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant.
[electronic resource]
by
Cappellini, M D
Martinez di Montemuros, F
Dotti, C
Tavazzi, D
Fiorelli, G
Producer:
19950511
In:
Human genetics
vol. 95
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