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Results of search for 'su:"Glucosephosphate Dehydrogenase Deficiency"', page 105 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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Results
2081.
Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.
[electronic resource]
by
Rinaldi, A
Filippi, G
Siniscalco, M
Producer:
19770103
In:
American journal of human genetics
vol. 28
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2082.
[Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Rumania: anthropogenetic significance].
[electronic resource]
by
Schneer, J H
Chipail, A
Producer:
19780218
In:
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi
vol. 81
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2083.
[Hereditary diseases of the blood system--erythrocytopathies].
[electronic resource]
by
Gavrilov, O K
Tokarev, Iu N
Producer:
19770428
In:
Vestnik Akademii meditsinskikh nauk SSSR
no. 8
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2084.
Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene.
[electronic resource]
by
Vulliamy, T
Beutler, E
Luzzatto, L
Producer:
19931006
In:
Human mutation
vol. 2
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2085.
Acute intravascular haemolysis following exchange transfusion with G-6-PD deficient blood.
[electronic resource]
by
Kumar, P
Sarkar, S
Narang, A
Producer:
19940517
In:
European journal of pediatrics
vol. 153
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2086.
Molecular genetics of glucose-6-phosphate dehydrogenase deficiency in Mexico.
[electronic resource]
by
Medina, M D
Vaca, G
Lopez-Guido, B
Westwood, B
Beutler, E
Producer:
19971003
In:
Blood cells, molecules & diseases
vol. 23
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2087.
The HLA system and G6PD deficiency in the Bulgarian population.
[electronic resource]
by
Minev, M
Bulanov, A G
Producer:
19810226
In:
Tissue antigens
vol. 15
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2088.
Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.
[electronic resource]
by
Wolfsdorf, J I
Holm, I A
Weinstein, D A
Producer:
20000118
In:
Endocrinology and metabolism clinics of North America
vol. 28
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2089.
METHEMOGLOBIN REDUCTION. STUDIES OF THE INTERACTION BETWEEN CELL POPULATIONS AND OF THE ROLE OF METHYLENE BLUE.
[electronic resource]
by
BEUTLER, E
BALUDA, M C
Producer:
19961201
In:
Blood
vol. 22
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2090.
THE MECHANISM OF HAEMOLYSIS IN FAVISM. SOME ANALOGY IN THE ACTIVITY OF PRIMAQUINE AND FAVA JUICE.
[electronic resource]
by
PANIZON, F
ZACCHELLO, F
Producer:
19961201
In:
Acta haematologica
vol. 33
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2091.
G6PD deficient alleles and haplotype analysis of human G6PD locus in São Tomé e Príncipe (West Africa).
[electronic resource]
by
Manco, Licínio
Botigué, Laura R
Ribeiro, M Letícia
Abade, Augusto
Producer:
20080625
In:
Human biology
vol. 79
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2092.
G6PD deficiency in autism: a case-series from Saudi Arabia.
[electronic resource]
by
Al-Salehi, Saleh M
Ghaziuddin, Mohammad
Producer:
20090713
In:
European child & adolescent psychiatry
vol. 18
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2093.
Potential risks of hemolysis after short-term administration of analgesics in children with glucose-6-phosphate dehydrogenase deficiency.
[electronic resource]
by
Najafi, Nadia
Van de Velde, Anne
Poelaert, Jan
Producer:
20111230
In:
The Journal of pediatrics
vol. 159
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2094.
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation.
[electronic resource]
by
Minucci, Angelo
De Luca, Daniele
Torti, Eleonora
Concolino, Paola
Maurizi, Palma
Giardina, Bruno
Zuppi, Cecilia
Capoluongo, Ettore
Producer:
20110906
In:
Annals of clinical biochemistry
vol. 48
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2095.
A young man with severe acute haemolytic anaemia.
[electronic resource]
by
Chen, Xi
He, Yongshu
Miao, Yinglei
Yang, Zhaoqing
Cui, Liwang
Producer:
20171130
In:
BMJ (Clinical research ed.)
vol. 359
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2096.
Reference levels for glucose-6-phosphate dehydrogenase enzyme activity in infants 7-90 days old in Taiwan.
[electronic resource]
by
Yang, Wen-Chien
Tai, Shin
Hsu, Chu-Ling
Fu, Chun-Min
Chou, An-Kuo
Shao, Pei-Lan
Li, Meng-Ju
Producer:
20200701
In:
Journal of the Formosan Medical Association = Taiwan yi zhi
vol. 119
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2097.
[Phenotypic and genotypic spectra of patients with glucose-6-phosphate dehydrogenase deficiency gene known pathogenic variants: a single-center study].
[electronic resource]
by
Chen, X
Yang, L
Wang, H J
Wu, B B
Lu, Y L
Dong, X R
Zhou, W H
Producer:
20190401
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 56
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2098.
Hyperhaemolytic and vascular occlusive crises in sickle cell disease. A case report with brief review of literature.
[electronic resource]
by
Phadke, M A
Kate, S L
Sainami, G S
Mutalik, G S
Phadke, M V
Baxi, A J
Producer:
19760209
In:
The Journal of the Association of Physicians of India
vol. 23
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2099.
Frequency of ABO blood groups, sickle-cell haemoglobin, G-6-PD deficiency and their relation with malaria in scheduled castes and scheduled tribes of Kheda District, Gujarat.
[electronic resource]
by
Pant, C S
Gupta, D K
Sharma, R C
Gautam, A S
Bhatt, R M
Producer:
19930330
In:
Indian journal of malariology
vol. 29
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2100.
Increased incidence of hyperbilirubinaemia in 'unchallenged' glucose-6-phosphate dehydrogenase deficiency in term Saudi newborns.
[electronic resource]
by
Yaish, H M
Niazi, G A
al Shaalan, M
Khan, S
Ahmed, G S
Producer:
19911204
In:
Annals of tropical paediatrics
vol. 11
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