-
1
-
-
0025831986
-
Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: Prevalence among 1 286 000 Greek newborn infants
-
Missiou-Tsagaraki S. Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: prevalence among 1 286 000 Greek newborn infants J Pediatr 1993;119:293-9.
-
(1993)
J Pediatr
, vol.119
, pp. 293-299
-
-
Missiou-Tsagaraki, S.1
-
2
-
-
79956318785
-
Drug-induced haemolytic anaemia and non-spherocytic haemolytic anaemia
-
Yoshida A, Beutler E, editors. Orlando: Academic
-
Beutler E. Drug-induced haemolytic anaemia and non-spherocytic haemolytic anaemia. In: Yoshida A, Beutler E, editors. Glucose-6-phosphate dehydrogenase. Orlando: Academic, 3-12.
-
Glucose-6-phosphate Dehydrogenase
, pp. 3-12
-
-
Beutler, E.1
-
3
-
-
0024604628
-
Incidence and causes of sepsis in glucose-6-phosphate dehydrogenase-deficient newborn infants
-
Abu-Osba YK, Mallouh AA, Hann RW. Incidence and causes of sepsis in glucose-6-phosphate dehydrogenase-deficient newborn infants. J Peditatr 1989;114:748-52.
-
(1989)
J Peditatr
, vol.114
, pp. 748-752
-
-
Abu-Osba, Y.K.1
Mallouh, A.A.2
Hann, R.W.3
-
4
-
-
0013963946
-
A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency and glutathione reductase deficiency
-
Beutler E. A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency and glutathione reductase deficiency. Blood 1966; 28:553-62.
-
(1966)
Blood
, vol.28
, pp. 553-562
-
-
Beutler, E.1
-
5
-
-
0012640767
-
Special modification of the fluorescent screening method for G6PD deficiency
-
Beutler E and Mitchell M. Special modification of the fluorescent screening method for G6PD deficiency. Blood 1968;32:826-35.
-
(1968)
Blood
, vol.32
, pp. 826-835
-
-
Beutler, E.1
Mitchell, M.2
-
6
-
-
0001585429
-
Glucose-6-phosphate dehydrogenase deficiency
-
Scriver CR, Beaudet AL, Sly WS, et al, editors. USA: McGraw-Hill publishers
-
Luzzatto L, Mahta A. Glucose-6-phosphate dehydrogenase deficiency. In: Scriver CR, Beaudet AL, Sly WS, et al, editors. The metabolic and molecular basis of inherited disease. USA: McGraw-Hill publishers, 1995:3367-98.
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 3367-3398
-
-
Luzzatto, L.1
Mahta, A.2
-
7
-
-
79956326732
-
G-6-PD diagnosis: Modification of the standard method eliminates the need for an additional haemoglobin determination
-
Reclos GJ, Hatzidakis CJ, Kruithof RA. G-6-PD diagnosis: modification of the standard method eliminates the need for an additional haemoglobin determination. Pharmakeftiki 1999;12:26-32.
-
(1999)
Pharmakeftiki
, vol.12
, pp. 26-32
-
-
Reclos, G.J.1
Hatzidakis, C.J.2
Kruithof, R.A.3
-
8
-
-
0014578097
-
Incidence and mechanism of neonatal jaundice related to glucose-6-phosphate dehydrogenase deficiency
-
Valaes T, Karaklis A, Stavrakakis D, et al. Incidence and mechanism of neonatal jaundice related to glucose-6-phosphate dehydrogenase deficiency. Pediatr Res 1969;3: 448-58.
-
(1969)
Pediatr Res
, vol.3
, pp. 448-458
-
-
Valaes, T.1
Karaklis, A.2
Stavrakakis, D.3
-
9
-
-
0002826398
-
The normal human female as a mosaic of X-chromosome activity: Studies using the gene for G-6-PD deficiency as a marker
-
Beutler E, Yeh M, Fairbanks VF. The normal human female as a mosaic of X-chromosome activity: studies using the gene for G-6-PD deficiency as a marker. Proc Natl Acad Sci USA 1962;48:9-16.
-
(1962)
Proc Natl Acad Sci USA
, vol.48
, pp. 9-16
-
-
Beutler, E.1
Yeh, M.2
Fairbanks, V.F.3
-
10
-
-
75449129733
-
Demonstration of two populations of cells in the human female heterozygous for glucose-6-phosphate dehydrogenase variants
-
Davidson RG, Nitowsky HM, Childs B. Demonstration of two populations of cells in the human female heterozygous for glucose-6-phosphate dehydrogenase variants. Proc Natl Acad Sci USA 1963;50:48-485.
-
(1963)
Proc Natl Acad Sci USA
, vol.50
, pp. 48-485
-
-
Davidson, R.G.1
Nitowsky, H.M.2
Childs, B.3
-
14
-
-
79956334134
-
Comparison between quantitative and qualitative G6PD screening of neonatal dried blood spots
-
Vienna, Austria
-
Tourna Å, Kruithof RA, Reclos GJ. Comparison between quantitative and qualitative G6PD screening of neonatal dried blood spots. Proceedings of the Seventh International Congress of Inborn Errors of Metabolism, Vienna, Austria, 1997:121.
-
(1997)
Proceedings of the Seventh International Congress of Inborn Errors of Metabolism
, pp. 121
-
-
Tourna, Å.1
Kruithof, R.A.2
Reclos, G.J.3
-
15
-
-
0033977661
-
An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis
-
Nicole JCL, Zielenski J, Tsui L-C, et al. An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis. FASEB 2000;14:111-27.
-
(2000)
FASEB
, vol.14
, pp. 111-127
-
-
Nicole, J.C.L.1
Zielenski, J.2
Tsui, L.-C.3
-
16
-
-
0021222591
-
Glucose-6-phosphate dehydrogenase deficiency: An easy and sensitive quantitative assay for the detection of female heterozygotes in red blood cells
-
Solem E. Glucose-6-phosphate dehydrogenase deficiency: an easy and sensitive quantitative assay for the detection of female heterozygotes in red blood cells. Clin Chim Acta 1984;142:135-45.
-
(1984)
Clin Chim Acta
, vol.142
, pp. 135-145
-
-
Solem, E.1
-
17
-
-
79956312517
-
G-6-PD deficiency: A new analyte for neonatal screening programmes?
-
Havana, Cuba
-
Neto EC, Becker D, Leile L. G-6-PD deficiency: a new analyte for neonatal screening programmes? Proceedings of Immunoensayo/97, Havana, Cuba, 1997.
-
(1997)
Proceedings of Immunoensayo/97
-
-
Neto, E.C.1
Becker, D.2
Leile, L.3
|