-
1
-
-
0025166591
-
Pathophysiology of haemolysis in glucose-6-phosphate dehydrogenase deficiency
-
Arese, P. & De Flora, A. (1990) Pathophysiology of haemolysis in glucose-6-phosphate dehydrogenase deficiency. Seminars in Haematology, 27, 1-39.
-
(1990)
Seminars in Haematology
, vol.27
, pp. 1-39
-
-
Arese, P.1
De Flora, A.2
-
2
-
-
0014284669
-
Variants of red cell glucose-6-phosphate dehydrogenase among Asiatic Indians
-
Azevedo, E., Kirkman, H.N., Morrow, A.C. & Motulsky, A.G. (1968) Variants of red cell glucose-6-phosphate dehydrogenase among Asiatic Indians. Annals of Human Genetics, 31, 373-379.
-
(1968)
Annals of Human Genetics
, vol.31
, pp. 373-379
-
-
Azevedo, E.1
Kirkman, H.N.2
Morrow, A.C.3
Motulsky, A.G.4
-
3
-
-
0029933131
-
G6PD: Population genetics and clinical manifestations
-
Beutler, E. (1996) G6PD: population genetics and clinical manifestations. Blood Reviews, 10, 53-58.
-
(1996)
Blood Reviews
, vol.10
, pp. 53-58
-
-
Beutler, E.1
-
5
-
-
0015812776
-
Seroepidemiological evidence of eradication of malaria from Mauritius
-
Bruce-Chwatt, L.J. & Draper, C.C. (1973) Seroepidemiological evidence of eradication of malaria from Mauritius. Lancet, ii, 547-551.
-
(1973)
Lancet
, vol.2
, pp. 547-551
-
-
Bruce-Chwatt, L.J.1
Draper, C.C.2
-
6
-
-
0027520218
-
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single strand conformation and sequence analysis
-
Calabrò, V., Mason, P.J., Filosa, S., Civitelli, D., Cittadella, R., Tagarelli, A., Martini, G., Brancti, C. & Luzzatto, L. (1993) Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single strand conformation and sequence analysis. American Journal of Human Genetics, 52, 527-563.
-
(1993)
American Journal of Human Genetics
, vol.52
, pp. 527-563
-
-
Calabrò, V.1
Mason, P.J.2
Filosa, S.3
Civitelli, D.4
Cittadella, R.5
Tagarelli, A.6
Martini, G.7
Brancti, C.8
Luzzatto, L.9
-
8
-
-
0013633952
-
-
Mahatma Gandhi Institute, Moka, Mauritius
-
Deerpalsingh, S. & Carter, M. (1994) In: Select Documents on Indian Immigration, Mauritius, Vol. 1, pp. 1834-1926. Mahatma Gandhi Institute, Moka, Mauritius.
-
(1994)
Select Documents on Indian Immigration, Mauritius
, vol.1
, pp. 1834-1926
-
-
Deerpalsingh, S.1
Carter, M.2
-
9
-
-
0025190032
-
High prevalence of NIDDM and impaired glucose tolerance in Indian, Creole, and Chinese Mauritians
-
Dowse, G.K., Gareeboo, H., Zimmet, P.Z., Alberti, G.M.M., Tuomilehto, J. Fareed, D, Brissonnette, L.G. & Finch, C.F. (1990) High prevalence of NIDDM and impaired glucose tolerance in Indian, Creole, and Chinese Mauritians. Diabetes, 39, 390-396.
-
(1990)
Diabetes
, vol.39
, pp. 390-396
-
-
Dowse, G.K.1
Gareeboo, H.2
Zimmet, P.Z.3
Alberti, G.M.M.4
Tuomilehto, J.5
Fareed, D.6
Brissonnette, L.G.7
Finch, C.F.8
-
11
-
-
0021347505
-
A new glucose-6-phosphate dehydrogenase variant (G6PD Kalyan) found in a Koli family
-
Ishwad, C.S. & Naik, S.N. (1984) A new glucose-6-phosphate dehydrogenase variant (G6PD Kalyan) found in a Koli family. Human Genetics, 66, 171-175.
-
(1984)
Human Genetics
, vol.66
, pp. 171-175
-
-
Ishwad, C.S.1
Naik, S.N.2
-
12
-
-
85038192029
-
-
(eds Bissoondoyal and Servansing). Mahatma Gandhi Institute, Moka, Mauritius
-
Jha, J.C. (1986) In: Indian Labour Immigration (eds Bissoondoyal and Servansing). Mahatma Gandhi Institute, Moka, Mauritius.
-
(1986)
Indian Labour Immigration
-
-
Jha, J.C.1
-
13
-
-
0013587360
-
A new glucose 6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala→Gly), is a major polymorphic variant in tribal populations in India
-
Kaeda, J.S., Chhotray, G.P., Ranjit, M.R., Bautista, J.M., Reddy, P.H., Stevens, D., Naidu, J.M., Britt, R.P., Vulliamy, T.J., Luzzatto, L. & Mason, P.J. (1995) A new glucose 6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala→Gly), is a major polymorphic variant in tribal populations in India. American Journal of Human Genetics, 47, 1013-1019.
-
(1995)
American Journal of Human Genetics
, vol.47
, pp. 1013-1019
-
-
Kaeda, J.S.1
Chhotray, G.P.2
Ranjit, M.R.3
Bautista, J.M.4
Reddy, P.H.5
Stevens, D.6
Naidu, J.M.7
Britt, R.P.8
Vulliamy, T.J.9
Luzzatto, L.10
Mason, P.J.11
-
14
-
-
0023075908
-
The sickle gene is widespread in India
-
Kar, B.C., Devi, S., Dash, K.C. & Das, M. (1987) The sickle gene is widespread in India. Transactions of the Royal Society of Medicine and Hygiene, 81, 273-275.
-
(1987)
Transactions of the Royal Society of Medicine and Hygiene
, vol.81
, pp. 273-275
-
-
Kar, B.C.1
Devi, S.2
Dash, K.C.3
Das, M.4
-
15
-
-
0029073256
-
Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island
-
Kotea, N., Baligadoo, S., Surrun, S.K., Ramasawmy, R., Lu, C.Y., Ducrocq, R., Labie, D., Krishnamoorthy, R. & Nagel, R.L. (1995) Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island. Blood, 86, 407-408.
-
(1995)
Blood
, vol.86
, pp. 407-408
-
-
Kotea, N.1
Baligadoo, S.2
Surrun, S.K.3
Ramasawmy, R.4
Lu, C.Y.5
Ducrocq, R.6
Labie, D.7
Krishnamoorthy, R.8
Nagel, R.L.9
-
16
-
-
0025242265
-
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD Mediterranean) in the Middle East
-
Kurdi-Haidar, B., Mason, P.J., Berriebi, A., Ankra-Badu, G., Al-Ali, A., Oppenheim, A. & Luzzatto, L. (1990) Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD Mediterranean) in the Middle East. American Journal of Human Genetics, 47, 1013-1019.
-
(1990)
American Journal of Human Genetics
, vol.47
, pp. 1013-1019
-
-
Kurdi-Haidar, B.1
Mason, P.J.2
Berriebi, A.3
Ankra-Badu, G.4
Al-Ali, A.5
Oppenheim, A.6
Luzzatto, L.7
-
17
-
-
0002770999
-
Glucose-6-phosphate dehydrogenase deficiency and haemolytic anaemia
-
(ed. by D. G. Nathan and F. A. Oski). Saunders, Philadelphia
-
Luzzatto, L. (1993) Glucose-6-phosphate dehydrogenase deficiency and haemolytic anaemia. Haematology of Infancy and Childhood (ed. by D. G. Nathan and F. A. Oski), pp. 674-691. Saunders, Philadelphia.
-
(1993)
Haematology of Infancy and Childhood
, pp. 674-691
-
-
Luzzatto, L.1
-
18
-
-
0001585429
-
Glucose-6-phosphate dehydrogenase deficiency
-
(ed. by C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle). McGraw-Hill, London
-
Luzzatto, L. & Mehta, A. (1995) Glucose-6-phosphate dehydrogenase deficiency. In: The Metabolic Basis of Inherited Disease (ed. by C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle). McGraw-Hill, London.
-
(1995)
The Metabolic Basis of Inherited Disease
-
-
Luzzatto, L.1
Mehta, A.2
-
19
-
-
0029757639
-
New insights into G6PD deficiency
-
Mason, P.J. (1996) New insights into G6PD deficiency. British Journal of Haematology. 94, 585-591.
-
(1996)
British Journal of Haematology
, vol.94
, pp. 585-591
-
-
Mason, P.J.1
-
20
-
-
0023638805
-
Neonatal jaundice and severity of glucose 6-phosphate dehydrogenase in Sardinian babies
-
Meloni, T., Cutillo, S., Testa, U. & Luzzatto, L. (1987) Neonatal jaundice and severity of glucose 6-phosphate dehydrogenase in Sardinian babies. Early Human Development, 15, 317-322.
-
(1987)
Early Human Development
, vol.15
, pp. 317-322
-
-
Meloni, T.1
Cutillo, S.2
Testa, U.3
Luzzatto, L.4
-
22
-
-
0028143967
-
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria
-
Nafa, K., Reghis, A., Osmani, N., Baghli, L., Aòt-Abes, H., Benabadji, M., Kaplan, J.C., Vulliamy, T. & Luzzatto, L. (1994) At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria. Human Genetics, 94, 513-517.
-
(1994)
Human Genetics
, vol.94
, pp. 513-517
-
-
Nafa, K.1
Reghis, A.2
Osmani, N.3
Baghli, L.4
Aòt-Abes, H.5
Benabadji, M.6
Kaplan, J.C.7
Vulliamy, T.8
Luzzatto, L.9
-
23
-
-
0027537149
-
G6PD Aures: A new mutation (48Ile→Thr) causing mild G6PD deficiency is associated with favism
-
Nafa, K., Reghis, A., Osmani, N., Baghli, L., Benabadji, M., Vulliamy, T. & Luzzatto, L. (1993) G6PD Aures: a new mutation (48Ile→Thr) causing mild G6PD deficiency is associated with favism. Human Molecular Genetics, 2, 81-82.
-
(1993)
Human Molecular Genetics
, vol.2
, pp. 81-82
-
-
Nafa, K.1
Reghis, A.2
Osmani, N.3
Baghli, L.4
Benabadji, M.5
Vulliamy, T.6
Luzzatto, L.7
-
24
-
-
0029879674
-
Glucose-6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme
-
Naylor, C.E., Rowland, P., Basak, A.K., Gover, S., Mason, P.J., Bautista, J.M., Vulliamy, T.J., Luzzatto, L. & Adams, M.J. (1996) Glucose-6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme. Blood, 87, 2974-2982.
-
(1996)
Blood
, vol.87
, pp. 2974-2982
-
-
Naylor, C.E.1
Rowland, P.2
Basak, A.K.3
Gover, S.4
Mason, P.J.5
Bautista, J.M.6
Vulliamy, T.J.7
Luzzatto, L.8
Adams, M.J.9
-
25
-
-
0020841311
-
DNA in heritable disease
-
Sykes, B.C. (1983) DNA in heritable disease. Lancet, ii, 787-788.
-
(1983)
Lancet
, vol.2
, pp. 787-788
-
-
Sykes, B.C.1
|