-
1
-
-
0024951961
-
Glucose-6-phosphate dehydrogenase deficiency
-
WHO Working Group
-
Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group. Bull World Health Organ. 1989;67:601-611.
-
(1989)
Bull World Health Organ
, vol.67
, pp. 601-611
-
-
-
2
-
-
0015542451
-
The epidemiology of favism
-
Belsey MA. The epidemiology of favism. Bull World Health Organ. 1973;48:1-13.
-
(1973)
Bull World Health Organ
, vol.48
, pp. 1-13
-
-
Belsey, M.A.1
-
3
-
-
0029933131
-
G6PD: Population genetics and clinical manifestations
-
Beutler E. G6PD: population genetics and clinical manifestations. Blood Rev. 1996;10:45-52.
-
(1996)
Blood Rev
, vol.10
, pp. 45-52
-
-
Beutler, E.1
-
4
-
-
0027940492
-
G6PD deficiency
-
Beutler E. G6PD deficiency. Blood. 1994;84:3613-3636.
-
(1994)
Blood
, vol.84
, pp. 3613-3636
-
-
Beutler, E.1
-
5
-
-
0014002412
-
Haemolysis due to glucose-6-phosphate dehydrogenase deficiency in Malaya
-
Lie-Injo LE, Pillay RP, Virik HK. Haemolysis due to glucose-6-phosphate dehydrogenase deficiency in Malaya. Trans R Soc Trop Med Hyg. 1966;60:262-266.
-
(1966)
Trans R Soc Trop Med Hyg
, vol.60
, pp. 262-266
-
-
Lie-Injo, L.E.1
Pillay, R.P.2
Virik, H.K.3
-
7
-
-
84920211306
-
Letter: Diagnosis of G-6-PD deficiency
-
Wood TA, Tooze JA, Dunbar E. Letter: diagnosis of G-6-PD deficiency. Lancet. 1975;2:657.
-
(1975)
Lancet
, vol.2
, pp. 657
-
-
Wood, T.A.1
Tooze, J.A.2
Dunbar, E.3
-
8
-
-
0029442158
-
Glucose-6-phosphate dehydrogenase deficiency in the newborn: Its prevalence and relation to neonatal jaundice
-
Tanphaichitr VS, Pung-amritt P, Yodthong S, Soongswang J, Mahasandana C, Suvatte V. Glucose-6-phosphate dehydrogenase deficiency in the newborn: its prevalence and relation to neonatal jaundice. Southeast Asian J Trop Med Public Health. 1995;26(suppl 1):137-141.
-
(1995)
Southeast Asian J Trop Med Public Health
, vol.26
, Issue.SUPPL. 1
, pp. 137-141
-
-
Tanphaichitr, V.S.1
Pung-amritt, P.2
Yodthong, S.3
Soongswang, J.4
Mahasandana, C.5
Suvatte, V.6
-
9
-
-
0019627835
-
Glucose-6-phosphate dehydrogenase deficiency, 2: Tropical Asia
-
Panich V. Glucose-6-phosphate dehydrogenase deficiency, 2: tropical Asia. Clin Haematol. 1981;10:800-814.
-
(1981)
Clin Haematol
, vol.10
, pp. 800-814
-
-
Panich, V.1
-
11
-
-
0036306730
-
Hematologically important mutations: Glucose-6-phosphate dehydrogenase
-
Beutler E, Vulliamy TJ. Hematologically important mutations: glucose-6-phosphate dehydrogenase. Blood Cells Mol Dis. 2002;28:93-103.
-
(2002)
Blood Cells Mol Dis
, vol.28
, pp. 93-103
-
-
Beutler, E.1
Vulliamy, T.J.2
-
12
-
-
0036481467
-
Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871 G>A) is the most common deficiency variant in the Thai population
-
Nuchprayoon I, Sanpavat S, Nuchprayoon S. Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871 G>A) is the most common deficiency variant in the Thai population. Hum Mutat. 2002;19:185-190.
-
(2002)
Hum Mutat
, vol.19
, pp. 185-190
-
-
Nuchprayoon, I.1
Sanpavat, S.2
Nuchprayoon, S.3
-
13
-
-
13844250277
-
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind)
-
Laosombat V, Sattayasevana B, Janejindamai W, et al. Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind). Blood Cells Mol Dis. 2005;34:191-196.
-
(2005)
Blood Cells Mol Dis
, vol.34
, pp. 191-196
-
-
Laosombat, V.1
Sattayasevana, B.2
Janejindamai, W.3
-
14
-
-
0014040790
-
Standardization of procedures for the study of glucose-6-phosphate dehydrogenase: Report of a WHO Scientific Group
-
Standardization of procedures for the study of glucose-6-phosphate dehydrogenase: report of a WHO Scientific Group. World Health Organ Tech Rep Ser. 1967;366:1-53.
-
(1967)
World Health Organ Tech Rep Ser
, vol.366
, pp. 1-53
-
-
-
15
-
-
0030031242
-
Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants
-
Huang CS, Hung KL, Huang MJ, Li YC, Liu TH, Tang TK. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants. Am J Hematol. 1996;51:19-25.
-
(1996)
Am J Hematol
, vol.51
, pp. 19-25
-
-
Huang, C.S.1
Hung, K.L.2
Huang, M.J.3
Li, Y.C.4
Liu, T.H.5
Tang, T.K.6
-
16
-
-
0036264433
-
Identification of G6PD Mediterranean mutation by amplification refractory mutation system
-
Maffi D, Pasquino MT, Caprari P, et al. Identification of G6PD Mediterranean mutation by amplification refractory mutation system. Clin Chim Acta. 2002;321:43-47.
-
(2002)
Clin Chim Acta
, vol.321
, pp. 43-47
-
-
Maffi, D.1
Pasquino, M.T.2
Caprari, P.3
-
17
-
-
0033108129
-
Studies on a G6PD polymorphic site, cDNA C1311T
-
Ren X, Du C, Lin Q. Studies on a G6PD polymorphic site, cDNA C1311T [in Chinese]. Zhonghua Xue Ye Xue Za Zhi. 1999;20:197-199.
-
(1999)
Zhonghua Xue Ye Xue Za Zhi
, vol.20
, pp. 197-199
-
-
Ren, X.1
Du, C.2
Lin, Q.3
-
18
-
-
0014575143
-
G6PD deficiency and favism in the island of Rhodes
-
Kattamis CA, Chaidas A, Chaidas S. G6PD deficiency and favism in the island of Rhodes (Greece). J Med Genet. 1969;6:286-291.
-
(1969)
J Med Genet
, vol.6
, pp. 286-291
-
-
Kattamis, C.A.1
Chaidas, A.2
Chaidas, S.3
-
19
-
-
36949071079
-
Favism and thalassaemia in Sardinia and their relationship to malaria
-
Siniscalco M, Bernini L, Latte B, Motulski AG. Favism and thalassaemia in Sardinia and their relationship to malaria. Nature. 1961;190:1179-1180.
-
(1961)
Nature
, vol.190
, pp. 1179-1180
-
-
Siniscalco, M.1
Bernini, L.2
Latte, B.3
Motulski, A.G.4
-
20
-
-
0026568987
-
Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education: The northern Sardinian experience
-
Meloni T, Forteleoni G, Meloni GF. Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education: the northern Sardinian experience. Acta Haematol. 1992;87:29-31.
-
(1992)
Acta Haematol
, vol.87
, pp. 29-31
-
-
Meloni, T.1
Forteleoni, G.2
Meloni, G.F.3
-
21
-
-
0020628953
-
Favism and hemolytic anemia in glucose-6-phosphate dehydrogenase- deficient subjects in North Sardinia
-
Meloni T, Forteleoni G, Dore A, Cutillo S. Favism and hemolytic anemia in glucose-6-phosphate dehydrogenase-deficient subjects in North Sardinia. Acta Haematol. 1983;70:83-90.
-
(1983)
Acta Haematol
, vol.70
, pp. 83-90
-
-
Meloni, T.1
Forteleoni, G.2
Dore, A.3
Cutillo, S.4
-
24
-
-
0033254047
-
Hemolytic crisis after excessive ingestion of fava beans in a male infant with G6PD Canton
-
Shibuya A, Hirono A, Ishii S, Fujii H, Miwa S. Hemolytic crisis after excessive ingestion of fava beans in a male infant with G6PD Canton. Int J Hematol. 1999;70:233-235.
-
(1999)
Int J Hematol
, vol.70
, pp. 233-235
-
-
Shibuya, A.1
Hirono, A.2
Ishii, S.3
Fujii, H.4
Miwa, S.5
-
25
-
-
0027537149
-
G6PD Aures: A new mutation (48 Ile→Thr) causing mild G6PD deficiency is associated with favism
-
Nafa K, Reghis A, Osmani N, et al. G6PD Aures: a new mutation (48 Ile→Thr) causing mild G6PD deficiency is associated with favism. Hum Mol Genet. 1993;2:81-82.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 81-82
-
-
Nafa, K.1
Reghis, A.2
Osmani, N.3
-
26
-
-
0028962122
-
Haptoglobin therapy for acute favism: A Japanese boy with glucose-6-phosphate dehydrogenase Guadalajara
-
Ohga S, Higashi E, Nomura A, et al. Haptoglobin therapy for acute favism: a Japanese boy with glucose-6-phosphate dehydrogenase Guadalajara. Br J Haematol. 1995;89:421-423.
-
(1995)
Br J Haematol
, vol.89
, pp. 421-423
-
-
Ohga, S.1
Higashi, E.2
Nomura, A.3
-
27
-
-
0015933602
-
Characterization of glucose-6-phosphate dehydrogenase in Thailand: The occurrence of 6 variants among 50 G-6-PD deficient Thai
-
Panich V, Sungnate T. Characterization of glucose-6-phosphate dehydrogenase in Thailand: the occurrence of 6 variants among 50 G-6-PD deficient Thai. Humangenetik. 1973;18:39-46.
-
(1973)
Humangenetik
, vol.18
, pp. 39-46
-
-
Panich, V.1
Sungnate, T.2
-
29
-
-
0025831075
-
Two commonly occurring nucleotide base substitutions in Chinese G6PD variants
-
Chiu DT, Zuo L, Chen E, et al. Two commonly occurring nucleotide base substitutions in Chinese G6PD variants. Biochem Biophys Res Commun. 1991;180:988-993.
-
(1991)
Biochem Biophys Res Commun
, vol.180
, pp. 988-993
-
-
Chiu, D.T.1
Zuo, L.2
Chen, E.3
-
30
-
-
0032041102
-
Molecular characterization of Chinese G6PD deficiency by using polymerase chain reaction/single strand conformation polymorphism
-
Chen BH, Lin SR, Chiang CH, Chao MC. Molecular characterization of Chinese G6PD deficiency by using polymerase chain reaction/single strand conformation polymorphism. Kaohsiung J Med Sci. 1998;14:197-202.
-
(1998)
Kaohsiung J Med Sci
, vol.14
, pp. 197-202
-
-
Chen, B.H.1
Lin, S.R.2
Chiang, C.H.3
Chao, M.C.4
-
31
-
-
0034891012
-
The genotype analysis of glucose-6-phosphate dehydrogenase deficiency in Yunnan province
-
Yang Z, Chu J, Ban G, Huang X, Xu S, Li M. The genotype analysis of glucose-6-phosphate dehydrogenase deficiency in Yunnan province [in Chinese]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001;18:259-263.
-
(2001)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.18
, pp. 259-263
-
-
Yang, Z.1
Chu, J.2
Ban, G.3
Huang, X.4
Xu, S.5
Li, M.6
-
32
-
-
1842858287
-
The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province
-
Yang Z, Chu J, Xu S, Lin K, Tao Y, Shi L. The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province [in Chinese]. Zhonghua Xue Ye Xue Za Zhi. 2000;21:509-511.
-
(2000)
Zhonghua Xue Ye Xue Za Zhi
, vol.21
, pp. 509-511
-
-
Yang, Z.1
Chu, J.2
Xu, S.3
Lin, K.4
Tao, Y.5
Shi, L.6
-
33
-
-
1842858996
-
Comparative study of three common G6PD gene mutations in Yao and Han People in Guangxi
-
Liu J, Ren X, Chen Q, et al. Comparative study of three common G6PD gene mutations in Yao and Han People in Guangxi [in Chinese]. Zhonghua Xue Ye Xue Za Zhi. 2000;21:190-191.
-
(2000)
Zhonghua Xue Ye Xue Za Zhi
, vol.21
, pp. 190-191
-
-
Liu, J.1
Ren, X.2
Chen, Q.3
-
34
-
-
0033011104
-
Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system
-
Du CS, Ren X, Chen L, Jiang W, He Y, Yang M. Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system. Hum Hered. 1999;49:133-138.
-
(1999)
Hum Hered
, vol.49
, pp. 133-138
-
-
Du, C.S.1
Ren, X.2
Chen, L.3
Jiang, W.4
He, Y.5
Yang, M.6
-
35
-
-
0026629648
-
Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: Five mutations account for most G6PD deficiency cases in Taiwan
-
Chang JG, Chiou SS, Perng LI, et al. Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan. Blood. 1992;80:1079-1082.
-
(1992)
Blood
, vol.80
, pp. 1079-1082
-
-
Chang, J.G.1
Chiou, S.S.2
Perng, L.I.3
-
36
-
-
0033209615
-
Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese
-
Ainoon O, Joyce J, Boo NY, Cheong SK, Zainal ZA, Hamidah NH. Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese. Hum Mutat. 1999;14:352-359.
-
(1999)
Hum Mutat
, vol.14
, pp. 352-359
-
-
Ainoon, O.1
Joyce, J.2
Boo, N.Y.3
Cheong, S.K.4
Zainal, Z.A.5
Hamidah, N.H.6
-
37
-
-
0027940286
-
Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in Singapore Chinese
-
Saha S, Saha N, Tay JS, Jeyaseelan K, Basair JB, Chew SE. Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in Singapore Chinese. Am J Hematol. 1994;47:273-277.
-
(1994)
Am J Hematol
, vol.47
, pp. 273-277
-
-
Saha, S.1
Saha, N.2
Tay, J.S.3
Jeyaseelan, K.4
Basair, J.B.5
Chew, S.E.6
-
38
-
-
0015407561
-
G-6-PD Mahidol: The most common glucose-6-phosphate dehydrogenase variant in Thailand
-
Panich V, Sungnate T, Wasi P, Na-Nakorn S. G-6-PD Mahidol: the most common glucose-6-phosphate dehydrogenase variant in Thailand. J Med Assoc Thai. 1972;55:576-585.
-
(1972)
J Med Assoc Thai
, vol.55
, pp. 576-585
-
-
Panich, V.1
Sungnate, T.2
Wasi, P.3
Na-Nakorn, S.4
-
39
-
-
0026591865
-
Glucose-6-phosphate dehydrogenase variants in Hawaii
-
Beutler E, Westwood B, Kuhl W, Hsia YE. Glucose-6-phosphate dehydrogenase variants in Hawaii. Hum Hered. 1992;42:327-329.
-
(1992)
Hum Hered
, vol.42
, pp. 327-329
-
-
Beutler, E.1
Westwood, B.2
Kuhl, W.3
Hsia, Y.E.4
-
40
-
-
17844388327
-
Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia
-
Iwai K, Hirono A, Matsuoka H, et al. Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia. Hum Genet. 2001;108:445-449.
-
(2001)
Hum Genet
, vol.108
, pp. 445-449
-
-
Iwai, K.1
Hirono, A.2
Matsuoka, H.3
-
41
-
-
0037208823
-
Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays
-
Ainoon O, Yu YH, Amir Muhriz AL, Boo NY, Cheong SK, Hamidah NH. Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays. Hum Mutat. 2003;21:101-109.
-
(2003)
Hum Mutat
, vol.21
, pp. 101-109
-
-
Ainoon, O.1
Yu, Y.H.2
Amir Muhriz, A.L.3
Boo, N.Y.4
Cheong, S.K.5
Hamidah, N.H.6
-
42
-
-
1842868529
-
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Malays in Malaysia
-
Yusoff NM, Shirakawa T, Nishiyama K, et al. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Malays in Malaysia. Int J Hematol. 2002;76:149-152.
-
(2002)
Int J Hematol
, vol.76
, pp. 149-152
-
-
Yusoff, N.M.1
Shirakawa, T.2
Nishiyama, K.3
-
43
-
-
0026357097
-
Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD "LeJeune."
-
Beutler E, Westwood B, Kuhl W. Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD "LeJeune." Acta Haematol. 1991;86:179-182.
-
(1991)
Acta Haematol
, vol.86
, pp. 179-182
-
-
Beutler, E.1
Westwood, B.2
Kuhl, W.3
-
44
-
-
0025203513
-
The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia
-
Beutler E, Kuhl W. The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia. Am J Hum Genet. 1990;47:1008-1012.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 1008-1012
-
-
Beutler, E.1
Kuhl, W.2
-
45
-
-
0025242265
-
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East
-
Kurdi-Haidar B, Mason PJ, Berrebi A, et al. Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. Am J Hum Genet. 1990;47:1013-1019.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 1013-1019
-
-
Kurdi-Haidar, B.1
Mason, P.J.2
Berrebi, A.3
-
47
-
-
0020049014
-
Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favism
-
Vives Corrons JL, Pujades A. Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favism. Hum Genet. 1982;60:216-221.
-
(1982)
Hum Genet
, vol.60
, pp. 216-221
-
-
Vives Corrons, J.L.1
Pujades, A.2
-
48
-
-
0017170066
-
Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type
-
Kahn A, Marie J, Desbois JC, Boivin P. Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type. Acta Haematol. 1976;56:58-64.
-
(1976)
Acta Haematol
, vol.56
, pp. 58-64
-
-
Kahn, A.1
Marie, J.2
Desbois, J.C.3
Boivin, P.4
-
49
-
-
2442721505
-
G6PD Aures: A rare mutant of G6PD in Saudi Arabia-molecular and clinical presentations
-
Niazi GA, Adeyokunnu A, Westwood B, Beutler E. G6PD Aures: a rare mutant of G6PD in Saudi Arabia-molecular and clinical presentations. Saudi Med J. 1996;17:311-314.
-
(1996)
Saudi Med J
, vol.17
, pp. 311-314
-
-
Niazi, G.A.1
Adeyokunnu, A.2
Westwood, B.3
Beutler, E.4
-
50
-
-
0032762791
-
Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism
-
Jablonska-Skwiecinska E, Lewandowska I, Plochocka D, et al. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism. Hum Mutat. 1999;14:477-484.
-
(1999)
Hum Mutat
, vol.14
, pp. 477-484
-
-
Jablonska-Skwiecinska, E.1
Lewandowska, I.2
Plochocka, D.3
-
51
-
-
0742324497
-
Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase
-
van Wijk R, Huizinga EG, Prins I, et al. Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase. Blood Cells Mol Dis. 2004;32:112-117.
-
(2004)
Blood Cells Mol Dis
, vol.32
, pp. 112-117
-
-
Van Wijk, R.1
Huizinga, E.G.2
Prins, I.3
-
52
-
-
0025121962
-
Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-)
-
Galiano S, Gaetani GF, Barabino A, et al. Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-). BMJ. 1990;300:236.
-
(1990)
BMJ
, vol.300
, pp. 236
-
-
Galiano, S.1
Gaetani, G.F.2
Barabino, A.3
|