-
1
-
-
0023112573
-
Hemoglobinopathies in Southeast Asia
-
Fucharoen S, Winichagoon P: Hemoglobinopathies in Southeast Asia. Hemoglobin 1987;11:65-88.
-
(1987)
Hemoglobin
, vol.11
, pp. 65-88
-
-
Fucharoen, S.1
Winichagoon, P.2
-
2
-
-
0036402894
-
Hb Paksé [(α2) codon 142 (TAA→TAT or Term→Tyr)] in Thai patients with EABart's disease and Hb H disease
-
Sanchaisuriya K, Fucharoen G, Fucharoen S: Hb Paksé [(α2) codon 142 (TAA→TAT or Term→Tyr)] in Thai patients with EABart's disease and Hb H disease. Hemoglobin 2002;26:227-235.
-
(2002)
Hemoglobin
, vol.26
, pp. 227-235
-
-
Sanchaisuriya, K.1
Fucharoen, G.2
Fucharoen, S.3
-
3
-
-
0036180261
-
Clinical phenotypes and molecular characterization of Hb H-Paksé disease
-
Viprakasit V, Tanphaichitr VS, Pung-Amritt P, Petrarat S, Suwantol L, Fischer C, Higgs DR: Clinical phenotypes and molecular characterization of Hb H-Paksé disease. Haematologica 2002;87:117-125.
-
(2002)
Haematologica
, vol.87
, pp. 117-125
-
-
Viprakasit, V.1
Tanphaichitr, V.S.2
Pung-Amritt, P.3
Petrarat, S.4
Suwantol, L.5
Fischer, C.6
Higgs, D.R.7
-
4
-
-
0018751682
-
Hemoglobin Suan-Dok (α2 109 (G16) Leu replaced by Arg β2): An unstable variant associated with α-thalassemia
-
Sanguansermsri T, Matragoon S, Changloah L, Flatz G: Hemoglobin Suan-Dok (α2 109 (G16) Leu replaced by Arg β2): An unstable variant associated with α-thalassemia. Hemoglobin 1979;3:161-174.
-
(1979)
Hemoglobin
, vol.3
, pp. 161-174
-
-
Sanguansermsri, T.1
Matragoon, S.2
Changloah, L.3
Flatz, G.4
-
5
-
-
0027051443
-
Hb Q-Thailand [α74(EF3)Asp→His]: Gene organization, molecular structure and DNA diagnosis
-
Zeng FY, Fucharoen S, Huang SZ, Rodgers GP: Hb Q-Thailand [α74(EF3)Asp→His]: Gene organization, molecular structure and DNA diagnosis. Hemoglobin 1992;16:481-491.
-
(1992)
Hemoglobin
, vol.16
, pp. 481-491
-
-
Zeng, F.Y.1
Fucharoen, S.2
Huang, S.Z.3
Rodgers, G.P.4
-
8
-
-
0031850660
-
α- and β-thalassemia in Thailand
-
Fucharoen S, Winichagoon P, Sirithanaratkul N, Chowthaworn J, Pootrakul P: α-and β-thalassemia in Thailand. Ann NY Acad Sci 1998;850:412-414.
-
(1998)
Ann NY Acad Sci
, vol.850
, pp. 412-414
-
-
Fucharoen, S.1
Winichagoon, P.2
Sirithanaratkul, N.3
Chowthaworn, J.4
Pootrakul, P.5
-
9
-
-
0002225638
-
Hemoglobin analysis
-
Weatherall DJ (ed): New York, Churchill-Livingstone
-
Wood WG: Hemoglobin analysis; in Weatherall DJ (ed): The Thalassemia. New York, Churchill-Livingstone, 1983, pp 31-37.
-
(1983)
The Thalassemia
, pp. 31-37
-
-
Wood, W.G.1
-
10
-
-
0028123021
-
Rapid and simultaneous non-radioactive method for detecting α-thalassemia 1 (SEA type) and hemoglobin Constant Spring gene
-
Fucharoen G, Fucharoen S: Rapid and simultaneous non-radioactive method for detecting α-thalassemia 1 (SEA type) and hemoglobin Constant Spring gene. Eur J Haematol 1994;53:186-187.
-
(1994)
Eur J Haematol
, vol.53
, pp. 186-187
-
-
Fucharoen, G.1
Fucharoen, S.2
-
12
-
-
0027939934
-
A simple non-radioactive assay for hemoglobin E gene in prenatal diagnosis
-
Fucharoen S, Fucharoen G, Ratanasiri T, Jetsrisuparb A, Fukumaki Y: A simple non-radioactive assay for hemoglobin E gene in prenatal diagnosis. Clin Chim Acta 1994;229:197-203.
-
(1994)
Clin Chim Acta
, vol.229
, pp. 197-203
-
-
Fucharoen, S.1
Fucharoen, G.2
Ratanasiri, T.3
Jetsrisuparb, A.4
Fukumaki, Y.5
-
13
-
-
0025135102
-
Locus assignment of human α globin mutations by selective amplification and direct sequencing
-
Dode C, Rochette J, Krishnamoorthy R: Locus assignment of human α globin mutations by selective amplification and direct sequencing. Br J Haematol 1990;76:275-281.
-
(1990)
Br J Haematol
, vol.76
, pp. 275-281
-
-
Dode, C.1
Rochette, J.2
Krishnamoorthy, R.3
-
14
-
-
0037542682
-
Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family
-
Fucharoen S, Changtrakun Y, Ratanasiri T, Fucharoen G, Sanchaisuriya K: Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family. Eur J Haematol 2003;70:304-309.
-
(2003)
Eur J Haematol
, vol.70
, pp. 304-309
-
-
Fucharoen, S.1
Changtrakun, Y.2
Ratanasiri, T.3
Fucharoen, G.4
Sanchaisuriya, K.5
-
15
-
-
0024509622
-
A review of the molecular genetics of the human α-globin gene cluster
-
Higgs DR, Vickers MA, Wilkie AOM, Pretorius IM, Jarman AP, Weatherall DJ: A review of the molecular genetics of the human α-globin gene cluster. Blood 1989;73:1081-1104.
-
(1989)
Blood
, vol.73
, pp. 1081-1104
-
-
Higgs, D.R.1
Vickers, M.A.2
Wilkie, A.O.M.3
Pretorius, I.M.4
Jarman, A.P.5
Weatherall, D.J.6
-
16
-
-
0023873763
-
Correlation of clinical phenotype to genotype in haemoglobin H disease
-
Kattamis C, Tzotzos S, Kanavakis E, Synodinos J, Metaxotou-Mavrommati A: Correlation of clinical phenotype to genotype in haemoglobin H disease. Lancet 1988;i:442-444.
-
(1988)
Lancet
, vol.1
, pp. 442-444
-
-
Kattamis, C.1
Tzotzos, S.2
Kanavakis, E.3
Synodinos, J.4
Metaxotou-Mavrommati, A.5
-
18
-
-
0026686425
-
Hb H disease in Sardinia: Molecular, hematological and clinical aspects
-
Galanello R, Aru B, Dessi C, Addis M, Paglietti E, Melis MA, Cocco S, Massa P, Giagu N, Barella S, Turco MP, Maccioni L, Cao A: Hb H disease in Sardinia: Molecular, hematological and clinical aspects. Acta Haematol 1992;88:1-6.
-
(1992)
Acta Haematol
, vol.88
, pp. 1-6
-
-
Galanello, R.1
Aru, B.2
Dessi, C.3
Addis, M.4
Paglietti, E.5
Melis, M.A.6
Cocco, S.7
Massa, P.8
Giagu, N.9
Barella, S.10
Turco, M.P.11
Maccioni, L.12
Cao, A.13
-
19
-
-
0034710582
-
Genetic and clinical features of hemoglobin H disease in Chinese patients
-
Chen FE, Ooi C, Ha SY, Cheung BMY, Todd D, Liang R, Chan TK, Chan V: Genetic and clinical features of hemoglobin H disease in Chinese patients. N Engl J Med 2000;343:544-550.
-
(2000)
N Engl J Med
, vol.343
, pp. 544-550
-
-
Chen, F.E.1
Ooi, C.2
Ha, S.Y.3
Cheung, B.M.Y.4
Todd, D.5
Liang, R.6
Chan, T.K.7
Chan, V.8
-
20
-
-
0034897265
-
Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases
-
Waye J, Eng B, Patterson M, Walker L, Carcao MD, Olivieri NF, Chui DHK: Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases. Am J Hematol 2001;68:11-15.
-
(2001)
Am J Hematol
, vol.68
, pp. 11-15
-
-
Waye, J.1
Eng, B.2
Patterson, M.3
Walker, L.4
Carcao, M.D.5
Olivieri, N.F.6
Chui, D.H.K.7
-
21
-
-
0034492252
-
Phenotype and molecular diversity of haemoglobin H disease: A Greek experience
-
Kanavakis E, Papassotiriou I, Karagiorga M, Vrettou C, Metaxotou-Mavrommati A, Stamoulakatou A, Kattamis C, Traeger-Synodinos J: Phenotype and molecular diversity of haemoglobin H disease: A Greek experience. Br J Haematol 2000;111:915-923.
-
(2000)
Br J Haematol
, vol.111
, pp. 915-923
-
-
Kanavakis, E.1
Papassotiriou, I.2
Karagiorga, M.3
Vrettou, C.4
Metaxotou-Mavrommati, A.5
Stamoulakatou, A.6
Kattamis, C.7
Traeger-Synodinos, J.8
-
22
-
-
0028224578
-
Molecular basis and hematological characterization of hemoglobin H disease in Southeast Asia
-
Liu TC, Chiou SS, Lin SF, Chen TP, Tseng WP, Chen PH, Chang JG: Molecular basis and hematological characterization of hemoglobin H disease in Southeast Asia. Am J Hematol 1994;45:293-297.
-
(1994)
Am J Hematol
, vol.45
, pp. 293-297
-
-
Liu, T.C.1
Chiou, S.S.2
Lin, S.F.3
Chen, T.P.4
Tseng, W.P.5
Chen, P.H.6
Chang, J.G.7
-
23
-
-
0033752241
-
Phenotype-genotype correlation in Sicilian patients with Hb H
-
Mirabile E, Samperi P, Di Cataldo A, Poli A, La Spina M, Schilir G: Phenotype-genotype correlation in Sicilian patients with Hb H. Eur J Haematol 2000;65:306-309.
-
(2000)
Eur J Haematol
, vol.65
, pp. 306-309
-
-
Mirabile, E.1
Samperi, P.2
Di Cataldo, A.3
Poli, A.4
La Spina, M.5
Schilir, G.6
-
24
-
-
0022964477
-
Molecular basis for Hb H disease in Italy: Geographical distribution of deletional and nondeletional α-thalassemia haplotypes
-
Di Rienzo A, Novelletto A, Aliquo MC, Bianco I, Tagarelli A, Brancati C, Columbo B, Felicetti L: Molecular basis for Hb H disease in Italy: Geographical distribution of deletional and nondeletional α-thalassemia haplotypes. Am J Hum Genet 1986;39:631-639.
-
(1986)
Am J Hum Genet
, vol.39
, pp. 631-639
-
-
Di Rienzo, A.1
Novelletto, A.2
Aliquo, M.C.3
Bianco, I.4
Tagarelli, A.5
Brancati, C.6
Columbo, B.7
Felicetti, L.8
-
26
-
-
0031032788
-
The unusual pathobiology of hemoglobin Constant Spring red blood cells
-
Schrier SL, Bunyaratvej A, Khuhapinant A, Fucharoen S, Aljurf M, Snyder LM, Keifer CR, Ma L, Mohandas N: The unusual pathobiology of hemoglobin Constant Spring red blood cells. Blood 1997;89:1762-1769.
-
(1997)
Blood
, vol.89
, pp. 1762-1769
-
-
Schrier, S.L.1
Bunyaratvej, A.2
Khuhapinant, A.3
Fucharoen, S.4
Aljurf, M.5
Snyder, L.M.6
Keifer, C.R.7
Ma, L.8
Mohandas, N.9
-
28
-
-
0031053941
-
Molecular defects in Hb H hydrops fetalis
-
Chan V, Chan WY, Tang M, Lau K, Todd D, Chan TK: Molecular defects in Hb H hydrops fetalis. Br J Haematol 1997;96:224-228.
-
(1997)
Br J Haematol
, vol.96
, pp. 224-228
-
-
Chan, V.1
Chan, W.Y.2
Tang, M.3
Lau, K.4
Todd, D.5
Chan, T.K.6
-
29
-
-
0037305250
-
Hemoglobin H disease: Not necessarily a benign disorder
-
Chui DHK, Fucharoen S, Chan V: Hemoglobin H disease: Not necessarily a benign disorder. Blood 2003;101:791-800.
-
(2003)
Blood
, vol.101
, pp. 791-800
-
-
Chui, D.H.K.1
Fucharoen, S.2
Chan, V.3
-
30
-
-
0023515184
-
Clinical and hematologic manifestations of AEBart's disease
-
Fucharoen S, Winichagoon P, Prayoonwiwat W, Pootrakul P, Piankijagum A, Wasi P: Clinical and hematologic manifestations of AEBart's disease. Birth Defects Original Article Ser 1988;23/5A:327-332.
-
(1988)
Birth Defects Original Article Ser
, vol.23
, Issue.5 A
, pp. 327-332
-
-
Fucharoen, S.1
Winichagoon, P.2
Prayoonwiwat, W.3
Pootrakul, P.4
Piankijagum, A.5
Wasi, P.6
|