-
1
-
-
0004252205
-
The clinical features of sickle cell disease
-
In: Bearn AG, Black DAK, Hiatt HH, editors., Vol. Amsterdam: North-Holland Publishing Company
-
Serjeant GR. The clinical features of sickle cell disease. In: Bearn AG, Black DAK, Hiatt HH, editors. Clinical Studies, Vol. 4. Amsterdam: North-Holland Publishing Company; 1974. p. 59.
-
(1974)
Clinical Studies
, vol.4
, pp. 59
-
-
Serjeant, G.R.1
-
2
-
-
0014619771
-
A new sickling disorder resulting from interaction of the genes of hemoglobin S and alpha-thalassaemia
-
Weatherall DJ, Clegg JB, Blankson J, McNeil JR. A new sickling disorder resulting from interaction of the genes of hemoglobin S and alpha-thalassaemia. Br J Hematol 1969;17:517-526.
-
(1969)
Br J Hematol
, vol.17
, pp. 517-526
-
-
Weatherall, D.J.1
Clegg, J.B.2
Blankson, J.3
McNeil, J.R.4
-
3
-
-
84896132093
-
Osteoblastic activity in sickle cell disease
-
Afonja OA. Osteoblastic activity in sickle cell disease. Clin Chem Newsletter 1982;3:161-163.
-
(1982)
Clin Chem Newsletter
, vol.3
, pp. 161-163
-
-
Afonja, O.A.1
-
6
-
-
84857482383
-
Sickle cell- β thalassemia
-
Serjeant GR, editor., Third edition. Oxford: Oxford University Press
-
Serjeant GR. Sickle cell- β thalassemia. In: Serjeant GR, editor. Sickle Cell Disease, Third edition. Oxford: Oxford University Press; 2001.
-
(2001)
Sickle Cell Disease
-
-
Serjeant, G.R.1
-
8
-
-
85047692316
-
Thalassemia intermedia in Cyprus. The interaction of alpha and beta thalassemia
-
Wainscoat JS, Kanavakis E, Wood WG, et al. Thalassemia intermedia in Cyprus. The interaction of alpha and beta thalassemia. Br J Haematol 1983;53:411-416.
-
(1983)
Br J Haematol
, vol.53
, pp. 411-416
-
-
Wainscoat, J.S.1
Kanavakis, E.2
Wood, W.G.3
-
9
-
-
0024338661
-
Molecular analysis of β0-thalassemia intermedia in Sardinia
-
Galanello R, Dessi E, Melis MA, et al., Molecular analysis of β0-thalassemia intermedia in Sardinia. Blood 1989;74:823-827.
-
(1989)
Blood
, vol.74
, pp. 823-827
-
-
Galanello, R.1
Dessi, E.2
Melis, M.A.3
-
10
-
-
0020531669
-
The triplicated alpha gene locus and β-thalassemia
-
Kanavakis E, Metaxotou-Mavromati A, Kattamis C, Wainscoat JS, Wood WG. The triplicated alpha gene locus and β-thalassemia. Br J Haematol 1983;54:201-207.
-
(1983)
Br J Haematol
, vol.54
, pp. 201-207
-
-
Kanavakis, E.1
Metaxotou-Mavromati, A.2
Kattamis, C.3
Wainscoat, J.S.4
Wood, W.G.5
-
11
-
-
85047689933
-
Thalassemia intermedia: Interaction of the triple alpha-globin gene arrangement and heterozygous ß-halassemia
-
Kulozik AE, Thein SL, Wainscoat JS, et al., Thalassemia intermedia: Interaction of the triple alpha-globin gene arrangement and heterozygous ß-halassemia. Br J Haematol 1987;66:109-112.
-
(1987)
Br J Haematol
, vol.66
, pp. 109-112
-
-
Kulozik, A.E.1
Thein, S.L.2
Wainscoat, J.S.3
-
12
-
-
0029964907
-
The triplicated α-globin gene locus in ß-thalassemia heterozygotes: Clinical, haematological, biosynthetic and molecular studies
-
Traeger-Synodinos J, Kanavakis E, Vrettou C, et al. The triplicated α-globin gene locus in ß-thalassemia heterozygotes: Clinical, haematological, biosynthetic and molecular studies. Br J Haematol 1996;95:467-471.
-
(1996)
Br J Haematol
, vol.95
, pp. 467-471
-
-
Traeger-Synodinos, J.1
Kanavakis, E.2
Vrettou, C.3
-
15
-
-
0021011759
-
The triplicated alpha gene locus and heterozygous beta thalassemia: A case of thalassemia intermedia
-
Sampietro M, Cazzola M, Cappelini MD, Fiorelli G. The triplicated alpha gene locus and heterozygous beta thalassemia: A case of thalassemia intermedia. Br J Haematol 1983;55:709-710.
-
(1983)
Br J Haematol
, vol.55
, pp. 709-710
-
-
Sampietro, M.1
Cazzola, M.2
Cappelini, M.D.3
Fiorelli, G.4
-
16
-
-
0028888675
-
Molecular basis and prenatal diagnosis of hemoglobinopathies in Turkey
-
Altay C, Basak AN. Molecular basis and prenatal diagnosis of hemoglobinopathies in Turkey. Int J Pediatr Hematol Oncol 1995;2:283-290.
-
(1995)
Int J Pediatr Hematol Oncol
, vol.2
, pp. 283-290
-
-
Altay, C.1
Basak, A.N.2
-
17
-
-
0031012244
-
Genetic analysis of β thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype
-
Rund D, Oron-Karni V, Filon D, Goldfarb A, Rachmilewitz E, Oppenheim A. Genetic analysis of β thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype. Am J Hematol 1997;54:16-22.
-
(1997)
Am J Hematol
, vol.54
, pp. 16-22
-
-
Rund, D.1
Oron-Karni, V.2
Filon, D.3
Goldfarb, A.4
Rachmilewitz, E.5
Oppenheim, A.6
-
18
-
-
0028247096
-
Severe thalassemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for ß0-thalassemia
-
Oron V, Filon D, Oppenheim A, Rund D. Severe thalassemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for ß0-thalassemia. Br J Haematol 1994;86:377-379.
-
(1994)
Br J Haematol
, vol.86
, pp. 377-379
-
-
Oron, V.1
Filon, D.2
Oppenheim, A.3
Rund, D.4
-
19
-
-
0022476657
-
Organization of the zeta-alpha genes in Chinese
-
Chan V, Chan TK, Cheng MY, Kan YW, Todd D. Organization of the zeta-alpha genes in Chinese. Br J Haematol 1986;64:97-105.
-
(1986)
Br J Haematol
, vol.64
, pp. 97-105
-
-
Chan, V.1
Chan, T.K.2
Cheng, M.Y.3
Kan, Y.W.4
Todd, D.5
-
21
-
-
0028263783
-
Detection of common deletional alpha thalassemia-2 determinants by Gap-PCR
-
Baysal E, Huisman THJ. Detection of common deletional alpha thalassemia-2 determinants by Gap-PCR. Am J Hematol. 1994;46:208-213.
-
(1994)
Am J Hematol.
, vol.46
, pp. 208-213
-
-
Baysal, E.1
Huisman, T.H.J.2
-
22
-
-
0029861119
-
Detection of alpha-thalassemia-2. (-3.7 kb) and its corresponding triplication ααα (anti-3.7 kb) by PCR: An improved technical change
-
Smetanina NS, Huisman TH. Detection of alpha-thalassemia-2. (-3.7 kb) and its corresponding triplication ααα (anti-3.7 kb) by PCR: An improved technical change. Am J Hematol. 1996;53(3):202-203.
-
(1996)
Am J Hematol.
, vol.53
, Issue.3
, pp. 202-203
-
-
Smetanina, N.S.1
Huisman, T.H.2
-
23
-
-
0348110520
-
Determination of the breakpoint and molecular diagnosis of a common alpha thalassemia-1deletion in the Indian population
-
Shaji RV, Eunice SE, Baidya S, Srivastava A, Chandy M. Determination of the breakpoint and molecular diagnosis of a common alpha thalassemia-1deletion in the Indian population. Br J Haematol 2003;123:942-947.
-
(2003)
Br J Haematol
, vol.123
, pp. 942-947
-
-
Shaji, R.V.1
Eunice, S.E.2
Baidya, S.3
Srivastava, A.4
Chandy, M.5
-
24
-
-
0025850971
-
Rapid diagnosis of alpha thalassemia-1 of Southeast Asia type and hydrops fetalis by polymerase chain reaction
-
Chang JG, Lee LS, Lin CP, Chen PH, Chen CP. Rapid diagnosis of alpha thalassemia-1 of Southeast Asia type and hydrops fetalis by polymerase chain reaction. Blood 1991;78:853-854.
-
(1991)
Blood
, vol.78
, pp. 853-854
-
-
Chang, J.G.1
Lee, L.S.2
Lin, C.P.3
Chen, P.H.4
Chen, C.P.5
-
25
-
-
0025887115
-
The spectrum of beta thalassemia mutations on the Indian subcontinent: The basis for prenatal diagnosis
-
Varawalla NY, Old JM, Sarkar R, Venkatesan R, Weatherall DJ. The spectrum of beta thalassemia mutations on the Indian subcontinent: The basis for prenatal diagnosis. Br J Haematol 1991;78:242-247.
-
(1991)
Br J Haematol
, vol.78
, pp. 242-247
-
-
Varawalla, N.Y.1
Old, J.M.2
Sarkar, R.3
Venkatesan, R.4
Weatherall, D.J.5
-
26
-
-
78650119843
-
Microdrepanocito-anemia in un soggetto di razza Bianca
-
Silvestroni E, Bianco I. Microdrepanocito-anemia in un soggetto di razza Bianca. Boll A Acad Med Roma 1944;70:347-351.
-
(1944)
Boll A Acad Med Roma
, vol.70
, pp. 347-351
-
-
Silvestroni, E.1
Bianco, I.2
-
27
-
-
70350303518
-
Aberrant hetrosis in hemoglobinopathies with special reference to beta thalassemia and structurally abnormal hemoglobins E and S in Orissa, India
-
Balagir RS. Aberrant hetrosis in hemoglobinopathies with special reference to beta thalassemia and structurally abnormal hemoglobins E and S in Orissa, India. J Clin Diagn Res 2007;1(3):122-130.
-
(2007)
J Clin Diagn Res
, vol.1
, Issue.3
, pp. 122-130
-
-
Balagir, R.S.1
-
29
-
-
0031943287
-
Effect of α-gene numbers on the expression of ß-thalassemia intermedia, ß-thalassemia and (δß)0-thalassemia traits
-
Altay C, Oner C, Oner R, Gümrük F, Mergen H, Gürgey A. Effect of α-gene numbers on the expression of ß-thalassemia intermedia, ß-thalassemia and (δß)0-thalassemia traits. Hum Hered 1998;48:121-125.
-
(1998)
Hum Hered
, vol.48
, pp. 121-125
-
-
Altay, C.1
Oner, C.2
Oner, R.3
Gümrük, F.4
Mergen, H.5
Gürgey, A.6
-
30
-
-
0019402140
-
Alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia
-
Altay C, Gravely ME, Joseph BR, Williams DF. Alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia. Pediatr Res 1981;15:1093-1096.
-
(1981)
Pediatr Res
, vol.15
, pp. 1093-1096
-
-
Altay, C.1
Gravely, M.E.2
Joseph, B.R.3
Williams, D.F.4
-
31
-
-
0842308839
-
Genetic insights into the clinical diversity of beta thalassaemia
-
Thein SL. Genetic insights into the clinical diversity of beta thalassaemia. Br J Haematol 2004;124:264-274.
-
(2004)
Br J Haematol
, vol.124
, pp. 264-274
-
-
Thein, S.L.1
-
32
-
-
0035320886
-
Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias
-
Weatherall DJ. Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias. Nat Rev Genet 2001;2:245-255.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 245-255
-
-
Weatherall, D.J.1
-
33
-
-
7044235524
-
Risk factors and prediction of outcomes in children and adolescents who have sickle cell anemia
-
Quinn CT, Miller ST. Risk factors and prediction of outcomes in children and adolescents who have sickle cell anemia. Hematol Oncol Clin North Am 2004;18:1339-1354.
-
(2004)
Hematol Oncol Clin North Am
, vol.18
, pp. 1339-1354
-
-
Quinn, C.T.1
Miller, S.T.2
-
34
-
-
0034773529
-
Pathophysiology of sickle cell disease: Role of cellular and genetic modifiers
-
Steinberg MH, Rodgers GP. Pathophysiology of sickle cell disease: Role of cellular and genetic modifiers. Semin Hematol 2001;38:299-306.
-
(2001)
Semin Hematol
, vol.38
, pp. 299-306
-
-
Steinberg, M.H.1
Rodgers, G.P.2
-
35
-
-
20044367676
-
Predicting clinical severity in sickle cell anaemia
-
Steinberg MH. Predicting clinical severity in sickle cell anaemia. Br J Haematol 2005;129:465-481.
-
(2005)
Br J Haematol
, vol.129
, pp. 465-481
-
-
Steinberg, M.H.1
-
36
-
-
59249088084
-
Genetic modifiers in hemoglobinopathies
-
Rund D, Fucharoen S. Genetic modifiers in hemoglobinopathies. Curr Mol Med 2008;8(7):600-608.
-
(2008)
Curr Mol Med
, vol.8
, Issue.7
, pp. 600-608
-
-
Rund, D.1
Fucharoen, S.2
-
37
-
-
0033953189
-
Clinical and hematologic aspects of hemoglobin E [beta]-thalassemia
-
Fucharoen S, Winichagoon P. Clinical and hematologic aspects of hemoglobin E [beta]-thalassemia. Curr Opin Hemat 2000;7(2):106-112.
-
(2000)
Curr Opin Hemat
, vol.7
, Issue.2
, pp. 106-112
-
-
Fucharoen, S.1
Winichagoon, P.2
-
38
-
-
0033205732
-
Variable clinical severity of Hb E beta-thalassemia among Indians
-
Nadkarni A, Ghosh K, Gorakshakar A, Colah R, Mohanty D. Variable clinical severity of Hb E beta-thalassemia among Indians. J Assoc Physicians India 1999;47(10):966-968.
-
(1999)
J Assoc Physicians India
, vol.47
, Issue.10
, pp. 966-968
-
-
Nadkarni, A.1
Ghosh, K.2
Gorakshakar, A.3
Colah, R.4
Mohanty, D.5
-
39
-
-
84896141382
-
-
Other Significant Heoglobinopathies. In: Bain BJ, editor., First edition. London: Blackwell Science
-
Other Significant Heoglobinopathies. In: Bain BJ, editor. Hemoglobinopathy Diagnosis, First edition. London: Blackwell Science; 2001. p. 154-186.
-
(2001)
Hemoglobinopathy Diagnosis
, pp. 154-186
-
-
-
40
-
-
18644377508
-
Hemoglobin E-beta thalassemia: Factors affecting phenotype
-
Panigrahi I, Agarwal S, Gupta T, Singhal P, Pradhan M. Hemoglobin E-beta thalassemia: Factors affecting phenotype. Indian Pediatr 2005;42(4):357-362.
-
(2005)
Indian Pediatr
, vol.42
, Issue.4
, pp. 357-362
-
-
Panigrahi, I.1
Agarwal, S.2
Gupta, T.3
Singhal, P.4
Pradhan, M.5
-
41
-
-
84859813409
-
Genotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients
-
Pandey S, Pandey SW, Sharma M, Mishra RM, Saxena R. Genotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients. Korean J Hematol 2011;46:192-195.
-
(2011)
Korean J Hematol
, vol.46
, pp. 192-195
-
-
Pandey, S.1
Pandey, S.W.2
Sharma, M.3
Mishra, R.M.4
Saxena, R.5
-
42
-
-
0028875253
-
The instability of the membrane skeleton in thalassemic red blood cells
-
Yuan J, Bunyaratvej A, Fucharoen S, Fung C, Shinar E, Schrier SL. The instability of the membrane skeleton in thalassemic red blood cells. Blood 1995;86:3945-3950.
-
(1995)
Blood
, vol.86
, pp. 3945-3950
-
-
Yuan, J.1
Bunyaratvej, A.2
Fucharoen, S.3
Fung, C.4
Shinar, E.5
Schrier, S.L.6
|