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Volumn 134, Issue 10, 2011, Pages 507-521

Past, present & future scenario of thalassaemic care & control in India

Author keywords

Blood transfusion; Bone marrow transplantation; Carrier screening; Chelation; Control; Cord blood storage; Prenatal diagnosis; Prevention; Thalassaemia care

Indexed keywords

ALPHA GLOBIN; BETA GLOBIN; DEFERASIROX; DEFERIPRONE; DEFEROXAMINE MESYLATE; HEMOGLOBIN E; HYDROXYUREA; ZOLEDRONIC ACID;

EID: 80455168753     PISSN: 09715916     EISSN: 09715916     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (61)

References (135)
  • 1
    • 0002341637 scopus 로고
    • Series of cases of splenomegaly in children with anemia and peculiar bone changes
    • Cooley TB, Lee P. Series of cases of splenomegaly in children with anemia and peculiar bone changes. Tr Am Pediatr Soc 1925; 37: 19.
    • (1925) Tr Am Pediatr Soc , vol.37 , pp. 19
    • Cooley, T.B.1    Lee, P.2
  • 2
    • 64849096191 scopus 로고
    • Cooley's anaemia (erythroblastic or Mediterranean anaemia)
    • Mukherji, M. Cooley's anaemia (erythroblastic or Mediterranean anaemia). Indian J Pediatr 1938; 5: 1-7.
    • (1938) Indian J Pediatr , vol.5 , pp. 1-7
    • Mukherji, M.1
  • 3
    • 85001466899 scopus 로고
    • Erythroblastic anemia- Cooley's anemia
    • Coelho C. Erythroblastic anemia- Cooley's anemia. Med Bull Bombay 1939; 7: 291-3.
    • (1939) Med Bull Bombay , vol.7 , pp. 291-293
    • Coelho, C.1
  • 5
    • 65749311895 scopus 로고
    • Erythroblastic anaemia with kyphosis and cirrhosis of liver
    • Patel ND, Bhende YM. Erythroblastic anaemia with kyphosis and cirrhosis of liver. Indian J Pediatr 1939; 6: 217-22.
    • (1939) Indian J Pediatr , vol.6 , pp. 217-222
    • Patel, N.D.1    Bhende, Y.M.2
  • 7
    • 51649137602 scopus 로고
    • Erythroblastic anaemia of Cooley
    • Chaudhuri KC. Erythroblastic anaemia of Cooley. Indian J Pediatr 1947; 14: 76-80.
    • (1947) Indian J Pediatr , vol.14 , pp. 76-80
    • Chaudhuri, K.C.1
  • 8
    • 0040790924 scopus 로고
    • Hemoglobinopathies in north India - 1. Hemoglobin D trait and hemoglobin D thalassemia
    • Ghai OP, Varma KP, Taneja PN. Hemoglobinopathies in north India - 1. Hemoglobin D trait and hemoglobin D thalassemia. Indian J Child Health 1961; 10: 334-41.
    • (1961) Indian J Child Health , vol.10 , pp. 334-341
    • Ghai, O.P.1    Varma, K.P.2    Taneja, P.N.3
  • 13
    • 0019294926 scopus 로고
    • Spectrum of haemolytic anaemias in Punjab, North India
    • Dash S, Dash RJ. Spectrum of haemolytic anaemias in Punjab, North India. Trop Geogr Med 1980; 32: 312-6.
    • (1980) Trop Geogr Med , vol.32 , pp. 312-316
    • Dash, S.1    Dash, R.J.2
  • 14
    • 0021499019 scopus 로고
    • Prevalence of abnormal haemoglobin, thalassaemia & G-6 PD deficiency among the hospital population of Udaipur (Rajasthan)
    • Jain RC. Prevalence of abnormal haemoglobin, thalassaemia & G-6 PD deficiency among the hospital population of Udaipur (Rajasthan). Indian J Med Res 1984; 80: 332-8.
    • (1984) Indian J Med Res , vol.80 , pp. 332-338
    • Jain, R.C.1
  • 16
    • 70449144558 scopus 로고
    • Fatal hemolytic anemia presumably due to the combination of sickle cell and thalassemia gene; case report
    • Naik SK, Kothari BV, Jhaveri CL, Sukumaran PK, Sanghvi LD. Fatal hemolytic anemia presumably due to the combination of sickle cell and thalassemia gene; case report. Indian J Med Sci 1957; 11: 244-9.
    • (1957) Indian J Med Sci , vol.11 , pp. 244-249
    • Naik, S.K.1    Kothari, B.V.2    Jhaveri, C.L.3    Sukumaran, P.K.4    Sanghvi, L.D.5
  • 17
    • 0013918880 scopus 로고
    • Haemoglobins E and K and thalassemia in an Indian family with evidence of interaction between haemoglobin E and thalassaemia
    • Swarup S, Ghosh SK, Chatterjee JB. Haemoglobins E and K and thalassemia in an Indian family with evidence of interaction between haemoglobin E and thalassaemia. J Indian Med Assoc 1966; 46: 587-90.
    • (1966) J Indian Med Assoc , vol.46 , pp. 587-590
    • Swarup, S.1    Ghosh, S.K.2    Chatterjee, J.B.3
  • 18
    • 0015445559 scopus 로고
    • Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families
    • Sukumaran PK, Merchant SM, Desai MP, Wiltshire BG, Lehmann H. Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. J Med Genet 1972; 9: 436-42.
    • (1972) J Med Genet , vol.9 , pp. 436-442
    • Sukumaran, P.K.1    Merchant, S.M.2    Desai, M.P.3    Wiltshire, B.G.4    Lehmann, H.5
  • 19
    • 0017502567 scopus 로고
    • Genetic interaction of beta-thalassaemia (Hb βT-) & haemoglobin E (Hb βE) in populations of Eastern India
    • Ajmani M, Sharma A, Talukder G, Bhattacharyya DK. Genetic interaction of beta-thalassaemia (Hb βT-) & haemoglobin E (Hb βE) in populations of Eastern India. Indian J Exp Biol 1977; 15: 455-7.
    • (1977) Indian J Exp Biol , vol.15 , pp. 455-457
    • Ajmani, M.1    Sharma, A.2    Talukder, G.3    Bhattacharyya, D.K.4
  • 21
    • 0013975221 scopus 로고
    • Haemoglobinopathies, glucose-6-phosphate dehydrogenase deficiency and allied problems in the Indian subcontinent
    • Chatterjee JB. Haemoglobinopathies, glucose-6-phosphate dehydrogenase deficiency and allied problems in the Indian subcontinent. Bull World Health Organ 1966; 35: 837-56.
    • (1966) Bull World Health Organ , vol.35 , pp. 837-856
    • Chatterjee, J.B.1
  • 23
    • 0021176154 scopus 로고
    • Partial deletion of the beta-globin gene: A common beta-thalassaemia allele in Asian Indians
    • Wood S, Daya M, Allanson JE, Kirby L, Coupland R, Gray GR. Partial deletion of the beta-globin gene: a common beta-thalassaemia allele in Asian Indians. Can J Genet Cytol 1984; 26: 296-301.
    • (1984) Can J Genet Cytol , vol.26 , pp. 296-301
    • Wood, S.1    Daya, M.2    Allanson, J.E.3    Kirby, L.4    Coupland, R.5    Gray, G.R.6
  • 24
    • 0021248997 scopus 로고
    • Population and genetic studies suggest a single origin for the Indian deletion beta thalassaemia
    • Thein SL, Old JM, Wainscoat JS, Petrou M, Modell B, Weatherall DJ. Population and genetic studies suggest a single origin for the Indian deletion beta thalassaemia. Br J Haematol 1984; 57: 271-8.
    • (1984) Br J Haematol , vol.57 , pp. 271-278
    • Thein, S.L.1    Old, J.M.2    Wainscoat, J.S.3    Petrou, M.4    Modell, B.5    Weatherall, D.J.6
  • 25
    • 85047690630 scopus 로고
    • Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations
    • Old JM, Petrou M, Modell B, Weatherall DJ. Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations. Br J Haematol 1984; 57: 255-63.
    • (1984) Br J Haematol , vol.57 , pp. 255-263
    • Old, J.M.1    Petrou, M.2    Modell, B.3    Weatherall, D.J.4
  • 26
    • 0023741186 scopus 로고
    • The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: Application to prenatal diagnosis
    • Thein SL, Hesketh C, Wallace RB, Weatherall DJ. The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis. Br J Haematol 1988; 70: 225-31.
    • (1988) Br J Haematol , vol.70 , pp. 225-231
    • Thein, S.L.1    Hesketh, C.2    Wallace, R.B.3    Weatherall, D.J.4
  • 27
    • 0025090944 scopus 로고
    • Rapid detection and prenatal diagnosis of β-thalassaemia: Studies in Indian and Cypriot populations in the UK
    • Old JM, Varawalla NY, Weatherall DJ. Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet 1990; 336: 834-7.
    • (1990) Lancet , vol.336 , pp. 834-837
    • Old, J.M.1    Varawalla, N.Y.2    Weatherall, D.J.3
  • 28
    • 0025887115 scopus 로고
    • The spectrum of β-thalassaemia mutations on the Indian subcontinent: The basis for prenatal diagnosis
    • Varawalla NY, Old JM, Sarkar R, Venkatesan R, Weatherall DJ. The spectrum of β-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis. Br J Haematol 1991; 78: 242-7.
    • (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
  • 29
    • 0030754149 scopus 로고    scopus 로고
    • Regional distribution of β-thalassemia mutations in India
    • Verma IC, Saxena R, Thomas E, Jain PK. Regional distribution of β-thalassemia mutations in India. Hum Genet 1997; 100: 109-13.
    • (1997) Hum Genet , vol.100 , pp. 109-113
    • Verma, I.C.1    Saxena, R.2    Thomas, E.3    Jain, P.K.4
  • 30
    • 0033847656 scopus 로고    scopus 로고
    • Distribution of β-thalassemia mutations in the Indian population referred to a diagnostic center
    • Vaz FE, Thakur CB, Banerjee MK, Gangal SG. Distribution of β-thalassemia mutations in the Indian population referred to a diagnostic center. Hemoglobin 2000; 24: 181-94.
    • (2000) Hemoglobin , vol.24 , pp. 181-194
    • Vaz, F.E.1    Thakur, C.B.2    Banerjee, M.K.3    Gangal, S.G.4
  • 33
    • 0026494873 scopus 로고
    • β-Thalassaemia mutations and their linkage to β-haplotypes in Tamil Nadu in southern India
    • Venkatesan R, Sarkar R, Old JM. β-Thalassaemia mutations and their linkage to β-haplotypes in Tamil Nadu in southern India. Clin Genet 1992; 42: 251-6.
    • (1992) Clin Genet , vol.42 , pp. 251-256
    • Venkatesan, R.1    Sarkar, R.2    Old, J.M.3
  • 34
    • 0028133515 scopus 로고
    • Characterization of β-thalassaemia mutations in 57 β-thalassaemia families seen at Lucknow
    • Agarwal S, Naveed M, Gupta UR, Kishore P, Agarwal SS. Characterization of β-thalassaemia mutations in 57 β-thalassaemia families seen at Lucknow. Indian J Med Res 1994; 100: 106-10.
    • (1994) Indian J Med Res , vol.100 , pp. 106-110
    • Agarwal, S.1    Naveed, M.2    Gupta, U.R.3    Kishore, P.4    Agarwal, S.S.5
  • 35
    • 0028244389 scopus 로고
    • The molecular basis of β thalassaemia in Punjabi and Maharashtran Indians includes a multilocus aetiology involving triplicated alpha-globin loci
    • Garewal G, Fearon CW, Warren TC, Marwaha N, Marwaha RK, Mahadik C, et al. The molecular basis of β thalassaemia in Punjabi and Maharashtran Indians includes a multilocus aetiology involving triplicated alpha-globin loci. Br J Haematol 1994; 86: 372-6.
    • (1994) Br J Haematol , vol.86 , pp. 372-376
    • Garewal, G.1    Fearon, C.W.2    Warren, T.C.3    Marwaha, N.4    Marwaha, R.K.5    Mahadik, C.6
  • 36
    • 0037406326 scopus 로고    scopus 로고
    • Rapid detection of β-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis
    • Shaji RV, Edison ES, Poonkuzhali B, Srivastava A, Chandy M. Rapid detection of β-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis. Clin Chem 2003; 49: 777-81.
    • (2003) Clin Chem , vol.49 , pp. 777-781
    • Shaji, R.V.1    Edison, E.S.2    Poonkuzhali, B.3    Srivastava, A.4    Chandy, M.5
  • 37
    • 40749097760 scopus 로고    scopus 로고
    • Analysis of β globin mutations in the Indian population: Presence of rare and novel mutations and region-wise heterogeneity
    • Edison ES, Shaji RV, Devi SG, Moses A, Viswabandhya A, Mathews V, et al. Analysis of β globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity. Clin Genet 2008; 73: 331-7.
    • (2008) Clin Genet , vol.73 , pp. 331-337
    • Edison, E.S.1    Shaji, R.V.2    Devi, S.G.3    Moses, A.4    Viswabandhya, A.5    Mathews, V.6
  • 38
    • 0028877634 scopus 로고
    • Clinical heterogeneity of silent-gene β-thalassemia among Indians
    • Nadkarni A, Pawar A, Mudera VC, Mohanty D, Colah R. Clinical heterogeneity of silent-gene β-thalassemia among Indians. Ann Hematol 1995; 70: 61-4.
    • (1995) Ann Hematol , vol.70 , pp. 61-64
    • Nadkarni, A.1    Pawar, A.2    Mudera, V.C.3    Mohanty, D.4    Colah, R.5
  • 39
    • 18244409133 scopus 로고    scopus 로고
    • A multi-center study in order to further define the molecular basis of β-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction
    • Old JM, Khan SN, Verma I, Fucharoen S, Kleanthous M, Ioannou P, et al. A multi-center study in order to further define the molecular basis of β-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction. Hemoglobin 2001; 25: 397-407.
    • (2001) Hemoglobin , vol.25 , pp. 397-407
    • Old, J.M.1    Khan, S.N.2    Verma, I.3    Fucharoen, S.4    Kleanthous, M.5    Ioannou, P.6
  • 40
    • 77951622783 scopus 로고    scopus 로고
    • Profiling β-thalassaemia mutations in India at state and regional levels: Implications for genetic education, screening and counselling programmes
    • Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, et al. Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. Hugo J 2009; 3: 51-62.
    • (2009) Hugo J , vol.3 , pp. 51-62
    • Sinha, S.1    Black, M.L.2    Agarwal, S.3    Colah, R.4    Das, R.5    Ryan, K.6
  • 41
    • 34848848420 scopus 로고    scopus 로고
    • Origin of the codon 47 (+A) β-thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India
    • Gorakshakar AC, Das MK, Phanasgaokar SP, Nadkarni AH, Colah RB, Mohanty D. Origin of the codon 47 (+A) β-thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India. Br J Haematol 2007; 139: 345-6.
    • (2007) Br J Haematol , vol.139 , pp. 345-346
    • Gorakshakar, A.C.1    Das, M.K.2    Phanasgaokar, S.P.3    Nadkarni, A.H.4    Colah, R.B.5    Mohanty, D.6
  • 42
    • 79960843856 scopus 로고    scopus 로고
    • ThalInd, a β-thalassemia and hemoglobinopathies database for India: Defining a model country-specific and disease-centric bioinformatics resource
    • Sinha S, Black ML, Agarwal S, Das R, Bittles AH, Bellgard M. ThalInd, a β-thalassemia and hemoglobinopathies database for India: defining a model country-specific and disease-centric bioinformatics resource. Hum Mutat 2011; 32: 887-93.
    • (2011) Hum Mutat , vol.32 , pp. 887-893
    • Sinha, S.1    Black, M.L.2    Agarwal, S.3    Das, R.4    Bittles, A.H.5    Bellgard, M.6
  • 43
    • 0023840573 scopus 로고
    • The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene
    • Kulozik AE, Kar BC, Serjeant GR, Serjeant BE, Weatherall DJ. The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. Blood 1988; 71: 467-72.
    • (1988) Blood , vol.71 , pp. 467-472
    • Kulozik, A.E.1    Kar, B.C.2    Serjeant, G.R.3    Serjeant, B.E.4    Weatherall, D.J.5
  • 45
    • 71049121392 scopus 로고    scopus 로고
    • The expanding spectrum of thalassemia intermedia
    • Panigrahi I, Marwaha RK, Kulkarni K. The expanding spectrum of thalassemia intermedia. Hematology 2009; 14: 311-4.
    • (2009) Hematology , vol.14 , pp. 311-314
    • Panigrahi, I.1    Marwaha, R.K.2    Kulkarni, K.3
  • 46
    • 36249009162 scopus 로고    scopus 로고
    • Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations
    • Verma IC, Kleanthous M, Saxena R, Fucharoen S, Winichagoon P, Raizuddin S, et al. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations. Hemoglobin 2007; 31: 439-52.
    • (2007) Hemoglobin , vol.31 , pp. 439-452
    • Verma, I.C.1    Kleanthous, M.2    Saxena, R.3    Fucharoen, S.4    Winichagoon, P.5    Raizuddin, S.6
  • 47
    • 80052647585 scopus 로고    scopus 로고
    • Xmn1- (G) γ polymorphism and clinical predictors of severity of disease in β-thalassemia intermedia
    • Oberoi S, Das R, Panigrahi I, Kaur J, Marwaha RK. Xmn1- (G) γ polymorphism and clinical predictors of severity of disease in β-thalassemia intermedia. Pediatr Blood Cancer 2011; 57: 1025-8.
    • (2011) Pediatr Blood Cancer , vol.57 , pp. 1025-1028
    • Oberoi, S.1    Das, R.2    Panigrahi, I.3    Kaur, J.4    Marwaha, R.K.5
  • 50
    • 78049472245 scopus 로고    scopus 로고
    • Growing up with the families of β-thalassaemia major using an accelerated longitudinal design
    • Khairkar P, Malhotra S, Marwaha RK. Growing up with the families of β-thalassaemia major using an accelerated longitudinal design. Indian J Med Res 2010; 132: 428-37.
    • (2010) Indian J Med Res , vol.132 , pp. 428-437
    • Khairkar, P.1    Malhotra, S.2    Marwaha, R.K.3
  • 52
    • 33745883771 scopus 로고    scopus 로고
    • Progress in the management of thalassemia
    • Lokeshwar MR. Progress in the management of thalassemia. Indian Pediatr 2006; 43: 503-6.
    • (2006) Indian Pediatr , vol.43 , pp. 503-506
    • Lokeshwar, M.R.1
  • 53
    • 50249128697 scopus 로고    scopus 로고
    • Current trends in the management of beta thalassemia
    • Dubey AP, Parakh A, Dublish S. Current trends in the management of beta thalassemia. Indian J Pediatr 2008; 75: 739-43.
    • (2008) Indian J Pediatr , vol.75 , pp. 739-743
    • Dubey, A.P.1    Parakh, A.2    Dublish, S.3
  • 54
    • 63549101289 scopus 로고    scopus 로고
    • Advances in management of thalassemia
    • Agarwal MB. Advances in management of thalassemia. Indian J Pediatr 2009; 76: 177-84.
    • (2009) Indian J Pediatr , vol.76 , pp. 177-184
    • Agarwal, M.B.1
  • 55
    • 77649184194 scopus 로고    scopus 로고
    • Whole blood and component use in resource poor settings
    • Marwaha N. Whole blood and component use in resource poor settings. Biologicals 2010; 38: 68-71.
    • (2010) Biologicals , vol.38 , pp. 68-71
    • Marwaha, N.1
  • 56
    • 84859104948 scopus 로고    scopus 로고
    • accessed on August 5
    • http://www.indianredcross.org, accessed on August 5, 2011.
    • (2011)
  • 57
    • 0035050973 scopus 로고    scopus 로고
    • A study report of 174 units of placental umbilical cord whole blood transfusion in 62 patients as a rich source of fetal hemoglobin supply in different indications of blood transfusion
    • Bhattacharya N, Mukherijee K, Chettri MK, Banerjee T, Mani U, Bhattacharya S. A study report of 174 units of placental umbilical cord whole blood transfusion in 62 patients as a rich source of fetal hemoglobin supply in different indications of blood transfusion. Clin Exp Obstet Gynecol 2001; 28: 47-52.
    • (2001) Clin Exp Obstet Gynecol , vol.28 , pp. 47-52
    • Bhattacharya, N.1    Mukherijee, K.2    Chettri, M.K.3    Banerjee, T.4    Mani, U.5    Bhattacharya, S.6
  • 59
    • 0025336901 scopus 로고
    • HBV & HIV seropositivity in multi-transfused haemophilics & thalassaemics in eastern India
    • De M, Banerjee D, Chandra S, Bhattacharya DK. HBV & HIV seropositivity in multi-transfused haemophilics & thalassaemics in eastern India. Indian J Med Res 1990; 91: 63-6.
    • (1990) Indian J Med Res , vol.91 , pp. 63-66
    • De, M.1    Banerjee, D.2    Chandra, S.3    Bhattacharya, D.K.4
  • 60
    • 0029563807 scopus 로고
    • Hepatitis B, C & D viral markers in multitransfused thalassemic children: Long-term complications and present managemen
    • Choudhry VP, Acharya SK. Hepatitis B, C & D viral markers in multitransfused thalassemic children: long-term complications and present management. Indian J Pediatr 1995; 62: 655-68.
    • (1995) Indian J Pediat , vol.62 , pp. 655-668
    • Choudhry, V.P.1    Acharya, S.K.2
  • 61
    • 0032106790 scopus 로고    scopus 로고
    • Dr. P. C. Sen Memorial Award Paper. A study of HIV infection in thalassaemia patients of rural Bengal
    • Sur D, Chakraborty AK, Mukhopadhyay SP. Dr. P. C. Sen Memorial Award Paper. A study of HIV infection in thalassaemia patients of rural Bengal. Indian J Public Health 1998; 42: 81-7.
    • (1998) Indian J Public Health , vol.42 , pp. 81-87
    • Sur, D.1    Chakraborty, A.K.2    Mukhopadhyay, S.P.3
  • 62
    • 0041837446 scopus 로고    scopus 로고
    • Seroprevalence of hepatitis C and B virus in multiply transfused beta-thalassemics: Results from a thalassemic day care unit in north India
    • Marwaha RK, Bansal D, Sharma S, Kumar S, Trehan A, Duseja A, et al. Seroprevalence of hepatitis C and B virus in multiply transfused beta-thalassemics: results from a thalassemic day care unit in north India. Vox Sang 2003; 85: 119-20.
    • (2003) Vox Sang , vol.85 , pp. 119-120
    • Marwaha, R.K.1    Bansal, D.2    Sharma, S.3    Kumar, S.4    Trehan, A.5    Duseja, A.6
  • 63
    • 80455169511 scopus 로고    scopus 로고
    • Need to change present regulatory framework for blood banks in India
    • Chaudhury N. Need to change present regulatory framework for blood banks in India. Asian J Trans Med 2011; 5: 1-2.
    • (2011) Asian J Trans Med , vol.5 , pp. 1-2
    • Chaudhury, N.1
  • 64
    • 70350672581 scopus 로고    scopus 로고
    • The proceedings of the 17th International Conference on Chelation: Application of effective chelation therapies in iron loading and non iron loading conditions, and the gap in the prevention and treatment policies on thalassemia between developed and developing countries
    • Kontoghiorghes GJ. The proceedings of the 17th International Conference on Chelation: application of effective chelation therapies in iron loading and non iron loading conditions, and the gap in the prevention and treatment policies on thalassemia between developed and developing countries. Hemoglobin 2009; 33: 283-6.
    • (2009) Hemoglobin , vol.33 , pp. 283-286
    • Kontoghiorghes, G.J.1
  • 65
    • 0026668939 scopus 로고
    • Long-term assessment of efficacy and safety of L1, an oral iron chelator, in transfusion dependent thalassaemia: Indian trial
    • Agarwal MB, Gupte SS, Viswanathan C, Vasandani D, Ramanathan J, Desai N, et al. Long-term assessment of efficacy and safety of L1, an oral iron chelator, in transfusion dependent thalassaemia: Indian trial. Br J Haematol 1992; 82: 460-6.
    • (1992) Br J Haematol , vol.82 , pp. 460-466
    • Agarwal, M.B.1    Gupte, S.S.2    Viswanathan, C.3    Vasandani, D.4    Ramanathan, J.5    Desai, N.6
  • 66
    • 0027484892 scopus 로고
    • Oral iron chelation: A review with special emphasis on Indian work on deferiprone (L1)
    • Agarwal MB. Oral iron chelation: a review with special emphasis on Indian work on deferiprone (L1). Indian J Pediatr 1993; 60: 509-16.
    • (1993) Indian J Pediatr , vol.60 , pp. 509-516
    • Agarwal, M.B.1
  • 67
    • 0029094988 scopus 로고
    • Efficacy and safety of oral iron chelating agent deferiprone in beta-thalassemia and hemoglobin E-beta thalassemia
    • Adhikari D, Roy TB, Biswas A, Chakraborty ML, Bhattacharya B, Maitra TK, et al. Efficacy and safety of oral iron chelating agent deferiprone in beta-thalassemia and hemoglobin E-beta thalassemia. Indian Pediatr 1995; 32: 855-61.
    • (1995) Indian Pediatr , vol.32 , pp. 855-861
    • Adhikari, D.1    Roy, T.B.2    Biswas, A.3    Chakraborty, M.L.4    Bhattacharya, B.5    Maitra, T.K.6
  • 68
    • 0032417990 scopus 로고    scopus 로고
    • Oral deferiprone--controversies on its efficacy and safety
    • Choudhry VP. Oral deferiprone--controversies on its efficacy and safety. Indian J Pediatr 1998; 65: 825-8.
    • (1998) Indian J Pediatr , vol.65 , pp. 825-828
    • Choudhry, V.P.1
  • 69
    • 0942298725 scopus 로고    scopus 로고
    • Comparative efficacy of desferrioxamine, deferiprone and in combination on iron chelation in thalassemic children
    • Gomber S, Saxena R, Madan N. Comparative efficacy of desferrioxamine, deferiprone and in combination on iron chelation in thalassemic children. Indian Pediatr 2004; 41: 21-7.
    • (2004) Indian Pediatr , vol.41 , pp. 21-27
    • Gomber, S.1    Saxena, R.2    Madan, N.3
  • 70
    • 48749087262 scopus 로고    scopus 로고
    • Long-term efficacy of oral deferiprone in management of iron overload in beta thalassemia major
    • Goel H, Girisha KM, Phadke SR. Long-term efficacy of oral deferiprone in management of iron overload in beta thalassemia major. Hematology 2008; 13: 77-82.
    • (2008) Hematology , vol.13 , pp. 77-82
    • Goel, H.1    Girisha, K.M.2    Phadke, S.R.3
  • 71
    • 34548304042 scopus 로고    scopus 로고
    • Deferasirox: The new oral iron chelator
    • Dubey AP, Sudha S, Parakh A. Deferasirox: the new oral iron chelator. Indian Pediatr 2007; 44: 603-7.
    • (2007) Indian Pediatr , vol.44 , pp. 603-607
    • Dubey, A.P.1    Sudha, S.2    Parakh, A.3
  • 72
    • 77749316834 scopus 로고    scopus 로고
    • Deferasirox: Oral, once daily iron chelator - an expert opinion
    • Agarwal MB. Deferasirox: oral, once daily iron chelator - an expert opinion. Indian J Pediatr 2010; 77: 185-91.
    • (2010) Indian J Pediatr , vol.77 , pp. 185-191
    • Agarwal, M.B.1
  • 73
    • 79551664069 scopus 로고    scopus 로고
    • Safety and efficacy of deferasirox in multitransfused Indian children with β-thalassaemia major
    • Chandra J, Chaudhary H, Pemde H, Singh V, Dutta AK. Safety and efficacy of deferasirox in multitransfused Indian children with β-thalassaemia major. Ann Trop Paediatr 2011; 31: 47-51.
    • (2011) Ann Trop Paediatr , vol.31 , pp. 47-51
    • Chandra, J.1    Chaudhary, H.2    Pemde, H.3    Singh, V.4    Dutta, A.K.5
  • 74
    • 3342943276 scopus 로고    scopus 로고
    • Wheat grass juice reduces transfusion requirement in patients with thalassemia major: A pilot study
    • Marawaha RK, Bansal D, Kaur S, Trehan A. Wheat grass juice reduces transfusion requirement in patients with thalassemia major: a pilot study. Indian Pediatr 2004; 41: 716-20.
    • (2004) Indian Pediatr , vol.41 , pp. 716-720
    • Marawaha, R.K.1    Bansal, D.2    Kaur, S.3    Trehan, A.4
  • 76
    • 76649122206 scopus 로고    scopus 로고
    • Effect of wheat grass tablets on the frequency of blood transfusions in thalassemia major
    • Singh K, Pannu MS, Singh P, Singh J. Effect of wheat grass tablets on the frequency of blood transfusions in thalassemia major. Indian J Pediatr 2010; 77: 90-1.
    • (2010) Indian J Pediatr , vol.77 , pp. 90-91
    • Singh, K.1    Pannu, M.S.2    Singh, P.3    Singh, J.4
  • 77
    • 0030872518 scopus 로고    scopus 로고
    • Hematological responses to hydroxyurea therapy in multitransfused thalassemic children
    • Choudhry VP, Lal A, Pati HP, Arya LS. Hematological responses to hydroxyurea therapy in multitransfused thalassemic children. Indian J Pediatr 1997; 64: 395-8.
    • (1997) Indian J Pediatr , vol.64 , pp. 395-398
    • Choudhry, V.P.1    Lal, A.2    Pati, H.P.3    Arya, L.S.4
  • 80
    • 33751564490 scopus 로고    scopus 로고
    • Relation of Xmn-1 polymorphism and five common Indian mutations of thalassaemia with phenotypic presentation in β-thalassaemia
    • Raina A, Verma IC, Saxena R, Kaul D, Khanna VK. Relation of Xmn-1 polymorphism and five common Indian mutations of thalassaemia with phenotypic presentation in β-thalassaemia. J K Sci 2006; 8: 139-43.
    • (2006) J K Sci , vol.8 , pp. 139-143
    • Raina, A.1    Verma, I.C.2    Saxena, R.3    Kaul, D.4    Khanna, V.K.5
  • 81
    • 50549092908 scopus 로고    scopus 로고
    • Stem cell transplantation in India
    • Chandy M. Stem cell transplantation in India. Bone Marrow Transplant 2008; 42: S81-4.
    • (2008) Bone Marrow Transplant , vol.42
    • Chandy, M.1
  • 82
    • 59549106857 scopus 로고    scopus 로고
    • Allogeneic hematopoietic SCT performed in non-HEPA filter rooms: Initial experience from a single center in India
    • Kumar R, Naithani R, Mishra P, Mahapatra M, Seth T, Dolai TK, et al. Allogeneic hematopoietic SCT performed in non-HEPA filter rooms: initial experience from a single center in India. Bone Marrow Transplant 2009; 43: 115-9.
    • (2009) Bone Marrow Transplant , vol.43 , pp. 115-119
    • Kumar, R.1    Naithani, R.2    Mishra, P.3    Mahapatra, M.4    Seth, T.5    Dolai, T.K.6
  • 83
    • 34147145789 scopus 로고    scopus 로고
    • Asian Indian donor marrow registry: All India Institute of Medical Sciences experience
    • Kanga U, Panigrahi A, Kumar S, Mehra NK. Asian Indian donor marrow registry: All India Institute of Medical Sciences experience. Transplant Proc 2007; 39: 719-20.
    • (2007) Transplant Proc , vol.39 , pp. 719-720
    • Kanga, U.1    Panigrahi, A.2    Kumar, S.3    Mehra, N.K.4
  • 84
    • 80455157375 scopus 로고    scopus 로고
    • Marrow donors on the rise, but they are not enough
    • Mumbai. May 12
    • Suryanarayan D. Marrow donors on the rise, but they are not enough. DNA, Mumbai. May 12, 2010.
    • (2010) DNA
    • Suryanarayan, D.1
  • 85
    • 84859104499 scopus 로고    scopus 로고
    • accessed on October 4
    • http://www.relicord.com, accessed on October 4, 2011.
    • (2011)
  • 86
    • 84859109731 scopus 로고    scopus 로고
    • accessed on August 5
    • http://www.bmdw.org/, accessed on August 5, 2011.
    • (2011)
  • 87
    • 84859102786 scopus 로고    scopus 로고
    • accessed on August 5
    • http://www.worldmarrow.org/, accessed on August 5, 2011.
    • (2011)
  • 88
    • 33845910650 scopus 로고    scopus 로고
    • Physical growth patterns and dental caries in thalassemia
    • Gomber S, Dewan P. Physical growth patterns and dental caries in thalassemia. Indian Pediatr 2006; 43: 1064-9.
    • (2006) Indian Pediatr , vol.43 , pp. 1064-1069
    • Gomber, S.1    Dewan, P.2
  • 89
    • 79958276399 scopus 로고    scopus 로고
    • Evaluation of growth, puberty and endocrine dysfunctions in relation to iron overload in multi transfused Indian thalassemia patients
    • Merchant RH, Shirodkar A, Ahmed J. Evaluation of growth, puberty and endocrine dysfunctions in relation to iron overload in multi transfused Indian thalassemia patients. Indian J Pediatr 2011; 78: 679-83.
    • (2011) Indian J Pediatr , vol.78 , pp. 679-683
    • Merchant, R.H.1    Shirodkar, A.2    Ahmed, J.3
  • 90
    • 0031260908 scopus 로고    scopus 로고
    • Development of secondary sex characteristics in multitransfused thalassemic children
    • George A, Bhaduri A, Choudhry VP. Development of secondary sex characteristics in multitransfused thalassemic children. Indian J Pediatr 1997; 64: 855-9.
    • (1997) Indian J Pediatr , vol.64 , pp. 855-859
    • George, A.1    Bhaduri, A.2    Choudhry, V.P.3
  • 91
    • 80054735357 scopus 로고    scopus 로고
    • Assessment of glucose tolerance in multi-transfused adolescent and young adult patients with beta thalassemia
    • Khairwa A, Chaudhary A, Jat KR. Assessment of glucose tolerance in multi-transfused adolescent and young adult patients with beta thalassemia. Indian J Pediatr 2011; 78: 1297-8.
    • (2011) Indian J Pediatr , vol.78 , pp. 1297-1298
    • Khairwa, A.1    Chaudhary, A.2    Jat, K.R.3
  • 92
    • 72449149285 scopus 로고    scopus 로고
    • Bone recovery after zoledronate therapy in thalassemia-induced osteoporosis: A meta-analysis and systematic review
    • Mamtani M, Kulkarni H. Bone recovery after zoledronate therapy in thalassemia-induced osteoporosis: a meta-analysis and systematic review. Osteoporos Int 2010; 21: 183-7.
    • (2010) Osteoporos Int , vol.21 , pp. 183-187
    • Mamtani, M.1    Kulkarni, H.2
  • 94
    • 80455133651 scopus 로고
    • Guidelines for control of hemoglobin disorders, WHO/HDP/HB/gl/94.1. Geneva: WHO
    • Guidelines for control of hemoglobin disorders. World Health Organization hereditary disease program. WHO/HDP/HB/gl/94.1. Geneva: WHO; 1994.
    • (1994) World Health Organization Hereditary Disease Program
  • 95
    • 0032415999 scopus 로고    scopus 로고
    • Prenatal diagnosis and screening of the haemoglobinopathies
    • Cao A, Galanello R, Rosatelli MC. Prenatal diagnosis and screening of the haemoglobinopathies. Baillieres Clin Haematol 1998; 11: 215-38.
    • (1998) Baillieres Clin Haematol , vol.11 , pp. 215-238
    • Cao, A.1    Galanello, R.2    Rosatelli, M.C.3
  • 96
  • 97
    • 0019363539 scopus 로고
    • Prevention of thalassemia in Cyprus
    • Angastiniotis MA, Model B. Prevention of thalassemia in Cyprus. Lancet 1981; 1: 369-70.
    • (1981) Lancet , vol.1 , pp. 369-370
    • Angastiniotis, M.A.1    Model, B.2
  • 99
    • 0002616532 scopus 로고
    • Probelms of screening and counseling in the hemoglobinopathies
    • Motulsky AG, Lenz W, editors, Amsterdam: Excerpta Medica
    • Stamatoyannopoulos G. Probelms of screening and counseling in the hemoglobinopathies. In: Motulsky AG, Lenz W, editors. Birth defects. Amsterdam: Excerpta Medica; 1974. p. 268-76.
    • (1974) Birth Defects , pp. 268-276
    • Stamatoyannopoulos, G.1
  • 100
    • 0025916638 scopus 로고
    • Reproductive behavior of families segregating for Cooley's anaemia before and after the availability of prenatal diagnosis
    • Gamberini MR, Lucci M, Vullo C, Anderson B, Canella R, Barrai I. Reproductive behavior of families segregating for Cooley's anaemia before and after the availability of prenatal diagnosis. J Med Genet 1991; 28: 523-9.
    • (1991) J Med Genet , vol.28 , pp. 523-529
    • Gamberini, M.R.1    Lucci, M.2    Vullo, C.3    Anderson, B.4    Canella, R.5    Barrai, I.6
  • 101
    • 8744272457 scopus 로고    scopus 로고
    • Iranian national thalassemia screening programme
    • Samavat A, Modell B. Iranian national thalassemia screening programme. BMJ 2004; 329: 1134-7.
    • (2004) BMJ , vol.329 , pp. 1134-1137
    • Samavat, A.1    Modell, B.2
  • 102
    • 20644467771 scopus 로고    scopus 로고
    • Couple screening to avoid thalassemia: Successful in Iran and instructive for us all
    • Haddow JE. Couple screening to avoid thalassemia: successful in Iran and instructive for us all. J Med Screen 2005; 12: 55-6.
    • (2005) J Med Screen , vol.12 , pp. 55-56
    • Haddow, J.E.1
  • 104
    • 0021259895 scopus 로고
    • A private view of heterozygosity:Eight year follow-up study on carriers of Tay - Sachs gene detected by high- school screening in Montreal
    • Zeesman S, Clow CL, Cartier L, Scriver CR. A private view of heterozygosity:eight year follow-up study on carriers of Tay - Sachs gene detected by high- school screening in Montreal. Am J Med Genet 1984; 18: 769-78.
    • (1984) Am J Med Genet , vol.18 , pp. 769-778
    • Zeesman, S.1    Clow, C.L.2    Cartier, L.3    Scriver, C.R.4
  • 105
    • 33749258721 scopus 로고    scopus 로고
    • 'Rakter dosh' - corrupting blood: The challenges of preventing thalassemia in Bengal, India
    • Chattopadhyay S. 'Rakter dosh' - corrupting blood: The challenges of preventing thalassemia in Bengal, India. Soc Sci Med 2006; 63: 2661-73.
    • (2006) Soc Sci Med , vol.63 , pp. 2661-2673
    • Chattopadhyay, S.1
  • 106
    • 59449095626 scopus 로고    scopus 로고
    • Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India
    • Tamhankar PM, Agarwal S, Arya V, Kumar R, Gupta UR, Agarwal SS. Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India. Prenat Diagn 2009; 29: 83-8.
    • (2009) Prenat Diagn , vol.29 , pp. 83-88
    • Tamhankar, P.M.1    Agarwal, S.2    Arya, V.3    Kumar, R.4    Gupta, U.R.5    Agarwal, S.S.6
  • 107
    • 0016784526 scopus 로고
    • Screening for microcytemia in Italy: Analysis of data collected in the past 30 years
    • Silverstroni E, Bianco I. Screening for microcytemia in Italy: Analysis of data collected in the past 30 years. Am J Hum Genet 1975; 27: 198-212.
    • (1975) Am J Hum Genet , vol.27 , pp. 198-212
    • Silverstroni, E.1    Bianco, I.2
  • 108
    • 0015730819 scopus 로고
    • Diagnosis of heterozygous beta-thalassemia in a population with high prevalence of iron deficiency
    • Mehta BC, Iyer PD, Gandhi SG, Ramnath SR, Patel JC. Diagnosis of heterozygous beta-thalassemia in a population with high prevalence of iron deficiency. Indian J Med Sci 1973; 27: 832-5.
    • (1973) Indian J Med Sci , vol.27 , pp. 832-835
    • Mehta, B.C.1    Iyer, P.D.2    Gandhi, S.G.3    Ramnath, S.R.4    Patel, J.C.5
  • 109
    • 0031445359 scopus 로고    scopus 로고
    • Validity of Nestroft in screening and diagnosis of β-thalassemia trait
    • Gomber S, Madan N. Validity of Nestroft in screening and diagnosis of β-thalassemia trait. J Trop Pediatr 1997; 43: 363-6.
    • (1997) J Trop Pediatr , vol.43 , pp. 363-366
    • Gomber, S.1    Madan, N.2
  • 110
    • 36849033896 scopus 로고    scopus 로고
    • Is NESTROFT sufficient for mass screening for beta-thalassaemia trait?
    • Mamtani M, Das K, Jawahirani A, Rughwani V, Kulkarni H. Is NESTROFT sufficient for mass screening for beta-thalassaemia trait? J Med Screen 2007; 14: 169-73.
    • (2007) J Med Screen , vol.14 , pp. 169-173
    • Mamtani, M.1    Das, K.2    Jawahirani, A.3    Rughwani, V.4    Kulkarni, H.5
  • 111
    • 0023775613 scopus 로고
    • Iron status in heterozygous beta-thalassemia: Detection of coexisting iron deficiency by transferrin saturation and serum ferritin
    • Saraya AK, Kumar R, Sehgal AK. Iron status in heterozygous beta-thalassemia: detection of coexisting iron deficiency by transferrin saturation and serum ferritin. Birth Defects Orig Artic Ser 1988; 23: 9-18.
    • (1988) Birth Defects Orig Artic Ser , vol.23 , pp. 9-18
    • Saraya, A.K.1    Kumar, R.2    Sehgal, A.K.3
  • 112
    • 0030345410 scopus 로고    scopus 로고
    • Frequency of coincident iron deficiency and beta-thalassaemia trait
    • Madan N, Sikka M, Sharma S, Rusia U. Frequency of coincident iron deficiency and beta-thalassaemia trait. J Clin Pathol 1996; 49: 1021.
    • (1996) J Clin Pathol , vol.49 , pp. 1021
    • Madan, N.1    Sikka, M.2    Sharma, S.3    Rusia, U.4
  • 113
    • 0031696475 scopus 로고    scopus 로고
    • Phenotypic expression of hemoglobin A2 in β-thalassemia trait with iron deficiency
    • Madan N, Sikka M, Sharma S, Rusia U. Phenotypic expression of hemoglobin A2 in β-thalassemia trait with iron deficiency. Ann Hematol 1998; 77: 93-6.
    • (1998) Ann Hematol , vol.77 , pp. 93-96
    • Madan, N.1    Sikka, M.2    Sharma, S.3    Rusia, U.4
  • 114
    • 2342462983 scopus 로고    scopus 로고
    • Development and validation of an ELISA for hemoglobin-A2: A novel method for β-thalassemia screening in developing countries
    • Menon SR, Khatkhatay MI, Dandekar SP, Patel ZM. Development and validation of an ELISA for hemoglobin-A2: a novel method for β-thalassemia screening in developing countries. J Immunoassay Immunochem 2004; 25: 135-46.
    • (2004) J Immunoassay Immunochem , vol.25 , pp. 135-146
    • Menon, S.R.1    Khatkhatay, M.I.2    Dandekar, S.P.3    Patel, Z.M.4
  • 115
    • 12844261653 scopus 로고    scopus 로고
    • Beta-thalassaemia carrier detection by ELISA: A simple screening strategy for developing countries
    • Ravindran MS, Patel ZM, Khatkhatay MI, Dandekar SP. Beta-thalassaemia carrier detection by ELISA: a simple screening strategy for developing countries. J Clin Lab Anal 2005; 19: 22-5.
    • (2005) J Clin Lab Anal , vol.19 , pp. 22-25
    • Ravindran, M.S.1    Patel, Z.M.2    Khatkhatay, M.I.3    Dandekar, S.P.4
  • 116
    • 34848894803 scopus 로고    scopus 로고
    • Assessing the impact of screening and counselling high school children for β-thalassaemia in India
    • Colah R, Thomas M, Mayekar P. Assessing the impact of screening and counselling high school children for β-thalassaemia in India. J Med Screen 2007; 14: 158.
    • (2007) J Med Screen , vol.14 , pp. 158
    • Colah, R.1    Thomas, M.2    Mayekar, P.3
  • 117
    • 0037057643 scopus 로고    scopus 로고
    • Screening extended families for genetic hemoglobin disorders in Pakistan
    • Ahmed S, Saleem M, Modell B, Petrou M. Screening extended families for genetic hemoglobin disorders in Pakistan. N Engl J Med 2002; 347: 1162-8.
    • (2002) N Engl J Med , vol.347 , pp. 1162-1168
    • Ahmed, S.1    Saleem, M.2    Modell, B.3    Petrou, M.4
  • 118
    • 0037057597 scopus 로고    scopus 로고
    • Effect of consanguinity on screening of thalassemia
    • Cao A, Galanello R. Effect of consanguinity on screening of thalassemia. N Engl J Med 2002; 347: 1200-2.
    • (2002) N Engl J Med , vol.347 , pp. 1200-1202
    • Cao, A.1    Galanello, R.2
  • 119
    • 73649121687 scopus 로고    scopus 로고
    • Cascade screening for beta-thalassemia: A practical approach for identifying and counseling carriers in India
    • Gorakshakar AC, Colah RB. Cascade screening for beta-thalassemia: A practical approach for identifying and counseling carriers in India. Indian J Community Med 2009; 34: 354-6.
    • (2009) Indian J Community Med , vol.34 , pp. 354-356
    • Gorakshakar, A.C.1    Colah, R.B.2
  • 120
    • 0031306226 scopus 로고    scopus 로고
    • Post counseling follow up of thalassemia in high risk communities
    • Yagnik H. Post counseling follow up of thalassemia in high risk communities. Indian Pediatr 1997; 34: 1115-8.
    • (1997) Indian Pediatr , vol.34 , pp. 1115-1118
    • Yagnik, H.1
  • 121
    • 0036095130 scopus 로고    scopus 로고
    • Feasibility of thalassaemia control by extended family screening in Indian context
    • Saxena A, Phadke SR. Feasibility of thalassaemia control by extended family screening in Indian context. J Health Popul Nutr 2002; 20: 31-5.
    • (2002) J Health Popul Nutr , vol.20 , pp. 31-35
    • Saxena, A.1    Phadke, S.R.2
  • 122
    • 80455157376 scopus 로고    scopus 로고
    • Indian Red Cross Society (IRCS, Annual Report 2009-2010. Ahmedabad: IRCS, Gujarat State Branch
    • Indian Red Cross Society (IRCS), Gujarat State Branch. Annual Report 2009-2010. Ahmedabad: IRCS, Gujarat State Branch; 2010.
    • (2010) Gujarat State Branch
  • 123
    • 45549083312 scopus 로고    scopus 로고
    • Carrier screening for beta-thalassemia during pregnancy in India: A 7-year evaluation
    • Colah R, Surve R, Wadia M, Solanki P, Mayekar P, Thomas M, et al. Carrier screening for beta-thalassemia during pregnancy in India: a 7-year evaluation. Genet Test 2008; 12: 181-5.
    • (2008) Genet Test , vol.12 , pp. 181-185
    • Colah, R.1    Surve, R.2    Wadia, M.3    Solanki, P.4    Mayekar, P.5    Thomas, M.6
  • 126
    • 0031963304 scopus 로고    scopus 로고
    • Prenatal diagnosis of beta-thalassaemia: Experience in a developing country
    • Saxena R, Jain PK, Thomas E, Verma IC. Prenatal diagnosis of beta-thalassaemia: experience in a developing country. Prenat Diagn 1998; 18: 1-7.
    • (1998) Prenat Diagn , vol.18 , pp. 1-7
    • Saxena, R.1    Jain, P.K.2    Thomas, E.3    Verma, I.C.4
  • 127
    • 0034030336 scopus 로고    scopus 로고
    • Prenatal diagnosis of beta-thalassaemia and other haemoglobinopathies in India
    • Thakur C, Vaz F, Banerjee M, Kapadia C, Natrajan PG, Yagnik H, et al. Prenatal diagnosis of beta-thalassaemia and other haemoglobinopathies in India. Prenat Diagn 2000; 20:194-201.
    • (2000) Prenat Diagn , vol.20 , pp. 194-201
    • Thakur, C.1    Vaz, F.2    Banerjee, M.3    Kapadia, C.4    Natrajan, P.G.5    Yagnik, H.6
  • 128
    • 23244432186 scopus 로고    scopus 로고
    • Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India
    • Garewal G, Das R, Ahluwalia J, Marwaha RK, Varma S. Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India. Am J Hematol 2005; 79: 252-6.
    • (2005) Am J Hematol , vol.79 , pp. 252-256
    • Garewal, G.1    Das, R.2    Ahluwalia, J.3    Marwaha, R.K.4    Varma, S.5
  • 129
    • 35048865291 scopus 로고    scopus 로고
    • The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians
    • Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians. Eur J Haematol 2007; 79: 417-21.
    • (2007) Eur J Haematol , vol.79 , pp. 417-421
    • Garewal, G.1    Das, R.2    Awasthi, A.3    Ahluwalia, J.4    Marwaha, R.K.5
  • 131
    • 0036189033 scopus 로고    scopus 로고
    • Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of beta-thalassemia
    • Wadia MR, Phanasgaokar SP, Nadkarni AH, Surve RR, Gorakshakar AC, Colah RB, et al. Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of beta-thalassemia. Prenat Diagn 2002; 22: 153-7.
    • (2002) Prenat Diagn , vol.22 , pp. 153-157
    • Wadia, M.R.1    Phanasgaokar, S.P.2    Nadkarni, A.H.3    Surve, R.R.4    Gorakshakar, A.C.5    Colah, R.B.6
  • 132
    • 66949159895 scopus 로고    scopus 로고
    • Use of HbA estimation by CE-HPLC for prenatal diagnosis of beta-thalassemia; experience from a tertiary care centre in north India: A brief report
    • Rao S, Saxena R, Deka D, Kabra M. Use of HbA estimation by CE-HPLC for prenatal diagnosis of beta-thalassemia; experience from a tertiary care centre in north India: a brief report. Hematology 2009; 14: 122-4.
    • (2009) Hematology , vol.14 , pp. 122-124
    • Rao, S.1    Saxena, R.2    Deka, D.3    Kabra, M.4
  • 133
    • 84859102784 scopus 로고    scopus 로고
    • accessed on October 4
    • http://www.who.int/healthinfo/global_burden_disease/en/, accessed on October 4, 2011.
    • (2011)
  • 134
    • 84859102785 scopus 로고    scopus 로고
    • accessed on October 4
    • http://data.worldbank.org/about/country-classifications, accessed on October 4, 2011.
    • (2011)
  • 135
    • 29744452838 scopus 로고    scopus 로고
    • Keynote address: The challenge of thalassemia for the developing countries
    • Weatherall DJ. Keynote address: The challenge of thalassemia for the developing countries. Ann N Y Acad Sci 2005; 1054: 11-7.
    • (2005) Ann N Y Acad Sci , vol.1054 , pp. 11-17
    • Weatherall, D.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.