-
1
-
-
0002341637
-
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
-
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
-
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
-
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
-
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
-
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
-
11
-
-
0014553071
-
Haemoglobinopathy in Orissa
-
Praharaj KC, Mohanta KD, Kar RS, Swain U, Nanda BK. Haemoglobinopathy in Orissa. Indian Pediatr 1969; 6: 533-7.
-
(1969)
Indian Pediatr
, vol.6
, pp. 533-537
-
-
Praharaj, K.C.1
Mohanta, K.D.2
Kar, R.S.3
Swain, U.4
Nanda, B.K.5
-
13
-
-
0019294926
-
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
-
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
-
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
-
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
-
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
-
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
-
20
-
-
34548493450
-
Case report of HbC/β0-thalassemia from India
-
Kumar S, Rana M, Handoo A, Saxena R, Verma IC, Bhargava M, et al. Case report of HbC/β0-thalassemia from India. Int J Lab Hematol 2007; 29: 381-5.
-
(2007)
Int J Lab Hematol
, vol.29
, pp. 381-385
-
-
Kumar, S.1
Rana, M.2
Handoo, A.3
Saxena, R.4
Verma, I.C.5
Bhargava, M.6
-
21
-
-
0013975221
-
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
-
22
-
-
0021399557
-
Molecular characterization of seven beta-thalassemia mutations in Asian Indians
-
Kazazian HH Jr, Orkin SH, Antonarakis SE, Sexton JP, Boehm CD, Goff SC, et al. Molecular characterization of seven beta-thalassemia mutations in Asian Indians. EMBO J 1984; 3: 593-6.
-
(1984)
EMBO J
, vol.3
, pp. 593-596
-
-
Kazazian Jr., H.H.1
Orkin, S.H.2
Antonarakis, S.E.3
Sexton, J.P.4
Boehm, C.D.5
Goff, S.C.6
-
23
-
-
0021176154
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
31
-
-
64849083131
-
Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population
-
Colah R, Gorakshakar A, Nadkarni A, Phanasgaonkar S, Surve R, Sawant P, et al. Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population. Blood Cells Mol Dis 2009; 42: 241-6.
-
(2009)
Blood Cells Mol Dis
, vol.42
, pp. 241-246
-
-
Colah, R.1
Gorakshakar, A.2
Nadkarni, A.3
Phanasgaonkar, S.4
Surve, R.5
Sawant, P.6
-
32
-
-
10844263355
-
Profile of β-thalassemia in eastern India and its prenatal diagnosis
-
Bandyopadhyay A, Bandyopadhyay S, Basak J, Mondal BC, Sarkar AA, Majumdar S, et al. Profile of β-thalassemia in eastern India and its prenatal diagnosis. Prenat Diagn 2004; 24: 992-6.
-
(2004)
Prenat Diagn
, vol.24
, pp. 992-996
-
-
Bandyopadhyay, A.1
Bandyopadhyay, S.2
Basak, J.3
Mondal, B.C.4
Sarkar, A.A.5
Majumdar, S.6
-
33
-
-
0026494873
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
48
-
-
0025194995
-
Thalassemia in Bombay: The role of medical genetics in developing countries
-
Sangani B, Sukumaran PK, Mahadik C, Yagnik H, Telang S, Vas F, et al. Thalassemia in Bombay: the role of medical genetics in developing countries. Bull World Health Organ 1990; 68: 75-81.
-
(1990)
Bull World Health Organ
, vol.68
, pp. 75-81
-
-
Sangani, B.1
Sukumaran, P.K.2
Mahadik, C.3
Yagnik, H.4
Telang, S.5
Vas, F.6
-
50
-
-
78049472245
-
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
-
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
-
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
-
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
-
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
-
-
accessed on August 5
-
http://www.indianredcross.org, accessed on August 5, 2011.
-
(2011)
-
-
-
57
-
-
0035050973
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
72
-
-
77749316834
-
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
-
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
-
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
-
75
-
-
67349123315
-
Effect of wheat grass therapy on transfusion requirement in beta-thalassemia major
-
Choudhary DR, Naithani R, Panigrahi I, Kumar R, Mahapatra M, Pati HP, et al. Effect of wheat grass therapy on transfusion requirement in beta-thalassemia major. Indian J Pediatr 2009; 76: 375-6.
-
(2009)
Indian J Pediatr
, vol.76
, pp. 375-376
-
-
Choudhary, D.R.1
Naithani, R.2
Panigrahi, I.3
Kumar, R.4
Mahapatra, M.5
Pati, H.P.6
-
76
-
-
76649122206
-
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
-
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
-
78
-
-
23244436397
-
Do alpha deletions influence hydroxyurea response in thalassemia intermedia?
-
Panigrahi I, Dixit A, Arora S, Kabra M, Mahapatra M, Choudhry VP, et al. Do alpha deletions influence hydroxyurea response in thalassemia intermedia? Hematology 2005; 10: 61-3.
-
(2005)
Hematology
, vol.10
, pp. 61-63
-
-
Panigrahi, I.1
Dixit, A.2
Arora, S.3
Kabra, M.4
Mahapatra, M.5
Choudhry, V.P.6
-
79
-
-
67749088379
-
Response to hydroxyurea in β-thalassemia major and intermedia: Experience in western India
-
Italia KY, Jijina FJ, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, et al. Response to hydroxyurea in β-thalassemia major and intermedia: experience in western India. Clin Chim Acta 2009; 407: 10-5.
-
(2009)
Clin Chim Acta
, vol.407
, pp. 10-15
-
-
Italia, K.Y.1
Jijina, F.J.2
Merchant, R.3
Panjwani, S.4
Nadkarni, A.H.5
Sawant, P.M.6
-
80
-
-
33751564490
-
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
-
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
-
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
-
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
-
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
-
-
accessed on October 4
-
http://www.relicord.com, accessed on October 4, 2011.
-
(2011)
-
-
-
86
-
-
84859109731
-
-
accessed on August 5
-
http://www.bmdw.org/, accessed on August 5, 2011.
-
(2011)
-
-
-
87
-
-
84859102786
-
-
accessed on August 5
-
http://www.worldmarrow.org/, accessed on August 5, 2011.
-
(2011)
-
-
-
88
-
-
33845910650
-
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
-
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
-
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
-
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
-
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
-
93
-
-
0031659246
-
Cost benefit analysis of a national thalassemia prevention programme in Israel
-
Ginsberg G, Tulchinsky T, Filon D, Goldfarb A, Abramov L, Rachmilevitz EA. Cost benefit analysis of a national thalassemia prevention programme in Israel. J Med Screening 1998; 5: 120-6.
-
(1998)
J Med Screening
, vol.5
, pp. 120-126
-
-
Ginsberg, G.1
Tulchinsky, T.2
Filon, D.3
Goldfarb, A.4
Abramov, L.5
Rachmilevitz, E.A.6
-
94
-
-
80455133651
-
-
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
-
-
-
97
-
-
0019363539
-
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
-
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
-
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
-
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
-
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
-
103
-
-
34447540222
-
Premarital screening for β-thalassaemia in Southern Iran:Options for improving the programme
-
Karimi M, Jamalian N, Yarmohammadi H, Askarnejad A, Afrasiabi A, Hashemi A. Premarital screening for β-thalassaemia in Southern Iran:options for improving the programme J Med Screen 2007; 14: 62-6.
-
(2007)
J Med Screen
, vol.14
, pp. 62-66
-
-
Karimi, M.1
Jamalian, N.2
Yarmohammadi, H.3
Askarnejad, A.4
Afrasiabi, A.5
Hashemi, A.6
-
104
-
-
0021259895
-
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
-
'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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
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
-
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
-
125
-
-
0030090607
-
Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique
-
Muralitharan S, Srivastava A, Shaji RV, Mathai M, Srivastava VM, Dennison D, et al. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique. Natl Med J India 1996; 9: 70-1.
-
(1996)
Natl Med J India
, vol.9
, pp. 70-71
-
-
Muralitharan, S.1
Srivastava, A.2
Shaji, R.V.3
Mathai, M.4
Srivastava, V.M.5
Dennison, D.6
-
126
-
-
0031963304
-
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
-
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
-
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
-
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
-
130
-
-
0024605518
-
Analysis of any point mutation in DNA - the amplification refractory mutation system (ARMS)
-
Newton CR, Graham A, Heptinstall LE, Powell SJ, Summers C, Kalsheker N, et al. Analysis of any point mutation in DNA - the amplification refractory mutation system (ARMS). Nucleic Acids Res 1989; 17: 2503-16.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 2503-2516
-
-
Newton, C.R.1
Graham, A.2
Heptinstall, L.E.3
Powell, S.J.4
Summers, C.5
Kalsheker, N.6
-
131
-
-
0036189033
-
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
-
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
-
-
accessed on October 4
-
http://www.who.int/healthinfo/global_burden_disease/en/, accessed on October 4, 2011.
-
(2011)
-
-
-
134
-
-
84859102785
-
-
accessed on October 4
-
http://data.worldbank.org/about/country-classifications, accessed on October 4, 2011.
-
(2011)
-
-
-
135
-
-
29744452838
-
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
|