-
1
-
-
20444498614
-
Outcome of holistic care in Nigerian patients with sickle cell anaemia
-
Akinyanju, O.O., Otaigbe, A.I. & Ibidapo, M.O. (2005) Outcome of holistic care in Nigerian patients with sickle cell anaemia. Clinical & Laboratory Haematology, 27, 195-199.
-
(2005)
Clinical & Laboratory Haematology
, vol.27
, pp. 195-199
-
-
Akinyanju, O.O.1
Otaigbe, A.I.2
Ibidapo, M.O.3
-
3
-
-
0025776299
-
Reproductive behavior and health in consanguineous marriages
-
Bittles, A.H., Mason, W.M., Greene, J. & Rao, N.A. (1991) Reproductive behavior and health in consanguineous marriages. Science, 252, 789-794.
-
(1991)
Science
, vol.252
, pp. 789-794
-
-
Bittles, A.H.1
Mason, W.M.2
Greene, J.3
Rao, N.A.4
-
4
-
-
20844460608
-
Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine
-
Borgna-Pignatti, C., Rugolotto, S., De Stefano, P., Zhao, H., Cappellini, M.D., Del Vecchio, G.C., Romeo, M.A., Forni, G.L., Gamberini, M.R., Ghilardi, R., Piga, A. & Cnaan, A. (2004) Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. Haematologica, 89, 1187-1193.
-
(2004)
Haematologica
, vol.89
, pp. 1187-1193
-
-
Borgna-Pignatti, C.1
Rugolotto, S.2
De Stefano, P.3
Zhao, H.4
Cappellini, M.D.5
Del Vecchio, G.C.6
Romeo, M.A.7
Forni, G.L.8
Gamberini, M.R.9
Ghilardi, R.10
Piga, A.11
Cnaan, A.12
-
5
-
-
0028059813
-
Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major
-
Brittenham, G.M., Griffith, P.M., Nienhuis, A.W., McLaren, C.E., Young, N.S., Tucker, E.E., Allen, C.J., Farrell, D.E. & Harris, J.W. (1994) Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major. New England Journal of Medicine, 331, 567-573.
-
(1994)
New England Journal of Medicine
, vol.331
, pp. 567-573
-
-
Brittenham, G.M.1
Griffith, P.M.2
Nienhuis, A.W.3
McLaren, C.E.4
Young, N.S.5
Tucker, E.E.6
Allen, C.J.7
Farrell, D.E.8
Harris, J.W.9
-
6
-
-
1542708757
-
Lessons from anti-thalassemia campaigns in Italy, before prenatal diagnosis
-
Canali, S. & Corbellini, G. (2002) Lessons from anti-thalassemia campaigns in Italy, before prenatal diagnosis. Med Secoli, 14, 739-771.
-
(2002)
Med Secoli
, vol.14
, pp. 739-771
-
-
Canali, S.1
Corbellini, G.2
-
7
-
-
0032415999
-
Prenatal diagnosis and screening of the haemoglobinopathies
-
Bailliere Tindall, London.
-
Cao, A., Galanello, R. & Rosatelli, M.C. (1998) Prenatal diagnosis and screening of the haemoglobinopathies. Bailliere's Clinical Haematology, 11, 215-238, Bailliere Tindall, London.
-
(1998)
Bailliere's Clinical Haematology
, vol.11
, pp. 215-238
-
-
Cao, A.1
Galanello, R.2
Rosatelli, M.C.3
-
8
-
-
77952634429
-
Epidemiology of beta-thalassaemia in Western India: mapping the frequncies and mutations in sub-regions of Maharashtra and Gujarat
-
Colah, R., Gorakshakar, A., Phanasgaonkar, S., D'Souza, E., Nadkarni, A., Surve, R., Sawant, P., Master, D., Patel, R., Ghosh, K. & Mohanty, D. (2010) Epidemiology of beta-thalassaemia in Western India: mapping the frequncies and mutations in sub-regions of Maharashtra and Gujarat. British Journal of Haematology, 149, 739-747.
-
(2010)
British Journal of Haematology
, vol.149
, pp. 739-747
-
-
Colah, R.1
Gorakshakar, A.2
Phanasgaonkar, S.3
D'Souza, E.4
Nadkarni, A.5
Surve, R.6
Sawant, P.7
Master, D.8
Patel, R.9
Ghosh, K.10
Mohanty, D.11
-
9
-
-
84932638322
-
Hemoglobin E disorders
-
eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall Cambridge University Press, Cambridge.
-
Fucharoen, S. & Weatherall, D.J. (2009) Hemoglobin E disorders. In: Disorders of Hemoglobin (eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall), pp. 417-433. Cambridge University Press, Cambridge.
-
(2009)
Disorders of Hemoglobin
, pp. 417-433
-
-
Fucharoen, S.1
Weatherall, D.J.2
-
10
-
-
0022977959
-
Sickle cell disease in Orissa State, India
-
1198.
-
Kar, B.C., Satapathy, R.K., Kulozik, A.E., Kulozik, M., Sirr, S., Serjeant, B.E. & Serjeant, G.R. (1986) Sickle cell disease in Orissa State, India. Lancet, ii, 1198.
-
(1986)
Lancet
, vol.2
-
-
Kar, B.C.1
Satapathy, R.K.2
Kulozik, A.E.3
Kulozik, M.4
Sirr, S.5
Serjeant, B.E.6
Serjeant, G.R.7
-
11
-
-
0022547280
-
s-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation
-
s-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation. American Journal of Human Genetics, 39, 239-244.
-
(1986)
American Journal of Human Genetics
, vol.39
, pp. 239-244
-
-
Kulozik, A.E.1
Wainscoat, J.S.2
Serjeant, G.R.3
Kar, B.C.4
Al-Awamy, B.5
Essan, G.J.F.6
Falusi, A.G.7
Haque, S.K.8
Hilali, A.M.9
Kate, S.10
Ranasinghe, W.A.E.P.11
Weatherall, D.J.12
-
13
-
-
79951924307
-
Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania
-
Makani, J., Cox, S.E., Soka, D., Komba, A.N., Oruo, J., Mwamtemi, H., Magesa, P., Rwezaula, S., Meda, E., Mgaya, J., Lowe, B., Muturi, D., Roberts, D.J., Williams, T.N., Pallangyo, K., Kitundu, J., Fegan, G., Kirkham, F.J., Marsh, K. & Newton, C.R. (2011) Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania. PLoS ONE, 6, e14699.
-
(2011)
PLoS ONE
, vol.6
-
-
Makani, J.1
Cox, S.E.2
Soka, D.3
Komba, A.N.4
Oruo, J.5
Mwamtemi, H.6
Magesa, P.7
Rwezaula, S.8
Meda, E.9
Mgaya, J.10
Lowe, B.11
Muturi, D.12
Roberts, D.J.13
Williams, T.N.14
Pallangyo, K.15
Kitundu, J.16
Fegan, G.17
Kirkham, F.J.18
Marsh, K.19
Newton, C.R.20
more..
-
14
-
-
44949128064
-
Global epidemiology of haemoglobin disorders and derived service indicators
-
Modell, B. & Darlison, M. (2008) Global epidemiology of haemoglobin disorders and derived service indicators. Bulletin of the World Health Organization, 86, 480-487.
-
(2008)
Bulletin of the World Health Organization
, vol.86
, pp. 480-487
-
-
Modell, B.1
Darlison, M.2
-
15
-
-
0025826185
-
Services for thalassaemia as a model for cost-benefit analysis of genetics services
-
Modell, B. & Kuliev, A.M. (1991) Services for thalassaemia as a model for cost-benefit analysis of genetics services. Journal of Inherited Metabolic Disease, 14, 640-651.
-
(1991)
Journal of Inherited Metabolic Disease
, vol.14
, pp. 640-651
-
-
Modell, B.1
Kuliev, A.M.2
-
16
-
-
0027230044
-
A scientific basis for cost-benefit analysis of genetics services
-
Modell, B. & Kuliev, A.M. (1993) A scientific basis for cost-benefit analysis of genetics services. Trends in Genetics, 9, 46-52.
-
(1993)
Trends in Genetics
, vol.9
, pp. 46-52
-
-
Modell, B.1
Kuliev, A.M.2
-
17
-
-
0002186805
-
The history of community genetics: the contribution of the haemoglobin disorders
-
Modell, B. & Kuliev, A. (1998) The history of community genetics: the contribution of the haemoglobin disorders. Community Genetics, 1, 3-11.
-
(1998)
Community Genetics
, vol.1
, pp. 3-11
-
-
Modell, B.1
Kuliev, A.2
-
19
-
-
0003433982
-
-
Harvard University Press, Cambridge, MA.
-
Murray, C.J.L. & Lopez, A.D. (1996) The Global Burden of Disease: A comprehensive Assessment of Mortality and Disability from Diseases, Injuries and Risk Factors in 1990 and Projected to 2020. Harvard University Press, Cambridge, MA.
-
(1996)
The Global Burden of Disease: A comprehensive Assessment of Mortality and Disability from Diseases, Injuries and Risk Factors in 1990 and Projected to 2020
-
-
Murray, C.J.L.1
Lopez, A.D.2
-
20
-
-
84932611834
-
Clinical aspects of beta thalassemia and related disorders
-
(eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall) Cambridge University Press, Cambridge.
-
Olivieri, N.F. & Weatherall, D.J. (2009) Clinical aspects of beta thalassemia and related disorders. In: Disorders of Hemoglobin (eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall), pp. 357-416. Cambridge University Press, Cambridge.
-
(2009)
Disorders of Hemoglobin
, pp. 357-416
-
-
Olivieri, N.F.1
Weatherall, D.J.2
-
21
-
-
0028086414
-
Survival of medically treated patients with homozygous β thalassemia
-
Olivieri, N.F., Nathan, D.G., MacMillan, J.H., Wayne, A.S., Liu, P.P., McGee, A., Martin, M., Koren, G. & Cohen, A.R. (1994) Survival of medically treated patients with homozygous β thalassemia. New England Journal of Medicine, 331, 574-578.
-
(1994)
New England Journal of Medicine
, vol.331
, pp. 574-578
-
-
Olivieri, N.F.1
Nathan, D.G.2
MacMillan, J.H.3
Wayne, A.S.4
Liu, P.P.5
McGee, A.6
Martin, M.7
Koren, G.8
Cohen, A.R.9
-
22
-
-
77955893564
-
Emerging insights in the management of hemoglobin E beta thalassemia
-
Olivieri, N.F., Thayalsuthan, V., O'Donnell, A., Premawardena, A., Rigobon, C., Muraca, G., Fisher, C. & Weatherall, D.J. (2010) Emerging insights in the management of hemoglobin E beta thalassemia. Annals of the New York Academy of Sciences, 1202, 155-157.
-
(2010)
Annals of the New York Academy of Sciences
, vol.1202
, pp. 155-157
-
-
Olivieri, N.F.1
Thayalsuthan, V.2
O'Donnell, A.3
Premawardena, A.4
Rigobon, C.5
Muraca, G.6
Fisher, C.7
Weatherall, D.J.8
-
23
-
-
77954607742
-
Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management
-
O'Riordan, S., Hien, T.T., Miles, K., Allen, A., Quyen, N.N., Hung, N.Q., Anh do, Q., Tuyen, L.N., Khoa, D.B., Thai, C.Q., Triet, D.M., Phu, N.H., Dunstan, S., Peto, T., Clegg, J., Farrar, J. & Weatherall, D. (2010) Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management. British Journal of Haematology, 150, 359-364.
-
(2010)
British Journal of Haematology
, vol.150
, pp. 359-364
-
-
O'Riordan, S.1
Hien, T.T.2
Miles, K.3
Allen, A.4
Quyen, N.N.5
Hung, N.Q.6
Anh do, Q.7
Tuyen, L.N.8
Khoa, D.B.9
Thai, C.Q.10
Triet, D.M.11
Phu, N.H.12
Dunstan, S.13
Peto, T.14
Clegg, J.15
Farrar, J.16
Weatherall, D.17
-
24
-
-
75849133408
-
Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean
-
Penman, B.S., Pybus, O.G., Weatherall, D.J. & Gupta, S. (2009) Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean. Proceedings of the National Academy of Sciences of the United States of America, 106, 21242-21246.
-
(2009)
Proceedings of the National Academy of Sciences of the United States of America
, vol.106
, pp. 21242-21246
-
-
Penman, B.S.1
Pybus, O.G.2
Weatherall, D.J.3
Gupta, S.4
-
25
-
-
78650101852
-
Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis
-
Piel, F.B., Patil, A.P., Howes, R.E., Nyangiri, O.A., Gething, P.W., Williams, T.N., Weatherall, D.J. & Hay, S.I. (2010) Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis. Nature Communications, 1, 104.
-
(2010)
Nature Communications
, vol.1
, pp. 104
-
-
Piel, F.B.1
Patil, A.P.2
Howes, R.E.3
Nyangiri, O.A.4
Gething, P.W.5
Williams, T.N.6
Weatherall, D.J.7
Hay, S.I.8
-
26
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
Platt, O.S., Brambilla, D.J., Rosse, W.F., Milner, P.F., Castro, O., Steinberg, M.H. & Klug, P.P. (1994) Mortality in sickle cell disease. Life expectancy and risk factors for early death. New England Journal of Medicine, 330, 1639-1644.
-
(1994)
New England Journal of Medicine
, vol.330
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
Castro, O.5
Steinberg, M.H.6
Klug, P.P.7
-
27
-
-
58349100878
-
Newborn screening for sickle cell disease in the Republic of Benin
-
Rahimy, M.C., Gangbo, A., Ahouignan, G. & Alihonou, E. (2009) Newborn screening for sickle cell disease in the Republic of Benin. Journal of Clinical Pathology, 62, 46-48.
-
(2009)
Journal of Clinical Pathology
, vol.62
, pp. 46-48
-
-
Rahimy, M.C.1
Gangbo, A.2
Ahouignan, G.3
Alihonou, E.4
-
28
-
-
0030860293
-
Genetic counselling among Muslims: questions remain unanswered
-
Salihu, H.M. (1997) Genetic counselling among Muslims: questions remain unanswered. Lancet, 350, 1035-1036.
-
(1997)
Lancet
, vol.350
, pp. 1035-1036
-
-
Salihu, H.M.1
-
30
-
-
0034603546
-
Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group
-
de Silva, S., Fisher, C.A., Premawardhena, A., Lamabadusuriya, S.P., Peto, T.E., Perera, G., Old, J.M., Clegg, J.B., Olivieri, N.F. & Weatherall, D.J. (2000) Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group. Lancet, 355, 786-791.
-
(2000)
Lancet
, vol.355
, pp. 786-791
-
-
de Silva, S.1
Fisher, C.A.2
Premawardhena, A.3
Lamabadusuriya, S.P.4
Peto, T.E.5
Perera, G.6
Old, J.M.7
Clegg, J.B.8
Olivieri, N.F.9
Weatherall, D.J.10
-
31
-
-
77950436431
-
Genetic modulation of sickle cell disease and thalassemia
-
(eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall) Cambridge University Press, Cambridge.
-
Steinberg, M.H. & Nagel, R.L. (2009) Genetic modulation of sickle cell disease and thalassemia. In: Disorders of Hemoglobin (eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall), pp. 638-657. Cambridge University Press, Cambridge.
-
(2009)
Disorders of Hemoglobin
, pp. 638-657
-
-
Steinberg, M.H.1
Nagel, R.L.2
-
32
-
-
84932641769
-
Clinical and pathophysiological aspects of sickle cell anaemia
-
eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall Cambridge University Press, Cambridge.
-
Steinberg, M.H., Ohene-Frempong, K. & Heeney, M.M. (2009) Clinical and pathophysiological aspects of sickle cell anaemia. In: Disorders of Hemoglobin (eds by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall), pp. 437-496. Cambridge University Press, Cambridge.
-
(2009)
Disorders of Hemoglobin
, pp. 437-496
-
-
Steinberg, M.H.1
Ohene-Frempong, K.2
Heeney, M.M.3
-
33
-
-
79951553407
-
Optimal management of beta thalassaemia intermedia
-
Taher, A.T., Musallam, K.M., Cappellini, M.D. & Weatherall, D.J. (2011) Optimal management of beta thalassaemia intermedia. British Journal of Haematology, 152, 512-523.
-
(2011)
British Journal of Haematology
, vol.152
, pp. 512-523
-
-
Taher, A.T.1
Musallam, K.M.2
Cappellini, M.D.3
Weatherall, D.J.4
-
34
-
-
42049110421
-
Genetic variation and susceptibility to infection: the red cell and malaria
-
Weatherall, D.J. (2008) Genetic variation and susceptibility to infection: the red cell and malaria. British Journal of Haematology, 141, 276-286.
-
(2008)
British Journal of Haematology
, vol.141
, pp. 276-286
-
-
Weatherall, D.J.1
-
35
-
-
77952592557
-
The importance of micromapping the gene frequencies for the common inherited disorders of haemoglobin
-
Weatherall, D.J. (2010a) The importance of micromapping the gene frequencies for the common inherited disorders of haemoglobin. British Journal of Haematology, 149, 635-637.
-
(2010)
British Journal of Haematology
, vol.149
, pp. 635-637
-
-
Weatherall, D.J.1
-
37
-
-
77953952024
-
The inherited diseases of hemoglobin are an emerging global health burden
-
Weatherall, D.J. (2010c) The inherited diseases of hemoglobin are an emerging global health burden. Blood, 115, 4331-4336.
-
(2010)
Blood
, vol.115
, pp. 4331-4336
-
-
Weatherall, D.J.1
-
39
-
-
34247143171
-
Inherited disorders of Hemoglobin
-
eds by D.T. Jamison, J.G. Breman, A.R. Measham, G. Alleyne, M. Claeson, D.B. Evans, P. Jha, A. Mills & P. Musgrove. Oxford University Press and the World Bank, New York, Washington.
-
Weatherall, D.J., Akinyanju, O., Fucharoen, S., Olivieri, N.F. & Musgrove, P. (2006) Inherited disorders of Hemoglobin. In: Disease Control Priorities in Developing Countries eds by D.T. Jamison, J.G. Breman, A.R. Measham, G. Alleyne, M. Claeson, D.B. Evans, P. Jha, A. Mills & P. Musgrove, pp. 663-680. Oxford University Press and the World Bank, New York, Washington.
-
(2006)
Disease Control Priorities in Developing Countries
, pp. 663-680
-
-
Weatherall, D.J.1
Akinyanju, O.2
Fucharoen, S.3
Olivieri, N.F.4
Musgrove, P.5
-
41
-
-
60249084909
-
-
WHO. In: 118th Session of the WHO Executive Board, WHO, Geneva, Switzerland.
-
WHO (2006) Thalassaemia and the Haemoglobinopathies. In: 118th Session of the WHO Executive Board, WHO, Geneva, Switzerland.
-
(2006)
Thalassaemia and the Haemoglobinopathies
-
-
-
44
-
-
0029858255
-
High incidence of malaria in α-thalassaemic children
-
Williams, T.N., Maitland, K., Bennett, S., Ganczakowski, M., Peto, T.E.A., Newbold, C.I., Bowden, D.K., Weatherall, D.J. & Clegg, J.B. (1996) High incidence of malaria in α-thalassaemic children. Nature, 383, 522-525.
-
(1996)
Nature
, vol.383
, pp. 522-525
-
-
Williams, T.N.1
Maitland, K.2
Bennett, S.3
Ganczakowski, M.4
Peto, T.E.A.5
Newbold, C.I.6
Bowden, D.K.7
Weatherall, D.J.8
Clegg, J.B.9
-
45
-
-
27644566200
-
Negative epistasis between the malaria-protective effects of alpha+-thalassemia and the sickle cell trait
-
Williams, T.N., Mwangi, T.W., Wambua, S., Peto, T.E., Weatherall, D.J., Gupta, S., Recker, M., Penman, B.S., Uyoga, S., Macharia, A., Mwacharo, J.K., Snow, R.W. & Marsh, K. (2005) Negative epistasis between the malaria-protective effects of alpha+-thalassemia and the sickle cell trait. Nature Genetics, 37, 1253-1257.
-
(2005)
Nature Genetics
, vol.37
, pp. 1253-1257
-
-
Williams, T.N.1
Mwangi, T.W.2
Wambua, S.3
Peto, T.E.4
Weatherall, D.J.5
Gupta, S.6
Recker, M.7
Penman, B.S.8
Uyoga, S.9
Macharia, A.10
Mwacharo, J.K.11
Snow, R.W.12
Marsh, K.13
-
46
-
-
70349869344
-
Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case-control study
-
Williams, T.N., Uyoga, S., Macharia, A., Ndila, C., McAuley, C.F., Opi, D.H., Mwarumba, S., Makani, J., Komba, A., Ndiritu, M.N., Sharif, S.K., Marsh, K., Berkley, J.A. & Scott, J.A. (2009) Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case-control study. Lancet, 374, 1364-1370.
-
(2009)
Lancet
, vol.374
, pp. 1364-1370
-
-
Williams, T.N.1
Uyoga, S.2
Macharia, A.3
Ndila, C.4
McAuley, C.F.5
Opi, D.H.6
Mwarumba, S.7
Makani, J.8
Komba, A.9
Ndiritu, M.N.10
Sharif, S.K.11
Marsh, K.12
Berkley, J.A.13
Scott, J.A.14
|