-
1
-
-
12844276479
-
A case for developing North-South partnerships for research in sickle cell disease
-
Weatherall D, Hofman K, Rogers G, Ruffin J, Hrynkow S. A case for developing North-South partnerships for research in sickle cell disease. Blood 2005; 105:921-923.
-
(2005)
Blood
, vol.105
, pp. 921-923
-
-
Weatherall, D.1
Hofman, K.2
Rogers, G.3
Ruffin, J.4
Hrynkow, S.5
-
3
-
-
84872062977
-
Global epidemiology of sickle haemoglobin in neonates: A contemporary geostatistical model-based map and population estimates
-
Piel FB, Patil AP, Howes RE, Nyangiri OA, Gething PW, Dewi M, Temperley WH, Williams TN, Weatherall DJ, Hay SI. Global epidemiology of sickle haemoglobin in neonates: A contemporary geostatistical model-based map and population estimates. Lancet 2013; 381:142-151.
-
(2013)
Lancet
, vol.381
, pp. 142-151
-
-
Piel, F.B.1
Patil, A.P.2
Howes, R.E.3
Nyangiri, O.A.4
Gething, P.W.5
Dewi, M.6
Temperley, W.H.7
Williams, T.N.8
Weatherall, D.J.9
Hay, S.I.10
-
4
-
-
84903385956
-
Sickle cell anemia: An underappreciated and unaddressed contributor to global childhood mortality
-
McGann PT. Sickle cell anemia: An underappreciated and unaddressed contributor to global childhood mortality. J Pediatr 2014; 165:18-22.
-
(2014)
J Pediatr
, vol.165
, pp. 18-22
-
-
McGann, P.T.1
-
5
-
-
34548753905
-
Clinical outcomes in children with sickle cell disease living in England: A neonatal cohort in East London
-
Telfer P, Coen P, Chakravorty S, Wilkey O, Evans J, Newell H, Smalling B, Stephens A, Rogers D, Kirkham F. Clinical outcomes in children with sickle cell disease living in England: A neonatal cohort in East London. Haematologica 2007; 92:905-912.
-
(2007)
Haematologica
, vol.92
, pp. 905-912
-
-
Telfer, P.1
Coen, P.2
Chakravorty, S.3
Wilkey, O.4
Evans, J.5
Newell, H.6
Smalling, B.7
Stephens, A.8
Rogers, D.9
Kirkham, F.10
-
6
-
-
77951712618
-
Improved survival of children and adolescents with sickle cell disease
-
Quinn CT, Rogers ZR, McCavitt TL, Buchanan GR. Improved survival of children and adolescents with sickle cell disease. Blood 2010; 115:3447-3452.
-
(2010)
Blood
, vol.115
, pp. 3447-3452
-
-
Quinn, C.T.1
Rogers, Z.R.2
McCavitt, T.L.3
Buchanan, G.R.4
-
7
-
-
77953057530
-
The risks and benefits of long-term hydroxyurea in sickle cell anemia: A 17.5 year follow-up
-
Steinberg MH, McCarthy WF, Castro O, Ballas SK, Armstrong FD, Smith W, Swerdlow P, Kutlar A, DeCastro L, Waclawiw MA. The risks and benefits of long-term hydroxyurea in sickle cell anemia: A 17.5 year follow-up. Am J Hematol 2010; 85:403-408.
-
(2010)
Am J Hematol
, vol.85
, pp. 403-408
-
-
Steinberg, M.H.1
McCarthy, W.F.2
Castro, O.3
Ballas, S.K.4
Armstrong, F.D.5
Smith, W.6
Swerdlow, P.7
Kutlar, A.8
DeCastro, L.9
Waclawiw, M.A.10
-
8
-
-
71849118976
-
Allogeneic hematopoieitic stem-cell transplantation for sickle cell disease
-
Hsieh MM, Kang EM, Fitzhugh CD, Link MB, Bolan CD, Kurlander R, Childs RW, Rodgers GP, Powell JD, Tisdale JF. Allogeneic hematopoieitic stem-cell transplantation for sickle cell disease. N Engl J Med 2009; 361:2309-2317.
-
(2009)
N Engl J Med
, vol.361
, pp. 2309-2317
-
-
Hsieh, M.M.1
Kang, E.M.2
Fitzhugh, C.D.3
Link, M.B.4
Bolan, C.D.5
Kurlander, R.6
Childs, R.W.7
Rodgers, G.P.8
Powell, J.D.9
Tisdale, J.F.10
-
9
-
-
85009813220
-
Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease
-
Wang WC, Dwan K. Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease. Cochrane Database Syst Rev 2013; 11:CD003146.
-
(2013)
Cochrane Database Syst Rev
, vol.11
, pp. CD003146
-
-
Wang, W.C.1
Dwan, K.2
-
10
-
-
81355163446
-
Sickle cell disease in Africa: A neglected cause of early childhood mortality
-
Grosse SD, Odame I, Atrash HK, Amendah DD, Piel FB, Williams TN. Sickle cell disease in Africa: A neglected cause of early childhood mortality. Am J Prev Med 2010; 41:S398-S405.
-
(2010)
Am J Prev Med
, vol.41
, pp. S398-S405
-
-
Grosse, S.D.1
Odame, I.2
Atrash, H.K.3
Amendah, D.D.4
Piel, F.B.5
Williams, T.N.6
-
11
-
-
0034889014
-
Inherited haemoglobin disorders: An increasing global health problem
-
Weatherall DJ, Clegg JB. Inherited haemoglobin disorders: An increasing global health problem. Bull World Health Organ 2001; 79:704-712.
-
(2001)
Bull World Health Organ
, vol.79
, pp. 704-712
-
-
Weatherall, D.J.1
Clegg, J.B.2
-
12
-
-
70349869344
-
Bacteraemia in Kenyan children with sickle-cell anaemia: A retrospective cohort and case-control study
-
Williams TN, Uyoga S, Macharia A, Ndila C, McAuley CF, Opi DH, Makain J, Ndiriru MN, Sharif SK, Marsh K, Berkley JA, Scott JA. Bacteraemia in Kenyan children with sickle-cell anaemia: A retrospective cohort and case-control study. Lancet 2009; 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
Makain, J.7
Ndiriru, M.N.8
Sharif, S.K.9
Marsh, K.10
Berkley, J.A.11
Scott, J.A.12
-
13
-
-
77949441790
-
Developing a global agenda for sickle cell disease: Report of an international symposium and workshop in Cotonou, Republic of Benin
-
Odame I. Developing a global agenda for sickle cell disease: Report of an international symposium and workshop in Cotonou, Republic of Benin. Am J Prev Med 2010; 38:S571-S575.
-
(2010)
Am J Prev Med
, vol.38
, pp. S571-S575
-
-
Odame, I.1
-
14
-
-
84881220584
-
Global burden of sickle cell anaemia in children under five, 2010-2050: Modelling based on demographics, excess mortality, and interventions
-
Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anaemia in children under five, 2010-2050: Modelling based on demographics, excess mortality, and interventions. PLoS Med 2013; 10:e1001484.
-
(2013)
PLoS Med
, vol.10
, pp. e1001484
-
-
Piel, F.B.1
Hay, S.I.2
Gupta, S.3
Weatherall, D.J.4
Williams, T.N.5
-
16
-
-
58349117668
-
Neonatal screening for sickle cell anaemia in the Democratic Republic of the Congo: Experience from a pioneer project on 31 204 newborns
-
Tshilolo L, Aissi LM, Lukusa D, Kinsiama C, Wembonyama S, Gulbis B, Vertongen F. Neonatal screening for sickle cell anaemia in the Democratic Republic of the Congo: Experience from a pioneer project on 31 204 newborns. J Clin Pathol 2009; 62:35-38.
-
(2009)
J Clin Pathol
, vol.62
, pp. 35-38
-
-
Tshilolo, L.1
Aissi, L.M.2
Lukusa, D.3
Kinsiama, C.4
Wembonyama, S.5
Gulbis, B.6
Vertongen, F.7
-
17
-
-
84888028647
-
A prospective newborn screening and treatment program for sickle cell anemia in Luanda, Angola
-
McGann PT, Ferris MG, Ramamurthy U, Santos B, de Oliveira V, Bernardino L, Ware RE. A prospective newborn screening and treatment program for sickle cell anemia in Luanda, Angola. Am J Hematol 2013; 88:984-989.
-
(2013)
Am J Hematol
, vol.88
, pp. 984-989
-
-
McGann, P.T.1
Ferris, M.G.2
Ramamurthy, U.3
Santos, B.4
de Oliveira, V.5
Bernardino, L.6
Ware, R.E.7
-
18
-
-
84919344025
-
Sickle cell disease: A neglected chronic disease of increasing global importance
-
Chakravorty S, Williams TN. Sickle cell disease: A neglected chronic disease of increasing global importance. Arch Dis Child 2015; 100:48-53.
-
(2015)
Arch Dis Child
, vol.100
, pp. 48-53
-
-
Chakravorty, S.1
Williams, T.N.2
-
19
-
-
79955011693
-
Hydroxyurea for sickle cell anemia: What have we learned and what questions still remain?
-
McGann PT, Ware RE. Hydroxyurea for sickle cell anemia: What have we learned and what questions still remain? Curr Opin Hematol 2011; 18:158-165.
-
(2011)
Curr Opin Hematol
, vol.18
, pp. 158-165
-
-
McGann, P.T.1
Ware, R.E.2
-
20
-
-
80855133522
-
Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia
-
Ware RE, Despotovic JM, Mortier NA, Flanagan JM, He J, Smelzer MP, Kimble AC, Aygun B, Wu S, Howard T, Sparreboom A. Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia. Blood 2011; 118:4885-4991.
-
(2011)
Blood
, vol.118
, pp. 4885-4991
-
-
Ware, R.E.1
Despotovic, J.M.2
Mortier, N.A.3
Flanagan, J.M.4
He, J.5
Smelzer, M.P.6
Kimble, A.C.7
Aygun, B.8
Wu, S.9
Howard, T.10
Sparreboom, A.11
-
21
-
-
1542376824
-
Chemical and functional analysis of hydroxyurea oral solutions
-
Heeney MH, Whorton MR, Howard TA, Johnson CA, Ware RE. Chemical and functional analysis of hydroxyurea oral solutions. J Pediatr Hematol Oncol 2004; 26:179-184.
-
(2004)
J Pediatr Hematol Oncol
, vol.26
, pp. 179-184
-
-
Heeney, M.H.1
Whorton, M.R.2
Howard, T.A.3
Johnson, C.A.4
Ware, R.E.5
-
22
-
-
77955905049
-
How I use hydroxyurea to treat young patients with sickle cell anemia
-
Ware RE. How I use hydroxyurea to treat young patients with sickle cell anemia. Blood 2010; 115:5300-5311.
-
(2010)
Blood
, vol.115
, pp. 5300-5311
-
-
Ware, R.E.1
-
23
-
-
13044277572
-
Safety of hydroxyurea in children with sickle cell anemia: Results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group
-
Kinney TR, Helms RW, O'Branski EE, Ohene-Frempong K, Wang W, Daeschner C, Vichinsky E, Redding-Lallinger R, Gee B, Platt OS, Ware RE. Safety of hydroxyurea in children with sickle cell anemia: Results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group. Blood 1999; 94:1550-1554.
-
(1999)
Blood
, vol.94
, pp. 1550-1554
-
-
Kinney, T.R.1
Helms, R.W.2
O'Branski, E.E.3
Ohene-Frempong, K.4
Wang, W.5
Daeschner, C.6
Vichinsky, E.7
Redding-Lallinger, R.8
Gee, B.9
Platt, O.S.10
Ware, R.E.11
-
24
-
-
1542373662
-
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease
-
Zimmerman SA, Schultz WH, Davis JS, Pickens CV, Mortier NA, Howard TA, Ware RE. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood 2004; 103:2039-2045.
-
(2004)
Blood
, vol.103
, pp. 2039-2045
-
-
Zimmerman, S.A.1
Schultz, W.H.2
Davis, J.S.3
Pickens, C.V.4
Mortier, N.A.5
Howard, T.A.6
Ware, R.E.7
-
25
-
-
79955909191
-
Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG)
-
Wang WC, Ware RE, Miller ST, Iyer RV, Casella JF, Minniti CP, Rana S, Thornburg CD, Rogers ZR, Kalpatthi RV, Barredo JC, Brown RC, Sarnaik SA, Howard TH, Wynn LW, Kutlar A, Armstrong FD, Files BA, Goldsmith JC, Waclawiw MA, Huang X, Thompson BW. Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG). Lancet 2011; 377:1663-1672.
-
(2011)
Lancet
, vol.377
, pp. 1663-1672
-
-
Wang, W.C.1
Ware, R.E.2
Miller, S.T.3
Iyer, R.V.4
Casella, J.F.5
Minniti, C.P.6
Rana, S.7
Thornburg, C.D.8
Rogers, Z.R.9
Kalpatthi, R.V.10
Barredo, J.C.11
Brown, R.C.12
Sarnaik, S.A.13
Howard, T.H.14
Wynn, L.W.15
Kutlar, A.16
Armstrong, F.D.17
Files, B.A.18
Goldsmith, J.C.19
Waclawiw, M.A.20
Huang, X.21
Thompson, B.W.22
more..
-
26
-
-
0035666461
-
A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia
-
Wang WC, Wynn LW, Rogers ZR, Scott JP, Lane PA, Ware RE. A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia. J Pediatr 2001; 139:790-796.
-
(2001)
J Pediatr
, vol.139
, pp. 790-796
-
-
Wang, W.C.1
Wynn, L.W.2
Rogers, Z.R.3
Scott, J.P.4
Lane, P.A.5
Ware, R.E.6
-
27
-
-
0029025475
-
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
-
Charache S, Terrin ML, Moore RD, Dover GJ, Barton FB, Eckert SV, McMahon RP, Bonds DR. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med 1995; 332:1317-1322.
-
(1995)
N Engl J Med
, vol.332
, pp. 1317-1322
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
Dover, G.J.4
Barton, F.B.5
Eckert, S.V.6
McMahon, R.P.7
Bonds, D.R.8
-
28
-
-
77953057530
-
The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up
-
Steinberg MH, McCarthy WF, Castro, Ballas SK, Armstrong FD, Smith W, Ataga K, Swerdlow P, Kutlar A, DeCastro L, Waclawiw MA. The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up. Am J Hematol 2010; 85:403-408.
-
(2010)
Am J Hematol
, vol.85
, pp. 403-408
-
-
Steinberg, M.H.1
McCarthy, W.F.2
Castro, B.S.K.3
Armstrong, F.D.4
Smith, W.5
Ataga, K.6
Swerdlow, P.7
Kutlar, A.8
DeCastro, L.9
Waclawiw, M.A.10
-
29
-
-
77950622293
-
The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle-cell syndromes: Results of a 17-year, single center trial (LaSHS)
-
Voskaridou E, Christoulas D, Bilalis A, Plata E, Varvagiannis K, Stamatopoulos G, Sinopoulou K, Balassopoulou A, Loukopoulos D, Terpos E. The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle-cell syndromes: Results of a 17-year, single center trial (LaSHS). Blood 2010; 115:2354-2363.
-
(2010)
Blood
, vol.115
, pp. 2354-2363
-
-
Voskaridou, E.1
Christoulas, D.2
Bilalis, A.3
Plata, E.4
Varvagiannis, K.5
Stamatopoulos, G.6
Sinopoulou, K.7
Balassopoulou, A.8
Loukopoulos, D.9
Terpos, E.10
-
30
-
-
84878516824
-
The effect of hydroxycarbamide therapy on survival of children with sickle cell disease
-
Lobo CL, Pinto JF, Nascimento EM, Moura PG, Cardoso GP, Hankins JS. The effect of hydroxycarbamide therapy on survival of children with sickle cell disease. Br J Haematol 2013; 16:852-860.
-
(2013)
Br J Haematol
, vol.16
, pp. 852-860
-
-
Lobo, C.L.1
Pinto, J.F.2
Nascimento, E.M.3
Moura, P.G.4
Cardoso, G.P.5
Hankins, J.S.6
-
31
-
-
84907016412
-
Management of sickle cell disease: Summary of the 2014 evidence-based report by expert panel members
-
Yawn BP, Buchanan GR, Afenyi-Annan AN. Management of sickle cell disease: Summary of the 2014 evidence-based report by expert panel members. JAMA 2014; 312:1033-1048.
-
(2014)
JAMA
, vol.312
, pp. 1033-1048
-
-
Yawn, B.P.1
Buchanan, G.R.2
Afenyi-Annan, A.N.3
-
32
-
-
84925232855
-
Hydroxyurea for sickle-cell anaemia in Africa; mind the gap
-
Obaro SK. Hydroxyurea for sickle-cell anaemia in Africa; mind the gap. Lancet Global Health 2015; 3:e124-e125.
-
(2015)
Lancet Global Health
, vol.3
, pp. e124-e125
-
-
Obaro, S.K.1
-
33
-
-
81355153332
-
Concerted global effort to combat sickle cell disease: The first global congress on sickle cell disease in Accra, Ghana
-
Odame I. Concerted global effort to combat sickle cell disease: The first global congress on sickle cell disease in Accra, Ghana. J Prev Med 2011; 41:S417-S421.
-
(2011)
J Prev Med
, vol.41
, pp. S417-S421
-
-
Odame, I.1
-
34
-
-
79959326866
-
Sickle cell disease and morbidity: A tale with two tails
-
Williams TN, Obaro SK. Sickle cell disease and morbidity: A tale with two tails. Trends Parasitol 2011; 27:315-320.
-
(2011)
Trends Parasitol
, vol.27
, pp. 315-320
-
-
Williams, T.N.1
Obaro, S.K.2
-
35
-
-
84983162564
-
-
4th List. April, Geneva, Switzerland.
-
WHO Model List of Essential Medicines for Children, 4th List. April 2013, Geneva, Switzerland. http://www.who.int/medicines/publications/essentialmedicines/4th_EMLc_FINAL_web_8Jul13.pdf.
-
(2013)
-
-
-
36
-
-
84857862627
-
Impact of single centre status on estimates of intervention effects in trials with continuous outcomes: Meta-epidemiological study
-
Bafeta A, Dechartres A, Trinquart L, Yavchitz A, Boutron I, Ravaud P. Impact of single centre status on estimates of intervention effects in trials with continuous outcomes: Meta-epidemiological study. BMJ 2012; 344:e813.
-
(2012)
BMJ
, vol.344
, pp. e813
-
-
Bafeta, A.1
Dechartres, A.2
Trinquart, L.3
Yavchitz, A.4
Boutron, I.5
Ravaud, P.6
-
37
-
-
75749149540
-
An observational study of children with sickle cell disease in Kilifi, Kenya
-
Sadarangani M, Makani J, Komba AN, Alala-Agbo T, Newton CR, Marsh K, Williams TN. An observational study of children with sickle cell disease in Kilifi, Kenya. Br J Haematol 2009; 146:675-682.
-
(2009)
Br J Haematol
, vol.146
, pp. 675-682
-
-
Sadarangani, M.1
Makani, J.2
Komba, A.N.3
Alala-Agbo, T.4
Newton, C.R.5
Marsh, K.6
Williams, T.N.7
-
38
-
-
0024536437
-
Optimal Two-Stage Designs for Phase II Clinical Trials
-
Simon R. Optimal Two-Stage Designs for Phase II Clinical Trials. Control Clin Trials 1989; 10:1-10.
-
(1989)
Control Clin Trials
, vol.10
, pp. 1-10
-
-
Simon, R.1
-
39
-
-
49349115364
-
Predictive validity of a medication adherence measure for hypertension control
-
Morisky DE, Ang A, Krousel-Wood M, Ward H. Predictive validity of a medication adherence measure for hypertension control. J Clin Hypertens 2008; 10:348-354.
-
(2008)
J Clin Hypertens
, vol.10
, pp. 348-354
-
-
Morisky, D.E.1
Ang, A.2
Krousel-Wood, M.3
Ward, H.4
-
40
-
-
76749158307
-
Adherence to hydroxyurea therapy in children with sickle cell anemia
-
Thornburg CD, Calatroni A, Telen M, Kemper AR. Adherence to hydroxyurea therapy in children with sickle cell anemia. J Pediatr 2010; 156:415-419.
-
(2010)
J Pediatr
, vol.156
, pp. 415-419
-
-
Thornburg, C.D.1
Calatroni, A.2
Telen, M.3
Kemper, A.R.4
-
41
-
-
84983105587
-
-
Geneva, Switzerland
-
WHO 2012 Verbal Autopsy Instrument. World Health Organization 2012; Geneva, Switzerland. http://www.who.int/healthinfo/statistics/WHO_VA_2012_RC1_Instrument.pdf.
-
(2012)
-
-
-
42
-
-
84876062205
-
Routine paediatric sickle cell disease (SCD) outpatient care in a rural Kenyan hospital: Utilization and costs
-
Amendah DD, Mukamah G, Komba, Ndila C, Williams TN. Routine paediatric sickle cell disease (SCD) outpatient care in a rural Kenyan hospital: Utilization and costs. PLoS One 2013; 8:e61130.
-
(2013)
PLoS One
, vol.8
, pp. e61130
-
-
Amendah, D.D.1
Mukamah, G.2
Komba, N.C.3
Williams, T.N.4
|