-
1
-
-
0004252197
-
-
2nd edn. Oxford: Oxford University Press
-
Serjeant GR. Sickle Cell Disease, 2nd edn. Oxford: Oxford University Press, 1992.
-
(1992)
Sickle Cell Disease
-
-
Serjeant, G.R.1
-
2
-
-
0023908305
-
Nutritional support in sickle cell anaemia: Theoretical considerations
-
Enwonwu CO. Nutritional support in sickle cell anaemia: Theoretical considerations. J Natl Med Assoc 1988; 80:139-44.
-
(1988)
J Natl Med Assoc
, vol.80
, pp. 139-144
-
-
Enwonwu, C.O.1
-
3
-
-
0024450615
-
Delayed growth and sexual maturation in sickle cell disease
-
Wethers DL. Delayed growth and sexual maturation in sickle cell disease. Ann N Y Acad Sci 1989; 565:137-42.
-
(1989)
Ann N Y Acad Sci
, vol.565
, pp. 137-142
-
-
Wethers, D.L.1
-
4
-
-
0028186616
-
Transport proteins and acute phase reactant proteins in children with sickle cell anaemia
-
Warrier RP, Kuvibidila S, Gordon L, Humbert J. Transport proteins and acute phase reactant proteins in children with sickle cell anaemia. J Natl Med Assoc 1994; 86:33-9.
-
(1994)
J Natl Med Assoc
, vol.86
, pp. 33-39
-
-
Warrier, R.P.1
Kuvibidila, S.2
Gordon, L.3
Humbert, J.4
-
5
-
-
0028359724
-
Prevalence of impaired growth in children with homozygous sickle cell anaemia
-
Henderson RA, Saavedra JM, Dover GJ. Prevalence of impaired growth in children with homozygous sickle cell anaemia. Am J Med Sci 1994; 307:405-7.
-
(1994)
Am J Med Sci
, vol.307
, pp. 405-407
-
-
Henderson, R.A.1
Saavedra, J.M.2
Dover, G.J.3
-
7
-
-
0027273412
-
The clinical features of sickle cell disease
-
Serjeant GR. The clinical features of sickle cell disease. Baillières Clin Haematol 1993; 6:93-115.
-
(1993)
Baillières Clin Haematol
, vol.6
, pp. 93-115
-
-
Serjeant, G.R.1
-
8
-
-
6544262377
-
Studies in sickle-cell anaemia. VIII. Further observations on the clinical manifestations of sickle-cell anaemia in children
-
Scott RB, Ferguson AD, Jenkins ME, Clark HM. Studies in sickle-cell anaemia. VIII. Further observations on the clinical manifestations of sickle-cell anaemia in children. Am J Dis Child 1955; 90:682-91.
-
(1955)
Am J Dis Child
, vol.90
, pp. 682-691
-
-
Scott, R.B.1
Ferguson, A.D.2
Jenkins, M.E.3
Clark, H.M.4
-
9
-
-
0034146477
-
Impact of acute illness on nutritional status of infants and young children with sickle cell disease
-
Malinauskas BM, Gropper SS, Kawchak DA, Zemel BS, Ohene-Frempong K, Stallings VA. Impact of acute illness on nutritional status of infants and young children with sickle cell disease. J Am Diet Assoc 2000; 100:330-4.
-
(2000)
J Am Diet Assoc
, vol.100
, pp. 330-334
-
-
Malinauskas, B.M.1
Gropper, S.S.2
Kawchak, D.A.3
Zemel, B.S.4
Ohene-Frempong, K.5
Stallings, V.A.6
-
10
-
-
0035025047
-
Energy expenditure and intake in children with sickle cell disease during acute illness
-
Fung EB, Malinauskas BM, Kawchak DA, et al. Energy expenditure and intake in children with sickle cell disease during acute illness. Clin Nutr 2001; 20:131-8.
-
(2001)
Clin Nutr
, vol.20
, pp. 131-138
-
-
Fung, E.B.1
Malinauskas, B.M.2
Kawchak, D.A.3
-
11
-
-
0017648608
-
Heights and weights of Jamaican children with homozygous sickle cell disease
-
Lowry MF, Desai P, Ashcroft MT, Serjeant BF, Serjeant GR. Heights and weights of Jamaican children with homozygous sickle cell disease. Hum Biol 1977; 49:429-36.
-
(1977)
Hum Biol
, vol.49
, pp. 429-436
-
-
Lowry, M.F.1
Desai, P.2
Ashcroft, M.T.3
Serjeant, B.F.4
Serjeant, G.R.5
-
12
-
-
0029682285
-
Factors affecting prepubertal growth in homozygous sickle cell disease
-
Singhal A, Morris J, Thomas P, Dover G, Higgs D, Serjeant G. Factors affecting prepubertal growth in homozygous sickle cell disease. Arch Dis Child 1996; 74:502-6.
-
(1996)
Arch Dis Child
, vol.74
, pp. 502-506
-
-
Singhal, A.1
Morris, J.2
Thomas, P.3
Dover, G.4
Higgs, D.5
Serjeant, G.6
-
13
-
-
0027483349
-
Is there an acute-phase response in steady-state sickle cell disease?
-
Singhal A, Doherty JF, Raynes JG, et al. Is there an acute-phase response in steady-state sickle cell disease? Lancet 1993; 341:651-3.
-
(1993)
Lancet
, vol.341
, pp. 651-653
-
-
Singhal, A.1
Doherty, J.F.2
Raynes, J.G.3
-
14
-
-
19944367893
-
Proinflammatory cytokines and the hypermetabolism of children with sickle cell disease
-
Hibbert JM, Hsu LL, Bhathena SJ, et al. Proinflammatory cytokines and the hypermetabolism of children with sickle cell disease. Exp Biol Med (Maywood) 2005; 230:68-74.
-
(2005)
Exp Biol Med (Maywood)
, vol.230
, pp. 68-74
-
-
Hibbert, J.M.1
Hsu, L.L.2
Bhathena, S.J.3
-
15
-
-
0021833886
-
Growth retardation in sickle-cell disease treated by nutritional support
-
Heyman MB, Vichinsky E, Katz R, et al. Growth retardation in sickle-cell disease treated by nutritional support. Lancet 1985; 1:903-6.
-
(1985)
Lancet
, vol.1
, pp. 903-906
-
-
Heyman, M.B.1
Vichinsky, E.2
Katz, R.3
-
16
-
-
23944439931
-
Effect of long-term transfusion on growth in children with sickle cell anaemia: Results of the STOP trial
-
Wang WC, Morales KH, Scher CD, et al. Effect of long-term transfusion on growth in children with sickle cell anaemia: Results of the STOP trial. J Pediatr 2005; 147:244-7.
-
(2005)
J Pediatr
, vol.147
, pp. 244-247
-
-
Wang, W.C.1
Morales, K.H.2
Scher, C.D.3
-
17
-
-
0026031741
-
The effect of splenectomy on whole body protein turnover in homozygous sickle cell disease
-
Badaloo A, Emond A, Venugopal S, Serjeant G, Jackson AA. The effect of splenectomy on whole body protein turnover in homozygous sickle cell disease. Acta Paediatr Scand 1991; 80:103-5.
-
(1991)
Acta Paediatr Scand
, vol.80
, pp. 103-105
-
-
Badaloo, A.1
Emond, A.2
Venugopal, S.3
Serjeant, G.4
Jackson, A.A.5
-
18
-
-
0028906205
-
Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease
-
Singhal A, Thomas P, Kearney T, Venugopal S, Serjeant G. Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease. Arch Dis Child 1995; 72:227-9.
-
(1995)
Arch Dis Child
, vol.72
, pp. 227-229
-
-
Singhal, A.1
Thomas, P.2
Kearney, T.3
Venugopal, S.4
Serjeant, G.5
-
19
-
-
0035693851
-
Effect of hydroxyurea therapy on resting energy expenditure in children with sickle cell disease
-
Fung EB, Barden EM, Kawchak DA, Zemel BS, Ohene-Frempong K, Stallings VA. Effect of hydroxyurea therapy on resting energy expenditure in children with sickle cell disease. J Pediatr Hematol Oncol 2001; 23:604-8.
-
(2001)
J Pediatr Hematol Oncol
, vol.23
, pp. 604-608
-
-
Fung, E.B.1
Barden, E.M.2
Kawchak, D.A.3
Zemel, B.S.4
Ohene-Frempong, K.5
Stallings, V.A.6
-
20
-
-
27144448031
-
Long-term hydroxyurea therapy for infants with sickle cell anaemia: The HUSOFT extension study
-
Hankins JS, Ware RE, Rogers ZR, et al. Long-term hydroxyurea therapy for infants with sickle cell anaemia: The HUSOFT extension study. Blood 2005; 106:2269-75.
-
(2005)
Blood
, vol.106
, pp. 2269-2275
-
-
Hankins, J.S.1
Ware, R.E.2
Rogers, Z.R.3
-
21
-
-
0006175742
-
Habitus of patients with active sickle cell anaemia of long duration
-
Winsor T, Burch G. Habitus of patients with active sickle cell anaemia of long duration. Arch Intern Med 1945; 76:47-53.
-
(1945)
Arch Intern Med
, vol.76
, pp. 47-53
-
-
Winsor, T.1
Burch, G.2
-
22
-
-
0000802587
-
Growth status of children with sickle-cell anaemia
-
Whitten CF. Growth status of children with sickle-cell anaemia. Am J Dis Child 1961; 102:355-64.
-
(1961)
Am J Dis Child
, vol.102
, pp. 355-364
-
-
Whitten, C.F.1
-
23
-
-
0000223113
-
-
Jimenez CT, Scott RB, Henry LW, Sampson CC, Ferguson AD. Studies in sickle cell anaemia. XXVI. The effects of homozygous sickle cell disease on the onset of menarche, pregnancy, fertility, pubescent changes, and body growth in Negro subjects. Am J Dis Child 1966; 111:497-504.
-
Jimenez CT, Scott RB, Henry LW, Sampson CC, Ferguson AD. Studies in sickle cell anaemia. XXVI. The effects of homozygous sickle cell disease on the onset of menarche, pregnancy, fertility, pubescent changes, and body growth in Negro subjects. Am J Dis Child 1966; 111:497-504.
-
-
-
-
24
-
-
0017091813
-
Growth patterns of children with sickle-cell disease
-
McCormack MK, Dicker L, Katz SH, et al. Growth patterns of children with sickle-cell disease. Hum Biol 1976; 48:429-37.
-
(1976)
Hum Biol
, vol.48
, pp. 429-437
-
-
McCormack, M.K.1
Dicker, L.2
Katz, S.H.3
-
25
-
-
0342388222
-
Studies in sickle cell anaemia. Xxii. Clinical manifestations of sickle cell anaemia during the first two years of life
-
Booker CR, Scott RB, Ferguson AD. Studies in sickle cell anaemia. Xxii. Clinical manifestations of sickle cell anaemia during the first two years of life. Clin Pediatr (Phila) 1964; 3:111-15.
-
(1964)
Clin Pediatr (Phila)
, vol.3
, pp. 111-115
-
-
Booker, C.R.1
Scott, R.B.2
Ferguson, A.D.3
-
28
-
-
0021250668
-
Influence of sickle hemoglobinopathies on growth and development
-
Platt OS, Rosenstock W, Espeland MA. Influence of sickle hemoglobinopathies on growth and development. N Engl J Med 1984; 311:7-12.
-
(1984)
N Engl J Med
, vol.311
, pp. 7-12
-
-
Platt, O.S.1
Rosenstock, W.2
Espeland, M.A.3
-
29
-
-
0021248167
-
Growth patterns by age and sex in children with sickle cell disease
-
Phebus CK, Gloninger MF, Maciak BJ. Growth patterns by age and sex in children with sickle cell disease. J Pediatr 1984; 105:28-33.
-
(1984)
J Pediatr
, vol.105
, pp. 28-33
-
-
Phebus, C.K.1
Gloninger, M.F.2
Maciak, B.J.3
-
30
-
-
0033643542
-
Physical growth, sexual maturation, body image and sickle cell disease
-
Cepeda ML, Allen FH, Cepeda NJ, Yang YM. Physical growth, sexual maturation, body image and sickle cell disease. J Natl Med Assoc 2000; 92:10-14.
-
(2000)
J Natl Med Assoc
, vol.92
, pp. 10-14
-
-
Cepeda, M.L.1
Allen, F.H.2
Cepeda, N.J.3
Yang, Y.M.4
-
31
-
-
34247476032
-
Effects of delayed pubertal development, nutritional status, and disease severity on longitudinal patterns of growth failure in children with sickle cell disease
-
Zemel BS, Kawchak DA, Ohene-Frempong K, Schall JI, Stallings VA. Effects of delayed pubertal development, nutritional status, and disease severity on longitudinal patterns of growth failure in children with sickle cell disease. Pediatr Res 2007; 61:607-13.
-
(2007)
Pediatr Res
, vol.61
, pp. 607-613
-
-
Zemel, B.S.1
Kawchak, D.A.2
Ohene-Frempong, K.3
Schall, J.I.4
Stallings, V.A.5
-
32
-
-
0022454760
-
Prepubertal growth and skeletal maturation in children with sickle cell disease
-
Stevens MC, Maude GH, Cupidore L, Jackson H, Hayes RJ, Serjeant GR. Prepubertal growth and skeletal maturation in children with sickle cell disease. Pediatrics 1986; 78:124-32.
-
(1986)
Pediatrics
, vol.78
, pp. 124-132
-
-
Stevens, M.C.1
Maude, G.H.2
Cupidore, L.3
Jackson, H.4
Hayes, R.J.5
Serjeant, G.R.6
-
33
-
-
0036108631
-
Growth deficits in children with sickle cell disease
-
Silva CM, Viana MB. Growth deficits in children with sickle cell disease. Arch Med Res 2002; 33:308-12.
-
(2002)
Arch Med Res
, vol.33
, pp. 308-312
-
-
Silva, C.M.1
Viana, M.B.2
-
34
-
-
0027525007
-
Growth retardation in homozygous sickle cell disease: Role of calorie intake and possible gender-related differences
-
Modebe O, Ifenu SA. Growth retardation in homozygous sickle cell disease: Role of calorie intake and possible gender-related differences. Am J Hematol 1993; 44:149-54.
-
(1993)
Am J Hematol
, vol.44
, pp. 149-154
-
-
Modebe, O.1
Ifenu, S.A.2
-
35
-
-
0015382022
-
Heights, weights, and skeletal age of Jamaican adolescents with sickle cell anaemia
-
Ashcroft MT, Serjeant GR, Desai P. Heights, weights, and skeletal age of Jamaican adolescents with sickle cell anaemia. Arch Dis Child 1972; 47:519-24.
-
(1972)
Arch Dis Child
, vol.47
, pp. 519-524
-
-
Ashcroft, M.T.1
Serjeant, G.R.2
Desai, P.3
-
36
-
-
0019800414
-
Growth, morbidity, and mortality in a cohort of Jamaican adolescents with homozygous sickle cell disease
-
Ashcroft MT, Serjeant GR. Growth, morbidity, and mortality in a cohort of Jamaican adolescents with homozygous sickle cell disease. West Indian Med J 1981; 30:197-201.
-
(1981)
West Indian Med J
, vol.30
, pp. 197-201
-
-
Ashcroft, M.T.1
Serjeant, G.R.2
-
37
-
-
0020632345
-
Body shape in young children with homozygous sickle cell disease
-
Stevens MC, Hayes RJ, Serjeant GR. Body shape in young children with homozygous sickle cell disease. Pediatrics 1983; 71:610-14.
-
(1983)
Pediatrics
, vol.71
, pp. 610-614
-
-
Stevens, M.C.1
Hayes, R.J.2
Serjeant, G.R.3
-
38
-
-
0027973832
-
Delayed adolescent growth in homozygous sickle cell disease
-
Singhal A, Thomas P, Cook R, Wierenga K, Serjeant G. Delayed adolescent growth in homozygous sickle cell disease. Arch Dis Child 1994; 71:404-8.
-
(1994)
Arch Dis Child
, vol.71
, pp. 404-408
-
-
Singhal, A.1
Thomas, P.2
Cook, R.3
Wierenga, K.4
Serjeant, G.5
-
40
-
-
54349127564
-
Valores séricos de zinco em crianças com hemoglobinopatia (anaemia falciforme, beta talassemia e S-talassemia/serum zinc levels in children with homoglobinopathy (sickle cell anaemia, beta-talassemia and S-talassemia)
-
Souza NM, Tone LG, Collares EF, Souza IM. Valores séricos de zinco em crianças com hemoglobinopatia (anaemia falciforme, beta talassemia e S-talassemia/serum zinc levels in children with homoglobinopathy (sickle cell anaemia, beta-talassemia and S-talassemia). J Pediatr (Rio J) 1983; 55:385-8.
-
(1983)
J Pediatr (Rio J)
, vol.55
, pp. 385-388
-
-
Souza, N.M.1
Tone, L.G.2
Collares, E.F.3
Souza, I.M.4
-
41
-
-
54349104428
-
Anaemia drepanocítica y niveles sericos de zinc/Drepanocitic anaemia and zinc seric tenels
-
Figuera L, Carneiro L, Villarroel J. Anaemia drepanocítica y niveles sericos de zinc/Drepanocitic anaemia and zinc seric tenels. Arch Venez Pueric Pediatr 1994; 57:182-5.
-
(1994)
Arch Venez Pueric Pediatr
, vol.57
, pp. 182-185
-
-
Figuera, L.1
Carneiro, L.2
Villarroel, J.3
-
42
-
-
52549114697
-
Alterações no desenvolvimento somático e sexual na anaemia falciforme (SS) e traço falcêmico (AS) [Changes of the somatic and sexual development in sickle cell anaemia (SS) and sickling trace (AS)]
-
Britto MMS, Alves AFP, Rabelo MM. Alterações no desenvolvimento somático e sexual na anaemia falciforme (SS) e traço falcêmico (AS) [Changes of the somatic and sexual development in sickle cell anaemia (SS) and sickling trace (AS)]. Arq Bras Endocrinol Metab 1985; 29:111-14.
-
(1985)
Arq Bras Endocrinol Metab
, vol.29
, pp. 111-114
-
-
Britto, M.M.S.1
Alves, A.F.P.2
Rabelo, M.M.3
-
43
-
-
0027054133
-
Growth and sexual maturation of Brazilian patients with sickle cell diseases
-
Zago MA, Kerbauy J, Souza HM, et al. Growth and sexual maturation of Brazilian patients with sickle cell diseases. Trop Geogr Med 1992; 44:317-21.
-
(1992)
Trop Geogr Med
, vol.44
, pp. 317-321
-
-
Zago, M.A.1
Kerbauy, J.2
Souza, H.M.3
-
44
-
-
0029361853
-
Zinc, copper and iron and their interrelations in the growth of sickle cell patients (Zinc, cobre, hierro y su interrelación con el crescimiento de niños con anaemia falciforme)
-
Pellegrini-Braga J, Kerbauy J, Fisberg M. Zinc, copper and iron and their interrelations in the growth of sickle cell patients (Zinc, cobre, hierro y su interrelación con el crescimiento de niños con anaemia falciforme). Arch Latinoam Nutr 1995; 45:198-203.
-
(1995)
Arch Latinoam Nutr
, vol.45
, pp. 198-203
-
-
Pellegrini-Braga, J.1
Kerbauy, J.2
Fisberg, M.3
-
45
-
-
0033939795
-
Childhood and adolescent growth of patients with sickle cell disease in Aracaju, Sergipe, north-east Brazil
-
Cipolotti R, Caskey MF, Franco RP, et al. Childhood and adolescent growth of patients with sickle cell disease in Aracaju, Sergipe, north-east Brazil. Ann Trop Paediatr 2000; 20:109-13.
-
(2000)
Ann Trop Paediatr
, vol.20
, pp. 109-113
-
-
Cipolotti, R.1
Caskey, M.F.2
Franco, R.P.3
-
46
-
-
54349084503
-
Crecimiento y desarrollo en las hemoglobinopatias S (Growth and development in hemoglobinopathy-S)
-
Gonzáles-Fernándes P, Svarch E, Garriga E. Crecimiento y desarrollo en las hemoglobinopatias S (Growth and development in hemoglobinopathy-S). Rev Cuba Hematol Inmunol Hemoter 1992; 8:12-22.
-
(1992)
Rev Cuba Hematol Inmunol Hemoter
, vol.8
, pp. 12-22
-
-
Gonzáles-Fernándes, P.1
Svarch, E.2
Garriga, E.3
-
47
-
-
0024524485
-
A comparative study of the growth status of children with and without SS disease at Ilorin, Kwara State, Nigeria
-
Ebomoyi E, Adedoyin MA, Ogunlesi FO. A comparative study of the growth status of children with and without SS disease at Ilorin, Kwara State, Nigeria. Afr J Med Med Sci 1989; 18:69-74.
-
(1989)
Afr J Med Med Sci
, vol.18
, pp. 69-74
-
-
Ebomoyi, E.1
Adedoyin, M.A.2
Ogunlesi, F.O.3
-
48
-
-
0026132849
-
The health, growth and educational performance of sickle cell disease children
-
Oyedeji GA. The health, growth and educational performance of sickle cell disease children. East Afr Med J 1991; 68:181-9.
-
(1991)
East Afr Med J
, vol.68
, pp. 181-189
-
-
Oyedeji, G.A.1
-
49
-
-
0036651406
-
Anthropometric finding in Nigerian children with sickle cell disease
-
Oredugba FA, Savage KO. Anthropometric finding in Nigerian children with sickle cell disease. Pediatr Dent 2002; 24:321-5.
-
(2002)
Pediatr Dent
, vol.24
, pp. 321-325
-
-
Oredugba, F.A.1
Savage, K.O.2
-
50
-
-
29944438056
-
Body composition in Negro African children suffering from sickle cell disease. A mixed cross-sectional longitudinal study in Brazzaville, Congo
-
Mabiala-Babela JR, Massamba A, Tsiba JB, Moulongo JG, Nzingoula S, Senga P. Body composition in Negro African children suffering from sickle cell disease. A mixed cross-sectional longitudinal study in Brazzaville, Congo. Bull Soc Pathol Exot 2005; 98:394-9.
-
(2005)
Bull Soc Pathol Exot
, vol.98
, pp. 394-399
-
-
Mabiala-Babela, J.R.1
Massamba, A.2
Tsiba, J.B.3
Moulongo, J.G.4
Nzingoula, S.5
Senga, P.6
-
52
-
-
0030200789
-
Current aspects of sickle cell disease in children in Gabon
-
Thuilliez V, Ditsambou V, Mba JR, Mba Meyo S, Kitengue J. Current aspects of sickle cell disease in children in Gabon. Arch Pediatr 1996; 3:668-74.
-
(1996)
Arch Pediatr
, vol.3
, pp. 668-674
-
-
Thuilliez, V.1
Ditsambou, V.2
Mba, J.R.3
Mba Meyo, S.4
Kitengue, J.5
-
53
-
-
0027982139
-
The effect of sickle cell anaemia on adolescents and their growth and development - lessons from the sickle cell anaemia clinic
-
Athale UH, Chintu C. The effect of sickle cell anaemia on adolescents and their growth and development - lessons from the sickle cell anaemia clinic. J Trop Pediatr 1994; 40:246-52.
-
(1994)
J Trop Pediatr
, vol.40
, pp. 246-252
-
-
Athale, U.H.1
Chintu, C.2
-
54
-
-
0033046345
-
Growth and pubertal development in transfusion-dependent children and adolescents with thalassemia major and sickle cell disease: A comparative study
-
Soliman AT, el Zalabany M, Amer M, Ansari BM. Growth and pubertal development in transfusion-dependent children and adolescents with thalassemia major and sickle cell disease: A comparative study. J Trop Pediatr 1999; 45:23-30.
-
(1999)
J Trop Pediatr
, vol.45
, pp. 23-30
-
-
Soliman, A.T.1
el Zalabany, M.2
Amer, M.3
Ansari, B.M.4
-
55
-
-
0038692900
-
Influence of sickle hemoglobinopathy on growth and development of young adult males in Southern Iraq
-
Mansour AA. Influence of sickle hemoglobinopathy on growth and development of young adult males in Southern Iraq. Saudi Med J 2003; 24:544-6.
-
(2003)
Saudi Med J
, vol.24
, pp. 544-546
-
-
Mansour, A.A.1
-
56
-
-
0036130367
-
Sickle cell morbidity profile in Omani children
-
Jaiyesimi F, Pandey R, Bux D, Sreekrishna Y, Zaki F, Krishnamoorthy N. Sickle cell morbidity profile in Omani children. Ann Trop Paediatr 2002; 22:45-52.
-
(2002)
Ann Trop Paediatr
, vol.22
, pp. 45-52
-
-
Jaiyesimi, F.1
Pandey, R.2
Bux, D.3
Sreekrishna, Y.4
Zaki, F.5
Krishnamoorthy, N.6
-
58
-
-
12344338785
-
Physical growth of children with sickle cell disease
-
Mukherjee MB, Gangakhedkar RR. Physical growth of children with sickle cell disease. Indian J Hum Genet 2004; 10:70-2.
-
(2004)
Indian J Hum Genet
, vol.10
, pp. 70-72
-
-
Mukherjee, M.B.1
Gangakhedkar, R.R.2
-
59
-
-
0026644709
-
Growth and development in white patients with sickle cell diseases
-
Caruso-Nicoletti M, Mancuso M, Spadaro G, Samperi P, Consalvo C, Schiliro G. Growth and development in white patients with sickle cell diseases. Am J Pediatr Hematol Oncol 1992; 14:285-8.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 285-288
-
-
Caruso-Nicoletti, M.1
Mancuso, M.2
Spadaro, G.3
Samperi, P.4
Consalvo, C.5
Schiliro, G.6
-
60
-
-
0019452445
-
Sickle cell haemoglobinopathies in England
-
Mann JR. Sickle cell haemoglobinopathies in England. Arch Dis Child 1981; 56:676-83.
-
(1981)
Arch Dis Child
, vol.56
, pp. 676-683
-
-
Mann, J.R.1
-
61
-
-
0036789618
-
The importance of using ethnically appropriate reference ranges for growth assessment in sickle cell disease
-
Patey RA, Sylvester KP, Rafferty GF, Dick M, Greenough A. The importance of using ethnically appropriate reference ranges for growth assessment in sickle cell disease. Arch Dis Child 2002; 87:352-3.
-
(2002)
Arch Dis Child
, vol.87
, pp. 352-353
-
-
Patey, R.A.1
Sylvester, K.P.2
Rafferty, G.F.3
Dick, M.4
Greenough, A.5
-
62
-
-
0036297359
-
Body composition in children with sickle cell disease
-
Barden EM, Kawchak DA, Ohene-Frempong K, Stallings VA, Zemel BS. Body composition in children with sickle cell disease. Am J Clin Nutr 2002; 76:218-25.
-
(2002)
Am J Clin Nutr
, vol.76
, pp. 218-225
-
-
Barden, E.M.1
Kawchak, D.A.2
Ohene-Frempong, K.3
Stallings, V.A.4
Zemel, B.S.5
-
63
-
-
0024393875
-
Whole body protein turnover and resting metabolic rate in homozygous sickle cell disease
-
Badaloo A, Jackson AA, Jahoor F. Whole body protein turnover and resting metabolic rate in homozygous sickle cell disease. Clin Sci (Lond) 1989; 77:93-7.
-
(1989)
Clin Sci (Lond)
, vol.77
, pp. 93-97
-
-
Badaloo, A.1
Jackson, A.A.2
Jahoor, F.3
-
64
-
-
0027448378
-
Resting metabolic rate in homozygous sickle cell disease
-
Singhal A, Davies P, Sahota A, Thomas PW, Serjeant GR. Resting metabolic rate in homozygous sickle cell disease. Am J Clin Nutr 1993; 57:32-4.
-
(1993)
Am J Clin Nutr
, vol.57
, pp. 32-34
-
-
Singhal, A.1
Davies, P.2
Sahota, A.3
Thomas, P.W.4
Serjeant, G.R.5
-
66
-
-
0031936345
-
Alterations in basal nutrient metabolism increase resting energy expenditure in sickle cell disease
-
Borel MJ, Buchowski MS, Turner EA, Peeler BB, Goldstein RE, Flakoll PJ. Alterations in basal nutrient metabolism increase resting energy expenditure in sickle cell disease. Am J Physiol 1998; 274:e357-64.
-
(1998)
Am J Physiol
, vol.274
-
-
Borel, M.J.1
Buchowski, M.S.2
Turner, E.A.3
Peeler, B.B.4
Goldstein, R.E.5
Flakoll, P.J.6
-
67
-
-
0031690133
-
Protein turnover and energy expenditure increase during exogenous nutrient availability in sickle cell disease
-
Borel MJ, Buchowski MS, Turner EA, Goldstein RE, Flakoll PJ. Protein turnover and energy expenditure increase during exogenous nutrient availability in sickle cell disease. Am J Clin Nutr 1998; 68:607-14.
-
(1998)
Am J Clin Nutr
, vol.68
, pp. 607-614
-
-
Borel, M.J.1
Buchowski, M.S.2
Turner, E.A.3
Goldstein, R.E.4
Flakoll, P.J.5
-
68
-
-
0030840812
-
Is there an energy deficiency in homozygous sickle cell disease?
-
Singhal A, Davies P, Wierenga KJ, Thomas P, Serjeant G. Is there an energy deficiency in homozygous sickle cell disease? Am J Clin Nutr 1997; 66:386-90.
-
(1997)
Am J Clin Nutr
, vol.66
, pp. 386-390
-
-
Singhal, A.1
Davies, P.2
Wierenga, K.J.3
Thomas, P.4
Serjeant, G.5
-
69
-
-
0033911265
-
Total and resting energy expenditure in children with sickle cell disease
-
Barden EM, Zemel BS, Kawchak DA, Goran MI, Ohene-Frempong K, Stallings VA. Total and resting energy expenditure in children with sickle cell disease. J Pediatr 2000; 136:73-9.
-
(2000)
J Pediatr
, vol.136
, pp. 73-79
-
-
Barden, E.M.1
Zemel, B.S.2
Kawchak, D.A.3
Goran, M.I.4
Ohene-Frempong, K.5
Stallings, V.A.6
-
70
-
-
0025073194
-
Low plasma prealbumin and carotenoid levels in sickle cell disease patients
-
Jain SK, Ross JD, Duett J, Herbst JJ. Low plasma prealbumin and carotenoid levels in sickle cell disease patients. Am J Med Sci 1990; 299:13-15.
-
(1990)
Am J Med Sci
, vol.299
, pp. 13-15
-
-
Jain, S.K.1
Ross, J.D.2
Duett, J.3
Herbst, J.J.4
-
71
-
-
0030822169
-
Serum and urinary amino acid levels in sickle cell disease
-
Van der Jagt DJ, Kanellis GJ, Isichei C, Patuszyn A, Glew RH. Serum and urinary amino acid levels in sickle cell disease. J Trop Pediatr 1997; 43:220-5.
-
(1997)
J Trop Pediatr
, vol.43
, pp. 220-225
-
-
Van der Jagt, D.J.1
Kanellis, G.J.2
Isichei, C.3
Patuszyn, A.4
Glew, R.H.5
-
72
-
-
0031885129
-
Decreased polyunsaturated fatty acids in sickle cell anaemia
-
Enomoto TM, Isichei C, Van der Jagt DJ, Fry DE, Glew RH. Decreased polyunsaturated fatty acids in sickle cell anaemia. J Trop Pediatr 1998; 44:28-34.
-
(1998)
J Trop Pediatr
, vol.44
, pp. 28-34
-
-
Enomoto, T.M.1
Isichei, C.2
Van der Jagt, D.J.3
Fry, D.E.4
Glew, R.H.5
-
73
-
-
0029089462
-
Red cell genetic disorders and plasma lipids
-
el-Hazmi MA, Warsy AS, Al-Swailem A, Al-Swailem A, Bahakim H. Red cell genetic disorders and plasma lipids. J Trop Pediatr 1995; 41:202-5.
-
(1995)
J Trop Pediatr
, vol.41
, pp. 202-205
-
-
el-Hazmi, M.A.1
Warsy, A.S.2
Al-Swailem, A.3
Al-Swailem, A.4
Bahakim, H.5
-
74
-
-
0036017661
-
Hypocholesterolemia in Nigerian children with sickle cell disease
-
Van der Jagt DJ, Shores J, Okorodudu A, Okolo SN, Glew RH. Hypocholesterolemia in Nigerian children with sickle cell disease. J Trop Pediatr 2002; 48:156-61.
-
(2002)
J Trop Pediatr
, vol.48
, pp. 156-161
-
-
Van der Jagt, D.J.1
Shores, J.2
Okorodudu, A.3
Okolo, S.N.4
Glew, R.H.5
-
75
-
-
20144384638
-
Steady-state haemoglobin level in sickle cell anaemia increases with an increase in erythrocyte membrane n-3 fatty acids
-
Ren H, Obike I, Okpala I, Ghebremeskel K, Ugochukwu C, Crawford M. Steady-state haemoglobin level in sickle cell anaemia increases with an increase in erythrocyte membrane n-3 fatty acids. Prostaglandins Leukot Essent Fatty Acids 2005; 72:415-21.
-
(2005)
Prostaglandins Leukot Essent Fatty Acids
, vol.72
, pp. 415-421
-
-
Ren, H.1
Obike, I.2
Okpala, I.3
Ghebremeskel, K.4
Ugochukwu, C.5
Crawford, M.6
-
76
-
-
0035006311
-
Increased bone turnover is associated with protein and energy metabolism in adolescents with sickle cell anaemia
-
Buchowski MS, de la Fuente FA, Flakoll PJ, Chen KY, Turner EA. Increased bone turnover is associated with protein and energy metabolism in adolescents with sickle cell anaemia. Am J Physiol Endocrinol Metab 2001; 280:e518-27.
-
(2001)
Am J Physiol Endocrinol Metab
, vol.280
-
-
Buchowski, M.S.1
de la Fuente, F.A.2
Flakoll, P.J.3
Chen, K.Y.4
Turner, E.A.5
-
77
-
-
33750466901
-
Bone mineral density in children with sickle cell anaemia
-
Lal A, Fung EB, Pakbaz Z, Hackney-Stephens E, Vichinsky EP. Bone mineral density in children with sickle cell anaemia. Pediatr Blood Cancer 2006; 47:901-6.
-
(2006)
Pediatr Blood Cancer
, vol.47
, pp. 901-906
-
-
Lal, A.1
Fung, E.B.2
Pakbaz, Z.3
Hackney-Stephens, E.4
Vichinsky, E.P.5
-
78
-
-
0029922667
-
Protein and energy metabolism in prepubertal children with sickle cell anaemia
-
Salman EK, Haymond MW, Bayne E, et al. Protein and energy metabolism in prepubertal children with sickle cell anaemia. Pediatr Res 1996; 40:34-40.
-
(1996)
Pediatr Res
, vol.40
, pp. 34-40
-
-
Salman, E.K.1
Haymond, M.W.2
Bayne, E.3
-
79
-
-
5344259072
-
Oral glutamine supplementation decreases resting energy expenditure in children and adolescents with sickle cell anaemia
-
Williams R, Olivi S, Li CS, et al. Oral glutamine supplementation decreases resting energy expenditure in children and adolescents with sickle cell anaemia. J Pediatr Hematol Oncol 2004; 26:619-25.
-
(2004)
J Pediatr Hematol Oncol
, vol.26
, pp. 619-625
-
-
Williams, R.1
Olivi, S.2
Li, C.S.3
-
80
-
-
0016825006
-
Sexual maturation in subjects with sickle cell anaemia: Studies of serum gonadotropin concentration, height, weight, and skeletal age
-
Olambiwonnu NO, Penny R, Frasier SD. Sexual maturation in subjects with sickle cell anaemia: Studies of serum gonadotropin concentration, height, weight, and skeletal age. J Pediatr 1975; 87:459-64.
-
(1975)
J Pediatr
, vol.87
, pp. 459-464
-
-
Olambiwonnu, N.O.1
Penny, R.2
Frasier, S.D.3
-
81
-
-
0017110215
-
Gonadal function abnormalities in sickle cell anaemia. Studies in adult male patients
-
Abbasi AA, Prasad AS, Ortega J, Congco E, Oberleas D. Gonadal function abnormalities in sickle cell anaemia. Studies in adult male patients. Ann Intern Med 1976; 85:601-5.
-
(1976)
Ann Intern Med
, vol.85
, pp. 601-605
-
-
Abbasi, A.A.1
Prasad, A.S.2
Ortega, J.3
Congco, E.4
Oberleas, D.5
-
82
-
-
0028390396
-
The mechanism of low testosterone levels in homozygous sickle-cell disease
-
Parshad O, Stevens MC, Preece MA, Thomas PW, Serjeant GR. The mechanism of low testosterone levels in homozygous sickle-cell disease. West Indian Med J 1994; 43:12-14.
-
(1994)
West Indian Med J
, vol.43
, pp. 12-14
-
-
Parshad, O.1
Stevens, M.C.2
Preece, M.A.3
Thomas, P.W.4
Serjeant, G.R.5
-
83
-
-
0029264718
-
Testosterone deficiency and extreme retardation of puberty in homozygous sickle-cell disease
-
Singhal A, Gabay L, Serjeant GR. Testosterone deficiency and extreme retardation of puberty in homozygous sickle-cell disease. West Indian Med J 1995; 44:20-3.
-
(1995)
West Indian Med J
, vol.44
, pp. 20-23
-
-
Singhal, A.1
Gabay, L.2
Serjeant, G.R.3
-
85
-
-
0018909806
-
Endocrine function and haemoglobinopathies: Relation between the sickle cell gene and circulating plasma levels of testosterone, luteinising hormone (LH) and follicle stimulating hormone (FSH) in adult males
-
Dada OA, Nduka EU. Endocrine function and haemoglobinopathies: Relation between the sickle cell gene and circulating plasma levels of testosterone, luteinising hormone (LH) and follicle stimulating hormone (FSH) in adult males. Clin Chim Acta 1980; 105:269-73.
-
(1980)
Clin Chim Acta
, vol.105
, pp. 269-273
-
-
Dada, O.A.1
Nduka, E.U.2
-
86
-
-
0035515337
-
Sickle cell disease and age at menarche in Jamaican girls: Observations from a cohort study
-
Serjeant GR, Singhal A, Hambleton IR. Sickle cell disease and age at menarche in Jamaican girls: Observations from a cohort study. Arch Dis Child 2001; 85:375-8.
-
(2001)
Arch Dis Child
, vol.85
, pp. 375-378
-
-
Serjeant, G.R.1
Singhal, A.2
Hambleton, I.R.3
-
88
-
-
0022968447
-
Endocrine function and haemoglobinopathies: Biochemical assessment of thyroid function in children with sickle-cell disease
-
Lukanmbi FA, Adeyokunnu AA, Osifo BO, Bolodeoku JO, Dada OA. Endocrine function and haemoglobinopathies: Biochemical assessment of thyroid function in children with sickle-cell disease. Afr J Med Med Sci 1986; 15:25-8.
-
(1986)
Afr J Med Med Sci
, vol.15
, pp. 25-28
-
-
Lukanmbi, F.A.1
Adeyokunnu, A.A.2
Osifo, B.O.3
Bolodeoku, J.O.4
Dada, O.A.5
-
89
-
-
0029361250
-
Empty sella in short children with and without hypothalamic-pituitary abnormalities
-
Soliman AT, Darwish A, Asfour MG. Empty sella in short children with and without hypothalamic-pituitary abnormalities. Indian J Pediatr 1995; 62:597-603.
-
(1995)
Indian J Pediatr
, vol.62
, pp. 597-603
-
-
Soliman, A.T.1
Darwish, A.2
Asfour, M.G.3
-
90
-
-
0028808128
-
Circulating growth hormone (GH), insulin-like growth factor-I (IGF-I) and free thyroxine, GH response to clonidine provocation and CT scanning of the hypothalamic-pituitary area in children with sickle cell disease
-
Soliman AT, Darwish A, Mohammed SH, Bassiony MR, El-Banna N, Asfour M. Circulating growth hormone (GH), insulin-like growth factor-I (IGF-I) and free thyroxine, GH response to clonidine provocation and CT scanning of the hypothalamic-pituitary area in children with sickle cell disease. J Trop Pediatr 1995; 41:285-9.
-
(1995)
J Trop Pediatr
, vol.41
, pp. 285-289
-
-
Soliman, A.T.1
Darwish, A.2
Mohammed, S.H.3
Bassiony, M.R.4
El-Banna, N.5
Asfour, M.6
-
91
-
-
0030736415
-
Growth hormone secretion and circulating insulin-like growth factor-I (IGF-I) and IGF binding protein-3 concentrations in children with sickle cell disease
-
Soliman AT, El-Banna N, Al-Salmi I, De Silva V, Craig A, Asfour M. Growth hormone secretion and circulating insulin-like growth factor-I (IGF-I) and IGF binding protein-3 concentrations in children with sickle cell disease. Metabolism 1997; 46:1241-5.
-
(1997)
Metabolism
, vol.46
, pp. 1241-1245
-
-
Soliman, A.T.1
El-Banna, N.2
Al-Salmi, I.3
De Silva, V.4
Craig, A.5
Asfour, M.6
-
92
-
-
0031826766
-
Decreased bone mineral density in prepubertal children with sickle cell disease: Correlation with growth parameters, degree of siderosis and secretion of growth factors
-
Soliman AT, Bererhi H, Darwish A, Al-Zalabani MM, Wali Y, Ansari B. Decreased bone mineral density in prepubertal children with sickle cell disease: Correlation with growth parameters, degree of siderosis and secretion of growth factors. J Trop Pediatr 1998; 44:194-8.
-
(1998)
J Trop Pediatr
, vol.44
, pp. 194-198
-
-
Soliman, A.T.1
Bererhi, H.2
Darwish, A.3
Al-Zalabani, M.M.4
Wali, Y.5
Ansari, B.6
-
93
-
-
0034857606
-
Growth hormone and insulin-like growth factor I axis and growth of children with different sickle cell anaemia haplotypes
-
Luporini SM, Bendit I, Manhani R, Bracco OL, Manzella L, Giannella-Neto D. Growth hormone and insulin-like growth factor I axis and growth of children with different sickle cell anaemia haplotypes. J Pediatr Hematol Oncol 2001; 23:357-63.
-
(2001)
J Pediatr Hematol Oncol
, vol.23
, pp. 357-363
-
-
Luporini, S.M.1
Bendit, I.2
Manhani, R.3
Bracco, O.L.4
Manzella, L.5
Giannella-Neto, D.6
-
96
-
-
0023930499
-
Nutritional factors and growth in children with sickle cell disease
-
Finan AC, Elmer MA, Sasanow SR, McKinney S, Russell MO, Gill FM. Nutritional factors and growth in children with sickle cell disease. Am J Dis Child 1988; 142:237-40.
-
(1988)
Am J Dis Child
, vol.142
, pp. 237-240
-
-
Finan, A.C.1
Elmer, M.A.2
Sasanow, S.R.3
McKinney, S.4
Russell, M.O.5
Gill, F.M.6
-
97
-
-
0026516286
-
Nutritional status and dietary intake of children with sickle cell anaemia
-
Gray NT, Bartlett JM, Kolasa KM, Marcuard SP, Holbrook CT, Horner RD. Nutritional status and dietary intake of children with sickle cell anaemia. Am J Pediatr Hematol Oncol 1992; 14:57-61.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 57-61
-
-
Gray, N.T.1
Bartlett, J.M.2
Kolasa, K.M.3
Marcuard, S.P.4
Holbrook, C.T.5
Horner, R.D.6
-
99
-
-
34247360771
-
Adequacy of dietary intake declines with age in children with sickle cell disease
-
Kawchak DA, Schall JI, Zemel BS, Ohene-Frempong K, Stallings VA. Adequacy of dietary intake declines with age in children with sickle cell disease. J Am Diet Assoc 2007; 107:843-8.
-
(2007)
J Am Diet Assoc
, vol.107
, pp. 843-848
-
-
Kawchak, D.A.1
Schall, J.I.2
Zemel, B.S.3
Ohene-Frempong, K.4
Stallings, V.A.5
-
100
-
-
0006193762
-
Nutritional megaloblastic anaemia associated with sickle cell states
-
Jonsson U, Roath OS, Kirkpatrick CI. Nutritional megaloblastic anaemia associated with sickle cell states. Blood 1959; 14:535-47.
-
(1959)
Blood
, vol.14
, pp. 535-547
-
-
Jonsson, U.1
Roath, O.S.2
Kirkpatrick, C.I.3
-
101
-
-
0006145020
-
Sickle-cell anaemia complicated by megaloblastic anaemia of infancy
-
MacIver JE, Went LN. Sickle-cell anaemia complicated by megaloblastic anaemia of infancy. Br Med J 1960; 1:775-9.
-
(1960)
Br Med J
, vol.1
, pp. 775-779
-
-
MacIver, J.E.1
Went, L.N.2
-
102
-
-
0014123743
-
Folic acid deficiency complicating sickle cell anaemia. A study on the response to titrated doses of folic acid
-
Alperin JB. Folic acid deficiency complicating sickle cell anaemia. A study on the response to titrated doses of folic acid. Arch Intern Med 1967; 120:298-306.
-
(1967)
Arch Intern Med
, vol.120
, pp. 298-306
-
-
Alperin, J.B.1
-
103
-
-
0015605555
-
Recurrent folic acid deficiency in sickle cell disease
-
Lopez R, Shimizu N, Cooperman JM. Recurrent folic acid deficiency in sickle cell disease. Am J Dis Child 1973; 125:544-8.
-
(1973)
Am J Dis Child
, vol.125
, pp. 544-548
-
-
Lopez, R.1
Shimizu, N.2
Cooperman, J.M.3
-
104
-
-
54349107838
-
Folic acid deficiency in sickle-cell anaemia
-
Watson-Williams EJ. Folic acid deficiency in sickle-cell anaemia. East Afr Med J 1962; 39:213-21.
-
(1962)
East Afr Med J
, vol.39
, pp. 213-221
-
-
Watson-Williams, E.J.1
-
105
-
-
50549194013
-
Folic acid studies in sickle-cell anaemia
-
Pearson HA, Cobb WT. Folic acid studies in sickle-cell anaemia. J Lab Clin Med 1964; 64:913-21.
-
(1964)
J Lab Clin Med
, vol.64
, pp. 913-921
-
-
Pearson, H.A.1
Cobb, W.T.2
-
106
-
-
0016043305
-
Folate deficiency in children with sickle cell anaemia
-
Liu YK. Folate deficiency in children with sickle cell anaemia. Am J Dis Child 1974; 127:389-93.
-
(1974)
Am J Dis Child
, vol.127
, pp. 389-393
-
-
Liu, Y.K.1
-
107
-
-
0020533912
-
A trial of folate supplementation in children with homozygous sickle cell disease
-
Rabb LM, Grandison Y, Mason K, Hayes RJ, Serjeant B, Serjeant GR. A trial of folate supplementation in children with homozygous sickle cell disease. Br J Haematol 1983; 54:589-94.
-
(1983)
Br J Haematol
, vol.54
, pp. 589-594
-
-
Rabb, L.M.1
Grandison, Y.2
Mason, K.3
Hayes, R.J.4
Serjeant, B.5
Serjeant, G.R.6
-
108
-
-
0022365797
-
Treatment of sickle cell disease in early childhood in Jamaica
-
Serjeant GR. Treatment of sickle cell disease in early childhood in Jamaica. Am J Pediatr Hematol Oncol 1985; 7:235-9.
-
(1985)
Am J Pediatr Hematol Oncol
, vol.7
, pp. 235-239
-
-
Serjeant, G.R.1
-
109
-
-
0033510473
-
Role of nutritional supplement in sickle cell disease
-
Wang WC. Role of nutritional supplement in sickle cell disease. J Pediatr Hematol Oncol 1999; 21:176-8.
-
(1999)
J Pediatr Hematol Oncol
, vol.21
, pp. 176-178
-
-
Wang, W.C.1
-
112
-
-
0028991110
-
12 levels in patients with severe sickle cell disease
-
12 levels in patients with severe sickle cell disease. J Intern Med 1995; 237:551-5.
-
(1995)
J Intern Med
, vol.237
, pp. 551-555
-
-
Al-Momen, A.K.1
-
113
-
-
0027425890
-
Clinical trial of riboflavin in sickle cell disease
-
Ajayi OA, George BO, Ipadeola T. Clinical trial of riboflavin in sickle cell disease. East Afr Med J 1993; 70:418-21.
-
(1993)
East Afr Med J
, vol.70
, pp. 418-421
-
-
Ajayi, O.A.1
George, B.O.2
Ipadeola, T.3
-
114
-
-
21744448674
-
Homocysteine-lowering trials for prevention of heart disease and stroke
-
Clarke R. Homocysteine-lowering trials for prevention of heart disease and stroke. Semin Vasc Med 2005; 5:215-22.
-
(2005)
Semin Vasc Med
, vol.5
, pp. 215-222
-
-
Clarke, R.1
-
116
-
-
0036062012
-
-
Balasa VV, Kalinyak KA, Bean JA, Stroop D, Gruppo RA. Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease. J Pediatr Hematol Oncol 2002; 24:374-9.
-
Balasa VV, Kalinyak KA, Bean JA, Stroop D, Gruppo RA. Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease. J Pediatr Hematol Oncol 2002; 24:374-9.
-
-
-
-
117
-
-
54349125045
-
-
Marian TK. Folic Acid and Homocysteine Levels in Children with Sickle Cell Disease in The Gambia. Liverpool School of Tropical Medicine, UK: Master of Tropical Paediatrics thesis, 2001.
-
Marian TK. Folic Acid and Homocysteine Levels in Children with Sickle Cell Disease in The Gambia. Liverpool School of Tropical Medicine, UK: Master of Tropical Paediatrics thesis, 2001.
-
-
-
-
118
-
-
0030874635
-
Homocysteine in sickle cell disease: Relationship to stroke
-
Houston PE, Rana S, Sekhsaria S, Perlin E, Kim KS, Castro OL. Homocysteine in sickle cell disease: Relationship to stroke. Am J Med 1997; 103:192-6.
-
(1997)
Am J Med
, vol.103
, pp. 192-196
-
-
Houston, P.E.1
Rana, S.2
Sekhsaria, S.3
Perlin, E.4
Kim, K.S.5
Castro, O.L.6
-
119
-
-
0031049108
-
Thrombosis, megaloblastic anaemia, and sickle cell disease: A unified hypothesis
-
Ballas SK, Saidi P. Thrombosis, megaloblastic anaemia, and sickle cell disease: A unified hypothesis. Br J Haematol 1997; 96:879-80.
-
(1997)
Br J Haematol
, vol.96
, pp. 879-880
-
-
Ballas, S.K.1
Saidi, P.2
-
120
-
-
0036207289
-
Optimization of folic acid, vitamin B(12), and vitamin B(6) supplements in pediatric patients with sickle cell disease
-
van der Dijs FP, Fokkema MR, Dijck-Brouwer DA, et al. Optimization of folic acid, vitamin B(12), and vitamin B(6) supplements in pediatric patients with sickle cell disease. Am J Hematol 2002; 69:239-46.
-
(2002)
Am J Hematol
, vol.69
, pp. 239-246
-
-
van der Dijs, F.P.1
Fokkema, M.R.2
Dijck-Brouwer, D.A.3
-
121
-
-
54349083018
-
-
12 Supplmentation. Liverpool School of Tropical Medicine, UK: Master of Tropical Paediatrics thesis, 2002.
-
12 Supplmentation. Liverpool School of Tropical Medicine, UK: Master of Tropical Paediatrics thesis, 2002.
-
-
-
-
122
-
-
3242732330
-
Vitamin A status, hospitalizations, and other outcomes in young children with sickle cell disease
-
Schall JI, Zemel BS, Kawchak DA, Ohene-Frempong K, Stallings VA. Vitamin A status, hospitalizations, and other outcomes in young children with sickle cell disease. J Pediatr 2004; 145:99-106.
-
(2004)
J Pediatr
, vol.145
, pp. 99-106
-
-
Schall, J.I.1
Zemel, B.S.2
Kawchak, D.A.3
Ohene-Frempong, K.4
Stallings, V.A.5
-
124
-
-
0017319439
-
Trace elements in sickle cell disease
-
Prasad AS, Ortega J, Brewer GJ, Oberleas D, Schoomaker EB. Trace elements in sickle cell disease. JAMA 1976; 235:2396-8.
-
(1976)
JAMA
, vol.235
, pp. 2396-2398
-
-
Prasad, A.S.1
Ortega, J.2
Brewer, G.J.3
Oberleas, D.4
Schoomaker, E.B.5
-
125
-
-
0031917978
-
Plasma zinc status, growth, and maturation in children with sickle cell disease
-
Leonard MB, Zemel BS, Kawchak DA, Ohene-Frempong K, Stallings VA. Plasma zinc status, growth, and maturation in children with sickle cell disease. J Pediatr 1998; 132:467-71.
-
(1998)
J Pediatr
, vol.132
, pp. 467-471
-
-
Leonard, M.B.1
Zemel, B.S.2
Kawchak, D.A.3
Ohene-Frempong, K.4
Stallings, V.A.5
-
126
-
-
0036157449
-
Effect of zinc supplementation on growth and body composition in children with sickle cell disease
-
Zemel BS, Kawchak DA, Fung EB, Ohene-Frempong K, Stallings VA. Effect of zinc supplementation on growth and body composition in children with sickle cell disease. Am J Clin Nutr 2002; 75:300-7.
-
(2002)
Am J Clin Nutr
, vol.75
, pp. 300-307
-
-
Zemel, B.S.1
Kawchak, D.A.2
Fung, E.B.3
Ohene-Frempong, K.4
Stallings, V.A.5
-
127
-
-
0013392792
-
Studies on congenital hemolytic syndromes. III. Rates of destruction and production of erythrocytes in sickle cell anaemia
-
Erlandson ME, Schulman I, Smith CH. Studies on congenital hemolytic syndromes. III. Rates of destruction and production of erythrocytes in sickle cell anaemia. Pediatrics 1960; 25:629-44.
-
(1960)
Pediatrics
, vol.25
, pp. 629-644
-
-
Erlandson, M.E.1
Schulman, I.2
Smith, C.H.3
-
128
-
-
0017807133
-
Iron burden in sickle cell anaemia
-
O'Brien RT. Iron burden in sickle cell anaemia. J Pediatr 1978; 92:579-82.
-
(1978)
J Pediatr
, vol.92
, pp. 579-582
-
-
O'Brien, R.T.1
-
130
-
-
0023583227
-
An investigation into the iron status of children with sickle-cell disease in western Nigeria
-
Jeyakumar LH, Akpanyung EO, Akinyemi AA, Emerole GO. An investigation into the iron status of children with sickle-cell disease in western Nigeria. J Trop Pediatr 1987; 33:326-8.
-
(1987)
J Trop Pediatr
, vol.33
, pp. 326-328
-
-
Jeyakumar, L.H.1
Akpanyung, E.O.2
Akinyemi, A.A.3
Emerole, G.O.4
-
131
-
-
0019017254
-
Iron deficiency in sickle cell disease
-
Nagaraj Rao J, Sur AM. Iron deficiency in sickle cell disease. Acta Paediatr Scand 1980; 69:337-40.
-
(1980)
Acta Paediatr Scand
, vol.69
, pp. 337-340
-
-
Nagaraj Rao, J.1
Sur, A.M.2
-
132
-
-
0020147454
-
Iron deficiency in sickle cell anaemia in Nigerian children
-
Okeahialam TC, Obi GO. Iron deficiency in sickle cell anaemia in Nigerian children. Ann Trop Paediatr 1982; 2:89-92.
-
(1982)
Ann Trop Paediatr
, vol.2
, pp. 89-92
-
-
Okeahialam, T.C.1
Obi, G.O.2
-
134
-
-
0019805169
-
The diagnosis of iron deficiency anaemia in sickle cell disease
-
Vichinsky E, Kleman K, Embury S, Lubin B. The diagnosis of iron deficiency anaemia in sickle cell disease. Blood 1981; 58:963-8.
-
(1981)
Blood
, vol.58
, pp. 963-968
-
-
Vichinsky, E.1
Kleman, K.2
Embury, S.3
Lubin, B.4
-
135
-
-
0035181717
-
Iron status of children with sickle cell disease
-
Stettler N, Zemel BS, Kawchak DA, Ohene-Frempong K, Stallings VA. Iron status of children with sickle cell disease. J Parenter Enteral Nutr 2001; 25:36-8.
-
(2001)
J Parenter Enteral Nutr
, vol.25
, pp. 36-38
-
-
Stettler, N.1
Zemel, B.S.2
Kawchak, D.A.3
Ohene-Frempong, K.4
Stallings, V.A.5
-
136
-
-
0019194853
-
Haematological indices in normal negro children: A Jamaican cohort from birth to five years
-
Serjeant GR, Grandison Y, Mason K, Serjeant B, Sewell A, Vaidya S. Haematological indices in normal negro children: A Jamaican cohort from birth to five years. Clin Lab Haematol 1980; 2:169-78.
-
(1980)
Clin Lab Haematol
, vol.2
, pp. 169-178
-
-
Serjeant, G.R.1
Grandison, Y.2
Mason, K.3
Serjeant, B.4
Sewell, A.5
Vaidya, S.6
-
137
-
-
30644480296
-
Iron deficiency anaemia in Jamaican children, aged 1-5 years, with sickle cell disease
-
King L, Reid M, Forrester TE. Iron deficiency anaemia in Jamaican children, aged 1-5 years, with sickle cell disease. West Indian Med J 2005; 54:292-6.
-
(2005)
West Indian Med J
, vol.54
, pp. 292-296
-
-
King, L.1
Reid, M.2
Forrester, T.E.3
-
138
-
-
0016760932
-
Urinary iron in patients with sickle cell anaemia
-
Washington R, Boggs DR. Urinary iron in patients with sickle cell anaemia. J Lab Clin Med 1975; 86:17-23.
-
(1975)
J Lab Clin Med
, vol.86
, pp. 17-23
-
-
Washington, R.1
Boggs, D.R.2
-
139
-
-
0015914104
-
Iron-deficiency anaemia and sickle-cell disease: Hypothesis
-
Lincoln TL, Aroesty J, Morrison P. Iron-deficiency anaemia and sickle-cell disease: Hypothesis. Lancet 1973; 2:260-1.
-
(1973)
Lancet
, vol.2
, pp. 260-261
-
-
Lincoln, T.L.1
Aroesty, J.2
Morrison, P.3
-
140
-
-
0027930702
-
Improvement of sickle cell anaemia by iron-limited erythropoiesis
-
Castro O, Poillon WN, Finke H, Massac E. Improvement of sickle cell anaemia by iron-limited erythropoiesis. Am J Hematol 1994; 47:74-81.
-
(1994)
Am J Hematol
, vol.47
, pp. 74-81
-
-
Castro, O.1
Poillon, W.N.2
Finke, H.3
Massac, E.4
-
141
-
-
0034162841
-
Prevention of sickle cell crises with multiple phlebotomies
-
Bouchair N, Manigne P, Kanfer A, et al. Prevention of sickle cell crises with multiple phlebotomies. Arch Pediatr 2000; 7:249-55.
-
(2000)
Arch Pediatr
, vol.7
, pp. 249-255
-
-
Bouchair, N.1
Manigne, P.2
Kanfer, A.3
-
142
-
-
0019914185
-
Overt iron deficiency in sickle cell disease
-
Haddy TB, Castro O. Overt iron deficiency in sickle cell disease. Arch Intern Med 1982; 142:1621-4.
-
(1982)
Arch Intern Med
, vol.142
, pp. 1621-1624
-
-
Haddy, T.B.1
Castro, O.2
-
143
-
-
0037404579
-
-
Koduri PR. Iron in sickle cell disease: A review why less is better. Am J Hematol 2003; 73:59-63.
-
Koduri PR. Iron in sickle cell disease: A review why less is better. Am J Hematol 2003; 73:59-63.
-
-
-
-
144
-
-
0027243671
-
Iron deficiency in infancy and childhood
-
Oski FA. Iron deficiency in infancy and childhood. N Engl J Med 1993; 329:190-3.
-
(1993)
N Engl J Med
, vol.329
, pp. 190-193
-
-
Oski, F.A.1
-
145
-
-
0025305513
-
Nutritional deficiencies associated with vitamin E deficiency in sickle cell patients; the effect of vitamin supplementation
-
Sindel LJ, Baliga BS, Bendich A, Mankad V. Nutritional deficiencies associated with vitamin E deficiency in sickle cell patients; the effect of vitamin supplementation. Nutr Res 1990; 10:267-73.
-
(1990)
Nutr Res
, vol.10
, pp. 267-273
-
-
Sindel, L.J.1
Baliga, B.S.2
Bendich, A.3
Mankad, V.4
-
146
-
-
0025506552
-
Serum vitamin E and the sickling status in children with sickle cell anaemia
-
Ndombi IO, Kinoti SN. Serum vitamin E and the sickling status in children with sickle cell anaemia. East Afr Med J 1990; 67:720-5.
-
(1990)
East Afr Med J
, vol.67
, pp. 720-725
-
-
Ndombi, I.O.1
Kinoti, S.N.2
-
147
-
-
0034005021
-
Sickle cell disease and vitamin E deficiency in children in developing countries
-
Shukla P, Graham SM, Borgstein A, Nhlane A, Harper G, Brabin BJ. Sickle cell disease and vitamin E deficiency in children in developing countries. Trans R Soc Trop Med Hyg 2000; 94:109.
-
(2000)
Trans R Soc Trop Med Hyg
, vol.94
, pp. 109
-
-
Shukla, P.1
Graham, S.M.2
Borgstein, A.3
Nhlane, A.4
Harper, G.5
Brabin, B.J.6
-
148
-
-
0019314238
-
A decrease in irreversibly sickled erythrocytes in sickle cell anaemia patients given vitamin E
-
Natta CL, Machlin LJ, Brin M. A decrease in irreversibly sickled erythrocytes in sickle cell anaemia patients given vitamin E. Am J Clin Nutr 1980; 33:968-71.
-
(1980)
Am J Clin Nutr
, vol.33
, pp. 968-971
-
-
Natta, C.L.1
Machlin, L.J.2
Brin, M.3
-
149
-
-
0033828448
-
Ascorbate levels in red blood cells and urine in patients with sickle cell anaemia
-
Westerman MP, Zhang Y, McConnell JP, et al. Ascorbate levels in red blood cells and urine in patients with sickle cell anaemia. Am J Hematol 2000; 65:174-5.
-
(2000)
Am J Hematol
, vol.65
, pp. 174-175
-
-
Westerman, M.P.1
Zhang, Y.2
McConnell, J.P.3
-
150
-
-
7444220086
-
Low vitamin D status in children with sickle cell disease
-
Buison AM, Kawchak DA, Schall J, Ohene-Frempong K, Stallings VA, Zemel BS. Low vitamin D status in children with sickle cell disease. J Pediatr 2004; 145:622-7.
-
(2004)
J Pediatr
, vol.145
, pp. 622-627
-
-
Buison, A.M.1
Kawchak, D.A.2
Schall, J.3
Ohene-Frempong, K.4
Stallings, V.A.5
Zemel, B.S.6
-
151
-
-
7244242223
-
Serum ionized magnesium levels and ionized calcium-to-magnesium ratios in adult patients with sickle cell anaemia
-
Zehtabchi S, Sinert R, Rinnert S, et al. Serum ionized magnesium levels and ionized calcium-to-magnesium ratios in adult patients with sickle cell anaemia. Am J Hematol 2004; 77:215-22.
-
(2004)
Am J Hematol
, vol.77
, pp. 215-222
-
-
Zehtabchi, S.1
Sinert, R.2
Rinnert, S.3
-
152
-
-
0025308343
-
Selenium and glutathione peroxidase levels in sickle cell anaemia
-
Natta CL, Chen LC, Chow CK. Selenium and glutathione peroxidase levels in sickle cell anaemia. Acta Haematol 1990; 83:130-2.
-
(1990)
Acta Haematol
, vol.83
, pp. 130-132
-
-
Natta, C.L.1
Chen, L.C.2
Chow, C.K.3
-
153
-
-
0034191994
-
Sickle cell anaemia: A potential nutritional approach for a molecular disease
-
Ohnishi ST, Ohnishi T, Ogunmola GB. Sickle cell anaemia: A potential nutritional approach for a molecular disease. Nutrition 2000; 16:330-8.
-
(2000)
Nutrition
, vol.16
, pp. 330-338
-
-
Ohnishi, S.T.1
Ohnishi, T.2
Ogunmola, G.B.3
-
154
-
-
33644843002
-
Aged garlic extract is a potential therapy for sickle-cell anaemia
-
Takasu J, Uykimpang R, Sunga MA, Amagase H, Niihara Y. Aged garlic extract is a potential therapy for sickle-cell anaemia. J Nutr 2006; 136:803-5S.
-
(2006)
J Nutr
, vol.136
-
-
Takasu, J.1
Uykimpang, R.2
Sunga, M.A.3
Amagase, H.4
Niihara, Y.5
-
155
-
-
0034972252
-
Reduction of pain episodes and prothrombotic activity in sickle cell disease by dietary n-3 fatty acids
-
Tomer A, Kasey S, Connor WE, Clark S, Harker LA, Eckman JR. Reduction of pain episodes and prothrombotic activity in sickle cell disease by dietary n-3 fatty acids. Thromb Haemost 2001; 85:966-74.
-
(2001)
Thromb Haemost
, vol.85
, pp. 966-974
-
-
Tomer, A.1
Kasey, S.2
Connor, W.E.3
Clark, S.4
Harker, L.A.5
Eckman, J.R.6
-
156
-
-
26444514376
-
New therapies for sickle cell disease
-
Okpala IE. New therapies for sickle cell disease. Hematol Oncol Clin North Am 2005; 19:975-87, ix.
-
(2005)
Hematol Oncol Clin North Am
, vol.19
-
-
Okpala, I.E.1
-
157
-
-
0043204998
-
Arginine therapy: A new treatment for pulmonary hypertension in sickle cell disease?
-
Morris CR, Morris SM Jr, Hagar W, et al. Arginine therapy: A new treatment for pulmonary hypertension in sickle cell disease? Am J Respir Crit Care Med 2003; 168:63-9.
-
(2003)
Am J Respir Crit Care Med
, vol.168
, pp. 63-69
-
-
Morris, C.R.1
Morris Jr, S.M.2
Hagar, W.3
-
158
-
-
5044239523
-
Sickle-cell disease
-
Stuart MJ, Nagel RL. Sickle-cell disease. Lancet 2004; 364:1343-60.
-
(2004)
Lancet
, vol.364
, pp. 1343-1360
-
-
Stuart, M.J.1
Nagel, R.L.2
-
159
-
-
0034011397
-
Oral magnesium pidolate: Effects of long-term administration in patients with sickle cell disease
-
De Franceschi L, Bachir D, Galacteros F, et al. Oral magnesium pidolate: Effects of long-term administration in patients with sickle cell disease. Br J Haematol 2000; 108:284-9.
-
(2000)
Br J Haematol
, vol.108
, pp. 284-289
-
-
De Franceschi, L.1
Bachir, D.2
Galacteros, F.3
-
160
-
-
0031201124
-
Malnutrition in sickle cell disease patients
-
Prasad AS. Malnutrition in sickle cell disease patients. Am J Clin Nutr 1997; 66:423-4.
-
(1997)
Am J Clin Nutr
, vol.66
, pp. 423-424
-
-
Prasad, A.S.1
-
162
-
-
0043245973
-
Effect of a comprehensive clinical care program on disease course in severely ill children with sickle cell anaemia in a sub-Saharan African setting
-
Rahimy MC, Gangbo A, Ahouignan G, et al. Effect of a comprehensive clinical care program on disease course in severely ill children with sickle cell anaemia in a sub-Saharan African setting. Blood 2003; 102:834-8.
-
(2003)
Blood
, vol.102
, pp. 834-838
-
-
Rahimy, M.C.1
Gangbo, A.2
Ahouignan, G.3
-
163
-
-
0026947907
-
Growth and development in sickle hemoglobinopathies
-
Mankad VN. Growth and development in sickle hemoglobinopathies. Am J Pediatr Hematol Oncol 1992; 14:283-4.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 283-284
-
-
Mankad, V.N.1
-
164
-
-
0028783876
-
Factors associated with lowered intelligence in homozygous sickle cell disease
-
Knight S, Singhal A, Thomas P, Serjeant G. Factors associated with lowered intelligence in homozygous sickle cell disease. Arch Dis Child 1995; 73:316-20.
-
(1995)
Arch Dis Child
, vol.73
, pp. 316-320
-
-
Knight, S.1
Singhal, A.2
Thomas, P.3
Serjeant, G.4
-
165
-
-
0031724415
-
Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease
-
Zimmerman SA, Ware RE. Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease. Am J Hematol 1998; 59:267-72.
-
(1998)
Am J Hematol
, vol.59
, pp. 267-272
-
-
Zimmerman, S.A.1
Ware, R.E.2
-
166
-
-
0034944343
-
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease
-
Kutlar A, Kutlar F, Turker I, Tural C. The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease. Hemoglobin 2001; 25:213-17.
-
(2001)
Hemoglobin
, vol.25
, pp. 213-217
-
-
Kutlar, A.1
Kutlar, F.2
Turker, I.3
Tural, C.4
-
167
-
-
3042646355
-
Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia
-
Fawaz NA, Bashawery L, Al-Sheikh I, Qatari A, Al-Othman SS, Almawi WY. Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia. Am J Hematol 2004; 76:307-9.
-
(2004)
Am J Hematol
, vol.76
, pp. 307-309
-
-
Fawaz, N.A.1
Bashawery, L.2
Al-Sheikh, I.3
Qatari, A.4
Al-Othman, S.S.5
Almawi, W.Y.6
-
168
-
-
4544305476
-
A C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and G20210A mutation in the prothrombin gene of sickle cell anaemia patients from Northeast Brazil
-
Couto FD, Boas WV, Lyra I, et al. A C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and G20210A mutation in the prothrombin gene of sickle cell anaemia patients from Northeast Brazil. Hemoglobin 2004; 28:237-41.
-
(2004)
Hemoglobin
, vol.28
, pp. 237-241
-
-
Couto, F.D.1
Boas, W.V.2
Lyra, I.3
-
169
-
-
0035087298
-
Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anaemia
-
Nagel RL, Steinberg MH. Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anaemia. Pediatr Pathol Mol Med 2001; 20:123-36.
-
(2001)
Pediatr Pathol Mol Med
, vol.20
, pp. 123-136
-
-
Nagel, R.L.1
Steinberg, M.H.2
|