-
1
-
-
84865231169
-
Characterization of the complement sensitivity of density-fractionated sickle cells
-
Test ST, Kleman K, Lubin B. Characterization of the complement sensitivity of density-fractionated sickle cells. Blood 1991;78: 202a.
-
(1991)
Blood
, vol.78
-
-
Test, S.T.1
Kleman, K.2
Lubin, B.3
-
2
-
-
0020486107
-
Release of Spectrin-free Spicules on re- oxygenation of sickled erythrocytes
-
Allan D, Lumbrick AR, Thomas P, Westerman MP. Release of Spectrin-free Spicules on re- oxygenation of sickled erythrocytes. Nature 1982; 295: 612-13.
-
(1982)
Nature
, vol.295
, pp. 612-613
-
-
Allan, D.1
Lumbrick, A.R.2
Thomas, P.3
Westerman, M.P.4
-
3
-
-
0020045248
-
Exercise-induced haemolysis in Sickle cell anaemia: Shear sensitivity and erythrocyte dehydration
-
Platt OS. Exercise-induced haemolysis in Sickle cell anaemia: Shear sensitivity and erythrocyte dehydration: Blood 1982; 59: 1055-60.
-
(1982)
Blood
, vol.59
, pp. 1055-1060
-
-
Platt, O.S.1
-
4
-
-
0022572982
-
Excessive binding of natural anti-alpha galactosyl immunoglobulin G to sickle erythrocytes may contribute to extravascular cell destruction
-
Galili U, Clark MR, Shohat SB. Excessive binding of natural anti-alpha galactosyl immunoglobulin G to sickle erythrocytes may contribute to extravascular cell destruction J Clin Invest 1986: 77: 27-33.
-
(1986)
J Clin Invest
, vol.77
, pp. 27-33
-
-
Galili, U.1
Clark, M.R.2
Shohat, S.B.3
-
5
-
-
0023901188
-
Sickling-induced binding of immunoglobulin to sickle erythrocyte
-
Green GA, Kalra VK. Sickling-induced binding of immunoglobulin to sickle erythrocyte Blood 1988; 71: 636-9.
-
(1988)
Blood
, vol.71
, pp. 636-639
-
-
Green, G.A.1
Kalra, V.K.2
-
6
-
-
0022812367
-
Vaso-Occlusion by Sickle cells, evidence from selective trapping of dense red cells
-
Kaul DK, Fabry ME, Nagel RL. Vaso-Occlusion by Sickle cells, evidence from selective trapping of dense red cells Blood 1986: 68: 1162-6.
-
(1986)
Blood
, vol.68
, pp. 1162-1166
-
-
Kaul, D.K.1
Fabry, M.E.2
Nagel, R.L.3
-
7
-
-
0014645884
-
The irreversibly sickled cell,a determinant of haemolysis in sickle cell anaemias
-
Serjeant GR, Serjeant BE, Milner PF.The irreversibly sickled cell,a determinant of haemolysis in sickle cell anaemias. Br J Haematol 1969; 17: 527-33.
-
(1969)
Br J Haematol
, vol.17
, pp. 527-533
-
-
Serjeant, G.R.1
Serjeant, B.E.2
Milner, P.F.3
-
8
-
-
0021166235
-
Non-uniformity of intracellular polymer formation in sickle erythrocytes: possible correlation with severity of haemolytic anaemia
-
Noguchi CT, Schechter AN. Non-uniformity of intracellular polymer formation in sickle erythrocytes: possible correlation with severity of haemolytic anaemia. Am J Pediatr Hematoloncol 1984; 6: 46-50.
-
(1984)
Am J Pediatr Hematoloncol
, vol.6
, pp. 46-50
-
-
Noguchi, C.T.1
Schechter, A.N.2
-
9
-
-
0021931288
-
haemoglobin S polymerization: primary determinant of the haemolytic and clinical severity of sickling syndromes
-
Brittenham GM, Schechter AN, Noguchi CT. haemoglobin S polymerization: primary determinant of the haemolytic and clinical severity of sickling syndromes. Blood 1985; 65: 183-9.
-
(1985)
Blood
, vol.65
, pp. 183-189
-
-
Brittenham, G.M.1
Schechter, A.N.2
Noguchi, C.T.3
-
10
-
-
0020631382
-
Effects of blood transfusion on exercise capacity in patients with sickle cell anaemia
-
Charache S, Bleecker ER, Bross DS. Effects of blood transfusion on exercise capacity in patients with sickle cell anaemia. Am J Med 1983; 74: 757-64.
-
(1983)
Am J Med
, vol.74
, pp. 757-764
-
-
Charache, S.1
Bleecker, E.R.2
Bross, D.S.3
-
11
-
-
0017196848
-
Aprophylactic transfusion program for children with sickle cell anaemia complicated by CNS infarction
-
Lusher JM, Haglighat H, Khalifa AS. Aprophylactic transfusion program for children with sickle cell anaemia complicated by CNS infarction. Am J Hematol 1976; 1: 265-73.
-
(1976)
Am J Hematol
, vol.1
, pp. 265-273
-
-
Lusher, J.M.1
Haglighat, H.2
Khalifa, A.S.3
-
12
-
-
84942187010
-
Sickle cell crises treated by exchange transfusion
-
Green M, Hall RJC, Huntsman RG, et al. Sickle cell crises treated by exchange transfusion. JAMA 1975; 231: 948-50.
-
(1975)
JAMA
, vol.231
, pp. 948-950
-
-
Green, M.1
Hall, R.J.C.2
Huntsman, R.G.3
-
13
-
-
0021182135
-
Normal values of haemoglobin, packed cell volume and erythrocyte sedimentation rate in healthy Nigerian adults
-
Obi. GO. Normal values of haemoglobin, packed cell volume and erythrocyte sedimentation rate in healthy Nigerian adults. Afr J Med Med Sci 1984; 13: 1-6.
-
(1984)
Afr J Med Med Sci
, vol.13
, pp. 1-6
-
-
Obi, G.O.1
-
14
-
-
0022560281
-
Sickle cell anaemia patients have low erythropoietin levels for their degree of anaemia
-
Sherwood JB, Goldwesser E, Chilcoat R, Carmichael LD, Nagel RL. Sickle cell anaemia patients have low erythropoietin levels for their degree of anaemia Blood 1987; 67: 46-9.
-
(1987)
Blood
, vol.67
, pp. 46-49
-
-
Sherwood, J.B.1
Goldwesser, E.2
Chilcoat, R.3
Carmichael, L.D.4
Nagel, R.L.5
-
15
-
-
0025728010
-
The haematology of homozygous sickle cell disease after 40 years
-
Morris J. Dunn D, Beckford M, et al. The haematology of homozygous sickle cell disease after 40 years. Br J Haematol 1991; 77: 382-5.
-
(1991)
Br J Haematol
, vol.77
, pp. 382-385
-
-
Morris, J.1
Dunn, D.2
Beckford, M.3
-
16
-
-
0025770390
-
Pain in sickle cell disease. Rates and risk factors
-
Platt O, Thorington B, Brambilla D, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991; 325: 11-6.
-
(1991)
N Engl J Med
, vol.325
, pp. 11-16
-
-
Platt, O.1
Thorington, B.2
Brambilla, D.3
-
17
-
-
0025311897
-
Treatment of sickle cell anaemia with hydroxyurea and erythropoietin
-
Goldberg M, Burugara C, Dover G, et al. Treatment of sickle cell anaemia with hydroxyurea and erythropoietin. N Eng J Med 1990; 323: 366-72.
-
(1990)
N Eng J Med
, vol.323
, pp. 366-372
-
-
Goldberg, M.1
Burugara, C.2
Dover, G.3
-
18
-
-
0027452375
-
Sickle cell anaemia. Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression
-
Powers D, Hiti A. Sickle cell anaemia. Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression. Am J Dis Child 1993; 147: 1197-202.
-
(1993)
Am J Dis Child
, vol.147
, pp. 1197-1202
-
-
Powers, D.1
Hiti, A.2
-
19
-
-
0020081165
-
Concurrent sickle cell anaemia and alpha- thalassemia: effect on severity of anaemia
-
Embury SH, Dozy AM, Miller J, et al. Concurrent sickle cell anaemia and alpha- thalassemia: effect on severity of anaemia; N Engl J Med 1982; 306: 270-4.
-
(1982)
N Engl J Med
, vol.306
, pp. 270-274
-
-
Embury, S.H.1
Dozy, A.M.2
Miller, J.3
-
20
-
-
80955173605
-
Serum levels of leptin in Nigerian patients with sickle cell anaemia
-
Iwalokun BA, Iwalokun SO, Hodonou SO, Aina AO, Agomo PU. Serum levels of leptin in Nigerian patients with sickle cell anaemia. BMC Blood disord 2011; 11: 2.
-
(2011)
BMC Blood disord
, vol.11
, pp. 2
-
-
Iwalokun, B.A.1
Iwalokun, S.O.2
Hodonou, S.O.3
Aina, A.O.4
Agomo, P.U.5
-
21
-
-
31344482604
-
Haematological values in sickle cell anaemia in steady state and during vaso-occlusive crisis in Benin city, Nigeria
-
Omoti CE. Haematological values in sickle cell anaemia in steady state and during vaso-occlusive crisis in Benin city, Nigeria. Ann Afr Med 2005; 4: 62-7.
-
(2005)
Ann Afr Med
, vol.4
, pp. 62-67
-
-
Omoti, C.E.1
-
22
-
-
79952808284
-
Haematological indices of sickle cell anaemia patients with pulmonary tuberculosis in Northern Nigeria
-
Sagir G, Ahmed SG, Bukar AA, Jolayemi B. Haematological indices of sickle cell anaemia patients with pulmonary tuberculosis in Northern Nigeria. Mediterr J Hematol Infect Dis 2010; 2: e20100014.
-
(2010)
Mediterr J Hematol Infect Dis
, vol.2
-
-
Sagir, G.1
Ahmed, S.G.2
Bukar, A.A.3
Jolayemi, B.4
-
23
-
-
0020606642
-
Erythrocytes in sickle cell anaemia are heterogenous in their rheological and haemodynamic characteristics
-
Kaul DK, Fabry ME, Windisch P, Baez S, Nagel RL. Erythrocytes in sickle cell anaemia are heterogenous in their rheological and haemodynamic characteristics. J Clin invest 1983; 72: 22-31.
-
(1983)
J Clin invest
, vol.72
, pp. 22-31
-
-
Kaul, D.K.1
Fabry, M.E.2
Windisch, P.3
Baez, S.4
Nagel, R.L.5
-
24
-
-
0028961230
-
Plasma erythropoietin reference ranges in children
-
Kraff-Jacobs B, Williams J, Soldin SJ. Plasma erythropoietin reference ranges in children. J Paediatr 1995; 126: 601-3.
-
(1995)
J Paediatr
, vol.126
, pp. 601-603
-
-
Kraff-Jacobs, B.1
Williams, J.2
Soldin, S.J.3
-
25
-
-
84865392457
-
Hematological values in Nigerian children with steady state homozygous sickle cell disease
-
Momodu I, Suleiman K, Abdullahi S, Shehu UA. Hematological values in Nigerian children with steady state homozygous sickle cell disease. Intern J Academic Res 2011; 3: 501-6.
-
(2011)
Intern J Academic Res
, vol.3
, pp. 501-506
-
-
Momodu, I.1
Suleiman, K.2
Abdullahi, S.3
Shehu, U.A.4
-
26
-
-
80955173605
-
Serum levels of leptin in Nigerian patients with sickle cell anaemia
-
Iwalokun BA, Iwalokun SO, Hodonou SO, Aina AO, Agomo PU. Serum levels of leptin in Nigerian patients with sickle cell anaemia. BMC. Blood. Disord. 2011;11: 2.
-
(2011)
BMC. Blood. Disord
, vol.11
, pp. 2
-
-
Iwalokun, B.A.1
Iwalokun, S.O.2
Hodonou, S.O.3
Aina, A.O.4
Agomo, P.U.5
|