-
1
-
-
84856279998
-
Biomarkers in sickle cell disease
-
Rees D.C., Gibson J.S. Biomarkers in sickle cell disease. Br J Haematol 2012, 156(4):433-445.
-
(2012)
Br J Haematol
, vol.156
, Issue.4
, pp. 433-445
-
-
Rees, D.C.1
Gibson, J.S.2
-
2
-
-
5044239523
-
Sickle-cell disease
-
Stuart M.J., Nagel R.L. Sickle-cell disease. Lancet 2004, 364(9442):1343-1360.
-
(2004)
Lancet
, vol.364
, Issue.9442
, pp. 1343-1360
-
-
Stuart, M.J.1
Nagel, R.L.2
-
4
-
-
81055147553
-
Genetic modifiers of sickle cell disease
-
Thein S.L. Genetic modifiers of sickle cell disease. Hemoglobin 2011, 35(5-6):589-606.
-
(2011)
Hemoglobin
, vol.35
, Issue.5-6
, pp. 589-606
-
-
Thein, S.L.1
-
5
-
-
0001719775
-
Compound heterozygous and other sickle hemoglobinopathies
-
Cambridge University Press, Cambridge, UK, M.H. Steinberg, B.G. Forget, D.R. Higgs, R.L. Nagel (Eds.)
-
Steinberg M.H. Compound heterozygous and other sickle hemoglobinopathies. Disorders of hemoglobin: genetics, pathophysiology, and clinical management 2001, 786-810. Cambridge University Press, Cambridge, UK. 1st ed. M.H. Steinberg, B.G. Forget, D.R. Higgs, R.L. Nagel (Eds.).
-
(2001)
Disorders of hemoglobin: genetics, pathophysiology, and clinical management
, pp. 786-810
-
-
Steinberg, M.H.1
-
6
-
-
84878982472
-
Classification of the disorders of hemoglobin
-
Forget B.G., Bunn H.F. Classification of the disorders of hemoglobin. Cold Spring Harb Perspect Med 2013, 3(2):a011684.
-
(2013)
Cold Spring Harb Perspect Med
, vol.3
, Issue.2
, pp. a011684
-
-
Forget, B.G.1
Bunn, H.F.2
-
7
-
-
0035096303
-
Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemia
-
Rigano P., Rodgers G.P., Renda D., Renda M.C., Aquino A., Maggio A. Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemia. Hemoglobin 2001, 25(1):9-17.
-
(2001)
Hemoglobin
, vol.25
, Issue.1
, pp. 9-17
-
-
Rigano, P.1
Rodgers, G.P.2
Renda, D.3
Renda, M.C.4
Aquino, A.5
Maggio, A.6
-
8
-
-
45849104274
-
The Hb S/beta+-thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele
-
Schmugge M., Waye J.S., Basran R.K., Zurbriggen K., Frischknecht H. The Hb S/beta+-thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele. Hemoglobin 2008, 32(3):303-307.
-
(2008)
Hemoglobin
, vol.32
, Issue.3
, pp. 303-307
-
-
Schmugge, M.1
Waye, J.S.2
Basran, R.K.3
Zurbriggen, K.4
Frischknecht, H.5
-
9
-
-
0345327621
-
Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene
-
Lacan P., Ponceau B., Aubry M., Francina A. Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene. Hemoglobin 2003, 27(4):257-259.
-
(2003)
Hemoglobin
, vol.27
, Issue.4
, pp. 257-259
-
-
Lacan, P.1
Ponceau, B.2
Aubry, M.3
Francina, A.4
-
10
-
-
0028098232
-
Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations
-
Boletini E., Svobodova M., Divoky V., Baysal E., Curuk M.A., Dimovski A.J., et al. Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations. Hum Genet 1994, 93(2):182-187.
-
(1994)
Hum Genet
, vol.93
, Issue.2
, pp. 182-187
-
-
Boletini, E.1
Svobodova, M.2
Divoky, V.3
Baysal, E.4
Curuk, M.A.5
Dimovski, A.J.6
-
11
-
-
0025838154
-
Molecular characterization of Hb S(C) beta-thalassemia in American blacks
-
Gonzalez-Redondo J.M., Kutlar A., Kutlar F., McKie V.C., McKie K.M., Baysal E., et al. Molecular characterization of Hb S(C) beta-thalassemia in American blacks. Am J Hematol 1991, 38(1):9-14.
-
(1991)
Am J Hematol
, vol.38
, Issue.1
, pp. 9-14
-
-
Gonzalez-Redondo, J.M.1
Kutlar, A.2
Kutlar, F.3
McKie, V.C.4
McKie, K.M.5
Baysal, E.6
-
12
-
-
0027474960
-
A mild type of Hb S-beta(+)-thalassemia [-92(C→T)] in a Sicilian family
-
Divoky V., Baysal E., Schiliro G., Dibenedetto S.P., Huisman T.H. A mild type of Hb S-beta(+)-thalassemia [-92(C→T)] in a Sicilian family. Am J Hematol 1993, 42(2):225-226.
-
(1993)
Am J Hematol
, vol.42
, Issue.2
, pp. 225-226
-
-
Divoky, V.1
Baysal, E.2
Schiliro, G.3
Dibenedetto, S.P.4
Huisman, T.H.5
-
13
-
-
0000650711
-
Compound heterozygous states
-
Raven Press Ltd., New York, S.H. Embury, R.P. Hebbel, N. Mohandas, M.H. Steinberg (Eds.)
-
Kinney T.R., Ware R.E. Compound heterozygous states. Sickle cell disease: basic principles and clinical practice 1994, 437-451. Raven Press Ltd., New York. 1st ed. S.H. Embury, R.P. Hebbel, N. Mohandas, M.H. Steinberg (Eds.).
-
(1994)
Sickle cell disease: basic principles and clinical practice
, pp. 437-451
-
-
Kinney, T.R.1
Ware, R.E.2
-
14
-
-
79952138729
-
Hb S-beta-thalassemia: molecular, hematological and clinical comparisons
-
Serjeant G.R., Serjeant B.E., Fraser R.A., Hambleton I.R., Higgs D.R., Kulozik A.E., et al. Hb S-beta-thalassemia: molecular, hematological and clinical comparisons. Hemoglobin 2011, 35(1):1-12.
-
(2011)
Hemoglobin
, vol.35
, Issue.1
, pp. 1-12
-
-
Serjeant, G.R.1
Serjeant, B.E.2
Fraser, R.A.3
Hambleton, I.R.4
Higgs, D.R.5
Kulozik, A.E.6
-
15
-
-
84878959132
-
The natural history of sickle cell disease
-
Serjeant G.R. The natural history of sickle cell disease. Cold Spring Harb Perspect Med 2013, 3(10):a011783.
-
(2013)
Cold Spring Harb Perspect Med
, vol.3
, Issue.10
, pp. a011783
-
-
Serjeant, G.R.1
-
16
-
-
84930085319
-
Very mild forms of Hb S/beta+-thalassemia in Brazilian children
-
Belisario A.R., Sales R.R., Viana M.B. Very mild forms of Hb S/beta+-thalassemia in Brazilian children. Rev Bras Hematol Hemoter 2015, 37(3):198-201.
-
(2015)
Rev Bras Hematol Hemoter
, vol.37
, Issue.3
, pp. 198-201
-
-
Belisario, A.R.1
Sales, R.R.2
Viana, M.B.3
|