-
1
-
-
0029793542
-
Modulation of erythrocyte potassium-chloride cotransport, potassium content and density by dietary magnesium intake in trangenic SAD mouse
-
De Franceschi, L., Beuzard, Y., Jouault, H. & Brugnara, C. (1996) Modulation of erythrocyte potassium-chloride cotransport, potassium content and density by dietary magnesium intake in trangenic SAD mouse. Blood, 88, 2738-2744.
-
(1996)
Blood
, vol.88
, pp. 2738-2744
-
-
De Franceschi, L.1
Beuzard, Y.2
Jouault, H.3
Brugnara, C.4
-
2
-
-
0030964677
-
Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease
-
De Franceschi, L., Bachir, D., Galacteros, F., Tchernia, G., Cynober, T., Alper, S., Platt, O., Beuzard, Y. & Brugnara, C. (1997) Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease. Journal of Clinical Investigation, 100, 1847-1852.
-
(1997)
Journal of Clinical Investigation
, vol.100
, pp. 1847-1852
-
-
De Franceschi, L.1
Bachir, D.2
Galacteros, F.3
Tchernia, G.4
Cynober, T.5
Alper, S.6
Platt, O.7
Beuzard, Y.8
Brugnara, C.9
-
3
-
-
0034011397
-
Oral magnesium pidolate: effects of long-term administration in patients with sickle cell disease
-
De Franceschi, L., Bachir, D., Galacteros, F., Tchernia, G., Cynober, T., Neuberg, D., Beuzard, Y. & Brugnara, C. (2000) Oral magnesium pidolate: effects of long-term administration in patients with sickle cell disease. British Journal of Haematology, 108, 284-289.
-
(2000)
British Journal of Haematology
, vol.108
, pp. 284-289
-
-
De Franceschi, L.1
Bachir, D.2
Galacteros, F.3
Tchernia, G.4
Cynober, T.5
Neuberg, D.6
Beuzard, Y.7
Brugnara, C.8
-
4
-
-
36849065265
-
Phase I study of magnesium pidolate in combination with hydroxyurea for children with sickle cell anemia
-
Hankins, J., Wynn, L., Brugnara, C., Hillery, C., Li, C.-S. & Wang, W. (2007) Phase I study of magnesium pidolate in combination with hydroxyurea for children with sickle cell anemia. British Journal of Haematology, 140, 80-85.
-
(2007)
British Journal of Haematology
, vol.140
, pp. 80-85
-
-
Hankins, J.1
Wynn, L.2
Brugnara, C.3
Hillery, C.4
Li, C.-S.5
Wang, W.6
-
5
-
-
0034082976
-
Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and laminin
-
Hillery, C.A., Du, M.C., Wang, W.C. & Scott, J.P. (2000) Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and laminin. British Journal of Haematology, 109, 322-327.
-
(2000)
British Journal of Haematology
, vol.109
, pp. 322-327
-
-
Hillery, C.A.1
Du, M.C.2
Wang, W.C.3
Scott, J.P.4
-
6
-
-
0034102323
-
Maximum urine concentrating ability in children with Hb SC disease: effects of hydroxyurea
-
Iyer, R., Baliga, R., Nagel, R.L., Brugnara, C., Kirchner, K., Hogan, S. & Steinberg, M.H. (2000) Maximum urine concentrating ability in children with Hb SC disease: effects of hydroxyurea. American Journal of Hematology, 64, 47-52.
-
(2000)
American Journal of Hematology
, vol.64
, pp. 47-52
-
-
Iyer, R.1
Baliga, R.2
Nagel, R.L.3
Brugnara, C.4
Kirchner, K.5
Hogan, S.6
Steinberg, M.H.7
-
7
-
-
0034917427
-
Hydroxyurea therapy for pediatric patients with haemoglobin SC disease
-
Miller, M.K., Zimmerman, S.A., Schultz, W.H. & Ware, R.E. (2001) Hydroxyurea therapy for pediatric patients with haemoglobin SC disease. Journal of Pediatric Hematology Oncology, 23, 306-308.
-
(2001)
Journal of Pediatric Hematology Oncology
, vol.23
, pp. 306-308
-
-
Miller, M.K.1
Zimmerman, S.A.2
Schultz, W.H.3
Ware, R.E.4
-
8
-
-
0038713649
-
The paradox of hemoglobin SC disease
-
Nagel, R.L., Fabry, M.E. & Steinberg, M.H. (2003) The paradox of hemoglobin SC disease. Blood Reviews, 17, 167-178.
-
(2003)
Blood Reviews
, vol.17
, pp. 167-178
-
-
Nagel, R.L.1
Fabry, M.E.2
Steinberg, M.H.3
-
9
-
-
42149139084
-
Modulation of erythroid adhesion receptors expression by hydroxyurea in children with sickle cell disease
-
Odièvre, M.-H., Bony, V., Benkerrou, M., Lapouméroulie, C., Alberti, C., Ducrocq, R., Jacqz-Aigrain, E., Elion, J. & Cartron, J.-P. (2008) Modulation of erythroid adhesion receptors expression by hydroxyurea in children with sickle cell disease. Haematologica, 93, 502-510.
-
(2008)
Haematologica
, vol.93
, pp. 502-510
-
-
Odièvre, M.-H.1
Bony, V.2
Benkerrou, M.3
Lapouméroulie, C.4
Alberti, C.5
Ducrocq, R.6
Jacqz-Aigrain, E.7
Elion, J.8
Cartron, J.-P.9
-
10
-
-
0016799829
-
Sequential treatment assignment with balancing for prognostic factors in the controlled clinical trial
-
Pocock, S.J. & Simon, R. (1975) Sequential treatment assignment with balancing for prognostic factors in the controlled clinical trial. Biometrics, 31, 103-115.
-
(1975)
Biometrics
, vol.31
, pp. 103-115
-
-
Pocock, S.J.1
Simon, R.2
-
11
-
-
11144227632
-
Abnormal regulation of Mg2+ transport via Na/Mg exchange in sickle erythrocytes
-
Rivera, A., Ferreira, A., Bertoni, D., Romero, J.R. & Brugnara, C. (2005) Abnormal regulation of Mg2+ transport via Na/Mg exchange in sickle erythrocytes. Blood, 105, 382-386.
-
(2005)
Blood
, vol.105
, pp. 382-386
-
-
Rivera, A.1
Ferreira, A.2
Bertoni, D.3
Romero, J.R.4
Brugnara, C.5
-
12
-
-
0030768046
-
Cellular effects of hydroxyurea in Hb SC disease
-
Steinberg, M.H., Nagel, R.L. & Brugnara, C. (1997) Cellular effects of hydroxyurea in Hb SC disease. British Journal of Haematology, 98, 838-844.
-
(1997)
British Journal of Haematology
, vol.98
, pp. 838-844
-
-
Steinberg, M.H.1
Nagel, R.L.2
Brugnara, C.3
-
13
-
-
4544273781
-
Epinephrine acts through erythroid signaling pathways to activate sickle cell adhesion to endothelium via LW-αvβ3 interactions
-
Zennadi, R., Hines, P.C., De Castro, L.M., Cartron, J.-P., Parise, L.V. & Telen, M.J. (2004) Epinephrine acts through erythroid signaling pathways to activate sickle cell adhesion to endothelium via LW-αvβ3 interactions. Blood, 104, 3774-3781.
-
(2004)
Blood
, vol.104
, pp. 3774-3781
-
-
Zennadi, R.1
Hines, P.C.2
De Castro, L.M.3
Cartron, J.-P.4
Parise, L.V.5
Telen, M.J.6
|