-
1
-
-
0016491247
-
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
-
Zarkowsky HS, Mohandas N, Speaker CB, Shohet SB. A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane. Br J Haematol 1975;29:537-43.
-
(1975)
Br J Haematol
, vol.29
, pp. 537-543
-
-
Zarkowsky, H.S.1
Mohandas, N.2
Speaker, C.B.3
Shohet, S.B.4
-
2
-
-
1942445176
-
Hereditary Elliptocytosis: Spectrin and Protein 4.1R
-
DOI 10.1053/j.seminhematol.2004.01.003
-
Gallagher PG. Hereditary elliptocytosis: spectrin and protein 4.1. R. Semin Hematol 2004;41:142-64. (Pubitemid 38509639)
-
(2004)
Seminars in Hematology
, vol.41
, Issue.2
, pp. 142-164
-
-
Gallagher, P.G.1
-
4
-
-
33846274937
-
The molecular basis of hereditary red cell membrane disorders
-
DOI 10.1016/j.blre.2006.03.005, PII S0268960X06000257
-
Delaunay J. The molecular basis of hereditary red cell membrane disorders. Blood reviews 2007;21:1-20. (Pubitemid 46110925)
-
(2007)
Blood Reviews
, vol.21
, Issue.1
, pp. 1-20
-
-
Delaunay, J.1
-
5
-
-
0034124560
-
Les maladies hereditaires de la membrane erythrocytaire: Du tableau clinique aux mecanismes genetiques et moleculaires sous-jacents
-
Bichis M, Huber AR. Hereditary diseases of erythrocyte membrane: from clinical aspects to underlying genetical and molecular mechanisms. Ann Biol Clin 2000;58:277-89. (Pubitemid 30398814)
-
(2000)
Annales de Biologie Clinique
, vol.58
, Issue.3
, pp. 277-289
-
-
Bichis, M.1
Huber, A.R.2
-
6
-
-
33750378860
-
Une résistance globulaire osmotique normale n'exclut pas une membranopathie érythrocytaire! À propos d'un cas d'elliptocytose héréditaire
-
DOI 10.1684/abc.2006.0010
-
Perrin J, Marchand-Arvier M, Latger-Cannard V, Vigneron C, Lecompte T. Une résistance globulaire osmotique normale n'exclut pas une membranopathie érythrocytaire ! A propos d'un cas d'elliptocytose héréditaire. Ann Biol Clin 2006;64:491-5. (Pubitemid 44627915)
-
(2006)
Annales de Biologie Clinique
, vol.64
, Issue.5
, pp. 491-495
-
-
Perrin, J.1
Marchand-Arvier, M.2
Latger-Cannard, V.3
Vigneron, C.4
Lecompte, T.5
-
7
-
-
0034494630
-
Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia
-
DOI 10.1046/j.1365-2141.2000.02416.x
-
King MJ, Behrens J, Rogers C, Flynn C, Grennwood D, Chambers K. Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia. Br J Haematol 2000;111:924-33. (Pubitemid 32098933)
-
(2000)
British Journal of Haematology
, vol.111
, Issue.3
, pp. 924-933
-
-
King, M.-J.1
Behrens, J.2
Rogers, C.3
Flynn, C.4
Greenwood, D.5
Chambers, K.6
-
8
-
-
47549102275
-
Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis
-
DOI 10.1002/cyto.b.20413
-
King MJ, Telfer P, MacKinnon H, Langabeer L, McMahon C, Darbyshire P, et al. Using the eosin-5-maléimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoïkilocytosis. Cytometry Part B 2008;74B:244-50. (Pubitemid 352007322)
-
(2008)
Cytometry Part B - Clinical Cytometry
, vol.74
, Issue.4
, pp. 244-250
-
-
King, M.-J.1
Telfer, P.2
MacKinnon, H.3
Langabeer, L.4
McMahon, C.5
Darbyshire, P.6
Dhermy, D.7
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