Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
European Biophysics Journal : EBJ|April 8, 1999
Properties of normal and mutant polypeptide fragments from the dimer self-association sites of human red cell spectrinM C Lecomte, G Nicolas, D Dhermy, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|October 15, 1980
[Acute agranulocytosis. Clinical study of thirty-two cases (author's transl)]M Renoux, J F Bernard, D Dhermy, et al.
British Journal of Haematology|July 1, 1994
Spontaneous megakaryocyte colony formation in myeloproliferative disorders is not neutralizable by antibodies against IL3, IL6 and GM-CSFY Li, G Hetet, A M Maurer, et al.
British Journal of Haematology|November 1, 1983
A phenomenological difference between membrane skeletal protein complexes isolated from normal and hereditary spherocytosis erythrocytesJ C Pinder, D Dhermy, A J Baines, et al.
Blood Cells, Molecules & Diseases|August 26, 1998
Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin geneD Dhermy, C Galand, O Bournier, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|June 12, 2002
South-East Asian ovalocytosis among the population of the Highlands of Madagascar: a vestigé of the island's settlementT Rabe, R Jambou, L Rabarijaona, et al.
Nouvelle Revue Francaise D'Hematologie; Blood Cells|January 1, 1977
Cerebromeningeal localizations in acute myeloblastic leukemia of the adult. Clinical and pathological study of 15 casesM Renoux, D Dhermy, J F Bernard, et al.
Clinical and Laboratory Haematology|April 25, 2001
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis familyD Dhermy, J Steen-Johnsen, O Bournier, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|September 18, 1978
[Acute leukemia and primary Vaquez' polycythemia. 20 cases]J F Bernard, M Renoux, D Dhermy, et al.
The Biochemical Journal|May 13, 1998
Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosisG Nicolas, S Pedroni, C Fournier, et al.
Pageof 13