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D Dhermy

Showing results (61-70 of 109) with videos related to

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Blood|September 15, 1994
A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sôr)L Boulanger, D Dhermy, M Garbarz, 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.
Medicina|January 1, 1992
[Clinical and biochemical study of 9 patients with hereditary elliptocytosis]L Feldman, T Marick, S Cerone, et al.
Acta Haematologica|January 1, 1984
Hereditary elliptocytosis with a spectrin molecular defect in a white patientM C Lecomte, D Dhermy, M Garbarz, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 1, 1996
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysisM Garbarz, D Bibas, T Cynober, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|September 18, 1978
[Extramedullary lymphosarcoma, erythroblastopenia and gastric adenocarcinoma. Apropos of a case]J F Bernard, J L Harousseau, M Renoux, et al.
Blood|June 15, 1997
Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemiaC M Fournier, G Nicolas, P G Gallagher, et al.
British Journal of Haematology|November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variantsM C Lecomte, M Garbarz, H Gautero, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
Blood|September 15, 1994
A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sôr)L Boulanger, D Dhermy, M Garbarz, 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.
Medicina|January 1, 1992
[Clinical and biochemical study of 9 patients with hereditary elliptocytosis]L Feldman, T Marick, S Cerone, et al.
Acta Haematologica|January 1, 1984
Hereditary elliptocytosis with a spectrin molecular defect in a white patientM C Lecomte, D Dhermy, M Garbarz, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 1, 1996
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysisM Garbarz, D Bibas, T Cynober, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|September 18, 1978
[Extramedullary lymphosarcoma, erythroblastopenia and gastric adenocarcinoma. Apropos of a case]J F Bernard, J L Harousseau, M Renoux, et al.
Blood|June 15, 1997
Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemiaC M Fournier, G Nicolas, P G Gallagher, et al.
British Journal of Haematology|November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variantsM C Lecomte, M Garbarz, H Gautero, et al.
Pageof 11