C Feo|D Dhermy - JoVE Visualize

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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.

British Journal of Haematology|March 1, 1983

Immune disorders in agnogenic myeloid metaplasia: relations to myelofibrosisE Rondeau, P Solal-Celigny, D Dhermy, et al.

American Journal of Hematology|December 1, 1982

The effect of cell hydration on the deformability of normal and sickle erythrocytesM L Gulley, D W Ross, C Feo, et al.

European Journal of Pediatrics|August 13, 1999

Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhoodY Perel, D Dhermy, A Carrere, et al.

Nouvelle Revue Francaise D'Hematologie|January 1, 1983

[Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]D Dhermy, C Féo, M Garbarz, et al.

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Showing results (61-70 of 122) with videos related to

Sort By:

Pageof 13

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.

British Journal of Haematology|March 1, 1983

Immune disorders in agnogenic myeloid metaplasia: relations to myelofibrosisE Rondeau, P Solal-Celigny, D Dhermy, et al.

American Journal of Hematology|December 1, 1982

The effect of cell hydration on the deformability of normal and sickle erythrocytesM L Gulley, D W Ross, C Feo, et al.

European Journal of Pediatrics|August 13, 1999

Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhoodY Perel, D Dhermy, A Carrere, et al.

Nouvelle Revue Francaise D'Hematologie|January 1, 1983

[Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]D Dhermy, C Féo, M Garbarz, et al.

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