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D Dhermy

Showing results (71-80 of 109) with videos related to

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Presse Medicale (Paris, France : 1983)|November 26, 1983
[Neonatal hemolysis secondary to congenital poikilocytosis]F Gretillat, N Delepine, D Dhermy, 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.
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.
Human Genetics|December 1, 1986
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosisD Dhermy, M Garbarz, M C Lecomte, et al.
British Journal of Haematology|April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variantM C Lecomte, C Feo, H Gautero, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1996
Human erythroid spectrin alpha subunit and its SH3 domain are sensitive to acidic Plasmodium falciparum proteolytic activityS L Le Bonniec, C Fournier, C Deregnaucourt, et al.
Blood|January 9, 1999
Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosisD Dhermy, C Galand, O Bournier, et al.
Journal of Biochemical and Biophysical Methods|May 1, 1989
An efficient laboratory made apparatus for DNA amplificationO Bertrand, M H Delfau, M Garbarz, et al.
Blood|May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosisM C Lecomte, D Dhermy, C Solis, et al.
Pageof 11

Showing results (71-80 of 109) with videos related to

Sort By:
Pageof 11
Presse Medicale (Paris, France : 1983)|November 26, 1983
[Neonatal hemolysis secondary to congenital poikilocytosis]F Gretillat, N Delepine, D Dhermy, 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.
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.
Human Genetics|December 1, 1986
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosisD Dhermy, M Garbarz, M C Lecomte, et al.
British Journal of Haematology|April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variantM C Lecomte, C Feo, H Gautero, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1996
Human erythroid spectrin alpha subunit and its SH3 domain are sensitive to acidic Plasmodium falciparum proteolytic activityS L Le Bonniec, C Fournier, C Deregnaucourt, et al.
Blood|January 9, 1999
Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosisD Dhermy, C Galand, O Bournier, et al.
Journal of Biochemical and Biophysical Methods|May 1, 1989
An efficient laboratory made apparatus for DNA amplificationO Bertrand, M H Delfau, M Garbarz, et al.
Blood|May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosisM C Lecomte, D Dhermy, C Solis, et al.
Pageof 11