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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 myelofibrosis
E Rondeau, P Solal-Celigny, D Dhermy, et al.
European Journal of Pediatrics
|
August 13, 1999
Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhood
Y 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 elliptocytosis
D 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 variant
M 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 activity
S 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 elliptocytosis
D Dhermy, C Galand, O Bournier, et al.
Journal of Biochemical and Biophysical Methods
|
May 1, 1989
An efficient laboratory made apparatus for DNA amplification
O Bertrand, M H Delfau, M Garbarz, et al.
Blood
|
May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosis
M C Lecomte, D Dhermy, C Solis, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 109) with videos related to
Sort By:
Page
of 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 myelofibrosis
E Rondeau, P Solal-Celigny, D Dhermy, et al.
European Journal of Pediatrics
|
August 13, 1999
Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhood
Y 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 elliptocytosis
D 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 variant
M 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 activity
S 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 elliptocytosis
D Dhermy, C Galand, O Bournier, et al.
Journal of Biochemical and Biophysical Methods
|
May 1, 1989
An efficient laboratory made apparatus for DNA amplification
O Bertrand, M H Delfau, M Garbarz, et al.
Blood
|
May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosis
M C Lecomte, D Dhermy, C Solis, et al.
Page
of 11