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C Galand

Showing results (51-60 of 87) with videos related to

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La Presse Medicale|June 1, 1970
[Congenital deficiency erythrocyte adenylate-kinase]P Boivin, C Galand, J Hakim, et al.
La Presse Medicale|January 30, 1971
[A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency]P Boivin, C Galand, J Hakim, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|May 20, 1973
[Acute hemolytic anemia with methemoglobinemia due to phenacetin: a case]B Graisely, J Debray, M Krulik, et al.
Blood|July 1, 1982
A shortened variant of red cell membrane protein 4.1N Alloisio, E Dorléac, J Delaunay, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1974
[Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature]P Boivin, J Hakim, J Mandereau, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1977
A Spanish family with erythrocyte pyruvate kinase deficiency: contribution of various immunologic methods in the study of the mutant enzymeA Kahn, J L Vives-Corron, J Marie, et al.
Blood|November 1, 1976
Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesisA Kahn, D Cottreau, C Boyer, et al.
Human Genetics|September 1, 1993
Spectrin alpha IIa variant in dominant and non-dominant spherocytosisP Boivin, C Galand, I Devaux, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1988
[Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants]M C Lecomte, D Dhermy, H Gautero, et al.
Skeletal Radiology|December 23, 2008
Fracture-associated and idiopathic subchondral vertebral lesions: a magnetic resonance study in autopsy specimens with histologic correlationC A Peters, B C Vande Berg, C Galand, et al.
Pageof 9

Showing results (51-60 of 87) with videos related to

Sort By:
Pageof 9
La Presse Medicale|June 1, 1970
[Congenital deficiency erythrocyte adenylate-kinase]P Boivin, C Galand, J Hakim, et al.
La Presse Medicale|January 30, 1971
[A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency]P Boivin, C Galand, J Hakim, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|May 20, 1973
[Acute hemolytic anemia with methemoglobinemia due to phenacetin: a case]B Graisely, J Debray, M Krulik, et al.
Blood|July 1, 1982
A shortened variant of red cell membrane protein 4.1N Alloisio, E Dorléac, J Delaunay, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1974
[Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature]P Boivin, J Hakim, J Mandereau, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1977
A Spanish family with erythrocyte pyruvate kinase deficiency: contribution of various immunologic methods in the study of the mutant enzymeA Kahn, J L Vives-Corron, J Marie, et al.
Blood|November 1, 1976
Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesisA Kahn, D Cottreau, C Boyer, et al.
Human Genetics|September 1, 1993
Spectrin alpha IIa variant in dominant and non-dominant spherocytosisP Boivin, C Galand, I Devaux, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1988
[Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants]M C Lecomte, D Dhermy, H Gautero, et al.
Skeletal Radiology|December 23, 2008
Fracture-associated and idiopathic subchondral vertebral lesions: a magnetic resonance study in autopsy specimens with histologic correlationC A Peters, B C Vande Berg, C Galand, et al.
Pageof 9