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C Altay

Showing results (31-40 of 160) with videos related to

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The Journal of Laboratory and Clinical Medicine|July 1, 1971
Role of the lymphocyte in antihemophilic globulin production: a rise in antihemophilic globulin levels in a hemophilic subject with acute lymphoblastic leukemiaJ D Bouhasin, P Monteleone, C Altay
American Journal of Diseases of Children (1960)|December 1, 1971
Congenital factor 13 deficiency. Observation of two new cases in the newborn periodS Ozsoylu, C Altay, G Hi csönmez
British Journal of Haematology|March 23, 1999
Transferrin receptor on peripheral blood lymphocytes in iron deficiency anaemiaS T Kinik, A M Tuncer, C Altay
Journal of Clinical Ultrasound : JCU|May 1, 1981
Cholecystosonography in children with sickle cell disease: technical approach and clinical resultsJ J Cunningham, S M Houlihan, C Altay
Hemoglobin|January 1, 1976
Probable inclusion-body beta-thalassemia in a Chinese familyC Altay, T H Huisman, R R Moores
Journal of Medical Genetics|June 1, 1985
Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia IIA Gurgey, S Kayin, E Kansu, et al.
American Journal of Hematology|February 9, 2002
Importance of RDW value in differential diagnosis of hypochrome anemiasD Aslan, F Gümrük, A Gürgey, et al.
The Journal of Pediatrics|June 1, 1975
Plasma, erythrocyte, and leukocyte ascorbic acid concentrations in children with iron deficiency anemiaA Bingöl, C Altay, B Say, et al.
European Journal of Pediatrics|December 1, 1989
Role of protein C in childhood cerebrovascular occlusive accidentsS Uysal, B Anlar, C Altay, et al.
British Journal of Haematology|February 1, 1995
A new Turkish type of beta-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletions of the psi beta and beta genes and an intact delta geneC Oner, R Oner, A Gürgey, et al.
Pageof 16

Showing results (31-40 of 160) with videos related to

Sort By:
Pageof 16
The Journal of Laboratory and Clinical Medicine|July 1, 1971
Role of the lymphocyte in antihemophilic globulin production: a rise in antihemophilic globulin levels in a hemophilic subject with acute lymphoblastic leukemiaJ D Bouhasin, P Monteleone, C Altay
American Journal of Diseases of Children (1960)|December 1, 1971
Congenital factor 13 deficiency. Observation of two new cases in the newborn periodS Ozsoylu, C Altay, G Hi csönmez
British Journal of Haematology|March 23, 1999
Transferrin receptor on peripheral blood lymphocytes in iron deficiency anaemiaS T Kinik, A M Tuncer, C Altay
Journal of Clinical Ultrasound : JCU|May 1, 1981
Cholecystosonography in children with sickle cell disease: technical approach and clinical resultsJ J Cunningham, S M Houlihan, C Altay
Hemoglobin|January 1, 1976
Probable inclusion-body beta-thalassemia in a Chinese familyC Altay, T H Huisman, R R Moores
Journal of Medical Genetics|June 1, 1985
Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia IIA Gurgey, S Kayin, E Kansu, et al.
American Journal of Hematology|February 9, 2002
Importance of RDW value in differential diagnosis of hypochrome anemiasD Aslan, F Gümrük, A Gürgey, et al.
The Journal of Pediatrics|June 1, 1975
Plasma, erythrocyte, and leukocyte ascorbic acid concentrations in children with iron deficiency anemiaA Bingöl, C Altay, B Say, et al.
European Journal of Pediatrics|December 1, 1989
Role of protein C in childhood cerebrovascular occlusive accidentsS Uysal, B Anlar, C Altay, et al.
British Journal of Haematology|February 1, 1995
A new Turkish type of beta-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletions of the psi beta and beta genes and an intact delta geneC Oner, R Oner, A Gürgey, et al.
Pageof 16