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Acta Haematologica|January 1, 1979
Chronic myelomonocytic leukemia associated with hereditary pyruvate kinase deficiency and multiple acquired erythrocyte abnormalitiesJ L Vives-Corrons, L Florensa, J Muncunill, et al.Sangre|February 1, 1992
[Chronic myeloid leukemia beginning as thrombocythemia. Analysis of 5 cases]F Cervantes, I Alcorta, F Bosch, et al.Biorheology. Supplement : the Official Journal of the International Society of Biorheology|January 1, 1984
Viscometric methods for assessing red cell deformability and fragmentationL Berga, J Dolz, J L Vives-Corrons, et al.British Journal of Haematology|September 1, 1996
Haemoglobin Lleida: a new alpha 2-globin variant (12 bp deletion) with mild thalassaemic phenotypeS Ayala, D Colomer, A Pujades, 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.British Journal of Haematology|July 1, 1997
First description of a frameshift mutation in the alpha1-globin gene associated with alpha-thalassaemiaS Ayala, D Colomer, M Aymerich, et al.Medicina Clinica|March 23, 1991
[Paroxysmal cold hemoglobinuria: only in the textbooks?]L Escoda, A Pereira, A Graena, et al.Leukemia|July 1, 1996
Chronic myeloid leukemia of thrombocythemic onset: a CML subtype with distinct hematological and molecular features?F Cervantes, D Colomer, J L Vives-Corrons, et al.Humangenetik|October 7, 1975
Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: clinical and familial studiesJ L Vives-Corrons, C Rozman, A Kahn, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|April 2, 1979
Significance of the electrophoretic modifications of defective pyruvate kinase variants. Study of six new observationsJ Marie, A Zanella, J L Vives-Corrons, et al.Pageof 14