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L Florensa

Showing results (101-110 of 136) with videos related to

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Acta Haematologica|January 1, 1991
Acquired amegakaryocytic thrombocytopenic purpura associated with immunoglobulin deficiencyM Rovira, E Feliu, L Florensa, et al.
Haematologica|June 28, 2000
Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemiaB Espinet, F Solé, M Salido, et al.
Sangre|January 1, 1985
[Practical use of the platelet peroxidase reaction at the ultrastructural level in the characterization of an apparently undifferentiated blast cell population]R Lafuente, S Woessner, L Florensa, et al.
British Journal of Haematology|August 10, 2000
Translocation t(6;14)(p12;q32): a novel cytogenetic abnormality in splenic lymphoma with villous lymphocytesF Solé, B Espinet, M Salido, et al.
Medicina Clinica|April 16, 1998
[Cytogenetic study of 93 myelodysplastic syndromes]F Solé, S Woessner, L Florensa, et al.
Leukemia Research|August 1, 1993
Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity?F Solé, M Torrabadella, I Granada, et al.
The British Journal of Dermatology|September 27, 2005
Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndromeR M Pujol, M Gilaberte, A Toll, et al.
Medicina Clinica|October 20, 1984
[Acquired refractory anemia and neoplasms. Study of 11 cases]J Sans-Sabrafen, J Buxó, S Woessner, et al.
Sangre|October 1, 1995
[Cytogenetic abnormalities in seven patients with the Sezary syndrome]F Solé, S Woessner, T Vallespí, et al.
Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.
Pageof 14

Showing results (101-110 of 136) with videos related to

Sort By:
Pageof 14
Acta Haematologica|January 1, 1991
Acquired amegakaryocytic thrombocytopenic purpura associated with immunoglobulin deficiencyM Rovira, E Feliu, L Florensa, et al.
Haematologica|June 28, 2000
Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemiaB Espinet, F Solé, M Salido, et al.
Sangre|January 1, 1985
[Practical use of the platelet peroxidase reaction at the ultrastructural level in the characterization of an apparently undifferentiated blast cell population]R Lafuente, S Woessner, L Florensa, et al.
British Journal of Haematology|August 10, 2000
Translocation t(6;14)(p12;q32): a novel cytogenetic abnormality in splenic lymphoma with villous lymphocytesF Solé, B Espinet, M Salido, et al.
Medicina Clinica|April 16, 1998
[Cytogenetic study of 93 myelodysplastic syndromes]F Solé, S Woessner, L Florensa, et al.
Leukemia Research|August 1, 1993
Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity?F Solé, M Torrabadella, I Granada, et al.
The British Journal of Dermatology|September 27, 2005
Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndromeR M Pujol, M Gilaberte, A Toll, et al.
Medicina Clinica|October 20, 1984
[Acquired refractory anemia and neoplasms. Study of 11 cases]J Sans-Sabrafen, J Buxó, S Woessner, et al.
Sangre|October 1, 1995
[Cytogenetic abnormalities in seven patients with the Sezary syndrome]F Solé, S Woessner, T Vallespí, et al.
Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.
Pageof 14