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H Tamary

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Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1994
Chronic childhood idiopathic thrombocytopenia purpura: long-term follow-upH Tamary, C Kaplinsky, I Levy, et al.
Journal of Pediatric Hematology/Oncology|February 1, 1996
Hodgkin disease in children: reduced tailored chemotherapy for stage I-II diseaseI Yaniv, A Saab, I J Cohen, et al.
Pediatric Hematology and Oncology|January 1, 1990
Infantile idiopathic thrombocytopenic purpuraA Ballin, G Kenet, H Tamary, et al.
European Journal of Haematology|June 19, 2002
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adultsH Shalev, Y Kapleushnik, L Haeskelzon, et al.
British Journal of Haematology|September 21, 2001
Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and IIIE Zdebska, E Gołaszewska, J Fabijańska-Mitek, et al.
Medical and Pediatric Oncology|January 1, 1992
T-cell acute lymphoblastic leukemia following therapy of rhabdomyosarcomaC Kaplinsky, A Frisch, I J Cohen, et al.
Pediatric Hematology and Oncology|July 1, 1992
Childhood malignant thymoma: clinical, therapeutic, and immunohistochemical considerationsC Kaplinsky, C Mor, I J Cohen, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 1, 1994
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygousF Galacteros, E Girodon, A M'Rad, et al.
Radiology|May 1, 1991
Hepatic iron overload: quantitative MR imagingJ M Gomori, G Horev, H Tamary, et al.
American Journal of Human Genetics|May 23, 1998
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3H Tamary, L Shalmon, H Shalev, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1994
Chronic childhood idiopathic thrombocytopenia purpura: long-term follow-upH Tamary, C Kaplinsky, I Levy, et al.
Journal of Pediatric Hematology/Oncology|February 1, 1996
Hodgkin disease in children: reduced tailored chemotherapy for stage I-II diseaseI Yaniv, A Saab, I J Cohen, et al.
Pediatric Hematology and Oncology|January 1, 1990
Infantile idiopathic thrombocytopenic purpuraA Ballin, G Kenet, H Tamary, et al.
European Journal of Haematology|June 19, 2002
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adultsH Shalev, Y Kapleushnik, L Haeskelzon, et al.
British Journal of Haematology|September 21, 2001
Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and IIIE Zdebska, E Gołaszewska, J Fabijańska-Mitek, et al.
Medical and Pediatric Oncology|January 1, 1992
T-cell acute lymphoblastic leukemia following therapy of rhabdomyosarcomaC Kaplinsky, A Frisch, I J Cohen, et al.
Pediatric Hematology and Oncology|July 1, 1992
Childhood malignant thymoma: clinical, therapeutic, and immunohistochemical considerationsC Kaplinsky, C Mor, I J Cohen, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 1, 1994
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygousF Galacteros, E Girodon, A M'Rad, et al.
Radiology|May 1, 1991
Hepatic iron overload: quantitative MR imagingJ M Gomori, G Horev, H Tamary, et al.
American Journal of Human Genetics|May 23, 1998
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3H Tamary, L Shalmon, H Shalev, et al.
Pageof 5