Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Brok-Simoni

Showing results (61-70 of 73) with videos related to

Pageof 8
Sort By:
Acta Haematologica|January 1, 1989
Aplastic crisis due to human B19 parvovirus infection in red cell pyrimidine-5'-nucleotidase deficiencyG Rechavi, A Vonsover, Y Manor, et al.
British Journal of Haematology|December 1, 1995
Preferred usage of specific immunoglobulin gene segments in chronic lymphocytic leukaemia cells of three HLA-identical sistersI Hakim, N Amariglio, F Brok-Simoni, et al.
Clinical and Experimental Immunology|May 2, 2002
Activated macrophages for treating skin ulceration: gene expression in human monocytes after hypo-osmotic shockO Frenkel, E Shani, I Ben-Bassat, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 14, 1999
Plasma glutathione peroxidase deficiency and platelet insensitivity to nitric oxide in children with familial strokeG Kenet, J Freedman, B Shenkman, et al.
Leukemia|May 1, 1993
Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analysesS Izraeli, J W Janssen, O A Haas, et al.
Genome Research|May 1, 1996
The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced productsR Berger, L Theodor, J Shoham, et al.
Blood|November 9, 2000
Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13A Toren, G Rozenfeld-Granot, B Rocca, et al.
Leukemia|July 30, 2002
Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet) combined morphological and cytogenetical analysisA Shimoni, A Nagler, C Kaplinsky, et al.
Medical and Pediatric Oncology|February 1, 1997
Central nervous system involvement at diagnosis in a case of pediatric CD30+ anaplastic large cell lymphomaC Kaplinsky, A Toren, Y Neumann, et al.
Bone Marrow Transplantation|April 1, 1999
Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiencyA Toren, A Nagler, N Amariglio, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Acta Haematologica|January 1, 1989
Aplastic crisis due to human B19 parvovirus infection in red cell pyrimidine-5'-nucleotidase deficiencyG Rechavi, A Vonsover, Y Manor, et al.
British Journal of Haematology|December 1, 1995
Preferred usage of specific immunoglobulin gene segments in chronic lymphocytic leukaemia cells of three HLA-identical sistersI Hakim, N Amariglio, F Brok-Simoni, et al.
Clinical and Experimental Immunology|May 2, 2002
Activated macrophages for treating skin ulceration: gene expression in human monocytes after hypo-osmotic shockO Frenkel, E Shani, I Ben-Bassat, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 14, 1999
Plasma glutathione peroxidase deficiency and platelet insensitivity to nitric oxide in children with familial strokeG Kenet, J Freedman, B Shenkman, et al.
Leukemia|May 1, 1993
Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analysesS Izraeli, J W Janssen, O A Haas, et al.
Genome Research|May 1, 1996
The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced productsR Berger, L Theodor, J Shoham, et al.
Blood|November 9, 2000
Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13A Toren, G Rozenfeld-Granot, B Rocca, et al.
Leukemia|July 30, 2002
Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet) combined morphological and cytogenetical analysisA Shimoni, A Nagler, C Kaplinsky, et al.
Medical and Pediatric Oncology|February 1, 1997
Central nervous system involvement at diagnosis in a case of pediatric CD30+ anaplastic large cell lymphomaC Kaplinsky, A Toren, Y Neumann, et al.
Bone Marrow Transplantation|April 1, 1999
Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiencyA Toren, A Nagler, N Amariglio, et al.
Pageof 8