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H Tamary

Showing results (11-20 of 47) with videos related to

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The Journal of Pediatrics|July 1, 1997
Neonatal manifestations of congenital dyserythropoietic anemia type IH Shalev, H Tamary, D Shaft, et al.
Bulletin (Hospital for Joint Diseases (New York, N.Y.))|March 11, 2000
Increased operative bleeding during orthopaedic surgery in patients with type I Gaucher disease and bone involvementK Katz, H Tamary, J Lahav, et al.
Therapeutic Drug Monitoring|January 1, 1985
Analysis of 6-mercaptopurine in serum or plasma using high performance liquid chromatographyC E Whalen, H Tamary, M Greenberg, et al.
Pediatric Hematology and Oncology|February 24, 2001
Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasisD Marom, I Offer, H Tamary, et al.
Israel Journal of Medical Sciences|August 1, 1994
Ambulatory treatment with ceftriaxone in febrile neutropenic childrenC Kaplinsky, M Drucker, J Goshen, et al.
Transfusion|May 1, 1998
Viremia, genetic heterogeneity, and immunity to hepatitis G/GB-C virus in multiply transfused patients with thalassemiaR Zemel, R Dickman, H Tamary, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patientsY Fromovich-Amit, A Zivelin, N Rosenberg, et al.
The Journal of Pediatrics|June 1, 1982
GM1 gangliosidosis presenting as neonatal ascitesK I Abu-Dalu, H Tamary, N Livni, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 14, 1997
Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP)H Tamary, S Surrey, J Augustine, et al.
Annals of the New York Academy of Sciences|July 21, 1998
The diverse molecular basis and mild clinical picture of HbH disease in IsraelH Tamary, G Klinger, L Shalmon, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|July 1, 1997
Neonatal manifestations of congenital dyserythropoietic anemia type IH Shalev, H Tamary, D Shaft, et al.
Bulletin (Hospital for Joint Diseases (New York, N.Y.))|March 11, 2000
Increased operative bleeding during orthopaedic surgery in patients with type I Gaucher disease and bone involvementK Katz, H Tamary, J Lahav, et al.
Therapeutic Drug Monitoring|January 1, 1985
Analysis of 6-mercaptopurine in serum or plasma using high performance liquid chromatographyC E Whalen, H Tamary, M Greenberg, et al.
Pediatric Hematology and Oncology|February 24, 2001
Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasisD Marom, I Offer, H Tamary, et al.
Israel Journal of Medical Sciences|August 1, 1994
Ambulatory treatment with ceftriaxone in febrile neutropenic childrenC Kaplinsky, M Drucker, J Goshen, et al.
Transfusion|May 1, 1998
Viremia, genetic heterogeneity, and immunity to hepatitis G/GB-C virus in multiply transfused patients with thalassemiaR Zemel, R Dickman, H Tamary, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patientsY Fromovich-Amit, A Zivelin, N Rosenberg, et al.
The Journal of Pediatrics|June 1, 1982
GM1 gangliosidosis presenting as neonatal ascitesK I Abu-Dalu, H Tamary, N Livni, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 14, 1997
Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP)H Tamary, S Surrey, J Augustine, et al.
Annals of the New York Academy of Sciences|July 21, 1998
The diverse molecular basis and mild clinical picture of HbH disease in IsraelH Tamary, G Klinger, L Shalmon, et al.
Pageof 5