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A Shalev

Showing results (151-160 of 193) with videos related to

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American Journal of Infection Control|June 25, 2011
Glucose meters and opportunities for in-hospital transmission of infection: Quantitative assessment and management with and without patient assignmentWalter C Hellinger, Rhonda L Grant, Debra A Hernke, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|April 23, 2014
Surgical site infections after liver retransplantation: incidence and risk factorsHarshal Shah, Walter C Hellinger, Michael G Heckman, et al.
American Journal of Human Genetics|August 6, 2008
Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9Ortal Barel, Stavit A Shalev, Rivka Ofir, et al.
The Journal of Biological Chemistry|July 18, 2001
Saccharomyces cerevisiae protein Pci8p and human protein eIF3e/Int-6 interact with the eIF3 core complex by binding to cognate eIF3b subunitsA Shalev, L Valásek, C A Pise-Masison, et al.
European Journal of Medical Genetics|October 2, 2014
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 geneHanna Mandel, Ksenya Cohen Katsanelson, Morad Khayat, et al.
Blood|September 1, 1992
Quantification of a novel dense granule protein (granulophysin) in platelets of patients with dense granule storage pool deficiencyA Shalev, G Michaud, S J Israels, et al.
American Journal of Medical Genetics. Part A|May 7, 2016
KCNK9 imprinting syndrome-further delineation of a possible treatable disorderJohn M Graham, Neda Zadeh, Melissa Kelley, et al.
Journal of Medical Genetics|December 15, 2010
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndromeRonen Spiegel, Morad Khayat, Stavit A Shalev, et al.
European Journal of Medical Genetics|July 13, 2010
Expanding the clinical spectrum of SLC29A3 gene defectsRonen Spiegel, Simon T Cliffe, Michael F Buckley, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 11, 2011
Association of surgeon with surgical site infection after liver transplantationW C Hellinger, M G Heckman, J E Crook, et al.
Pageof 20

Showing results (151-160 of 193) with videos related to

Sort By:
Pageof 20
American Journal of Infection Control|June 25, 2011
Glucose meters and opportunities for in-hospital transmission of infection: Quantitative assessment and management with and without patient assignmentWalter C Hellinger, Rhonda L Grant, Debra A Hernke, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|April 23, 2014
Surgical site infections after liver retransplantation: incidence and risk factorsHarshal Shah, Walter C Hellinger, Michael G Heckman, et al.
American Journal of Human Genetics|August 6, 2008
Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9Ortal Barel, Stavit A Shalev, Rivka Ofir, et al.
The Journal of Biological Chemistry|July 18, 2001
Saccharomyces cerevisiae protein Pci8p and human protein eIF3e/Int-6 interact with the eIF3 core complex by binding to cognate eIF3b subunitsA Shalev, L Valásek, C A Pise-Masison, et al.
European Journal of Medical Genetics|October 2, 2014
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 geneHanna Mandel, Ksenya Cohen Katsanelson, Morad Khayat, et al.
Blood|September 1, 1992
Quantification of a novel dense granule protein (granulophysin) in platelets of patients with dense granule storage pool deficiencyA Shalev, G Michaud, S J Israels, et al.
American Journal of Medical Genetics. Part A|May 7, 2016
KCNK9 imprinting syndrome-further delineation of a possible treatable disorderJohn M Graham, Neda Zadeh, Melissa Kelley, et al.
Journal of Medical Genetics|December 15, 2010
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndromeRonen Spiegel, Morad Khayat, Stavit A Shalev, et al.
European Journal of Medical Genetics|July 13, 2010
Expanding the clinical spectrum of SLC29A3 gene defectsRonen Spiegel, Simon T Cliffe, Michael F Buckley, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 11, 2011
Association of surgeon with surgical site infection after liver transplantationW C Hellinger, M G Heckman, J E Crook, et al.
Pageof 20