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A Shalev

Showing results (121-130 of 193) with videos related to

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Prenatal Diagnosis|August 24, 2006
Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndromeS A Shalev, E Shalev, E Pras, et al.
Molecular Vision|December 13, 2012
A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophyBen Cohen, Elena Chervinsky, Haneen Jabaly-Habib, et al.
Transplantation|March 13, 2012
Association of cytomegalovirus infection and disease with recurrent hepatitis C after liver transplantationWendelyn Bosch, Michael G Heckman, Surakit Pungpapong, et al.
Journal of Inherited Metabolic Disease|March 21, 2007
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutationR Spiegel, A Shaag, A Gutman, et al.
Muscle & Nerve|August 22, 2009
Myotonia congenita in a large consanguineous Arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel CLCN1 geneAdel Shalata, Haya Furman, Vardit Adir, 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 cytomegalovirus infection and disease with death and graft loss after liver transplant in high-risk recipientsW Bosch, M G Heckman, N N Diehl, et al.
European Journal of Clinical Investigation|November 27, 2012
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemiaGianluca Caridi, Monica Dagnino, Francesca Lugani, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1983
Evidence for beta 2-microglobulin-like and H-2-like antigenic determinants in DrosophilaA Shalev, M Pla, T Ginsburger-Vogel, et al.
Clinical and Experimental Rheumatology|January 16, 2010
A painful train of events: increased prevalence of fibromyalgia in survivors of a major train crashD Buskila, J N Ablin, I Ben-Zion, et al.
Gene|December 14, 2012
A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathyZeynep Atay, Abdullah Bereket, Serap Turan, et al.
Pageof 20

Showing results (121-130 of 193) with videos related to

Sort By:
Pageof 20
Prenatal Diagnosis|August 24, 2006
Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndromeS A Shalev, E Shalev, E Pras, et al.
Molecular Vision|December 13, 2012
A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophyBen Cohen, Elena Chervinsky, Haneen Jabaly-Habib, et al.
Transplantation|March 13, 2012
Association of cytomegalovirus infection and disease with recurrent hepatitis C after liver transplantationWendelyn Bosch, Michael G Heckman, Surakit Pungpapong, et al.
Journal of Inherited Metabolic Disease|March 21, 2007
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutationR Spiegel, A Shaag, A Gutman, et al.
Muscle & Nerve|August 22, 2009
Myotonia congenita in a large consanguineous Arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel CLCN1 geneAdel Shalata, Haya Furman, Vardit Adir, 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 cytomegalovirus infection and disease with death and graft loss after liver transplant in high-risk recipientsW Bosch, M G Heckman, N N Diehl, et al.
European Journal of Clinical Investigation|November 27, 2012
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemiaGianluca Caridi, Monica Dagnino, Francesca Lugani, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1983
Evidence for beta 2-microglobulin-like and H-2-like antigenic determinants in DrosophilaA Shalev, M Pla, T Ginsburger-Vogel, et al.
Clinical and Experimental Rheumatology|January 16, 2010
A painful train of events: increased prevalence of fibromyalgia in survivors of a major train crashD Buskila, J N Ablin, I Ben-Zion, et al.
Gene|December 14, 2012
A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathyZeynep Atay, Abdullah Bereket, Serap Turan, et al.
Pageof 20