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Esther Leshinsky-Silver

Showing results (31-40 of 69) with videos related to

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The American Journal of Gastroenterology|January 26, 2005
A polymorphism in the TNF-alpha promoter gene is associated with pediatric onset and colonic location of Crohn's diseaseArie Levine, Amir Karban, Rami Eliakim, et al.
The Israel Medical Association Journal : IMAJ|March 21, 2006
Candidate gene polymorphism in cardiovascular disease: the BIP cohortEsther Leshinsky-Silver, Suzanne Cheng, Michael A Grow, et al.
Hormone Research|May 31, 2006
Congenital hyperreninemic hypoaldosteronism in Israel: sequence analysis of CYP11B2 geneEsther Leshinsky-Silver, Zohar Landau, Sema Unlubay, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasmsDorit Lev, Yuval Weigl, Mariana Hasan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Clinical Immunology (Orlando, Fla.)|June 1, 2011
Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndromeIlan Dalal, Diana Tasher, Raz Somech, et al.
American Journal of Medical Genetics. Part A|May 16, 2012
Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative regionMarina Michelson, Anat Ben-Sasson, Chana Vinkler, et al.
Acta Neuropathologica|July 4, 2012
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutationJohann Böhm, Esther Leshinsky-Silver, Stéphane Vassilopoulos, et al.
Fetal Diagnosis and Therapy|October 7, 2016
Familial Brain Periventricular PseudocystsShiri Shinar, Gustavo Malinger, Zvi Leibovitz, et al.
Digestive Diseases and Sciences|July 3, 2008
Disease behavior in children with Crohn's disease: the effect of disease duration, ethnicity, genotype, and phenotypeRon Shaoul, Amir Karban, Shimon Reif, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
The American Journal of Gastroenterology|January 26, 2005
A polymorphism in the TNF-alpha promoter gene is associated with pediatric onset and colonic location of Crohn's diseaseArie Levine, Amir Karban, Rami Eliakim, et al.
The Israel Medical Association Journal : IMAJ|March 21, 2006
Candidate gene polymorphism in cardiovascular disease: the BIP cohortEsther Leshinsky-Silver, Suzanne Cheng, Michael A Grow, et al.
Hormone Research|May 31, 2006
Congenital hyperreninemic hypoaldosteronism in Israel: sequence analysis of CYP11B2 geneEsther Leshinsky-Silver, Zohar Landau, Sema Unlubay, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasmsDorit Lev, Yuval Weigl, Mariana Hasan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Clinical Immunology (Orlando, Fla.)|June 1, 2011
Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndromeIlan Dalal, Diana Tasher, Raz Somech, et al.
American Journal of Medical Genetics. Part A|May 16, 2012
Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative regionMarina Michelson, Anat Ben-Sasson, Chana Vinkler, et al.
Acta Neuropathologica|July 4, 2012
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutationJohann Böhm, Esther Leshinsky-Silver, Stéphane Vassilopoulos, et al.
Fetal Diagnosis and Therapy|October 7, 2016
Familial Brain Periventricular PseudocystsShiri Shinar, Gustavo Malinger, Zvi Leibovitz, et al.
Digestive Diseases and Sciences|July 3, 2008
Disease behavior in children with Crohn's disease: the effect of disease duration, ethnicity, genotype, and phenotypeRon Shaoul, Amir Karban, Shimon Reif, et al.
Pageof 7