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A Shalev

Showing results (161-170 of 193) with videos related to

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Journal of Child and Adolescent Psychopharmacology|May 28, 2026
A Phase-2 Open-Label Trial of Cannabidiol to Treat Core and Associated Symptoms of Autism in Children and Adolescents Without Intellectual DisabilityJacqueline Lawson, Lauren Robinson, Greta R Conlon, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
The clinical spectrum of fetal Niemann-Pick type CRonen Spiegel, Annick Raas-Rothschild, Orit Reish, et al.
European Journal of Human Genetics : EJHG|January 16, 2014
Delineation of C12orf65-related phenotypes: a genotype-phenotype relationshipRonen Spiegel, Hanna Mandel, Ann Saada, et al.
Clinical Genetics|July 23, 2021
The landscape of autosomal recessive variants in an isolated community: Implications for population screening for reproductive purposesMorad Khayat, Nada Danial-Farran, Elena Chervinsky, et al.
Journal of Community Genetics|December 19, 2023
Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli populationChen Gafni-Amsalem, Olfat Aboleil-Zoubi, Elena Chervinsky, et al.
Journal of Genetic Counseling|August 26, 2023
The effect of a prior e-learning tool on genetic counseling outcomes in diverse ethnic couples with abnormal Down syndrome screening tests: A randomized controlled trialOlfat Aboleil-Zoubi, Chen Gafni-Amsalem, Lilach Peled-Perets, et al.
European Journal of Human Genetics : EJHG|August 25, 2018
Genetics of hearing loss in the Arab population of Northern IsraelNada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, et al.
Epilepsia|May 19, 2007
Founder effect with variable age at onset in Arab families with Lafora disease and EPM2A mutationCristina Gomez-Abad, Zaid Afawi, Amos D Korczyn, et al.
Transplantation|May 9, 2009
Surgical site infection after liver transplantation: risk factors and association with graft loss or deathWalter C Hellinger, Julia E Crook, Michael G Heckman, et al.
American Journal of Human Genetics|April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosaRob W J Collin, Christine Safieh, Karin W Littink, et al.
Pageof 20

Showing results (161-170 of 193) with videos related to

Sort By:
Pageof 20
Journal of Child and Adolescent Psychopharmacology|May 28, 2026
A Phase-2 Open-Label Trial of Cannabidiol to Treat Core and Associated Symptoms of Autism in Children and Adolescents Without Intellectual DisabilityJacqueline Lawson, Lauren Robinson, Greta R Conlon, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
The clinical spectrum of fetal Niemann-Pick type CRonen Spiegel, Annick Raas-Rothschild, Orit Reish, et al.
European Journal of Human Genetics : EJHG|January 16, 2014
Delineation of C12orf65-related phenotypes: a genotype-phenotype relationshipRonen Spiegel, Hanna Mandel, Ann Saada, et al.
Clinical Genetics|July 23, 2021
The landscape of autosomal recessive variants in an isolated community: Implications for population screening for reproductive purposesMorad Khayat, Nada Danial-Farran, Elena Chervinsky, et al.
Journal of Community Genetics|December 19, 2023
Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli populationChen Gafni-Amsalem, Olfat Aboleil-Zoubi, Elena Chervinsky, et al.
Journal of Genetic Counseling|August 26, 2023
The effect of a prior e-learning tool on genetic counseling outcomes in diverse ethnic couples with abnormal Down syndrome screening tests: A randomized controlled trialOlfat Aboleil-Zoubi, Chen Gafni-Amsalem, Lilach Peled-Perets, et al.
European Journal of Human Genetics : EJHG|August 25, 2018
Genetics of hearing loss in the Arab population of Northern IsraelNada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, et al.
Epilepsia|May 19, 2007
Founder effect with variable age at onset in Arab families with Lafora disease and EPM2A mutationCristina Gomez-Abad, Zaid Afawi, Amos D Korczyn, et al.
Transplantation|May 9, 2009
Surgical site infection after liver transplantation: risk factors and association with graft loss or deathWalter C Hellinger, Julia E Crook, Michael G Heckman, et al.
American Journal of Human Genetics|April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosaRob W J Collin, Christine Safieh, Karin W Littink, et al.
Pageof 20