Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ayelet Eran

Showing results (41-50 of 57) with videos related to

Pageof 6
Sort By:
Molecular Genetics & Genomic Medicine|December 31, 2021
Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variantsLimor Kalfon, Meirav Baydany, Nadra Samra, et al.
Brain Communications|June 24, 2026
Personalized tremor control targeting for MR-guided focused ultrasound using tractographyNoam Shalem, Alon Sinai, Gil Zur, et al.
Obesity Facts|July 26, 2021
Bariatric Surgery-Associated MyelopathySewar Asakly, Ramit Magen-Rimon, Ahmad Ighbariya, et al.
Human Genetics|January 23, 2015
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5Daniella Magen, Ayala Ofir, Liron Berger, et al.
Metabolic Brain Disease|January 15, 2019
Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and reviewYoav Zehavi, Hanna Mandel, Ayelet Eran, et al.
Human Genetics|January 7, 2015
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5Daniella Magen, Ayala Ofir, Liron Berger, et al.
Journal of Human Genetics|February 17, 2017
Erratum: PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorderTakeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, et al.
Journal of Human Genetics|January 13, 2017
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorderTakeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, et al.
Neurology|May 3, 2015
Absence of α- and β-dystroglycan is associated with Walker-Warburg syndromeMoniek Riemersma, Hanna Mandel, Ellen van Beusekom, et al.
Clinical Genetics|July 20, 2020
COG6-CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex developmentHanna Mandel, Nehama Cohen Kfir, Ayalla Fedida, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Molecular Genetics & Genomic Medicine|December 31, 2021
Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variantsLimor Kalfon, Meirav Baydany, Nadra Samra, et al.
Brain Communications|June 24, 2026
Personalized tremor control targeting for MR-guided focused ultrasound using tractographyNoam Shalem, Alon Sinai, Gil Zur, et al.
Obesity Facts|July 26, 2021
Bariatric Surgery-Associated MyelopathySewar Asakly, Ramit Magen-Rimon, Ahmad Ighbariya, et al.
Human Genetics|January 23, 2015
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5Daniella Magen, Ayala Ofir, Liron Berger, et al.
Metabolic Brain Disease|January 15, 2019
Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and reviewYoav Zehavi, Hanna Mandel, Ayelet Eran, et al.
Human Genetics|January 7, 2015
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5Daniella Magen, Ayala Ofir, Liron Berger, et al.
Journal of Human Genetics|February 17, 2017
Erratum: PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorderTakeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, et al.
Journal of Human Genetics|January 13, 2017
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorderTakeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, et al.
Neurology|May 3, 2015
Absence of α- and β-dystroglycan is associated with Walker-Warburg syndromeMoniek Riemersma, Hanna Mandel, Ellen van Beusekom, et al.
Clinical Genetics|July 20, 2020
COG6-CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex developmentHanna Mandel, Nehama Cohen Kfir, Ayalla Fedida, et al.
Pageof 6