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Lilach Shemer-Meiri

Showing results (1-10 of 7) with videos related to

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Epilepsy Research and Treatment|September 1, 2012
The ketogenic diet 2011: how it worksKeren Politi, Lilach Shemer-Meiri, Avinoam Shuper, et al.
Children (Basel, Switzerland)|August 26, 2023
Neurodevelopmental Outcome of Very Low Birth Weight Infants in the Northern District of Israel: A Cross-Sectional StudyMichal Molad, Ayala Gover, Zaki Marai, et al.
Molecular Genetics and Metabolism|November 12, 2013
Man made disease: clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse studyBen Pode-Shakked, Lilach Shemer-Meiri, Alon Harmelin, et al.
Frontiers in Pediatrics|June 1, 2026
Long-term headaches in children with idiopathic intracranial hypertension-a 10 years follow-upJacob Genizi, Moran Cymbrowicz, Lilach Shemer-Meiri, et al.
Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Brain : a Journal of Neurology|January 25, 2018
De novo mutations in GRIN1 cause extensive bilateral polymicrogyriaAndrew E Fry, Katherine A Fawcett, Nathanel Zelnik, et al.
Brain : a Journal of Neurology|April 4, 2022
Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsyMarieke M van der Knoop, Reza Maroofian, Yuko Fukata, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Epilepsy Research and Treatment|September 1, 2012
The ketogenic diet 2011: how it worksKeren Politi, Lilach Shemer-Meiri, Avinoam Shuper, et al.
Children (Basel, Switzerland)|August 26, 2023
Neurodevelopmental Outcome of Very Low Birth Weight Infants in the Northern District of Israel: A Cross-Sectional StudyMichal Molad, Ayala Gover, Zaki Marai, et al.
Molecular Genetics and Metabolism|November 12, 2013
Man made disease: clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse studyBen Pode-Shakked, Lilach Shemer-Meiri, Alon Harmelin, et al.
Frontiers in Pediatrics|June 1, 2026
Long-term headaches in children with idiopathic intracranial hypertension-a 10 years follow-upJacob Genizi, Moran Cymbrowicz, Lilach Shemer-Meiri, et al.
Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Brain : a Journal of Neurology|January 25, 2018
De novo mutations in GRIN1 cause extensive bilateral polymicrogyriaAndrew E Fry, Katherine A Fawcett, Nathanel Zelnik, et al.
Brain : a Journal of Neurology|April 4, 2022
Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsyMarieke M van der Knoop, Reza Maroofian, Yuko Fukata, et al.
Pageof 1