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Epilepsy Research and Treatment
|
September 1, 2012
The ketogenic diet 2011: how it works
Keren 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 Study
Michal 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 study
Ben 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-up
Jacob 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 palsy
Michal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Brain : a Journal of Neurology
|
January 25, 2018
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
Andrew 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 epilepsy
Marieke M van der Knoop, Reza Maroofian, Yuko Fukata, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Epilepsy Research and Treatment
|
September 1, 2012
The ketogenic diet 2011: how it works
Keren 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 Study
Michal 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 study
Ben 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-up
Jacob 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 palsy
Michal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Brain : a Journal of Neurology
|
January 25, 2018
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
Andrew 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 epilepsy
Marieke M van der Knoop, Reza Maroofian, Yuko Fukata, et al.
Page
of 1