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Rony Cohen

Showing results (31-40 of 36) with videos related to

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Journal of Neurology|August 24, 2014
Novel EXOSC3 mutation causes complicated hereditary spastic paraplegiaAyelet Halevy, Israela Lerer, Rony Cohen, et al.
Children (Basel, Switzerland)|July 29, 2023
High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri SyndromeJacob Genizi, Lotan Berger, Muhammad Mahajnah, 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 Neurology|October 14, 2015
Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasiaKarl Martin Klein, Manuela Pendziwiat, Rony Cohen, et al.
Neuromuscular Disorders : NMD|December 28, 2016
Congenital myasthenic syndrome in Israel: Genetic and clinical characterizationSharon Aharoni, Menachem Sadeh, Yehuda Shapira, et al.
American Journal of Human Genetics|July 31, 2020
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA ProcessingAnna Fliedner, Philipp Kirchner, Antje Wiesener, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Journal of Neurology|August 24, 2014
Novel EXOSC3 mutation causes complicated hereditary spastic paraplegiaAyelet Halevy, Israela Lerer, Rony Cohen, et al.
Children (Basel, Switzerland)|July 29, 2023
High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri SyndromeJacob Genizi, Lotan Berger, Muhammad Mahajnah, 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 Neurology|October 14, 2015
Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasiaKarl Martin Klein, Manuela Pendziwiat, Rony Cohen, et al.
Neuromuscular Disorders : NMD|December 28, 2016
Congenital myasthenic syndrome in Israel: Genetic and clinical characterizationSharon Aharoni, Menachem Sadeh, Yehuda Shapira, et al.
American Journal of Human Genetics|July 31, 2020
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA ProcessingAnna Fliedner, Philipp Kirchner, Antje Wiesener, et al.
Pageof 4