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Rony Cohen

Showing results (21-30 of 36) with videos related to

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Frontiers in Neurology|January 9, 2019
Use of Optical Coherence Tomography to Detect Retinal Nerve Fiber Loss in Children With Optic Pathway GliomaAlon Zahavi, Helen Toledano, Rony Cohen, et al.
Brain Sciences|February 25, 2023
Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor CerebriRony Cohen, Muhammad Mahajnah, Yulia Shlonsky, et al.
Neurogenetics|September 16, 2016
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2ARony Cohen, Ayelet Halevy, Sharon Aharoni, et al.
Seizure|February 5, 2011
The mystery of electroencephalography in acute lymphoblastic leukemiaHadassa Goldberg-Stern, Rony Cohen, Lea Pollak, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 22, 2021
Trametinib for orbital plexiform neurofibromas in young children with neurofibromatosis type 1Helen Toledano, Gad Dotan, Rivka Friedland, et al.
Neuropediatrics|November 29, 2013
Christianson syndrome: spectrum of neuroimaging findingsThangamadhan Bosemani, Ginevra Zanni, Adam L Hartman, et al.
Clinical Genetics|November 16, 2019
The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complexMika Shapira Rootman, Yael Goldberg, Rony Cohen, et al.
Gene Therapy|April 27, 2022
Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec -routine care evidenceSharon Aharoni, Jacob Bistritzer, Hagit Levine, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2014
Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22Rony Cohen, Lina Basel-Vanagaite, Hadassah Goldberg-Stern, et al.
Neuromuscular Disorders : NMD|November 21, 2020
Impact of a national population-based carrier-screening program on spinal muscular atrophy birthsSharon Aharoni, Yoram Nevo, Naama Orenstein, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Frontiers in Neurology|January 9, 2019
Use of Optical Coherence Tomography to Detect Retinal Nerve Fiber Loss in Children With Optic Pathway GliomaAlon Zahavi, Helen Toledano, Rony Cohen, et al.
Brain Sciences|February 25, 2023
Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor CerebriRony Cohen, Muhammad Mahajnah, Yulia Shlonsky, et al.
Neurogenetics|September 16, 2016
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2ARony Cohen, Ayelet Halevy, Sharon Aharoni, et al.
Seizure|February 5, 2011
The mystery of electroencephalography in acute lymphoblastic leukemiaHadassa Goldberg-Stern, Rony Cohen, Lea Pollak, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 22, 2021
Trametinib for orbital plexiform neurofibromas in young children with neurofibromatosis type 1Helen Toledano, Gad Dotan, Rivka Friedland, et al.
Neuropediatrics|November 29, 2013
Christianson syndrome: spectrum of neuroimaging findingsThangamadhan Bosemani, Ginevra Zanni, Adam L Hartman, et al.
Clinical Genetics|November 16, 2019
The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complexMika Shapira Rootman, Yael Goldberg, Rony Cohen, et al.
Gene Therapy|April 27, 2022
Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec -routine care evidenceSharon Aharoni, Jacob Bistritzer, Hagit Levine, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2014
Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22Rony Cohen, Lina Basel-Vanagaite, Hadassah Goldberg-Stern, et al.
Neuromuscular Disorders : NMD|November 21, 2020
Impact of a national population-based carrier-screening program on spinal muscular atrophy birthsSharon Aharoni, Yoram Nevo, Naama Orenstein, et al.
Pageof 4