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Manoj P Menezes

Showing results (51-60 of 68) with videos related to

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JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Ebiomedicine|September 29, 2022
Decreased cerebrospinal fluid kynurenic acid in epileptic spasms: A biomarker of response to corticosteroidsJingya Yan, Kavitha Kothur, Emily A Innes, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 10, 2022
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth diseaseEppie M Yiu, Paula Bray, Jonathan Baets, et al.
Brain : a Journal of Neurology|January 17, 2019
Erratum to: Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Brain : a Journal of Neurology|November 27, 2018
Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Ebiomedicine|April 29, 2023
CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammationJingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Charcot-Marie-Tooth disease type 1E: Clinical Natural History and Molecular Impact of <i>PMP22</i> VariantsKailee S Ward, Christopher P Ptak, Natalya Pashkova, et al.
Brain : a Journal of Neurology|June 9, 2025
Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of PMP22 variantsKailee S Ward, Christopher P Ptak, Natalya Pashkova, et al.
Neurology|September 8, 2021
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Sarah P Garnett, Kayla M D Cornett, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Ebiomedicine|September 29, 2022
Decreased cerebrospinal fluid kynurenic acid in epileptic spasms: A biomarker of response to corticosteroidsJingya Yan, Kavitha Kothur, Emily A Innes, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 10, 2022
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth diseaseEppie M Yiu, Paula Bray, Jonathan Baets, et al.
Brain : a Journal of Neurology|January 17, 2019
Erratum to: Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Brain : a Journal of Neurology|November 27, 2018
Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Ebiomedicine|April 29, 2023
CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammationJingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Charcot-Marie-Tooth disease type 1E: Clinical Natural History and Molecular Impact of <i>PMP22</i> VariantsKailee S Ward, Christopher P Ptak, Natalya Pashkova, et al.
Brain : a Journal of Neurology|June 9, 2025
Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of PMP22 variantsKailee S Ward, Christopher P Ptak, Natalya Pashkova, et al.
Neurology|September 8, 2021
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Sarah P Garnett, Kayla M D Cornett, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.
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