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Bindu Parayil Sankaran

Showing results (1-10 of 18) with videos related to

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Mitochondrion|October 23, 2021
Mitochondrial iron-sulfur cluster biogenesis and neurological disordersArthavan Selvanathan, Bindu Parayil Sankaran
Journal of Pediatric Hematology/Oncology|June 10, 2024
Hematologic Manifestations in Primary Mitochondrial DiseasesArthavan Selvanathan, Juliana Teo, Bindu Parayil Sankaran
Journal of the American Academy of Audiology|June 15, 2022
Audiological Findings in Children with PLA2G6-Associated NeurodegenerationValiyaparambath Purushothaman Vandana, Jeevendra Kumar Darshini, Bindu Parayil Sankaran
Neurology|August 11, 2021
Teaching NeuroImage: Bilateral Nucleus Tractus Solitarius Lesions in Neurogenic Respiratory FailureBindu Parayil Sankaran, Saskia B Wortmann, Michel A Willemsen, et al.
Journal of Paediatrics and Child Health|February 15, 2021
Purpuric, delayed child: Beyond septicaemia and into inborn errors of metabolismAshley Hertzog, Arthavan Selvanathan, Adviye A Tolun, et al.
Orphanet Journal of Rare Diseases|November 4, 2021
GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcomeBindu Parayil Sankaran, Sachin Gupta, Michel Tchan, et al.
Neurology|April 24, 2021
Child Neurology: Hereditary Folate MalabsorptionAkshata Huddar, Shwetha Chiplunkar, Madhu Nagappa, et al.
Journal of Child Neurology|March 18, 2020
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene PanelBindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar, et al.
Mitochondrion|February 27, 2021
Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteomeGajanan Sathe, Sekar Deepha, Narayanappa Gayathri, et al.
Brain & Development|May 8, 2023
Developmental delay and non-phenylketonuria (PKU) hyperphenylalaninemia in DNAJC12 deficiency: Case and approachRachel Sze Hui Wong, Shekeeb Mohammad, Bindu Parayil Sankaran, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Mitochondrion|October 23, 2021
Mitochondrial iron-sulfur cluster biogenesis and neurological disordersArthavan Selvanathan, Bindu Parayil Sankaran
Journal of Pediatric Hematology/Oncology|June 10, 2024
Hematologic Manifestations in Primary Mitochondrial DiseasesArthavan Selvanathan, Juliana Teo, Bindu Parayil Sankaran
Journal of the American Academy of Audiology|June 15, 2022
Audiological Findings in Children with PLA2G6-Associated NeurodegenerationValiyaparambath Purushothaman Vandana, Jeevendra Kumar Darshini, Bindu Parayil Sankaran
Neurology|August 11, 2021
Teaching NeuroImage: Bilateral Nucleus Tractus Solitarius Lesions in Neurogenic Respiratory FailureBindu Parayil Sankaran, Saskia B Wortmann, Michel A Willemsen, et al.
Journal of Paediatrics and Child Health|February 15, 2021
Purpuric, delayed child: Beyond septicaemia and into inborn errors of metabolismAshley Hertzog, Arthavan Selvanathan, Adviye A Tolun, et al.
Orphanet Journal of Rare Diseases|November 4, 2021
GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcomeBindu Parayil Sankaran, Sachin Gupta, Michel Tchan, et al.
Neurology|April 24, 2021
Child Neurology: Hereditary Folate MalabsorptionAkshata Huddar, Shwetha Chiplunkar, Madhu Nagappa, et al.
Journal of Child Neurology|March 18, 2020
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene PanelBindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar, et al.
Mitochondrion|February 27, 2021
Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteomeGajanan Sathe, Sekar Deepha, Narayanappa Gayathri, et al.
Brain & Development|May 8, 2023
Developmental delay and non-phenylketonuria (PKU) hyperphenylalaninemia in DNAJC12 deficiency: Case and approachRachel Sze Hui Wong, Shekeeb Mohammad, Bindu Parayil Sankaran, et al.
Pageof 2