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Arthavan Selvanathan

Showing results (1-10 of 23) 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 Pediatric Gastroenterology and Nutrition|April 9, 2020
Ornithine Transcarbamylase Deficiency Presenting as Acute Liver Failure in Girls: A Paediatric Case SeriesArthavan Selvanathan, Ashley Hertzog, Daniel A Lemberg, et al.
Translational Pediatrics|November 8, 2022
A narrative review of metabolomics in the era of "-omics": integration into clinical practice for inborn errors of metabolismAshley Hertzog, Arthavan Selvanathan, Beena Devanapalli, et al.
Journal of Inherited Metabolic Disease|January 12, 2026
The History and Nosology of the Glycine Disorders: A Framework for CliniciansArthavan Selvanathan, Ashley Hertzog, Curtis R Coughlin, et al.
JIMD Reports|September 6, 2021
Effectiveness of early hematopoietic stem cell transplantation in preventing neurocognitive decline in aspartylglucosaminuria: A case seriesArthavan Selvanathan, Jane Kinsella, Francesca Moore, et al.
JIMD Reports|April 29, 2026
Clinical Outcomes and Correlation With Biochemical Control in Hydroxocobalamin-Treated Patients With Early-Onset Cobalamin C DiseaseArthavan Selvanathan, Ashley Hertzog, Jacqui Russell, et al.
Frontiers in Genetics|December 23, 2022
Intronic variants in inborn errors of metabolism: Beyond the exomeAshley Hertzog, Arthavan Selvanathan, Elizabeth Farnsworth, et al.
JIMD Reports|November 7, 2022
3-Methylglutaconyl-CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosisAshley Hertzog, Arthavan Selvanathan, Dinusha Pandithan, et al.
JIMD Reports|July 13, 2022
A serendipitous journey to a promoter variant: The c.-106C>A variant and its role in late-onset ornithine transcarbamylase deficiencyAshley Hertzog, Arthavan Selvanathan, Rebecca Halligan, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
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 Pediatric Gastroenterology and Nutrition|April 9, 2020
Ornithine Transcarbamylase Deficiency Presenting as Acute Liver Failure in Girls: A Paediatric Case SeriesArthavan Selvanathan, Ashley Hertzog, Daniel A Lemberg, et al.
Translational Pediatrics|November 8, 2022
A narrative review of metabolomics in the era of "-omics": integration into clinical practice for inborn errors of metabolismAshley Hertzog, Arthavan Selvanathan, Beena Devanapalli, et al.
Journal of Inherited Metabolic Disease|January 12, 2026
The History and Nosology of the Glycine Disorders: A Framework for CliniciansArthavan Selvanathan, Ashley Hertzog, Curtis R Coughlin, et al.
JIMD Reports|September 6, 2021
Effectiveness of early hematopoietic stem cell transplantation in preventing neurocognitive decline in aspartylglucosaminuria: A case seriesArthavan Selvanathan, Jane Kinsella, Francesca Moore, et al.
JIMD Reports|April 29, 2026
Clinical Outcomes and Correlation With Biochemical Control in Hydroxocobalamin-Treated Patients With Early-Onset Cobalamin C DiseaseArthavan Selvanathan, Ashley Hertzog, Jacqui Russell, et al.
Frontiers in Genetics|December 23, 2022
Intronic variants in inborn errors of metabolism: Beyond the exomeAshley Hertzog, Arthavan Selvanathan, Elizabeth Farnsworth, et al.
JIMD Reports|November 7, 2022
3-Methylglutaconyl-CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosisAshley Hertzog, Arthavan Selvanathan, Dinusha Pandithan, et al.
JIMD Reports|July 13, 2022
A serendipitous journey to a promoter variant: The c.-106C>A variant and its role in late-onset ornithine transcarbamylase deficiencyAshley Hertzog, Arthavan Selvanathan, Rebecca Halligan, et al.
Pageof 3