Stroke in a Child with Dengue Encephalopathy

por Yoganathan, Sangeetha, Sudhakar, Sniya Valsa, Priyambada, Leena, Thomas, Maya
Publicado 2017

Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India

por Muthusamy, Karthik, Thomas, Maya, Yoganathan, Sangeetha, Sudhakar, Sniya Valsa
Publicado 2019

A tropical menace of co-infection of Japanese encephalitis and neurocysticercosis in two children

por Yoganathan, Sangeetha, Sudhakar, Sniya Valsa, Thomas, Maya Mary, Yadav, Vikas Kapildeo
Publicado 2016

Clinicoradiological Spectrum of L-2-Hydroxy Glutaric Aciduria: Typical and Atypical Findings in an Indian Cohort

por Muthusamy, Karthik, Sudhakar, Sniya Valsa, Christudass, Christhunesa S, Chandran, Mahalakshmi, Thomas, Maya, Gibikote, Sridhar
Publicado 2019

Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic Encephalopathy

por YOGANATHAN, Sangeetha, SUDHAKAR, SniyaVALSA, THOMAS, Maya, KUMAR DUTTA, Atanu, DANDA, Sumita, CHANDRAN, Mahalakshmi
Publicado 2018

Menkes disease and response to copper histidine: An Indian case series

por Yoganathan, Sangeetha, Sudhakar, Sniya Valsa, Arunachal, Gautham, Thomas, Maya, Subramanian, Annadurai, George, Renu, Danda, Sumita
Publicado 2017

Clinico-radiological phenotyping and diagnostic pathways in childhood neurometabolic disorders—a practical introductory guide

por Biswas, Asthik, Malhotra, Mukul, Mankad, Kshitij, Carney, Olivia, D’Arco, Felice, Muthusamy, Karthik, Sudhakar, Sniya Valsa
Publicado 2021

Revisiting magnetic resonance imaging pattern of Krabbe disease – Lessons from an Indian cohort

por Muthusamy, Karthik, Sudhakar, Sniya Valsa, Thomas, Maya, Yoganathan, Sangeetha, Christudass, Christhunesa S., Chandran, Mahalakshmi, Panwala, Hirenkumar, Gibikote, Sridhar
Publicado 2019

Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase Deficiency

por Yoganathan, Sangeetha, Arunachal, Gautham, Kratz, Lisa, Varman, Mugil, Thomas, Maya, Sudhakar, Sniya Valsa, Oommen, Samuel Philip, Danda, Sumita
Publicado 2020

Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder

por Yoganathan, Sangeetha, Srinivasaraghavan, Rangan, Chandran, Mahalakshmi, Kratz, Lisa, Koshy, Beena, Sudhakar, Sniya Valsa, Arunachal, Gautham, Thomas, Maya, Danda, Sumita
Publicado 2021

Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder

por Yoganathan, Sangeetha, Arunachal, Gautham, Kratz, Lisa, Varman, Mugil, Sudhakar, Sniya Valsa, Oommen, Samuel Philip, Jain, Shikha, Thomas, Maya, Babuji, Manimegalai
Publicado 2020

Cerebrotendinous xanthomatosis: Possibility of founder mutation in CYP27A1 gene (c.526delG) in Eastern Indian and Surinamese population

por Dutta, Atanu Kumar, Danda, Sumita, Muthusamy, Karthik, Alexander, Mathew, Sudhakar, Sniya Valsa, Hansdak, Samuel, Bandyopadhyay, Rini, Bakhya Shree, G.B., Rekha, L.
Publicado 2015