Natural History of Temporal Lobe Epilepsy: Antecedents and Progression

por Shukla, Garima, Prasad, Asuri N.
Publicado 2012

Menkes disease: what a multidisciplinary approach can do

por Ojha, Rahul, Prasad, Asuri N
Publicado 2016

Inborn Errors of Metabolism and Epilepsy: Current Understanding, Diagnosis, and Treatment Approaches

por Sharma, Suvasini, Prasad, Asuri N.
Publicado 2017

Fever, Seizures and Encephalopathy: From Bush Fires to Firestorms

por Kaur, Prabhjot, Sharma, Suvasini, Konanki, Ramesh, Prasad, Asuri N.
Publicado 2022

The expanding phenotype of MELAS caused by the m.3291T > C mutation in the MT-TL1 gene

por Keilland, E., Rupar, C.A., Prasad, Asuri N., Tay, K.Y., Downie, A., Prasad, C.
Publicado 2016

Response to: Letter to the Editor Regarding: The Expanding Phenotype of MELAS Caused by the m.3291 T > C tRNA Mutation E Kelland, C. A. Rupar, Asuri N. Prasad, K. Y. Tay, A. Downie...

por Kelland, E., Rupar, C.A., Prasad, Asuri N., Tay, K.Y., Downie, A., Prasad, C.
Publicado 2016

Pitfalls in Genetic Testing for Consanguineous Pediatric Populations

por Saleh, Maha, Colaiacovo, Samantha, Napier, Melanie P., Prasad, Asuri N., Rupar, C. Anthony, Prasad, Chitra
Publicado 2022

De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures

por Yang, Ping, Broadbent, Robert, Prasad, Chitra, Levin, Simon, Goobie, Sharan, Knoll, Joan H., Prasad, Asuri N.
Publicado 2021

A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report

por Almudhry, Montaha, Prasad, Asuri N., Rupar, C. Anthony, Tay, Keng Yeow, Ratko, Suzanne, Jenkins, Mary E., Prasad, Chitra
Publicado 2023

Parental psychosocial aspects and stressors involved in the management of inborn errors of metabolism

por Rajasekar, Prashanth, Gannavarapu, Srinitya, Napier, Melanie, Prasad, Asuri N., Vasudev, Akshya, Mantulak, Andrew, Potter, Beth K., Prasad, Chitra
Publicado 2020

High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses

por Jilani, Abdulhakim, Matviychuk, Diana, Blaser, Susan, Dyack, Sarah, Mathieu, Jean, Prasad, Asuri N., Prasad, Chitra, Kyriakopoulou, Lianna, Mercimek‐Andrews, Saadet
Publicado 2019

Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report

por Macintosh, Julia, Perrier, Stefanie, Pinard, Maxime, Tran, Luan T., Guerrero, Kether, Prasad, Chitra, Prasad, Asuri N., Pastinen, Tomi, Thiffault, Isabelle, Coulombe, Benoit, Bernard, Geneviève
Publicado 2023

A live-online mindfulness-based intervention for children living with epilepsy and their families: protocol for a randomized controlled trial of Making Mindfulness Matter©

por Puka, Klajdi, Bax, Karen, Andrade, Andrea, Devries-Rizzo, Margo, Gangam, Hema, Levin, Simon, Nouri, Maryam N., Prasad, Asuri N., Secco, Mary, Zou, Guangyong, Speechley, Kathy N.
Publicado 2020