Amitav Parida

Birmingham, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 15 publications

Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Journal: Nature genetics

Published: May 18, 2026

Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsy.

Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsy.

Journal: bioRxiv : the preprint server for biology

Published: March 27, 2026

Paramagnetic Rim Lesions in Pediatric Multiple Sclerosis and Their Association With Brain Tissue Atrophy.

Paramagnetic Rim Lesions in Pediatric Multiple Sclerosis and Their Association With Brain Tissue Atrophy.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: November 03, 2025

From Neonatal Encephalopathy to Adult Survival: Revisiting the Natural History of D-Bifunctional Protein Deficiency in a Multicentre International Case Series.

From Neonatal Encephalopathy to Adult Survival: Revisiting the Natural History of D-Bifunctional Protein Deficiency in a Multicentre International Case Series.

Journal: Journal of inherited metabolic disease

Published: September 24, 2025

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.

Journal: Nature genetics

Published: September 02, 2025

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Journal: Nature genetics

Published: August 18, 2025

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Journal: Nature genetics

Published: August 18, 2025

Slowly Expanding Lesions in Pediatric-Onset Multiple Sclerosis.

Slowly Expanding Lesions in Pediatric-Onset Multiple Sclerosis.

Journal: JAMA neurology

Published: August 11, 2025

Impact of rapid genomic testing on clinical outcomes of acutely unwell children presenting with severe epilepsy.

Impact of rapid genomic testing on clinical outcomes of acutely unwell children presenting with severe epilepsy.

Journal: European journal of human genetics : EJHG

Published: November 26, 2024

Reverse transcriptase inhibitors in Aicardi-Goutières syndrome: A crossover clinical trial.

Reverse transcriptase inhibitors in Aicardi-Goutières syndrome: A crossover clinical trial.

Journal: Developmental medicine and child neurology

Published: September 05, 2024

Cranial vault expansion in treatment of paediatric idiopathic intracranial hypertension.

Cranial vault expansion in treatment of paediatric idiopathic intracranial hypertension.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: March 22, 2024

Periportal necrosis and successful liver transplantation following Lamotrigine drug-induced liver injury in a child.

Periportal necrosis and successful liver transplantation following Lamotrigine drug-induced liver injury in a child.

Journal: BMJ case reports

Published: November 24, 2023

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Last Updated: 09/26/2026