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Amitav Parida

Clinical features, investigations, and outcomes of pediatric limbic encephalitis: A multicenter study
2022 · Saraswathy Sabanathan, Omar Abdel‐Mannan, et al. · Annals of Clinical and Translational Neurology · 25
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Isolated central nervous system familial hemophagocytic lymphohistiocytosis (fHLH) presenting as a mimic of demyelination in children
2021 · Amitav Parida, Omar Abdel-Mannan, et al. · Multiple Sclerosis Journal · 22
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Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes
2026 · Rocio Rius, Alexander J. M. Blakes, et al. · Nature Genetics · 10
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Reverse transcriptase inhibitors in Aicardi–Goutières syndrome: A crossover clinical trial
2024 · Yanick J. Crow, Tracy A. Briggs, et al. · Developmental Medicine & Child Neurology · 9
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Biallelic variants in RNU2-2 cause a remarkably frequent developmental epileptic encephalopathy
2025 · Adam Jackson, Alexander JM Blakes, et al. · medRxiv · 8
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Paramagnetic Rim Lesions in Pediatric Multiple Sclerosis and Their Association With Brain Tissue Atrophy
2025 · Riccardo Nistri, Ermelinda De Meo, et al. · Neurology Neuroimmunology & Neuroinflammation · 7
Slowly Expanding Lesions in Pediatric-Onset Multiple Sclerosis
2025 · Valeria Pozzilli, Ferran Prados Carrasco, et al. · JAMA Neurology · 6
Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes
2025 · Rocio Rius, Alexander JM Blakes, et al. · medRxiv · 5
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Periportal necrosis and successful liver transplantation following Lamotrigine drug-induced liver injury in a child
2023 · Michael Richard Couper, Rachel M Brown, et al. · BMJ Case Reports · 4
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Impact of rapid genomic testing on clinical outcomes of acutely unwell children presenting with severe epilepsy
2025 · Erina Sasaki, Philip Millington, et al. · European Journal of Human Genetics · 2
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Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy
2026 · Adam Jackson, Alexander J. M. Blakes, et al. · Nature Genetics · 1
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From Neonatal Encephalopathy to Adult Survival: Revisiting the Natural History of D‐Bifunctional Protein Deficiency in a Multicentre International Case Series
2025 · U. Diaz‐Moreno, S. L. C. Brothwell, et al. · Journal of Inherited Metabolic Disease · 1
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Cranial vault expansion in treatment of paediatric idiopathic intracranial hypertension
2024 · Fardad T. Afshari, Guirish A. Solanki, et al. · Child s Nervous System · 1
Myasthenia gravis complicating the surgical management of achondroplasia: a case-based update
2022 · Fardad T. Afshari, Amitav Parida, et al. · Child s Nervous System · 1
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G180(P) Review of the pathway for children with ‘swollen’ optic discs: a service evaluation and quality improvement study
2019 · L Christodoulou, A Parida, et al. · 1
A Multimodal Multiomics Machine Learning (MMM) approach for biomarker discovery and acceleration of clinical trial readiness for childhood-onset neurological disorders
2026 · Audrey Ker Shin Soo, Jenny Hällqvist, et al. · medRxiv
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes
2026 · Rocio Rius, Alexander J. M. Blakes, et al. · Nature Genetics
Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsy
2026 · Roberta Castelli, Carla Marini, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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P334: Deep phenotyping of thirty-one cases of Aicardi-Goutières syndrome
2025 · Samuel Thomas, Samuel Jack, et al. · Genetics in Medicine Open
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143 Is it ‘CLIPPERS’? Is it CNS Hemophagocytic Lymphohistiocytosis (HLH)?
2022 · Amitav Parida, Cheryl Hemingway, et al. · Journal of Neurology Neurosurgery & Psychiatry
Works count: 23
Citation count: 103
H-index: 6
I10-index: 3
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