Prab Prabhakar

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 41 publications

Biallelic variants in SUPV3L1 cause a variable leukodystrophy due to impaired mitochondrial degradosome function.

Biallelic variants in SUPV3L1 cause a variable leukodystrophy due to impaired mitochondrial degradosome function.

Journal: Research square
Published: July 17, 2026

Consensus recommendations for the assessment and management of idiopathic intracranial hypertension in children and young people.

Consensus recommendations for the assessment and management of idiopathic intracranial hypertension in children and young people.

Journal: Archives of disease in childhood
Published: November 28, 2023

Extended Phenotyping of Migraine in Children: A Cross-Sectional Study in a Specialist Children's Headache Clinic.

Extended Phenotyping of Migraine in Children: A Cross-Sectional Study in a Specialist Children's Headache Clinic.

Journal: Pediatric neurology
Published: August 04, 2023

Bi-allelic variants in INTS11 are associated with a complex neurological disorder.

Bi-allelic variants in INTS11 are associated with a complex neurological disorder.

Journal: American journal of human genetics
Published: January 05, 2023

Fifteen-minute consultation: Management of primary headaches in children.

Fifteen-minute consultation: Management of primary headaches in children.

Journal: Archives of disease in childhood. Education and practice edition
Published: November 10, 2022

STXBP1 Stop-Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy.

STXBP1 Stop-Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy.

Journal: Movement disorders clinical practice
Published: April 27, 2022

Headache in Children and Adolescents: A Focus on Uncommon Headache Disorders.

Headache in Children and Adolescents: A Focus on Uncommon Headache Disorders.

Journal: Indian pediatrics
Published: September 01, 2021

A recent surge of fulminant and early onset subacute sclerosing panencephalitis (SSPE) in the United Kingdom: An emergence in a time of measles.

A recent surge of fulminant and early onset subacute sclerosing panencephalitis (SSPE) in the United Kingdom: An emergence in a time of measles.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 16, 2020

Post-licensure observational safety study after meningococcal B vaccine 4CMenB (Bexsero) vaccination within the routine UK immunisation program.

Post-licensure observational safety study after meningococcal B vaccine 4CMenB (Bexsero) vaccination within the routine UK immunisation program.

Journal: Vaccine
Published: October 23, 2020

Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum.

Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum.

Journal: American journal of medical genetics. Part A
Published: July 15, 2020

Diagnostic algorithm for children presenting with epilepsia partialis continua.

Diagnostic algorithm for children presenting with epilepsia partialis continua.

Journal: Epilepsia
Published: April 13, 2020

Headache in children with Sturge-Weber syndrome - Prevalence, associations and impact.

Headache in children with Sturge-Weber syndrome - Prevalence, associations and impact.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: February 24, 2020
Showing 1-12 of 41

Last Updated: 09/26/2026