Hardev S. Pall

Birmingham, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 26 publications

Adult-Onset Bilateral Optic Neuropathy in a Patient with Non-Familial Childhood-Onset Generalized Dystonia Associated with Mitochondrial DNA 14459G>A Mutation: A Case Report and Review of Literature.

Adult-Onset Bilateral Optic Neuropathy in a Patient with Non-Familial Childhood-Onset Generalized Dystonia Associated with Mitochondrial DNA 14459G>A Mutation: A Case Report and Review of Literature.

Journal: Neuro-ophthalmology (Aeolus Press)

Published: April 07, 2025

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia.

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 10, 2022

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.

Journal: JAMA neurology

Published: August 30, 2021

Subthalamic deep brain stimulation under general anesthesia and neurophysiological guidance while on dopaminergic medication: comparative cohort study.

Subthalamic deep brain stimulation under general anesthesia and neurophysiological guidance while on dopaminergic medication: comparative cohort study.

Journal: Acta neurochirurgica

Published: October 16, 2017

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Journal: Nature genetics

Published: May 27, 2017

Patients' experiences of deep brain stimulation for Parkinson's disease: a qualitative systematic review and synthesis.

Patients' experiences of deep brain stimulation for Parkinson's disease: a qualitative systematic review and synthesis.

Journal: BMJ open

Published: June 25, 2016

Apathy in patients with Parkinson's disease following deep brain stimulation of the subthalamic nucleus.

Apathy in patients with Parkinson's disease following deep brain stimulation of the subthalamic nucleus.

Journal: CNS spectrums

Published: May 07, 2016

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Journal: Nature genetics

Published: April 19, 2016

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.

Journal: Nature genetics

Published: February 25, 2016

Subthalamic nucleus microelectrode recordings (MER) can be reliably detected despite general anaesthesia and dopaminergic treatment.

Subthalamic nucleus microelectrode recordings (MER) can be reliably detected despite general anaesthesia and dopaminergic treatment.

Journal: Acta neurochirurgica

Published: February 17, 2016

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.

Journal: Science translational medicine

Published: November 26, 2015

Phenotypic insights into ADCY5-associated disease.

Phenotypic insights into ADCY5-associated disease.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: August 19, 2015

Showing 1-12 of 26

Last Updated: 09/26/2026