Nichola Z. Lax

Framlington Place
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 31 publications

Delineating the mechanisms of cerebellar degeneration in paediatric and adult primary mitochondrial disease.

Delineating the mechanisms of cerebellar degeneration in paediatric and adult primary mitochondrial disease.

Journal: Acta neuropathologica

Published: April 01, 2025

Model systems informing mechanisms and drug discovery: a review of POLG-related disease models.

Model systems informing mechanisms and drug discovery: a review of POLG-related disease models.

Journal: Wellcome open research

Published: March 24, 2025

Astrocytic pathology in Alpers' syndrome.

Astrocytic pathology in Alpers' syndrome.

Journal: Acta neuropathologica communications

Published: March 23, 2023

A novel mouse model of mitochondrial disease exhibits juvenile-onset severe neurological impairment due to parvalbumin cell mitochondrial dysfunction.

A novel mouse model of mitochondrial disease exhibits juvenile-onset severe neurological impairment due to parvalbumin cell mitochondrial dysfunction.

Journal: Communications biology

Published: October 14, 2022

Delineating selective vulnerability of inhibitory interneurons in Alpers' syndrome.

Delineating selective vulnerability of inhibitory interneurons in Alpers' syndrome.

Journal: Neuropathology and applied neurobiology

Published: January 23, 2022

Forecasting stroke-like episodes and outcomes in mitochondrial disease.

Forecasting stroke-like episodes and outcomes in mitochondrial disease.

Journal: Brain : a journal of neurology

Published: May 10, 2021

Complex I reductions in the nucleus basalis of Meynert in Lewy body dementia: the role of Lewy bodies.

Complex I reductions in the nucleus basalis of Meynert in Lewy body dementia: the role of Lewy bodies.

Journal: Acta neuropathologica communications

Published: June 30, 2020

Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls.

Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls.

Journal: Acta neuropathologica

Published: October 31, 2019

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.

Journal: EMBO molecular medicine

Published: September 12, 2018

The role of astrocytes in seizure generation: insights from a novel in vitro seizure model based on mitochondrial dysfunction.

The role of astrocytes in seizure generation: insights from a novel in vitro seizure model based on mitochondrial dysfunction.

Journal: Brain : a journal of neurology

Published: May 29, 2018

Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological study.

Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological study.

Journal: Brain pathology (Zurich, Switzerland)

Published: March 28, 2018

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

Journal: EBioMedicine

Published: January 09, 2018

Showing 1-12 of 31

Last Updated: 09/26/2026