Browsing publications by Dr Nichola Lax

Newcastle AuthorsTitleYearFull text
Dr Nichola Lax
Dr John Grady
Dr Alex Laude
Felix Chan
Philippa Hepplewhite
et al.
Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease2015
Dr Nichola Lax
Dr Langping He
Gavin Falkous
Dr Bobby McFarland
Professor Robert Taylor
et al.
Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 Mutations2015
Dr Yi Ng
Dr John Grady
Dr Nichola Lax
Dr John Bourke
Charlotte Alston
et al.
Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults2015
Dr Anne Grunewald
Dr Nichola Lax
Dr Amy Reeve
Philippa Hepplewhite
Karolina Rygiel
et al.
Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue2014
Dr Yi Ng
Dr Nichola Lax
Dr Andrew Schaefer
Professor Robert Taylor
Professor Doug Turnbull
et al.
Sudden Unexpected Death in Adults with M.3243A>G Mutation2014
Dr Nichola Lax
Charlotte Alston
Dr Tuomo Polvikoski
Dr Evelyn Jaros
Dr John Yarham
et al.
Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA(Glu) (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study2013
Helen Bogle
Dr Nichola Lax
Dr Evelyn Jaros
Dr Bobby McFarland
Professor Robert Taylor
et al.
Neuropathological changes in Alpers' syndrome2013
Dr Amy Reeve
Dr Martin Meagher
Dr Nichola Lax
Dr Eve Simcox
Philippa Hepplewhite
et al.
The Impact of Pathogenic Mitochondrial DNA Mutations on Substantia Nigra Neurons2013
Dr Nichola Lax
Philippa Hepplewhite
Dr Amy Reeve
Dr Victoria Nesbitt
Dr Bobby McFarland
et al.
Cerebellar Ataxia in Patients With Mitochondrial DNA Disease: A Molecular Clinicopathological Study2012
Dr Nichola Lax
Graham Campbell
Dr Amy Reeve
Jessica Zambonin
Professor Robert Taylor
et al.
Loss of Myelin-Associated Glycoprotein in Kearns-Sayre Syndrome2012
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