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Browsing publications by Dr Andrew Morris

Newcastle AuthorsTitleYearFull text
Dr Andrew Morris
Dr Richard Martin
Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing2017
Dr Monika Olahova
Dr Steven Hardy
Dr John Yarham
William Wilson
Dr Charlotte Alston
et al.		LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population2015
Dr Monika Olahova
Dr Charlotte Alston
Jess Houghton
Dr Langping He
Dr Andrew Morris
et al.		A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency2015
Dr Elizabeth Jones
Dr Andrew Morris
Mosaic structural variation in children with developmental disorders2015
Professor Robert Taylor
Dr Angela Pyle
Dr Helen Griffin
Dr Jennifer Duff
Dr Langping He
et al.		Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies2014
Professor Bobby McFarland
Dr Andrew Morris
Professor Robert Taylor
SURF1 deficiency: a multi-centre natural history study2013
Dr Charlotte Alston
Dr Andrew Morris
Emeritus Professor Doug Turnbull
Professor Bobby McFarland
Professor Robert Taylor
Maternally inherited mitochondrial DNA disease in consanguineous families2011
Anna Butterworth
Dr Andrew Morris
Professor Robert Taylor
Mitochondrial DNA depletion syndrome due to mutations in the MPV17 gene2011
Dr Helen Tuppen
Dr Vanessa Hogan
Dr Langping He
Dr Mazhor Aldosary
Dr Gabriele Saretzki
et al.		The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families2010
Professor Bobby McFarland
Dr Helen Tuppen
Dr Andrew Morris
Dr Anita Devlin
Professor Robert Taylor
Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle2009
Dr Helen Tuppen
Professor Bobby McFarland
Professor Robert Taylor
Dr Andrew Morris
The Biochemical and Molecular Genetic Aetiology of Leigh Syndrome2009
Dr Martin Ward Platt
Dr Andrew Morris
Hypothesis: proposals for the management of a neonate at risk of hyperammonaemia due to a urea cycle disorder2008
Joanna Stewart
Dr Angela Pyle
Emeritus Professor Mike Sir Michael Rawlins
Professor Gavin Hudson
Dr Andrew Morris
et al.		Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.2008
Dr Morteza Pourfarzam
Emeritus Professor Doug Turnbull
Dr Andrew Morris
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency2007
Dr Andrew Morris
Rachel Appleton
Professor Robert Taylor
Emeritus Professor Doug Turnbull
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy2007
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