Browsing publications by Dr Andrew Morris

Newcastle AuthorsTitleYear
Charlotte Alston
Dr Andrew Morris
Professor Doug Turnbull
Dr Bobby McFarland
Professor Robert Taylor
et al.		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
Dr Bobby McFarland
Dr Helen Tuppen
Dr Andrew Morris
Dr Anita Devlin
Professor Robert Taylor
et al.		Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle2009
Dr Helen Tuppen
Dr 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 Michael Sir Michael Rawlins
Dr Gavin Hudson
Dr Andrew Morris
et al.		Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.2008
Dr Morteza Pourfarzam
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
Professor Doug Turnbull
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy2007
Dr Bobby McFarland
Professor Patrick Chinnery
Dr Andrew Schaefer
Dr Andrew Morris
Sharon Foster
et al.		Homoplasmy, heteroplasmy, and mitochondrial dystonia2007
1234