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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
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
Professor 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
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
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
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
Professor Bobby McFarland
Professor Patrick Chinnery
Dr Andrew Schaefer
Dr Andrew Morris
Sharon Foster
et al.
Homoplasmy, heteroplasmy, and mitochondrial dystonia2007
Professor Robert Taylor
Dr Margaret Johnson
Professor Zofia Chrzanowska-Lightowlers
Dr Andrew Morris
Emeritus Professor Doug Turnbull
et al.
A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome2004
Dr Anita Devlin
Dr Anil Gholkar OBE
Helen Fernandes
Dr Vankateswara Ramesh
Dr Andrew Morris
et al.
Cerebral edema associated with betaine treatment in classical homocystinuria2004
Dr Morteza Pourfarzam
Dr Andrew Morris
Dr Raul Dias
Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency2004
Dr Andrew Morris
Dr Sally Lynch
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome2004
Dr Andrew Morris
Emeritus Professor Doug Turnbull
Dr Morteza Pourfarzam
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency2003
Professor Robert Taylor
Dr Andrew Morris
Dr Michael Hutchinson
Emeritus Professor Doug Turnbull
Leigh disease associated with a novel mitochondrial DNA ND5 mutation2002
Dr Andrew Morris
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Clinical presentation and follow-up of 50 patients2002
Professor Bobby McFarland
Kim Clark
Dr Andrew Morris
Professor Robert Taylor
Dr Sheila MacPhail
et al.
Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation2002
Dr Katherine Eastham
Dr Jonathan Wyllie
Dr Sally Lynch
Dr Andrew Morris
ARC syndrome: An expanding range of phenotypes2001
Dr Andrew Morris
Mutation spectrum in patients with fructose-1,6-bisphosphatase deficiency2001
Dr Andrew Morris
Dr Simon Baudouin
Dr Michael Snow
Renal tubular acidosis and hypophosphataemia after treatment with nucleoside reverse transcriptase inhibitors2001
Dr Andrew Morris
Professor Robert Lightowlers
Can paternal mtDNA be inherited?2000
Dr Andrew Morris
Improving the outcome for fatty acid oxidation disorders2000
Dr Andrew Morris
Inborn errors of metabolism around time of birth2000
Dr Andrew Morris
Dr Timothy Cheetham
Infantile hypophosphatasia: disappointing results of treatment2000
Dr Andrew Morris
Professor Robert Lightowlers
Mitochondrial DNA recombination2000
Dr Andrew Morris
Neonatal screening for inborn errors of metabolism2000
Dr Andrew Morris
Changes in serum phenylalanine after overnight fasts in youngsters with phenylketonuria1999
Dr Andrew Morris
Glutaric aciduria and suspected child abuse1999
Dr Andrew Morris
HIV nucleoside analogues: new adverse effects on mitochondria?1999
Dr Andrew Morris
Mitochondrial depletion syndrome is expressed in amniotic fluid cell cultures1999
Dr Andrew Morris
Mitochondrial respiratory chain disorders and the liver1999
Dr Andrew Morris
Novel mutations in patients with fructose-1,6-bisphosphatase deficiency1999
Dr Andrew Morris
Emeritus Professor Robert Perry
Dr Paul Griffiths
Professor Alastair Burt
Emeritus Professor Doug Turnbull
et al.
Respiratory chain dysfunction in progressive neuronal degeneration of childhood with liver disease1996