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Browsing publications by Andrew Curtis.

Newcastle AuthorsTitleYearFull text
Andrew Curtis
Dr Ann Curtis
Professor Sir John Burn
Professor Patrick Chinnery
A novel FTL insertion causing neuroferritinopathy2010
Andrew Curtis
Professor Patrick Chinnery
Dr Ann Curtis
Professor Sir John Burn
Characterisation of a novel neuroferritinopathy mutation in a French family2008
Dr Christopher Morris
Andrew Curtis
Professor Sir John Burn
Preliminary observation of elevated levels of nanocrystalline iron oxide in the basal ganglia of neuroferritinopathy patients2007
Andrew Curtis
Adult-onset generalized dystonia due to a mutation in the neuroferritinopathy gene2005
Daniel Routledge
Andrew Curtis
Dr Ann Curtis
An evaluation of the Qiagen M48 DNA Extraction Robot2004
Professor Patrick Chinnery
Andrew Curtis
Constanze Fey
Dr Douglas Crompton
Professor Sir John Burn
et al.
Neuroferritinopathy in a French family with late onset dominant dystonia2003
Constanze Fey
Andrew Curtis
Professor Patrick Chinnery
Dr Christopher Morris
Dr Ann Curtis
et al.
Did neuroferritinopathy originate in France?2002
Professor Patrick Chinnery
Andrew Curtis
Constanze Fey
Dr Margaret Jackson
Emeritus Professor David Bates
et al.
Neuroferritinopathy2002
Dr Douglas Crompton
Professor Patrick Chinnery
Constanze Fey
Andrew Curtis
Dr Christopher Morris
et al.
Neuroferritinopathy: A window on the role of iron in neurodegeneration2002
Andrew Curtis
Palatal tremor and cognitive decline in neuroferritinopathy2002
Andrew Curtis
Constanze Fey
Dr Christopher Morris
Professor Laurence Bindoff
Professor Patrick Chinnery
et al.
Mutation in ferritin light chain causes dominant adult onset neurodegeneration2001
Andrew Curtis
Constanze Fey
Dr Christopher Morris
Professor Laurence Bindoff
Professor Patrick Chinnery
et al.
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease2001
Professor Sir John Burn
Andrew Curtis
Dr Matthew Jackson
Constanze Fey
Emeritus Professor David Bates
et al.
A novel autosomal dominant basal ganglia degeneration with cavitation on 19q can mimic Parkinson's disease and Huntington's disease2000