Publications by Andrew Curtis - ePrints

Browsing publications by Andrew Curtis.

Newcastle Authors	Title	Year
Andrew Curtis Dr Ann Curtis Professor Sir John Burn Professor Patrick Chinnery	A novel FTL insertion causing neuroferritinopathy	2010
Andrew Curtis Professor Patrick Chinnery Dr Ann Curtis Professor Sir John Burn	Characterisation of a novel neuroferritinopathy mutation in a French family	2008
Dr Christopher Morris Andrew Curtis Professor Sir John Burn	Preliminary observation of elevated levels of nanocrystalline iron oxide in the basal ganglia of neuroferritinopathy patients	2007
Andrew Curtis	Adult-onset generalized dystonia due to a mutation in the neuroferritinopathy gene	2005
Daniel Routledge Andrew Curtis Dr Ann Curtis	An evaluation of the Qiagen M48 DNA Extraction Robot	2004
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 dystonia	2003
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.	Neuroferritinopathy	2002
Dr Douglas Crompton Professor Patrick Chinnery Constanze Fey Andrew Curtis Dr Christopher Morris et al.	Neuroferritinopathy: A window on the role of iron in neurodegeneration	2002
Andrew Curtis	Palatal tremor and cognitive decline in neuroferritinopathy	2002
Andrew Curtis Constanze Fey Dr Christopher Morris Professor Laurence Bindoff Professor Patrick Chinnery et al.	Mutation in ferritin light chain causes dominant adult onset neurodegeneration	2001
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 disease	2001
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 disease	2000