D. Nicholl

Acetylator genotype and Parkinson's disease

P. Bennett, D. Nicholl, 1998, The Lancet.

No association between Parkinson's disease and low-activity alleles of catechol O-methyltransferase.

D. Collier, K. Chaudhuri, K. Aitchison, 1996, Biochemical and biophysical research communications.

family associated with anovel144basepair insertion oftheprion protein gene

R. Lathe, M. Dempster, J. Ironside, 2011 .

Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.

R. Lathe, S. Sawcer, O. Windl, 1995, Journal of neurology, neurosurgery, and psychiatry.

ACTIVATING MUTATIONS IN STIM1 AND ORAI1 CAUSE OVERLAPPING SYNDROMES OF TUBULAR AGGREGATE MYOPATHY AND CONGENITAL MIOSIS

K. Wierenga, A. Wills, F. Bremner, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

The HhaI polymorphism in the CYP2D6 gene is not associated with Parkinson's disease in a Caucasian population

S. Ho, D. Nicholl, D. Ramsden, 1995, European journal of neurology.