Publications by authors named "P D Holohan"

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The combination of nuclear and mitochondrial mutations as a risk factor for idiosyncratic toxicity.
Daria LaRocca, David F Lehmann, Andras Perl, Takayuki Ozawa, Peter D Holohan

Br J Clin Pharmacol· February 2007

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Association between conformational mutations in neuroserpin and onset and severity of dementia.
Richard L Davis, Antony E Shrimpton, Robin W Carrell, David A Lomas, Lieselotte Gerhard, Peter D Holohan

Lancet· June 2002

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Cognitive deficits associated with a recently reported familial neurodegenerative disease: familial encephalopathy with neuroserpin inclusion bodies.
C B Bradshaw, R L Davis, A E Shrimpton, P D Holohan, C B Rea

Arch Neurol· September 2001

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Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.
M Takao, M D Benson, J R Murrell, M Yazaki, P Piccardo, P D Holohan

J Neuropathol Exp Neurol· December 2000

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Familial encephalopathy with neuroserpin inclusion bodies.
R L Davis, P D Holohan, A E Shrimpton, A H Tatum, J Daucher

Am J Pathol· December 1999

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