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M.P. Clarke
M.P. Clarke
Email verificata su ncl.ac.uk
Titolo
Citata da
Citata da
Anno
Amblyopia
JM Holmes, MP Clarke
The Lancet 367 (9519), 1343-1351, 2006
5552006
The retina in Parkinson's disease
NK Archibald, MP Clarke, UP Mosimann, DJ Burn
Brain 132 (5), 1128-1145, 2009
4792009
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ...
Brain 133 (3), 771-786, 2010
4372010
Heterozygous mutations of OTX2 cause severe ocular malformations
NK Ragge, AG Brown, CM Poloschek, B Lorenz, RA Henderson, ...
The American Journal of Human Genetics 76 (6), 1008-1022, 2005
3352005
An efficient component model for the construction of adaptive middleware
M Clarke, GS Blair, G Coulson, N Parlavantzas
Middleware 2001: IFIP/ACM International Conference on Distributed Systems …, 2001
2762001
The ocular manifestations of the Sturge-Weber syndrome
TJ Sullivan, MP Clarke, JD Morin
Journal of Pediatric Ophthalmology & Strabismus 29 (6), 349-356, 1992
2741992
Discovery of radio emission from the brown dwarf LP944-20
E Berger, S Ball, KM Becker, M Clarke, DA Frail, TA Fukuda, IM Hoffman, ...
Nature 410 (6826), 338-340, 2001
2392001
Randomised controlled trial of treatment of unilateral visual impairment detected at preschool vision screening
MP Clarke, CM Wright, S Hrisos, JD Anderson, J Henderson, ...
Bmj 327 (7426), 1251, 2003
2342003
Visual symptoms in Parkinson's disease and Parkinson's disease dementia
NK Archibald, MP Clarke, UP Mosimann, DJ Burn
Movement disorders 26 (13), 2387-2395, 2011
2322011
The prevalence and natural history of dominant optic atrophy due to OPA1 mutations
P Yu-Wai-Man, PG Griffiths, A Burke, PW Sellar, MP Clarke, L Gnanaraj, ...
Ophthalmology 117 (8), 1538-1546. e1, 2010
2062010
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations
I Hanson, A Churchill, J Love, R Axton, T Moore, M Clarke, F Meire, ...
Human molecular genetics 8 (2), 165-172, 1999
1961999
International variations in amputation practice: a VASCUNET report
CA Behrendt, B Sigvant, Z Szeberin, B Beiles, N Eldrup, IA Thomson, ...
European Journal of Vascular and Endovascular Surgery 56 (3), 391-399, 2018
1692018
Retinal thickness in Parkinson's disease
NK Archibald, MP Clarke, UP Mosimann, DJ Burn
Parkinsonism & related disorders 17 (6), 431-436, 2011
1642011
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
KP Burdon, JD McKay, MM Sale, IM Russell-Eggitt, DA Mackey, MG Wirth, ...
The American Journal of Human Genetics 73 (5), 1120-1130, 2003
1502003
The emotional impact of amblyopia treatment in preschool children: randomized controlled trial
S Hrisos, MP Clarke, CM Wright
Ophthalmology 111 (8), 1550-1556, 2004
1492004
A semi‐structured interview to assess visual hallucinations in older people
UP Mosimann, D Collerton, R Dudley, TD Meyer, G Graham, JL Dean, ...
International Journal of Geriatric Psychiatry: A journal of the psychiatry …, 2008
1382008
The Newcastle Control Score: a new method of grading the severity of intermittent distance exotropia
H Haggerty, S Richardson, S Hrisos, NP Strong, MP Clarke
British Journal of Ophthalmology 88 (2), 233-235, 2004
1362004
Mitochondrial abnormalities in ageing macular photoreceptors
MJ Barron, MA Johnson, RM Andrews, MP Clarke, PG Griffiths, E Bristow, ...
Investigative ophthalmology & visual science 42 (12), 3016-3022, 2001
1262001
A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy
KP Langton, N McKie, A Curtis, JA Goodship, PM Bond, MD Barker, ...
Journal of Biological Chemistry 275 (35), 27027-27031, 2000
1072000
A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy
KP Langton, N McKie, A Curtis, JA Goodship, PM Bond, MD Barker, ...
Journal of Biological Chemistry 275 (35), 27027-27031, 2000
1072000
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