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Jump to: D | G | L | M | N | S | X
Number of items: 22.

D

Doherty, KM and Noyce, AJ and Silveira-Moriyama, L and Nisbet, A and Quinn, N and Lees, AJ (2012) Familial camptocormia: from dystonia to myopathy. J Neurol Neurosurg Psychiatry , 83 (3) 350 - 351. 10.1136/jnnp.2011.246561.

Doherty, KM and Silveira-Moriyama, L and Giladi, N and Bhatia, KP and Parton, M and Lees, AJ (2012) Camptocormia: Don't forget muscle disease in the movement disorder clinic. Journal of Neurology , 259 (8) 1752 - 1754.

Doherty, KM and Silveira-Moriyama, L and Giladi, N and Bhatia, KP and Parton, M and Lees, AJ (2012) Camptocormia: don't forget muscle disease in the movement disorder clinic. J Neurol , 259 (8) 1752 - 1754. 10.1007/s00415-012-6448-z.

G

Gardiner, AR and Bhatia, KP and Stamelou, M and Dale, RC and Kurian, MA and Schneider, SA and Wali, GM and Counihan, T and Schapira, AH and Spacey, SD and Valente, E-M and Silveira-Moriyama, L and Teive, HAG and Raskin, S and Sander, JW and Lees, A and Warner, T and Kullmann, DM and Wood, NW and Hanna, M and Houlden, H (2012) PRRT2 gene mutations From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. NEUROLOGY , 79 (21) 2115 - 2121.

Gardiner, AR and Bhatia, KP and Stamelou, M and Dale, RC and Kurian, MA and Schneider, SA and Wali, GM and Counihan, T and Schapira, AH and Spacey, SD and Valente, EM and Silveira-Moriyama, L and Teive, HA and Raskin, S and Sander, JW and Lees, A and Warner, T and Kullmann, DM and Wood, NW and Hanna, M and Houlden, H (2012) PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. Neurology , 79 (21) 2115 - 2121. 10.1212/WNL.0b013e3182752c5a.

Glass, P and Lees, A and Bacellar, A and Zijlmans, J and Katzenschlager, R and Silveira-Moriyama, L (2012) Clinical Features of Vascular Parkinsonism in Pathologically Confirmed Cases. In: NEUROLOGY.

Glass, PG and Lees, AJ and Bacellar, A and Zijlmans, J and Katzenschlager, R and Silveira-Moriyama, L (2012) The clinical features of pathologically confirmed vascular parkinsonism. J Neurol Neurosurg Psychiatry , 83 (10) 1027 - 1029. 10.1136/jnnp-2012-302828.

Glass, PG and Lees, AJ and Mathias, C and Mason, L and Best, C and Williams, DR and Katzenschlager, R and Silveira-Moriyama, L (2012) Olfaction in pathologically proven patients with multiple system atrophy. Movement Disorders , 27 (2) 327 - 328.

L

Liston, A and Bayford, R and Holder, D (2012) A cable theory based biophysical model of resistance change in crab peripheral nerve and human cerebral cortex during neuronal depolarisation: Implications for electrical impedance tomography of fast neural activity in the brain. Medical and Biological Engineering and Computing , 50 (5) 425 - 437.

Liston, A and Bayford, R and Holder, D (2012) A cable theory based biophysical model of resistance change in crab peripheral nerve and human cerebral cortex during neuronal depolarisation: implications for electrical impedance tomography of fast neural activity in the brain. Med Biol Eng Comput , 50 (5) 425 - 437. 10.1007/s11517-012-0901-0.

M

Morales-Briceño, H and Rodríguez-Violante, M and Cervantes-Arriaga, A and Irani, SR and Lees, AJ and Silveira-Moriyama, L (2012) Opsoclonus myoclonus syndrome associated with GQ1b antibodies. Mov Disord , 27 (13) 1615 - 1616. 10.1002/mds.25169.

Moscovich, M and Munhoz, RP and Teive, HA and Raskin, S and Carvalho, MDEJ and Barbosa, ER and Ranvaud, R and Liu, J and McFarland, K and Ashizawa, T and Lees, AJ and Silveira-Moriyama, L (2012) Olfactory impairment in familial ataxias. J Neurol Neurosurg Psychiatry , 83 (10) 970 - 974. 10.1136/jnnp-2012-302770.

Moscovich, M and Munhoz, RP and Teive, HA and Raskin, S and De Carvalho, MJ and Barbosa, ER and Ranvaud, R and Liu, J and McFarland, K and Ashizawa, T and Lees, AJ and Silveira-Moriyama, L (2012) Olfactory impairment in familial ataxias. Journal of Neurology, Neurosurgery and Psychiatry , 83 (10) 970 - 974.

N

Noyce, A and Bestwick, J and Hawkes, CH and Knowles, CH and Hardy, J and Lees, AJ and Silveira-Moriyama, L and Giovannoni, G and Schrag, A (2012) AN ALGORITHM TO IDENTIFY INDIVIDUALS AT HIGH-RISK OF PARKINSON'S DISEASE IN THE COMMUNITY. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY.

Noyce, A and Silveira-Moriyama, L and Lees, AJ and Schrag, A and Bestwick, J and Hawkes, CH and Giovannoni, G and Hardy, J and Knowles, CH (2012) A PILOT STUDY OF AN ALGORITHM DESIGNED TO IDENTIFY PARKINSON'S DISEASE IN THE EARLY, NON-MOTOR PHASE. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY.

Noyce, AJ and Bestwick, JP and Silveira-Moriyama, L and Hawkes, CH and Giovannoni, G and Lees, AJ and Schrag, A (2012) Meta-analysis of early nonmotor features and risk factors for Parkinson disease. Annals of Neurology , 72 (6) 893 - 901.

Noyce, AJ and Bestwick, JP and Silveira-Moriyama, L and Hawkes, CH and Giovannoni, G and Lees, AJ and Schrag, A (2012) Meta-analysis of early nonmotor features and risk factors for Parkinson disease. Ann Neurol , 72 (6) 893 - 901. 10.1002/ana.23687.

Noyce, AJ and Silveira-Moriyama, L and Gilpin, P and Ling, H and Howard, R and Lees, AJ (2012) Severe dysphagia as a presentation of Parkinson's disease. Mov Disord , 27 (3) 457 - 458. 10.1002/mds.24006.

S

Sheerin, UM and Charlesworth, G and Bras, J and Guerreiro, R and Bhatia, K and Foltynie, T and Limousin, P and Silveira-Moriyama, L and Lees, A and Wood, N (2012) Screening for VPS35 mutations in Parkinson's disease. Neurobiol Aging , 33 (4) 838.e1 - 838.e5. 10.1016/j.neurobiolaging.2011.10.032.

Silveira-Moriyama, L and Lees, AJ (2012) Tricks of the trade | Pulo do gato. Arquivos de Neuro-Psiquiatria , 70 (4) 245 - 245.
An open access publication

Stockner, H and Schwingenschuh, P and Djamshidian, A and Silveira-Moriyama, L and Katschnig, P and Seppi, K and Dickson, J and Edwards, MJ and Lees, AJ and Poewe, W and Bhatia, KP (2012) Is transcranial sonography useful to distinguish scans without evidence of dopaminergic deficit patients from Parkinson's disease? Mov Disord , 27 (9) 1182 - 1185. 10.1002/mds.25102.

X

Xiromerisiou, G and Houlden, H and Sailer, A and Silveira-Moriyama, L and Hardy, J and Lees, AJ (2012) Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease. Mov Disord , 27 (10) 1323 - ?. 10.1002/mds.24924.

This list was generated on Wed May 22 11:44:16 2013 BST.