Browse by UCL Department: listings for include files
- UCL (195485)
- UCL (195485)
- Provost and Vice Provost Offices (194260)
- School of Life and Medical Sciences (95391)
- Faculty of Brain Sciences (35370)
- UCL Queen Square Institute of Neurology (15184)
- Clinical Neuroscience (73)
- UCL Queen Square Institute of Neurology (15184)
- Faculty of Brain Sciences (35370)
- School of Life and Medical Sciences (95391)
- Provost and Vice Provost Offices (194260)
- UCL (195485)
Number of items at this level: 73.
Article
Antelmi, E;
Rocchi, L;
Cocco, A;
Erro, R;
Latorre, A;
Liguori, R;
Plazzi, G;
... Bhatia, KP; + view all
(2018)
Cerebellar and brainstem functional abnormalities in patients with primary orthostatic tremor.
Movement Disorders
10.1002/mds.27331.
(In press).
|
Balint, B;
Mulroy, E;
Gövert, F;
Latorre, A;
Di Lazarro, G;
Erro, R;
Batla, A;
... Bhatia, KP; + view all
(2021)
Development of parkinsonism after long-standing cervical dystonia – A cohort.
Journal of the Neurological Sciences
, 427
, Article 117477. 10.1016/j.jns.2021.117477.
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Balint, B;
Guerreiro, R;
Carmona, S;
Dehghani, N;
Latorre, A;
Cordivari, C;
Bhatia, KP;
(2020)
KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia.
European Journal of Neurology
, 27
(8)
pp. 1471-1477.
10.1111/ene.14228.
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Balint, B;
Killaspy, H;
Marston, L;
Barnes, T;
Latorre, A;
Joyce, E;
Clarke, CS;
... Martino, D; + view all
(2018)
Development and clinimetric assessment of a nurse-administered screening tool for movement disorders in psychosis.
BJPsych Open
, 4
(5)
pp. 404-410.
10.1192/bjo.2018.55.
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Balint, B;
Rispoli, V;
Latorre, A;
Bhatia, KP;
(2019)
Ataxia with Oculomotor Apraxia Type 1—New Mutation, Characteristic Phenotype.
Movement Disorders Clinical Practice
10.1002/mdc3.12725.
(In press).
|
Balint, B;
Wiethoff, S;
Martino, D;
Del Gamba, C;
Latorre, A;
Ganos, C;
Houlden, H;
(2018)
Quick Flicks: Association of Paroxysmal Kinesigenic Dyskinesia and Tics.
Movement Disorders Clinical Practice
, 5
(3)
pp. 317-320.
10.1002/mdc3.12615.
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Bettencourt, C;
Morris, HR;
Singleton, AB;
Hardy, J;
Houlden, H;
(2013)
Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment.
Journal of Neurology
, 260
(9)
pp. 2414-2416.
10.1007/s00415-013-7044-6.
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Bonomo, R;
Latorre, A;
Bhatia, KP;
(2021)
Reply to Comment on: Voluntary Inhibitory Control of Chorea.
Movement Disorders Clinical Practice
, 8
(4)
p. 636.
10.1002/mdc3.13189.
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Bonomo, R;
Latorre, A;
Balint, B;
Smilowska, K;
Rocchi, L;
Rothwell, JC;
Zappia, M;
(2020)
Voluntary Inhibitory Control of Chorea: A Case Series.
Movement Disorders Clinical Practice
10.1002/mdc3.12907.
(In press).
|
Bonomo, R;
Latorre, A;
Bhatia, KP;
(2019)
Self-Injurious Behaviour in SCA17: A New Clinical Observation.
Tremor and other Hyperkinetic Movements
, 2019
(9)
pp. 1-3.
10.7916/tohm.v0.672.
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Cani, I;
Latorre, A;
Cordivari, C;
Balint, B;
Bhatia, KP;
(2019)
Brachial Neuritis After Botulinum Toxin Injections for Cervical Dystonia: A Need for a Reappraisal?
Movement Disorders Clinical Practice
10.1002/mdc3.12710.
(In press).
|
Chio, A.;
Schymick, J. C.;
Restagno, G.;
Scholz, S. W.;
Lombardo, F.;
Lai, S.-L.;
Mora, G.;
... Traynor, B. J.; + view all
(2009)
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
Human Molecular Genetics
, 18
(8)
pp. 1524-1532.
10.1093/hmg/ddp059.
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Conte, A;
Rocchi, L;
Latorre, A;
Belvisi, D;
Rothwell, JC;
Berardelli, A;
(2019)
Ten-Year Reflections on the Neurophysiological Abnormalities of Focal Dystonias in Humans.
Movement Disorders
10.1002/mds.27859.
(In press).
|
Erro, R;
Antelmi, E;
Bhatia, KP;
Latorre, A;
Tinazzi, M;
Berardelli, A;
Rothwell, JC;
(2020)
Reversal of Temporal Discrimination in Cervical Dystonia after Low-Frequency Sensory Stimulation.
Movement Disorders
10.1002/mds.28369.
(In press).
|
Estevez-Fraga, C;
Magrinelli, F;
Latorre, A;
Cordivari, C;
Houlden, H;
Tinazzi, M;
Hemingway, C;
... Bhatia, KP; + view all
(2020)
A new family with GLRB-related hyperekplexia showing chorea in homo- and heterozygous variant carriers.
Parkinsonism and Related Disorders
, 79
pp. 97-99.
10.1016/j.parkreldis.2020.08.016.
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Ganos, C;
Rocchi, L;
Latorre, A;
Hockney, L;
Palmer, C;
Joyce, E;
Bhatia, K;
... Rothwell, J; + view all
(2018)
Motor cortical excitability during voluntary inhibition of involuntary tic movements.
Movement Disorders
, 33
(11)
pp. 1804-1809.
10.1002/mds.27479.
|
Jesús, S;
Latorre, A;
Vinuela, A;
Fahn, S;
Bhatia, KP;
Balint, B;
(2019)
Stimulus Sensitive Foot Myoclonus: A Clue to Coeliac Disease.
Movement Disorders Clinical Practice
, 6
(4)
pp. 320-323.
10.1002/mdc3.12753.
|
Jha, A;
Menozzi, E;
Oyekan, R;
Latorre, A;
Mulroy, E;
Schreglmann, SR;
Stamate, C;
... Bhatia, KP; + view all
(2020)
The CloudUPDRS smartphone software in Parkinson's study: cross-validation against blinded human raters.
npj Parkinson's Disease
, 6
(1)
, Article 36. 10.1038/s41531-020-00135-w.
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Koya Kutty, S;
Mulroy, E;
Magrinelli, F;
Di Lazzaro, G;
Latorre, A;
Bhatia, KP;
(2021)
Huntington disease-like phenotype in a patient with ANO3 mutation.
Parkinsonism & Related Disorders
, 90
pp. 120-122.
10.1016/j.parkreldis.2021.02.022.
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Lambon Ralph, M;
Garrard, P;
(2001)
Category-specific deficits: insights from semantic dementia and Alzheimer's disease.
Behavioral and Brain Sciences
, 24
(3)
485 - 486.
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Latorre, A;
Rocchi, L;
Sadnicka, A;
(2021)
The Expanding Horizon of Neural Stimulation for Hyperkinetic Movement Disorders.
Frontiers in Neurology
, 12
, Article 669690. 10.3389/fneur.2021.669690.
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Latorre, A;
Rothwell, JC;
(2020)
Myoclonus and COVID-19: A Challenge for the Present, a Lesson for the Future.
Movement Disorders Clinical Practice
, 7
(8)
pp. 888-890.
10.1002/mdc3.13103.
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Latorre, Anna;
Hale, Blake;
Rocchi, Lorenzo;
(2022)
How Do I Find Clues About Where Myoclonus Is Originating?
Movement Disorders Clinical Practice
, 9
(5)
pp. 721-722.
10.1002/mdc3.13472.
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Latorre, Anna;
Hallett, Mark;
Deuschl, Günther;
Bhatia, Kailash P;
(2022)
The MDS consensus tremor classification: The best way to classify patients with tremor at present.
Journal of the Neurological Sciences
, 435
, Article 120191. 10.1016/j.jns.2022.120191.
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Latorre, A;
Bhatia, KP;
(2020)
Treatment of Paroxysmal Dyskinesia.
Neurologic Clinics
, 38
(2)
pp. 433-447.
10.1016/j.ncl.2020.01.007.
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Latorre, A;
Cocco, A;
Bhatia, KP;
Erro, R;
Antelmi, E;
Conte, A;
Rothwell, JC;
(2020)
Defective Somatosensory Inhibition and Plasticity Are Not Required to Develop Dystonia.
Movement Disorders
10.1002/mds.28427.
(In press).
|
Latorre, A;
Del Gamba, C;
Menozzi, E;
Balint, B;
Brugger, F;
Bhatia, KP;
(2019)
Abnormal DaTSCAN and Atypical Parkinsonism in SCA12.
Movement Disorders Clinical Practice
, 6
(5)
pp. 400-402.
10.1002/mdc3.12751.
|
Latorre, A;
Rocchi, L;
Batla, A;
Berardelli, A;
Rothwell, JC;
Bhatia, KP;
(2021)
The Signature of Primary Writing Tremor Is Dystonic.
Movement Disorders
10.1002/mds.28579.
(In press).
|
Latorre, A;
Rocchi, L;
Berardelli, A;
Bhatia, KP;
Rothwell, JC;
(2019)
The interindividual variability of transcranial magnetic stimulation effects: Implications for diagnostic use in movement disorders.
Movement Disorders
, 34
(7)
pp. 936-949.
10.1002/mds.27736.
|
Latorre, A;
Rocchi, L;
Berardelli, A;
Bhatia, KP;
Rothwell, JC;
(2019)
The use of transcranial magnetic stimulation as a treatment for movement disorders: A critical review.
Movement Disorders
10.1002/mds.27705.
(In press).
|
Latorre, A;
Rocchi, L;
Berardelli, A;
Rothwell, JC;
Bhatia, KP;
Cordivari, C;
(2018)
Reappraisal of cortical myoclonus: A retrospective study of clinical neurophysiology.
Movement Disorders
, 33
(2)
pp. 339-341.
10.1002/mds.27234.
|
Latorre, A;
Rocchi, L;
Bhatia, KP;
(2020)
Delineating the electrophysiological signature of dystonia.
Experimental Brain Research
, 238
pp. 1685-1692.
10.1007/s00221-020-05863-2.
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Latorre, A;
Rocchi, L;
Cordivari, C;
Berardelli, A;
Bhatia, KP;
Rothwell, JC;
(2018)
Reply: “Reappraisal of cortical myoclonus: Electrophysiology is the gold standard”.
Movement Disorders
, 33
(7)
p. 1191.
10.1002/mds.27440.
|
Latorre, A;
Rocchi, L;
Magrinelli, F;
Mulroy, E;
Berardelli, A;
Rothwell, JC;
Bhatia, KP;
(2020)
Unravelling the enigma of cortical tremor and other forms of cortical myoclonus.
Brain
, 143
(9)
pp. 2653-2663.
10.1093/brain/awaa129.
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Latorre, A;
Rocchi, L;
Stamelou, M;
Batla, A;
Ciocca, M;
Balint, B;
Sidle, K;
... Bhatia, KP; + view all
(2019)
Tremor in motor neuron disease may be central rather than peripheral in origin.
European Journal of Neurology
, 26
(3)
394-e31.
10.1111/ene.13743.
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Latorre, A;
Salgado, P;
Salari, M;
Jesuthasan, A;
Bhatia, KP;
(2018)
Combined Dystonia With Self-Mutilation in 6-Pyruvoyl-Tetrahydropterin Synthase (PTPS) Deficiency: A Case Report.
Movement Disorders Clinical Practice
10.1002/mdc3.12698.
(In press).
|
Leodori, G;
De Bartolo, MI;
Guerra, A;
Fabbrini, A;
Rocchi, L;
Latorre, A;
Paparella, G;
... Berardelli, A; + view all
(2022)
Motor Cortical Network Excitability in Parkinson's Disease.
Movement Disorders
10.1002/mds.28914.
(In press).
|
Magrinelli, F;
Mehta, S;
Di Lazzaro, G;
Latorre, A;
Edwards, MJ;
Balint, B;
Basu, P;
... Bhatia, KP; + view all
(2021)
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.
Movement Disorders
10.1002/mds.28807.
(In press).
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Magrinelli, Francesca;
Rajapaksha, Ishani;
Kobylecki, Christopher;
Latorre, Anna;
Mulroy, Eoin;
Estevez-Fraga, Carlos;
Houlden, Henry;
... Bhatia, Kailash P; + view all
(2022)
Reply to: Juvenile PLA2G6-parkinsonism due to Indian 'Asian' p.R741Q mutation, and response to STN DBS.
Movement Disorders
10.1002/mds.28955.
(In press).
|
Magrinelli, F;
Latorre, A;
Balint, B;
Mackenzie, M;
Mulroy, E;
Stamelou, M;
Tinazzi, M;
(2020)
Isolated and combined genetic tremor syndromes: a critical appraisal based on the 2018 MDS criteria.
Parkinsonism & Related Disorders
, 77
pp. 121-140.
10.1016/j.parkreldis.2020.04.010.
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Magrinelli, F;
Mulroy, E;
Schneider, SA;
Latorre, A;
Di Lazzaro, G;
Hennig, A;
Grunewald, S;
... Bhatia, KP; + view all
(2020)
Criss-cross gait: A clue to glucose transporter type 1 deficiency syndrome.
Neurology
, 95
(11)
pp. 500-501.
10.1212/WNL.0000000000010502.
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Malaquias, Maria João;
Magrinelli, Francesca;
Quattrone, Andrea;
Neo, Ray Jen;
Latorre, Anna;
Mulroy, Eoin;
Bhatia, Kailash P;
(2023)
Presynaptic Hemiparkinsonism Following Cerebral Toxoplasmosis: Case Report and Literature Review.
Movement Disorders Clinical Practice
, 10
(2)
pp. 285-299.
10.1002/mdc3.13631.
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Menozzi, E;
Balint, B;
Latorre, A;
Valente, EM;
Rothwell, JC;
Bhatia, KP;
(2019)
Twenty years on: Myoclonus‐dystonia and ε‐sarcoglycan — neurodevelopment, channel, and signaling dysfunction.
Movement Disorders
10.1002/mds.27822.
(In press).
|
Menozzi, E;
Latorre, A;
Balint, B;
Bhatia, KP;
Dystonia in Handcuffs: A Picture Typical of Lesch-Nyhan Syndrome.
Movement Disorders Clinical Practice
10.1002/mdc3.12776.
(In press).
|
Mulroy, E;
Baschieri, F;
Magrinelli, F;
Latorre, A;
Cortelli, P;
Bhatia, KP;
(2021)
Movement Disorders and Liver Disease.
Movement Disorders Clinical Practice
, 8
(6)
pp. 828-842.
10.1002/mdc3.13238.
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Mulroy, E;
Ganos, C;
Latorre, A;
Terkelsen, AJ;
Balint, B;
Agarwal, PA;
Batla, A;
(2021)
Self-concocted, curious and creative coping strategies in movement disorders.
Parkinsonism & Related Disorders
, 83
pp. 140-143.
10.1016/j.parkreldis.2020.10.031.
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Mulroy, E;
Magrinelli, F;
Mohd Fauzi, NA;
Kutty, SK;
Latorre, A;
Bhatia, KP;
(2021)
Paroxysmal, exercise-induced, diurnally fluctuating dystonia: Expanding the phenotype of SPG8.
Parkinsonism & Related Disorders
, 85
pp. 26-28.
10.1016/j.parkreldis.2021.02.011.
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Mulroy, E;
Balint, B;
Latorre, A;
Schreglmann, S;
Menozzi, E;
Bhatia, KP;
Syringomyelia-Associated Dystonia: Case Series, Literature Review, and Novel Insights.
Movement Disorders Clinical Practice
10.1002/mdc3.12772.
(In press).
|
Mulroy, E;
Balint, B;
Menozzi, E;
Latorre, A;
Bhatia, KP;
(2019)
Benign tremulous parkinsonism of the young-consider Parkin.
[Letter].
Parkinsonism & Related Disorders
, 65
pp. 270-271.
10.1016/j.parkreldis.2019.05.027.
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Mulroy, E;
Jaunmuktane, Z;
Balint, B;
Erro, R;
Latorre, A;
Bhatia, KP;
(2020)
Some new and unexpected tauopathies in movement disorders.
Movement Disorders Clinical Practice
, 7
(6)
pp. 616-626.
10.1002/mdc3.12995.
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Mulroy, E;
Latorre, A;
Bhatia, KP;
(2019)
Parkinsonism in essential tremor cases: A clinicopathological study-were they really essential tremor?
Movement Disorders
, 34
(11)
p. 1749.
10.1002/mds.27835.
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Mulroy, E;
Latorre, A;
Magrinelli, F;
Bhatia, KP;
(2019)
Ciliary Dysfunction: The Hairy Explanation of Normal Pressure Hydrocephalus?
Movement Disorders Clinical Practice
10.1002/mdc3.12880.
(In press).
|
Mulroy, E;
Latorre, A;
Menozzi, E;
Teh, PC;
Magrinelli, F;
Bhatia, KP;
(2020)
Huntington disease like 2 (HDL-2) with parkinsonism and abnormal DAT-SPECT - A novel observation.
Parkinsonism & Related Disorders
, 71
pp. 46-48.
10.1016/j.parkreldis.2020.01.008.
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Rawji, V;
Latorre, A;
Sharma, N;
Rothwell, JC;
Rocchi, L;
(2020)
On the Use of TMS to Investigate the Pathophysiology of Neurodegenerative Diseases.
Frontiers in Neurology
, 11
, Article 584664. 10.3389/fneur.2020.584664.
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Rawji, V;
Modi, S;
Latorre, A;
Rocchi, L;
Hockey, L;
Bhatia, K;
Joyce, E;
... Jahanshahi, M; + view all
(2020)
Impaired automatic but intact volitional inhibition in primary tic disorders.
Brain
, 143
(3)
pp. 906-919.
10.1093/brain/awaa024.
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Rocchi, L;
Latorre, A;
Ibanez Pereda, J;
Spampinato, D;
Brown, KE;
Rothwell, J;
Bhatia, K;
(2019)
A case of congenital hypoplasia of the left cerebellar hemisphere and ipsilateral cortical myoclonus.
Movement Disorders
10.1002/mds.27881.
(In press).
|
Ros‐Castelló, V;
Latorre, A;
Álvarez‐Linera, J;
Martinez‐Castrillo, JC;
Bhatia, KP;
Pareés, I;
(2021)
Dystonia in a female fragile X premutation carrier: a case report.
Movement Disorders Clinical Practice
, 8
(5)
pp. 797-799.
10.1002/mdc3.13234.
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Sadnicka, Anna;
Rocchi, Lorenzo;
Latorre, Anna;
Antelmi, Elena;
Teo, James;
Pareés, Isabel;
Hoffland, Britt S;
... Rothwell, John C; + view all
(2022)
A Critical Investigation of Cerebellar Associative Learning in Isolated Dystonia.
Movement Disorders
10.1002/mds.28967.
(In press).
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Salgado, P;
Latorre, A;
Del Gamba, C;
Menozi, E;
Balint, B;
Bhatia, KP;
(2018)
SPG7: The Great Imitator of MSA‐C Within the ILOCAs.
Movement Disorders Clinical Practice
10.1002/mdc3.12711.
(In press).
|
Schrag, A.;
Jahanshahi, M.;
Quinn, N.P.;
(2001)
What contributes to depression in Parkinson's disease?
Psychological Medicine
, 31
(1)
pp. 65-73.
10.1017/S0033291799003141.
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Schreglmann, SR;
Wang, D;
Peach, RL;
Li, J;
Zhang, X;
Latorre, A;
Rhodes, E;
... Grossman, N; + view all
(2021)
Non-invasive suppression of essential tremor via phase-locked disruption of its temporal coherence.
Nature Communications
, 12
(1)
, Article 363. 10.1038/s41467-020-20581-7.
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Shahedah, KK;
Di Lazzaro, G;
Magrinelli, F;
Mulroy, E;
Latorre, A;
Bhatia, KP;
(2021)
Late‐Onset Chorea in JAK2‐Associated Essential Thrombocythemia.
Movement Disorders Clinical Practice
, 8
(1)
pp. 145-148.
10.1002/mdc3.13105.
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Tucker, H;
Osei‐Poku, F;
Ashton, D;
Lally, R;
Jesuthasan, A;
Latorre, A;
Bhatia, KP;
... Kobylecki, C; + view all
(2021)
Management of secondary poor response to botulinum toxin in cervical dystonia: a multicentre audit.
Movement Disorders Clinical Practice
(mdc3.131)
10.1002/mdc3.13181.
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Thesis
Bradley, L.;
(2006)
Mitochondrial abnormalities in remote tissues of patients with amyotrophic lateral sclerosis.
Doctoral thesis , University of London.
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Carroll, E.M.A.;
(2006)
Category- and modality-specificity in semantic dementia.
Doctoral thesis , University of London.
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Chakraborty, A.;
(2008)
The development of intra-operative ultrasound elasticity imaging techniques to assist during brain tumour resection.
Doctoral thesis , University of London.
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Higgins, A.;
(2008)
The impact of Deep Brain Stimulation of the subthalamic nucleus on reward responsiveness in patients with Parkinson's disease.
Doctoral thesis , University of London.
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Orth, M.;
(2005)
Molecular study of cell culture models of Parkinson's disease and Huntington's disease.
Doctoral thesis , University of London.
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Placzek, M.R.;
(2010)
Genetic mechanisms in primary dystonia.
Doctoral thesis , UCL (University College London).
|
Robertson, A.M.;
(1999)
The mechanism of neuropathy in peripheral myelin protein 22 mice.
Doctoral thesis , University of London.
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Swanton, J.;
(2009)
The investigation of early MRI in diagnosis and prognosis in patients presenting with a clinically isolated syndrome characteristic of demyelination.
Doctoral thesis , UCL (University College London).
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Turner, C.;
(2009)
The molecular pathogenesis of Huntington’s disease.
Doctoral thesis , UCL (University College London).
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Wilkinson, P.;
(2007)
A clinical, genetic and biochemical study of hereditary spastic paraplegia.
Doctoral thesis , University of London.
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