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Number of items: 33.
Article
Balint, B;
Charlesworth, G;
Stamelou, M;
Carr, L;
Mencacci, NE;
Wood, NW;
Bhatia, KP;
(2019)
Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy.
European Journal of Neurology
10.1111/ene.13956.
(In press).
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Batla, A;
Stamelou, M;
(2016)
Primary Familial Brain Calcification in the IBGC2 Kindred: All Linkage Roads Lead to SLC20A2.
Movement Disorders
, 31
(12)
pp. 1765-1766.
10.1002/mds.26873.
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Batla, A;
Stamelou, M;
Mencacci, N;
Schapira, AH;
Bhatia, KP;
(2013)
Ropinirole monotherapy induced severe reversible dyskinesias in Parkinson's disease.
Mov Disord
, 28
(8)
1159 - 1160.
10.1002/mds.25318.
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Bhatia, KP;
Bain, P;
Bajaj, N;
Elble, RJ;
Hallett, M;
Louis, ED;
Raethjen, J;
... Deuschl, G; + view all
(2017)
Consensus Statement on the Classification of Tremors. From the Task Force on Tremor of the International Parkinson and Movement Disorder Society.
Movement Disorders
, 33
(1)
pp. 75-87.
10.1002/mds.27121.
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Bhatia, KP;
Stamelou, M;
(2017)
Chapter Forty-Six - Nonmotor Features in Atypical Parkinsonism.
International Review of Neurobiology
, 134
pp. 1285-1301.
10.1016/bs.irn.2017.06.001.
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Brittain, C;
McCarthy, A;
Irizarry, MC;
McDermott, D;
Biglan, K;
Hoglinger, GU;
Lorenzl, S;
... Gerpen, JV; + view all
(2019)
Severity dependent distribution of impairments in PSP and CBS: Interactive visualizations.
Parkinsonism & Related Disorders
, 60
pp. 138-145.
10.1016/j.parkreldis.2018.08.025.
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Carecchio, M;
Mencacci, NE;
Iodice, A;
Pons, R;
Panteghini, C;
Zorzi, G;
Zibordi, F;
... Nardocci, N; + view all
(2017)
ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
PARKINSONISM & RELATED DISORDERS
, 41
pp. 37-43.
10.1016/j.parkreldis.2017.05.004.
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Charlesworth, G;
Angelova, PR;
Bartolomé-Robledo, F;
Ryten, M;
Trabzuni, D;
Stamelou, M;
Abramov, AY;
... Wood, NW; + view all
(2015)
Mutations in HPCA cause autosomal-recessive primary isolated dystonia.
American Journal of Human Genetics
, 96
(4)
pp. 657-665.
10.1016/j.ajhg.2015.02.007.
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Charlesworth, G;
Plagnol, V;
Holmström, KM;
Bras, J;
Sheerin, UM;
Preza, E;
Rubio-Agusti, I;
... Wood, NW; + view all
(2012)
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.
The American Journal of Human Genetics
, 91
(6)
1041 - 1050.
10.1016/j.ajhg.2012.10.024.
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Gardiner, AR;
Jaffer, F;
Dale, RC;
Labrum, R;
Erro, R;
Meyer, E;
Xiromerisiou, G;
... Houlden, H; + view all
(2015)
The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Brain
, 138
(Pt 12)
pp. 3567-3580.
10.1093/brain/awv310.
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Giagkou, N;
Bhatia, KP;
Höglinger, GU;
Stamelou, M;
(2019)
Chapter Thirteen - Genetic mimics of the non-genetic atypical parkinsonian disorders – the ‘atypical’ atypical.
International Review of Neurobiology
, 149
pp. 327-351.
10.1016/bs.irn.2019.10.008.
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Grimm, M-J;
Respondek, G;
Stamelou, M;
Arzberger, T;
Ferguson, L;
Gelpi, E;
Giese, A;
... Movement Disorder Society-endorsed PSP Study Group, .; + view all
(2019)
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy.
Movement Disorders
, 34
(8)
pp. 1228-1232.
10.1002/mds.27666.
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Haubenberger, D;
Abbruzzese, G;
Bain, PG;
Bajaj, N;
Benito-León, J;
Bhatia, KP;
Deuschl, G;
... Elble, RJ; + view all
(2016)
Transducer-based evaluation of tremor.
Movement Disorders
, 31
(9)
pp. 1327-1336.
10.1002/mds.26671.
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Hirschbichler, ST;
Erro, R;
Ganos, C;
Stamelou, M;
Batla, A;
Balint, B;
Bhatia, KP;
(2017)
"Atypical" atypical parkinsonism: Critical appraisal of a cohort.
Parkinsonism & Related Disorders
, 37
pp. 36-42.
10.1016/j.parkreldis.2016.12.006.
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Hoeglinger, GU;
Respondek, G;
Stamelou, M;
Kurz, C;
Josephs, KA;
Lang, AE;
Mollenhauer, B;
... Litvan, I; + view all
(2017)
Clinical Diagnosis of Progressive Supranuclear Palsy: The Movement Disorder Society Criteria.
Movement Disorders
, 32
(6)
pp. 853-864.
10.1002/mds.26987.
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Jinnah, HA;
Albanese, A;
Bhatia, KP;
Cardoso, F;
Da Prat, G;
de Koning, TJ;
Espay, AJ;
... Gatto, EM; + view all
(2018)
Treatable Inherited Rare Movement Disorders.
Movement Disorders
, 33
(1)
pp. 21-35.
10.1002/mds.27140.
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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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Martino, D;
Stamelou, M;
Bhatia, KP;
(2013)
The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.
Journal of Neurology, Neurosurgery and Psychiatry
, 84
(6)
650 -656.
10.1136/jnnp-2012-302532.
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Mencacci, NE;
Erro, R;
Wiethoff, S;
Hersheson, J;
Ryten, M;
Balint, B;
Ganos, C;
... Bhatia, KP; + view all
(2015)
ADCY5 mutations are another cause of benign hereditary chorea.
Neurology
, 85
(1)
pp. 80-88.
10.1212/WNL.0000000000001720.
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Mencacci, NE;
Isaias, IU;
Reich, MM;
Ganos, C;
Plagnol, V;
Polke, JM;
Bras, J;
... on behalf of the International Parkinson’s Disease Genomics Cons; + view all
(2014)
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.
Brain
, 137
(9)
pp. 2480-2492.
10.1093/brain/awu179.
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Mok, KY;
Schneider, SA;
Trabzuni, D;
Stamelou, M;
Edwards, M;
Kasperaviciute, D;
Pickering-Brown, S;
... Bhatia, KP; + view all
(2014)
Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.
Mov Disord
, 29
(2)
pp. 245-251.
10.1002/mds.25732.
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Mulroy, E;
Stamelou, M;
Bhatia, KP;
(2019)
How to approach a patient with parkinsonism – red flags for atypical parkinsonism.
International Review of Neurobiology
, 149
pp. 1-34.
10.1016/bs.irn.2019.10.001.
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Obeso, JA;
Stamelou, M;
Goetz, CG;
Poewe, W;
Lang, AE;
Weintraub, D;
Burn, D;
... Stoessl, AJ; + view all
(2017)
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy.
[Review].
Movement Disorders
, 32
(9)
pp. 1264-1310.
10.1002/mds.27115.
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Piot, I;
Schweyer, K;
Respondek, G;
Stamelou, M;
DescribePSP study group;
ProPSP study group;
MDS-endorsed PSP study group;
... Höglinger, GU; + view all
(2020)
The Progressive Supranuclear Palsy Clinical Deficits Scale.
Movement Disorders
10.1002/mds.27964.
(In press).
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Respondek, G;
Grimm, M-J;
Piot, I;
Arzberger, T;
Compta, Y;
Englund, E;
Ferguson, LW;
... Movement Disorder Society-Endorsed Progressive Supranuclear Pals; + view all
(2019)
Validation of the movement disorder society criteria for the diagnosis of 4‐repeat tauopathies.
Movement Disorders
10.1002/mds.27872.
(In press).
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Respondek, G;
Kurz, C;
Arzberger, T;
Compta, Y;
Englund, E;
Ferguson, LW;
Gelpi, E;
... Hoeglinger, GU; + view all
(2017)
Which Ante Mortem Clinical Features Predict Progressive Supranuclear Palsy Pathology?
Movement Disorders
, 32
(7)
pp. 995-1005.
10.1002/mds.27034.
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Schreglmann, SR;
Bhatia, KP;
Stamelou, M;
(2017)
Chapter Five - Advances in the Clinical Differential Diagnosis of Parkinson's Disease.
International Review of Neurobiology
, 132
pp. 79-127.
10.1016/bs.irn.2017.01.007.
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Sheerin, UM;
Schneider, SA;
Carr, L;
Deuschl, G;
Hopfner, F;
Stamelou, M;
Wood, NW;
(2014)
ALS2 mutations: Juvenile amyotrophic lateral sclerosis and generalized dystonia.
Neurology
, 82
(12)
pp. 1065-1067.
10.1212/WNL.0000000000000254.
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Stamelou, M;
Adams, M;
Davagnanam, I;
Batla, A;
Sheerin, U;
Talbot, K;
Bhatia, KP;
(2013)
Progressive ataxia and palatal tremor associated with dense pontine calcification: A unique case.
Mov Disord
, 28
(8)
pp. 1155-1157.
10.1002/mds.25310.
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Stamelou, M;
Charlesworth, G;
Cordivari, C;
Schneider, SA;
Kägi, G;
Sheerin, UM;
Rubio-Agusti, I;
... Bhatia, KP; + view all
(2014)
The phenotypic spectrum of DYT24 due to ANO3 mutations.
Mov Disord
, 29
(7)
pp. 928-934.
10.1002/mds.25802.
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Stamelou, M;
Hoeglinger, GU;
(2013)
Atypical parkinsonism: An Update.
Current Opinion in Neurology
, 26
(4)
401 - 405.
10.1097/WCO.0b013e3283632da6.
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Stamelou, M;
Saifee, TA;
Edwards, MJ;
Bhatia, KP;
(2012)
Psychogenic palatal tremor may be underrecognized: reappraisal of a large series of cases.
Mov Disord
, 27
(9)
1164 - 1168.
10.1002/mds.24948.
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Stamelou, M;
Schneider, SA;
Batla, A;
Bhatia, KP;
Lai, SC;
Yeh, T-H;
Lu, C-S;
... Houlden, H; + view all
(2013)
Dystonic opisthotonus: A "red flag" for neurodegeneration with brain iron accumulation syndromes?
Movement Disorders
, 28
(10)
1325 - 1329.
10.1002/mds.25490.
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