Papers authored by Niccolò Emanuele Mencacci
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Andreea Manole,
Stephanie Efthymiou,
Jana Vandrovcova,
Conceicao Bettencourt ,
Niccolò E. Mencacci ,
Christine Klein,
Michy P. Kelly,
Ceri H. Davies,
Haruhide Kimura,
Alfons Macaya,
Henry Houlden
A homozygous loss‐of‐function mutation in PDE2A associated to early‐onset hereditary chorea
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Marjan Jahanshahi,
Lisa Cipolotti,
Jonathan Hyam,
Ludvic Zrinzo,
Marwan Hariz,
John Hardy,
Patricia Limousin,
Tom Foltynie
GBA-Associated Parkinson’s Disease: Progression in a Deep Brain Stimulation Cohort
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Emerging Monogenic Complex Hyperkinetic Disorders
Download from link.springer.com
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Miryam Carecchio,
Davide Tonduti,
Veronica Saletti,
Celeste Panteghini,
Luisa Chiapparini,
Giovanna Zorzi,
Chiara Pantaleoni,
Barbara Garavaglia ,
Dimitri Krainc,
Steven J. Lubbe,
Nardo Nardocci,
Niccolò E. Mencacci
A PDE10A de novo mutation causes childhood‐onset chorea with diurnal fluctuations
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Niccolò E. Mencacci ,
Alessandro Iodice,
Roser Pons,
Celeste Panteghini,
Giovanna Zorzi,
Federica Zibordi ,
Anastasios Bonakis,
Argyris Dinopoulos,
Joseph Jankovic,
Leonidas Stefanis,
Kailash P. Bhatia,
Valentina Monti,
Lea R'Bibo ,
Liana Veneziano
and 5 other authors
Download from doi.org
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Ne Mencacci ,
Ch Hawkes,
Jm Masters,
Nicholas Wood ,
John Hardy,
Gavin Giovannoni,
Aj Lees,
Anette Schrag
PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease.
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Michel A. Willemsen,
Apostolos Papandreou,
David Arkadir,
Joanne Ng ,
Angela Barnicoat,
Andrea Cortese,
Hagai Bergman
and 69 other authors
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.
Download from www.nature.com
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Kin Y. Mok,
Bj J. Traynor,
Lucia Schottlaender,
Viorica Chelban,
Hr R. Morris
and 35 other authors
A genome-wide association study in multiple system atrophy
Download from www.neurology.org
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Miryam Carecchio
Recent advances in genetics of chorea:
Download from www.ncbi.nlm.nih.gov
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Lucinda Carr,
Nicholas W. Wood ,
Kailash P. Bhatia
SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy
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Erik-Jan Kamsteeg,
Kosuke Nakashima,
L. R'Bibo,
Lea R’Bibo,
David S. Lynch,
Bettina Balint,
Michèl A. A. P. Willemsen,
Sarah Wiethoff,
Matthew E. Adams,
Kazunori Suzuki,
Joanne Ng ,
Ceri H. Davies,
Esther Meyer,
Liana Veneziano
and 17 other authors
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions
Download from openaccess.sgul.ac.uk
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Kiran Mantripragada,
Karen M. Doherty,
Alastair J. Noyce,
Niccolo E. Mencacci ,
Steven J. Lubbe,
Caroline H. Williams Gray ,
Roger A. Barker,
Karin D. van Dijk,
Henk W. Berendse
and 24 other authors
Download from dx.doi.org
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Mencacci Ne,
N. E. Mencacci ,
Mallucci Gr,
G. R. Mallucci ,
S. H. Y. Loh,
Loh Sh,
Martins Lm,
L. Miguel Martins
Download from www.nature.com
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Niccolò Emmanuele Mencacci ,
Mencacci Ne,
Raquel Durán ,
Francisco Javier Barrero ,
Barrero Fj,
Francisco Escamilla-Sevilla,
Sarah Morgan ,
Jason Hehir ,
Francisco Vives,
John Hardy,
Pittman Am,
Alan M. Pittman
Analysis of the genetic variability in Parkinson's disease from Southern Spain
Download from www.researchgate.net
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K. P. Bhatia
Persistent chorea in DYT6, due to anticholinergic therapy
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Léa R'bibo,
Sara Bandres-Ciga,
Miryam Carecchio,
Giovanna Zorzi,
Nardo Nardocci,
Barbara Garavaglia ,
Amit Batla,
Kailash P. Bhatia,
Alan M. Pittman,
John Hardy,
Anne Weissbach,
Christine Klein,
Thomas Gasser,
Ebba Lohmann
and 1 other authors
Download from discovery.ucl.ac.uk
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John C. Morgan,
Sarah Wiethoff,
Roberto Erro,
Joshua Hersheson,
Julie A. Kurek,
Mina Ryten,
Bettina Balint,
Maria Stamelou,
Christos Ganos,
Jennie Davis,
Niall Quinn,
Nicholas W. Wood ,
Kapil D. Sethi,
Henry Houlden
and 1 other authors
ADCY5 mutations are another cause of benign hereditary chorea
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