Researcher
Thomas Wirth
Hôpitaux universitaires de Strasbourg
Statistics
43 papers found
Papers authored by Thomas Wirth
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Izzie Jacques Namer ,
Ben Monga,
Caroline Bund ,
Andra Valentina Iosif,
Odile Gebus,
Solveig Montaut,
Thomas Bogdan,
Laura Robelin,
Mathilde Renaud,
Stéphane Kremer,
Christine Tranchant ,
Mathieu Anheim
Progression of Nigrostriatal Denervation in Cerebellar Multiple System Atrophy
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,
Timothy Grover,
Francesca Preda,
Elina Tripoliti,
Jennifer Foley,
Emma Scelzo,
Antonella Macerollo,
Harith Akram ,
Jonathan Hyam,
Ludvic Zrinzo,
Patricia Limousin,
Thomas Foltynie
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Huw R. Morris
Revisiting the assessment of tremor: clinical review
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Thomas Wirth ,
Cécile Hubsch,
Andrea H. Németh,
Volkan Okur,
Mathieu Anheim,
Nathalie Drouot,
Christine Tranchant,
Gabrielle Rudolf ,
Jamel Chelly,
Katrina Tatton‐Brown,
Cornelis Blauwendraat,
Jean Paul G. Vonsattel,
Etty Cortes,
Roy N. Alcalay
and 1 other authors
Reply to “ PPP2R5D Genetic Mutations and Early Onset Parkinsonism”
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O. Lagha-Boukbiza,
Solveig Montaut,
Eric Bardinet,
Maeva Kyheng,
Anne‐Sophie-S. Rolland,
Thomas Wirth ,
Jimmy Voirin,
Sophie Drapier,
Franck Durif,
Alexandre Eusebio
and 18 other authors
Download from onlinelibrary.wiley.com
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Thomas Wirth ,
Cécile Hubsch,
Andrea H. Németh,
Volkan Okur,
Mathieu Anheim,
Nathalie Drouot,
Christine Tranchant,
Gabrielle Rudolf ,
Jamel Chelly,
Katrina Tatton‐Brown,
Cornelis Blauwendraat,
Jean Paul G. Vonsattel,
Etty Cortes,
Roy N. Alcalay
and 1 other authors
Early‐Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation
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Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia
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Matthieu Béreau ,
Wenshu XiangWei ,
Thomas Wirth ,
Daniel Amsallem,
Lauren Buisson,
Philippe Richard,
Nana Liu ,
Yuchen Xu ,
Scott J. Myers ,
Stephen F. Traynelis ,
Jameleddine Chelly,
Mathieu Anheim ,
Martine Raynaud ,
Lionel Van Maldergem
and 1 other authors
The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus
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Christine Tranchant,
Nathalie Drouot,
Boris Keren,
Cyril Mignot,
Laura Cif,
Romain Lefaucheur,
Laurence Lion-François,
Aurélie Méneret,
Domitille Gras,
Emmanuel Roze,
Cécile Laroche,
Pierre Burbaud,
Stéphanie Bannier,
Ouhaid Lagha-Boukbiza
and 9 other authors
Increased diagnostic yield in complex dystonia through exome sequencing
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Louise Laure Mariani ,
Gaber Bergant,
Michel Baulac,
Marie‐Odile Habert,
Nathalie Drouot,
Emmanuelle Ollivier,
Alenka Hodžić,
Gorazd Rudolf,
Patrick Nitschke,
Gabrielle Rudolf,
Jamel Chelly,
Christine Tranchant,
Mathieu Anheim,
Emmanuel Roze
Loss‐of‐function mutations in NR4A2 cause dopa‐responsive dystonia Parkinsonism
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S. Rivaud-Péchoux,
P. Charles,
C. Ewenczyk,
A. Meneret,
B. B. Monga,
M.-C. Fleury,
E. Hainque,
T. Maisonobe,
B. Degos,
A. Echaniz-Laguna,
M. Renaud,
T. Wirth ,
D. Grabli,
A. Brice
and 10 other authors
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