| Ident. | Authors (with country if any) | Title |
|---|
| 000041 |
Franziska Hopfner [Allemagne] ; Giovanni Stevanin ; Stefanie H. Müller ; Emeline Mundwiller ; May Bungeroth ; Alexandra Durr ; Manuela Pendziwiat ; Mathieu Anheim ; Susanne A. Schneider ; Lukas Tittmann ; Stephan Klebe ; Delia Lorenz ; Günther Deuschl ; Alexis Brice ; Gregor Kuhlenb Umer | The impact of rare variants in FUS in essential tremor. |
| 000063 |
Björn Br Ndl [Allemagne] ; Susanne A. Schneider ; Jeanne F. Loring ; John Hardy ; Philip Gribbon ; Franz-Josef Müller | Stem cell reprogramming: basic implications and future perspective for movement disorders. |
| 000156 |
Franziska Hopfner [Allemagne] ; Susanne A. Schneider [Allemagne] | Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family. |
| 000230 |
Miryam Carecchio [Italie] ; Susanne A. Schneider [Allemagne] | GTP cyclohydrolase 1 mutations and Parkinson's disease: new insights beyond DOPA-responsive dystonia. |
| 000245 |
Muthuraman Muthuraman [Allemagne] ; Günther Deuschl [Allemagne] ; Abdul Rauf Anwar [Allemagne] ; Kidist Gebremariam Mideksa [Allemagne] ; Friederike Von Helmolt [Allemagne] ; Susanne A. Schneider [Allemagne] | Essential and aging-related tremor: Differences of central control. |
| 000396 |
Maria Stamelou [Royaume-Uni] ; Gavin Charlesworth [Royaume-Uni] ; Carla Cordivari [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Georg K Gi [Royaume-Uni, Suisse] ; Una-Marie Sheerin [Royaume-Uni] ; Ignacio Rubio-Agusti [Royaume-Uni] ; Amit Batla [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | The Phenotypic Spectrum of DYT24 Due to ANO3 Mutations |
| 000766 |
Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider ; Günther Deuschl | Submandibular gland biopsy for the diagnosis of Parkinson's disease. |
| 000974 |
Kin Y. Mok [Royaume-Uni] ; Susanne A. Schneider [Allemagne, Royaume-Uni] ; Daniah Trabzuni [Royaume-Uni] ; Maria Stamelou [Royaume-Uni] ; Mark Edwards [Royaume-Uni] ; Dalia Kasperaviciute [Royaume-Uni] ; Stuart Pickering-Brown [Royaume-Uni] ; Monty Silverdale [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel |
| 000A13 |
Maria Stamelou [Royaume-Uni] ; Scarlett C. Lai [Taïwan] ; Annu Aggarwal [Inde] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Henry Houlden [Royaume-Uni] ; Tu-Hsueh Yeh [Taïwan] ; Amit Batla [Royaume-Uni] ; Chin-Song Lu [Taïwan] ; Mohit Bhatt [Inde] ; Kailash P. Bhatia [Royaume-Uni] | Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
| 000A38 |
Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider | De Novo mutations in the β-tubulin gene TUBB4: from DYT4 to leukoencephalopathy with hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC syndrome). |
| 000B97 |
Susanne A. Schneider [Allemagne] ; John Hardy ; Kailash P. Bhatia | Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations. |
| 000E92 |
Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider | Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations. |
| 000F04 |
Susanne A. Schneider [Allemagne] ; Laura Drude ; Meike Kasten ; Christine Klein ; Johann Hagenah | A study of subtle motor signs in early Parkinson's disease. |
| 000F69 |
Susanne A. Schneider [Allemagne, Royaume-Uni] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Syndromes of Neurodegeneration with Brain Iron Accumulation (NBIA): an Update on Clinical Presentations, Histological and Genetic Underpinnings, and Treatment Considerations |
| 001224 |
Susanne A. Schneider [Allemagne] ; Laura Drude [Allemagne] ; Meike Kasten [Allemagne] ; Christine Klein [Allemagne] ; Johann Hagenah [Allemagne] | A Study of Subtle Motor Signs in Early Parkinson's Disease |
| 001248 |
Susanne A. Schneider [Allemagne] ; Kailash P. Bhatia | Recognition of faciobrachial dystonic seizures allowing early intervention with and prevention of development of full-blown limbic encephalitis. |
| 001345 |
Susanne A. Schneider [Allemagne, Royaume-Uni] ; Peter G. Bain [Royaume-Uni] | The Wilson films — Bilateral postural tremor |
| 001431 |
Susanne A. Schneider [Allemagne] ; Kailash P. Bhatia [Royaume-Uni] | Recognition of faciobrachial dystonic seizures allowing early intervention with prevention of development of full‐blown limbic encephalitis |
| 001495 |
Jens T. Wuerfel [Allemagne] ; Guenter Seidel [Allemagne] ; Uwe Melchert [Allemagne] ; Andreas Sprenger [Allemagne] ; Cathrin Hansmann [Allemagne] ; Peter Trillenberg [Allemagne] ; Dirk Petersen [Allemagne] ; Rainer Schoenweiler [Allemagne] ; Susanne A. Schneider [Allemagne] | Palatal tremor visualized by cine MRI |
| 001524 |
Susanne A. Schneider [Allemagne] | NBIA due to FA2H gene mutations is allelic with hereditary spastic paraplegia (SPG35) and a form of familial leukodystrophy |
| 001534 |
Miryam Carecchio [Royaume-Uni, Italie] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Heidi Chan [Royaume-Uni] ; Robin Lachmann [Royaume-Uni] ; Philip J. Lee [Royaume-Uni] ; Elaine Murphy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Movement disorders in adult surviving patients with maple syrup urine disease |
| 001633 |
Susanne A. Schneider [Allemagne, Royaume-Uni] ; Alfredo Ramirez [Allemagne] ; Kaveh Shafiee [Iran] ; Frank J. Kaiser [Allemagne] ; Alev Erogullari [Allemagne] ; Norbert Brüggemann [Allemagne] ; Susen Winkler [Allemagne] ; Ideh Bahman [Iran] ; Alma Osmanovic [Allemagne] ; Mohammad A. Shafa [Iran] ; Kailish P. Bhatia [Royaume-Uni] ; Hossein Najmabadi [Iran] ; Christine Klein [Allemagne] ; Katja Lohmann [Allemagne] | Homozygous THAP1 mutations as cause of early‐onset generalized dystonia |
| 001651 |
Omar S. Mian [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Petra Schwingenschuh [Royaume-Uni, Autriche] ; Kailash P. Bhatia [Royaume-Uni] ; Brian L. Day [Royaume-Uni] | Gait in SWEDDs patients: Comparison with Parkinson's disease patients and healthy controls |
| 001B48 |
Georg K Gi [Royaume-Uni] ; Christine Klein [Allemagne] ; Nicholas W. Wood [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni] ; Peter P. Pramstaller [Allemagne, Italie] ; Vera Tadic [Allemagne] ; Niall P. Quinn [Royaume-Uni] ; Bart P. C. Van De Warrenburg [Royaume-Uni, Pays-Bas] ; Kailash P. Bhatia [Royaume-Uni] | Nonmotor symptoms in Parkin gene‐related parkinsonism |
| 001B78 |
Susanne A. Schneider [Royaume-Uni, Allemagne] ; Burkhard Pleger [Royaume-Uni, Allemagne] ; Bogdan Draganski [Royaume-Uni, Allemagne] ; Carla Cordivari [Royaume-Uni] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Ray J. Dolan [Royaume-Uni] | Modulatory effects of 5Hz rTMS over the primary somatosensory cortex in focal dystonia—An fMRI‐TMS study |
| 001C24 |
Annu Aggarwal [Inde] ; Susanne A. Schneider [Allemagne, Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Monty Silverdale [Royaume-Uni] ; Reema Paudel [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Shrinivas Desai [Inde] ; Mihir Munshi [Inde] ; Darshana Sanghvi [Inde] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Mohit Bhatt [Inde] | Indian‐subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms |
| 001D23 |
Coro Paisán-Ruiz [Royaume-Uni] ; Rocio Guevara [Royaume-Uni] ; Monica Federoff [Royaume-Uni] ; Hasmet Hanagasi [Turquie] ; Fardaz Sina [Iran] ; Elahe Elahi [Iran] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Petra Schwingenschuh [Allemagne] ; Nin Bajaj [Royaume-Uni] ; Murat Emre [Turquie] ; Andrew B. Singleton [États-Unis] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Allemagne] ; Sebastian Brandner [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; Henry Houlden [Royaume-Uni] | Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations |
| 001D43 |
Norbert Brüggemann [Allemagne] ; Susanne A. Schneider [Allemagne] ; Thurid Sander [Allemagne] ; Christine Klein [Allemagne] ; Johann Hagenah [Allemagne] | Distinct basal ganglia hyperechogenicity in idiopathic basal ganglia calcification |
| 001D90 |
Simone Zittel [Allemagne] ; Christian K. E. Moll [Allemagne] ; Norbert Brüggemann [Allemagne] ; Vera Tadic [Allemagne] ; Wolfgang Hamel [Allemagne] ; Meike Kasten [Allemagne] ; Katja Lohmann [Allemagne] ; Thora Lohnau [Allemagne] ; Susen Winkler [Allemagne] ; Christian Gerloff [Allemagne] ; Rainer Schönweiler [Allemagne] ; Johann Hagenah [Allemagne] ; Christine Klein [Allemagne] ; Alexander Münchau [Allemagne] ; Susanne A. Schneider [Allemagne] | Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families |
| 001E05 |
Susanne A. Schneider [Royaume-Uni, Allemagne] ; Anthony E. Lang [Canada] ; Elena Moro [Canada] ; Benedikt Bader [Allemagne] ; Adrian Danek [Allemagne] ; Kailash P. Bhatia [Royaume-Uni] | Characteristic head drops and axial extension in advanced chorea‐acanthocytosis |
| 001E75 |
Susanne A. Schneider [Royaume-Uni, Allemagne] ; Coro Paisan-Ruiz [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation |
| 001F55 |
Coro Paisan-Ruiz [Royaume-Uni] ; Rocio Guevara [Royaume-Uni] ; Monica Federoff [Royaume-Uni] ; Hasmet Hanagasi [Turquie] ; Fardaz Sina [Iran] ; Elahe Elahi [Iran] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Petra Schwingenschuh [Allemagne] ; Nin Bajaj [Royaume-Uni] ; Murat Emre [Turquie] ; Andrew B. Singleton [États-Unis] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Allemagne] ; Sebastian Brandner [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; Henry Houlden [Royaume-Uni] | Early-Onset L-dopa-Responsive Parkinsonism with Pyramidal Signs Due to ATP13A2, PLA2G6, FBX07 and Spatacsin Mutations |
| 002277 |
Christine Klein [Allemagne, Canada] ; Susanne A. Schneider [Allemagne, Royaume-Uni] ; Anthony E. Lang [Canada] | Hereditary parkinsonism: Parkinson disease look‐alikes—An algorithm for clinicians to “PARK” genes and beyond |
| 002296 |
Susanne A. Schneider [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Ines Garcia-Gorostiaga [Royaume-Uni, Espagne] ; Niall P. Quinn [Royaume-Uni] ; Yvonne G. Weber ; Holger Lerche [Allemagne] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | GLUT1 gene mutations cause sporadic paroxysmal exercise‐induced dyskinesias |
| 002835 |
Susanne A. Schneider [Royaume-Uni] ; Mary M. Robertson [Royaume-Uni] ; Renata Rizzo [Italie] ; Jeremy Turk [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Michael Orth [Royaume-Uni, Allemagne] | Fragile X syndrome associated with tic disorders |
