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Movement Disorders (revue)

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Susanne A. Schneider And NotAngleterre

List of bibliographic references

Number of relevant bibliographic references: 24.
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 UmerThe 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 MüllerStem 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
000462 Ali S. Shalash [Égypte] ; Solaf M. Elsayed ; Suzan Elnaghi ; Susanne A. Schneider ; Tawhida Y. Abdel GhaffarProminent extensor truncal dystonia in Egyptian patients with Wilson's disease.
000766 Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider ; Günther DeuschlSubmandibular gland biopsy for the diagnosis of Parkinson's disease.
000894 Petr Dusek [République tchèque] ; Susanne A. SchneiderNeurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determined.
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. SchneiderDe 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. BhatiaSyndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations.
000D02 Athanasia Alexoudi ; Susanne A. SchneiderMutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.
000D09 Susanne A. Schneider ; Michael R. JohnsonMonozygotic twins with LRRK2 mutations: genetically identical but phenotypically discordant.
000E92 Athanasia Alexoudi [Allemagne] ; Susanne A. SchneiderAlternating 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 HagenahA study of subtle motor signs in early Parkinson's disease.
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. BhatiaRecognition of faciobrachial dystonic seizures allowing early intervention with and 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
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
002672 James T. H. Teo [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni] ; Binith J. Cheeran [Royaume-Uni] ; Miguel Fernandez-Del-Olmo [Espagne] ; Paola Giunti [Royaume-Uni] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]Prolonged cortical silent period but normal sensorimotor plasticity in spinocerebellar ataxia 6
Wicri

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