Susanne A. Goldstein < Susanne A. Schneider < Susanne Asenbaum

Facettes :

List of bibliographic references indexed by Susanne A. Schneider

Number of relevant bibliographic references: 58.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000041 (2015)	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 (2015)	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 (2015)	Franziska Hopfner [Allemagne] ; Susanne A. Schneider [Allemagne]	Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family.
000230 (2015)	Miryam Carecchio [Italie] ; Susanne A. Schneider [Allemagne]	GTP cyclohydrolase 1 mutations and Parkinson's disease: new insights beyond DOPA-responsive dystonia.
000245 (2015)	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 (2014)	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 (2014)	Ali S. Shalash [Égypte] ; Solaf M. Elsayed ; Suzan Elnaghi ; Susanne A. Schneider ; Tawhida Y. Abdel Ghaffar	Prominent extensor truncal dystonia in Egyptian patients with Wilson's disease.
000483 (2014)	Amit Batla [Royaume-Uni] ; Roberto Erro ; Maria Stamelou ; Susanne A. Schneider ; Petra Schwingenschuh ; Christos Ganos ; Kailash P. Bhatia	Patients with scans without evidence of dopaminergic deficit: a long-term follow-up study.
000766 (2013)	Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider ; Günther Deuschl	Submandibular gland biopsy for the diagnosis of Parkinson's disease.
000894 (2013)	Petr Dusek [République tchèque] ; Susanne A. Schneider	Neurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determined.
000974 (2013)	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 (2013)	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 (2013)	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 (2012)	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.
000D02 (2012)	Athanasia Alexoudi ; Susanne A. Schneider	Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.
000D09 (2012)	Susanne A. Schneider ; Michael R. Johnson	Monozygotic twins with LRRK2 mutations: genetically identical but phenotypically discordant.
000D61 (2012)	Kailash P. Bhatia [Royaume-Uni] ; Susanne A. Schneider	Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia.
000E92 (2012)	Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider	Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations.
000F04 (2012)	Susanne A. Schneider [Allemagne] ; Laura Drude ; Meike Kasten ; Christine Klein ; Johann Hagenah	A study of subtle motor signs in early Parkinson's disease.
000F69 (2012)	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 (2012)	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

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