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

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 53.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000042 (2015)	Muthuraman Muthuraman ; Günther Deuschl ; Abdul Rauf Anwar ; Kidist Gebremariam Mideksa ; Friederike Von Helmolt ; Susanne A. Schneider	Essential and aging-related tremor: Differences of central control.
000146 (2015)	Franziska Hopfner ; Susanne A. Schneider	Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family.
000157 (2015)	Miryam Carecchio ; Susanne A. Schneider	GTP cyclohydrolase 1 mutations and Parkinson's disease: new insights beyond DOPA-responsive dystonia.
000284 (2015)	Franziska Hopfner ; 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.
000293 (2015)	Björn Br Ndl ; Susanne A. Schneider ; Jeanne F. Loring ; John Hardy ; Philip Gribbon ; Franz-Josef Müller	Stem cell reprogramming: basic implications and future perspective for movement disorders.
000359 (2014)	Amit Batla ; 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.
000606 (2014)	Maria Stamelou ; Gavin Charlesworth ; Carla Cordivari ; Susanne A. Schneider ; Georg K Gi ; Una-Marie Sheerin ; Ignacio Rubio-Agusti ; Amit Batla ; Henry Houlden ; Nicholas W. Wood ; Kailash P. Bhatia	The phenotypic spectrum of DYT24 due to ANO3 mutations.
000679 (2014)	Kin Y. Mok ; Susanne A. Schneider ; Daniah Trabzuni ; Maria Stamelou ; Mark Edwards ; Dalia Kasperaviciute ; Stuart Pickering-Brown ; Monty Silverdale ; John Hardy ; Kailash P. Bhatia	Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.
000770 (2014)	Ali S. Shalash ; Solaf M. Elsayed ; Suzan Elnaghi ; Susanne A. Schneider ; Tawhida Y. Abdel Ghaffar	Prominent extensor truncal dystonia in Egyptian patients with Wilson's disease.
000781 (2013)	Athanasia Alexoudi ; 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).
000825 (2013)	Petr Dusek ; Susanne A. Schneider	Neurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determined.
000886 (2013)	Maria Stamelou ; Scarlett C. Lai ; Annu Aggarwal ; Susanne A. Schneider ; Henry Houlden ; Tu-Hsueh Yeh ; Amit Batla ; Chin-Song Lu ; Mohit Bhatt ; Kailash P. Bhatia	Dystonic opisthotonus: a "red flag" for neurodegeneration with brain iron accumulation syndromes?
000890 (2013)	Athanasia Alexoudi ; Susanne A. Schneider ; Günther Deuschl	Submandibular gland biopsy for the diagnosis of Parkinson's disease.
000A01 (2012)	Athanasia Alexoudi ; Susanne A. Schneider	Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations.
000A52 (2012)	Athanasia Alexoudi ; Susanne A. Schneider	Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.
000C28 (2012)	Susanne A. Schneider ; Laura Drude ; Meike Kasten ; Christine Klein ; Johann Hagenah	A study of subtle motor signs in early Parkinson's disease.
000C51 (2012)	Susanne A. Schneider ; Michael R. Johnson	Monozygotic twins with LRRK2 mutations: genetically identical but phenotypically discordant.
000D65 (2012)	Kailash P. Bhatia ; Susanne A. Schneider	Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia.
000E67 (2011)	Susanne A. Schneider ; Kailash P. Bhatia	Recognition of faciobrachial dystonic seizures allowing early intervention with and prevention of development of full-blown limbic encephalitis.
000F83 (2012)	Susanne A. Schneider ; 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.
001059 (2011)	Susanne A. Schneider ; Peter G. Bain	The Wilson films--bilateral postural tremor.

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