Maria Soriano < Maria Stamelou < Maria Steinmayr

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 28.
[0-20] [0 - 20][0 - 28][20-27][20-40]

Ident.	Authors (with country if any)	Title
000009 (2015)	Gesine Respondek ; Günter U. Höglinger ; Maria Stamelou	From a single nucleotide polymorphism to tau pathology: Appoptosin is the missing link.
000301 (2015)	Roberto Erro ; Joshua Hersheson ; Christos Ganos ; Niccol E. Mencacci ; Maria Stamelou ; Amit Batla ; Stefanie Catherine Thust ; Jose M. Bras ; Rita J. Guerreiro ; John Hardy ; Niall P. Quinn ; Henry Houlden ; Kailash P. Bhatia	H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?
000356 (2014)	Gesine Respondek ; Maria Stamelou ; Carolin Kurz ; Leslie W. Ferguson ; Alexander Rajput ; Wan Zheng Chiu ; John C. Van Swieten ; Claire Troakes ; Safa Al Sarraj ; Ellen Gelpi ; Carles Gaig ; Eduardo Tolosa ; Wolfgang H. Oertel ; Armin Giese ; Sigrun Roeber ; Thomas Arzberger ; Stefan Wagenpfeil ; Günter U. Höglinger	The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases.
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.
000550 (2014)	Maria Stamelou	Commentary.
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.
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?
000889 (2013)	Maria Stamelou ; Niall P. Quinn ; Kailash P. Bhatia	"Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.
000945 (2013)	Maria Stamelou ; Christos Christodoulou ; Leonidas Stefanis	Dopamine agonists and delusional jealousy in Parkinson's disease: a cross-sectional prevalence study.
000955 (2013)	Maria Stamelou ; Giovanni Cossu ; Mark J. Edwards ; Daniela Murgia ; Isabel Pareés ; Maurizio Melis ; Kailash P. Bhatia	Familial psychogenic movement disorders.
000971 (2013)	Maria Stamelou	Commentary for "Slowing of saccadic eye movements in sporadic Creutzfeldt-Jakob disease".
000A17 (2013)	Maria Stamelou ; Matthew Adams ; Indran Davagnanam ; Amit Batla ; Una Sheerin ; Kevin Talbot ; Kailash P. Bhatia	Progressive ataxia and palatal tremor associated with dense pontine calcification: A unique case.
000A39 (2013)	Amit Batla ; Maria Stamelou ; Mark J. Edwards ; Isabel Pareés ; Tabish A. Saifee ; Zoe Fox ; Kailash P. Bhatia	Functional movement disorders are not uncommon in the elderly.
000A98 (2013)	Amit Batla ; Maria Stamelou ; Niccolo Mencacci ; Anthony H. Schapira ; Kailash P. Bhatia	Ropinirole monotherapy induced severe reversible dyskinesias in Parkinson's disease.
000C70 (2012)	Maria Stamelou ; Karin Tuschl ; W K Chong ; Andrew K. Burroughs ; Philippa B. Mills ; Kailash P. Bhatia ; Peter T. Clayton	Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder.
000C76 (2012)	Georgia Xiromerisiou ; Henry Houlden ; Nikolaos Scarmeas ; Maria Stamelou ; Eleanna Kara ; John Hardy ; Andrew J. Lees ; Prasad Korlipara ; Patricia Limousin ; Reema Paudel ; Georgios M. Hadjigeorgiou ; Kailash P. Bhatia	THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.
000D02 (2012)	Maria Stamelou ; Kailash P. Bhatia	A new treatable genetic disorder of manganese metabolism causing dystonia-parkinsonism and cirrhosis: the "new" Wilson's disease?
000D41 (2012)	Maria Stamelou ; Giuseppe Plazzi ; Elio Lugaresi ; Mark J. Edwards ; Kailash P. Bhatia	The distinct movement disorder in anti-NMDA receptor encephalitis may be related to Status Dissociatus: a hypothesis.
000D84 (2012)	Maria Stamelou ; Araceli Alonso-Canovas ; Kailash P. Bhatia	Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases.
000E29 (2012)	Maria Stamelou ; Tabish A. Saifee ; Mark J. Edwards ; Kailash P. Bhatia	Psychogenic palatal tremor may be underrecognized: reappraisal of a large series of cases.

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