Journal of neurology
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
Inhaltsverzeichnis
- 201
-
The full spectrum of ethical issues in the care of patients with ALS: a systematic qualitative reviewSeitzer, F. / Kahrass, H. / Neitzke, G. et al. | 2015
- 210
-
Vestibular-evoked myogenic potentials in central vestibular disordersOh, Sun-Young / Kim, Hyo-Jeong / Kim, Ji-Soo et al. | 2015
- 221
-
The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathiesGrimm, Alexander / Rasenack, Maria / Athanasopoulou, Ioanna M. et al. | 2015
- 231
-
Prognostic value of trans-thoracic echocardiography in patients with acute stroke and atrial fibrillation: findings from the RAF studyPaciaroni, Maurizio / Agnelli, Giancarlo / Falocci, Nicola et al. | 2015
- 238
-
The clinical relevance of cerebral microbleeds in patients with cerebral ischemia and atrial fibrillationHaji, Shamir / Planchard, Ryan / Zubair, Adeel et al. | 2015
- 245
-
Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome: a slowly progressive disorder with stereotypical presentationCazzato, Daniele / Bella, Eleonora Dalla / Dacci, Patrizia et al. | 2015
- 250
-
Pharmacodynamics of a low subacute levodopa dose helps distinguish between multiple system atrophy with predominant Parkinsonism and Parkinson’s diseaseCalandra-Buonaura, Giovanna / Doria, Andrea / Lopane, Giovanna et al. | 2015
- 257
-
Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient populationTatlisumak, Turgut / Putaala, Jukka / Innilä, Markus et al. | 2015
- 263
-
Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutationDi, Li / Chen, Hai / Da, Yuwei et al. | 2015
- 277
-
Predictors of outcome in HSV encephalitisSingh, Tarun D. / Fugate, Jennifer E. / Hocker, Sara et al. | 2015
- 290
-
Deep brain stimulation of the internal pallidum in Huntington’s disease patients: clinical outcome and neuronal firing patternsDelorme, Cécile / Rogers, Alister / Lau, Brian et al. | 2015
- 299
-
The relationship between the rate of brain volume loss during first 24 months and disability progression over 24 and 48 months in relapsing MSJeffery, Douglas R. / Di Cantogno, Elisabetta Verdun / Ritter, Shannon et al. | 2015
- 306
-
Domain-specific versus generalized cognitive screening in acute strokeDemeyere, Nele / Riddoch, M. J. / Slavkova, E. D. et al. | 2015
- 316
-
Pseudobulbar affect (PBA) in an incident ALS cohort: results from the Apulia registry (SLAP)Tortelli, Rosanna / Copetti, Massimiliano / Arcuti, Simona et al. | 2015
- 322
-
Rituximab in paediatric onset multiple sclerosis: a case seriesSalzer, Jonatan / Lycke, Jan / Wickström, Ronny et al. | 2015
- 327
-
Efficacy of fingolimod is superior to injectable disease modifying therapies in second-line therapy of relapsing remitting multiple sclerosisBraune, Stefan / Lang, M. / Bergmann, A. et al. | 2015
- 334
-
Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxiaSchwarz, N. / Hahn, A. / Bast, T. et al. | 2015
- 344
-
Brief intervention by general practitioners for medication-overuse headache, follow-up after 6 months: a pragmatic cluster-randomised controlled trialKristoffersen, Espen Saxhaug / Straand, Jørund / Vetvik, Kjersti Grøtta et al. | 2015
- 354
-
Onset of clinical and MRI efficacy occurs early after fingolimod treatment initiation in relapsing multiple sclerosisKappos, Ludwig / Radue, Ernst-Wilhelm / Chin, Peter et al. | 2015
- 361
-
NEFL N98S mutation: another cause of dominant intermediate Charcot–Marie–Tooth disease with heterogeneous early-onset phenotypeBerciano, José / Peeters, Kristien / García, Antonio et al. | 2015
- 370
-
Isolated new onset ‘atypical’ optic neuritis in the NMO clinic: serum antibodies, prognoses and diagnoses at follow-upPiccolo, L. / Woodhall, M. / Tackley, G. et al. | 2015
- 380
-
Progressive supranuclear palsy: progression and survivalArena, Julieta E. / Weigand, Stephen D. / Whitwell, Jennifer L. et al. | 2015
- 390
-
Clinical features and differential diagnosis of flail arm syndromeHübers, Annemarie / Hildebrandt, Viviane / Petri, Susanne et al. | 2015
- 396
-
Defining the phenotype of restless legs syndrome/Willis–Ekbom disease (RLS/WED): a clinical and polysomnographic studyRinaldi, Fabrizio / Galbiati, Andrea / Marelli, Sara et al. | 2016
- 403
-
Improvement of lateral axial dystonia following prismatic correction of oculomotor control disorders in Parkinson’s diseaseSantilli, Marco / Meglio, Michele / Varanese, Sara et al. | 2016
- 405
-
Paraneoplastic opsoclonus and cerebellar ataxia related to anti-Ma2 antibody: a case reportMélé, Nicolas / Hautefort, Charlotte / Toledano, Alain et al. | 2016
- 407
-
Key emerging issues in frontotemporal dementiaHopkins, Sarah A. A. / Chan, Dennis et al. | 2015
- 414
-
New ways of looking at an old disease: the reimagination of epilepsyMitchell, Clinton J. / Robertson, Neil P. et al. | 2016
- 417
-
József von Lenhossék (1818–1888)Triarhou, Lazaros C. et al. | 2015
- 419
-
Erratum to: The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegiaGuthrie, Grant / Pfeffer, Gerald / Bailie, Maura et al. | 2016