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Journal of Neurology|March 16, 2012
Presymptomatic genetic testing in CADASILS Reyes, A Kurtz, D Hervé, et al.Journal of Neurology|November 8, 2014
Diagnosis of muscle diseases presenting with early respiratory failureGerald Pfeffer, Marcus Povitz, G John Gibson, et al.Journal of Neurology|November 10, 2014
Compensatory eye and head movements of patients with homonymous hemianopia in the naturalistic setting of a driving simulationMarkus Bahnemann, Johanna Hamel, Sophie De Beukelaer, et al.Journal of Neurology|October 27, 2014
CADASIL in central Italy: a retrospective clinical and genetic study in 229 patientsSilvia Bianchi, Enza Zicari, Alessandra Carluccio, et al.Journal of Neurology|November 1, 2014
Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females onlyRobert Wilcox, Ingrid Brænne, Norbert Brüggemann, et al.Journal of Neurology|November 1, 2014
Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutationsCecilia Mancini, Stefano Nassani, Yiran Guo, et al.Journal of Neurology|November 12, 2014
Prognostic factors for the course of functional status of patients with ALS: a systematic reviewHuub Creemers, Hepke Grupstra, Frans Nollet, et al.Journal of Neurology|November 26, 2013
White matter damage is related to ataxia severity in SCA3J-S Kang, J C Klein, S Baudrexel, et al.Journal of Neurology|November 20, 2014
Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutationsGianluca Floris, Giuseppe Borghero, Antonino Cannas, et al.Journal of Neurology|February 24, 2001
Effects of parkinsonian medication on sleepD Schäfer, W GreulichPageof 1,108