Lingual dystonia etiology spectrum in a tertiary center
Objective: To describe a group of patients with LP regarding clinical presentation, etiology, and treatment. Background: Lingual dystonia (LD) is a rare, disabling and difficult…Isolated craniocervical dystonia without neuropsychiatric manifestations associated with NMDA-receptor antibodies
Objective: N-methyl-D-aspartate receptor (NMDAR) encephalitis classically spans neuropsychiatric disturbance, autonomic dysfunction and salient movement disorders. Attenuated presentations are increasingly recognised; however, presentations with an isolated…Changes in botulinum toxin dosing in cervical dystonia over 7 years
Objective: To assess changes in botulinum toxin dosing over the course of illness of cervical dystonia. Background: Muscle specific botulinum toxin injections remains the main…Spectrum of Movement disorders and Correlation with Functional Status in Children with Cerebral Palsy
Objective: We sought to detail the spectrum of movement disorders (MD) among children with cerebral palsy (CP) and assess impact on functional status. Background: Movement…Movement disorders in demyelination: A case series of ten patients
Objective: To observe the association of various movement disorder with demyelinating disease. Background: Movement disorders in demyelinating diseases are not an unheard entity, but besides…Neural Signals in the Cerebellar Nuclei Gate the Manifestation of Dystonia-Associated Symptoms in Mice
Objective: Define the differences in electrophysiological signatures of cerebellar output between mouse models of dystonia with diverse severity and manifestation. Background: Dystonia is heterogeneous movement…Blepharospasm – a network disorder
Objective: We present a case with apraxia of eyelid opening, orbicularis oculi spasms, increased blinking, which falls within the new paradigm that defines blepharospasm, that…Evaluation of abnormal cerebellar iron distribution in idiopathic cervical dystonia using quantitative susceptibility mapping
Objective: This study aimed to investigate abnormal cerebellar iron distribution in patients with idiopathic CD using quantitative susceptibility mapping (QSM). Background: Idiopathic CD is a…Clinical heterogeneity of DYT-KMT2B mutation in a family with monozygotic twins
Objective: We describe the clinical heterogeneity of a Danish family with complex dystonia and a variant in KMT2B not previously reported. Background: Heterozygous mutations in…Dystonia gravidarum: An emerging clinical entity
Objective: We describe a case of cervical dystonia in a 36 year-old, secundigravid, Caucasian woman at 8 weeks gestation. Background: Though uncommon, primary movement disorders…
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