Clinical and morphometric features of the tics
Objective: To evaluate clinical and morphometric features in patients with tics in association with OCD and ADHD Background: In recent years there have been reports…Hearing Evaluation (Peripheral and Central) in Patients with Sporadic Ataxia
Objective: To describe the audiological and electrophysiological results in patients with sporadic ataxia. Background: Patients with progressive non-familial adult ataxia are classified into a sporadic…Clinico-genetic correlation in Indian Spinocerebellar ataxia Type 1 (SCA1) patients
Objective: To conduct a clinical and genetic analysis of SCA 1 in Indian population. Background: Spinocerebellar ataxia type1 (SCA1) is a neurodegenerative disease caused by…Coexisting CACNA1A pathogenic variant and MJD expansion in the same family
Objective: Genetic investigation of a family with inherited cerebellar ataxia. Background: Despite the identification of an increasing number of genes causing dominant spinocerebellar ataxias (SCAs),…Rapidly progressive ataxia caused by an undetermined paraneoplastic disorder: A case report
Objective: To report the case of a 69-year-old woman with rapidly progressive ataxia. Background: Various cases exist in the literature of rapidly progressive ataxia secondary…Two cases of hemichorea-hemiballism in nonketotic hyperglycemia
Objective: We describe two cases of Hemichorea-Hemiballism (HCHB) associated with nonketotic hyperglycemia. Background: HCHB is defined as continuous, non-patterned, and involuntary movement involving one side…The clinical value of SPECT in identifying dystonic muscles of patients with cervical dystonia
Objective: The aim of this study is to compare the efficacy of selecting target muscles for botulinum toxin injection by abnormal movement pattern and by…Siblings with a PRKRA (DYT16) Mutation and Startle Myoclonus
Objective: To characterize and expand the phenotype of a family from North-East England with DYT16. Background: DYT16 is an autosomal recessive disease associated with mutations…Paroxysmal multifocal dystonia with hemiplegic migraine possibly related to novel CACNA1A mutation
Objective: To report a case of a unique clinical presentation of hemiplegic migraine associated with paroxysmal multifocal dystonia possibly related to a novel CACNA1A mutation.…Pilot trial of botulinum toxin and occupational therapy for Writer’s Cramp
Objective: We aimed to compare the effects of botulinum toxin (BoNT) therapy alone with a combination of BoNT and occupational therapy on patients with writer’s…
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