Results 61 to 70 of about 2,828,155 (151)

ATXN8OS Intermediate Expansion Acts as a Genetic Modifier in Spinocerebellar Ataxia Type 48 (SCA48/STUB1)

open access: yesMovement Disorders, EarlyView.
Abstract Background Association between monoallelic STUB1 variant and expanded ATXN8OS alleles was recently reported, suggesting a pathogenic interaction that may influence spinocerebellar ataxia type 48 (SCA48) phenotype. Objectives We investigated the frequency and clinical impact of ATXN8OS in a large cohort of STUB1 carriers compared to individuals
Charlotte Mouraux   +11 more
wiley   +1 more source

Psychogenic dystonia of the hand: A clinical case

open access: yesНеврология, нейропсихиатрия, психосоматика, 2016
The article describes a clinical case of psychogenic movement disorder appearing as fixed dystonia without pain. Over 5 years, a patient has had the right fingers being permanently clenched into a fist position at rest, which increased when fulfilling ...
A. I. Baidauletova, O. A. Shavlovskaya
doaj   +1 more source

Sensory Attenuation Assessed by Sensory Evoked Potentials in Functional Movement Disorders. [PDF]

open access: yesPLoS ONE, 2015
Functional (psychogenic) movement disorders (FMD) have features associated with voluntary movement (e.g. distractibility) but patients report movements to be out of their control.
Antonella Macerollo   +5 more
doaj   +1 more source

Clinical features of functional (psychogenic) eye movement disorders [PDF]

open access: yes, 2016
Despite increasing awareness of the high prevalence of functional neurological symptoms, there has been only one recent clinical evaluation of functional eye movement disorders, but this study reported only functional (psychogenic) oculogyric crises ...
Kaski, D, Bronstein, AM, Pradhan, V
core   +1 more source

Semiological features of epilepsy seizures and paroxysmal non‐epileptic events in children: A systematic review and meta‐analysis

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Pediatric paroxysmal non‐epileptic events (PNEs) are frequently misdiagnosed as epilepsy. We systematically reviewed and synthesized 40 studies, including 3123 video‐EEG monitored pediatric patients. Epileptic seizures in infants (1 month–3 years) typically presented as arrest, while in children and adolescents (1 month–21 years) they manifested as ...
Tímea Lőrincz‐Molnár   +8 more
wiley   +1 more source

Secondary tics and tourettism Tiques secundários e touretismo

open access: yesBrazilian Journal of Psychiatry, 2005
Motor and phonic tics are most frequently due to Tourette syndrome, but there are many other causes of tics. We analyzed data on 155 patients with tics and co-existent disorders (101M/54F; mean age 40.5 ± 20.2 years).
Nicte I Mejia, Joseph Jankovic
doaj   +1 more source

Scales for Antipsychotic-Associated Movement Disorders: Systematic Review, Critique, and Recommendations

open access: yes, 2023
BACKGROUND: Antipsychotic-associated movement disorders remain common and disabling. Their screening and assessment are challenging due to clinical heterogeneity and different use of nomenclature between psychiatrists and neurologists.
Bhidayasiri, R   +9 more
core   +1 more source

Developing a neuropsychiatry curriculum for clinical psychologists and neuropsychologists: An e‐Delphi study

open access: yesJournal of Neuropsychology, EarlyView.
Abstract Neuropsychiatric presentations are common across neurological and mental health services but they are often inadequately covered by core clinical psychology and clinical neuropsychology training. Consequently, we aimed to identify components for a neuropsychiatry curriculum for clinical psychologists using a Delphi process.
Keishema Kerr   +18 more
wiley   +1 more source

Epileptic–Dyskinetic Encephalopathy Associated with a PPP3CA Variant: Expansion of the Phenotypic Spectrum

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Bruno Antunes Contrucci   +10 more
wiley   +1 more source

Suspected hyperthyroidism‐associated myoclonus in a cat

open access: yesVeterinary Record Case Reports, Volume 14, Issue 4, November 2026.
Abstract A 10‐year‐old, male, neutered domestic shorthair cat presented with a 2‐week history of progressively worsening myoclonic jerks predominantly involving the head. Jerks were continuous and marked at rest, but became less intense during activity.
Magdalena Maria Dyrka   +5 more
wiley   +1 more source

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