Results 11 to 20 of about 10,678 (188)
Objective To summarize the clinical features of anti⁃leucine⁃rich⁃glioma⁃inactivation 1 (LGI1) antibody associated encephalitis. Methods and Results A total of 13 patients with anti ⁃ LGI1 antibody associated encephalitis were admitted to Huai'an No.
PAN He⁃yue +5 more
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Spotlight on Oculogyric Crisis: A Review
Background: Oculogyric crisis (OGC) is a form of acute dystonia characterized by sustained dystonic, conjugate, and upward deviation of the eyes. It was initially reported in patients with postencephalitic parkinsonism.
Pankaj Mahal +2 more
doaj +1 more source
Objective To study the clinical characteristics, diagnosis, treatment and prognosis of a patient with childhood⁃onset rapid⁃onset dystonia Parkinsonism (RDP) caused by ATP1A3 gene mutation, and review the related literature.
KANG Qing⁃yun +4 more
doaj +1 more source
Dystonia in childhood may be severely disabling and often un-remitting and un-recognised. Considered a rare disorder, dystonic symptoms in childhood are pervasive in many conditions including disorders of developmental delay, cerebral palsy, autism ...
Jean-Pierre Lin, Nardo Nardocci
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A Case of Peripherally Induced Task-Specific “Lipstick Dystonic Tremor”
Background: Peripherally induced movement disorders (PIMDs) represent a rare and debated complication of peripheral trauma. Phenomenology Shown: We report a case of task-specific “lipstick” jerky dystonic tremor as a consequence of traumatic shoulder ...
Francesco Cavallieri +4 more
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Dystonic Movement Disorders and Spinal Degenerative Disease
The occurrence of degenerative spinal disease subsequent to dystonic movement disorders has been neglected and has received more attention only recently. Spinal surgery is challenging with regard to continuous mechanical stress when treatment of the underlying movement disorder is insufficient.
Loher, Thomas J +2 more
openaire +3 more sources
Dopa-responsive dystonia [PDF]
Backgrround/Aim. Dystonia is considered to be a prolonged involuntary contractions of the muscles leading to twisting, repetitive movements or irregular postures. Etiologically, it could be classified as primary and secondary dystonia.
Đurić Gordana +3 more
doaj +1 more source
Diagnosis and Clinical Features in Autoimmune-Mediated Movement Disorders [PDF]
Movement disorders are common manifestations in autoimmune-mediated encephalitis. This group of diseases is suspected to be triggered by infection or neoplasm.
Pei-Chen Hsieh, Yih-Ru Wu
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Familial dystonic choreoathetosis with myokymia; a sleep responsive disorder. [PDF]
A family is presented with paroxysmal dystonic choreoathetosis transmitted as a dominant trait over five generations. The family is unusual in the marked responsiveness of the episodes to short periods of sleep in several members, in the very variable age of onset, and in the association with prominent myokymia in some cases.
E, Byrne, O, White, M, Cook
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Effect of Botulinum Toxin on Non-Motor Symptoms in Cervical Dystonia
Patients with cervical dystonia (CD) may display non-motor symptoms, including psychiatric disturbances, pain, and sleep disorders. Intramuscular injection of botulinum toxin type A (BoNT-A) is the most efficacious treatment for motor symptoms in CD, but
Matteo Costanzo +12 more
doaj +1 more source

