Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Dystonic movements"'
Publikováno v:
International Medical Case Reports Journal, Vol Volume 17, Pp 1037-1040 (2024)
Mohamed Farah Gabobe Nor,1 Rayan Mohamed Salah,2 Mohammed AM Ahmed,3 Sakariye Abdullahi Hassan,4 Mohamed Farah Yusuf Mohamud1,5,6 1Faculty of Medicine, Mogadishu University, Mogadishu, Somalia; 2Department of Pediatric, Kalkaal Hospital, Mogadishu, S
Externí odkaz:
https://doaj.org/article/dadedb699d804b55ad9a3d38cef05154
Autor:
Monica Volz, Jill L. Ostrem, Kristen A. Dodenhoff, Philip A. Starr, Leslie C. Markun, Marta San Luciano, Ian O. Bledsoe
Publikováno v:
Movement disorders clinical practice, vol 7, iss 5
Mov Disord Clin Pract
Mov Disord Clin Pract
BACKGROUND: The pallidum has been the preferred DBS target for dystonia, but recent studies have shown equal or greater improvement in patients implanted in the STN.(1) Transient stimulation‐induced dyskinesia (SID) is frequently observed when stim
Publikováno v:
The Journal of the International Society of Physical and Rehabilitation Medicine. 4:156-158
This case describes success using high-dose submotor threshold electrical stimulation (EStim) therapy for the management of dystonia in a chronic stroke patient. The authors find this novel EStim treatment is safe and offers the potential to manage p
Publikováno v:
Journal of Anaesthesiology Clinical Pharmacology, Vol 28, Iss 3, Pp 371-373 (2012)
Dystonic movements after general anesthesia are very rare. The differential diagnosis includes adverse drug reaction, local anesthetic reaction, emergence delirium, hysterical response, and shivering. We present a case of a 10-year-old, otherwise hea
Externí odkaz:
https://doaj.org/article/a3dac68814664c1292b4fc1427389301
Akademický článek
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Publikováno v:
Case Reports in Dentistry, Vol 2021 (2021)
Case Reports in Dentistry
Case Reports in Dentistry
Mandibular parasymphysis fracture is very commonly observed especially in old age when there is resorptions of the alveolar ridges. In cervical dystonia, there is centrally mediated disease in which there is uncontrolled and spasmodic contraction of
Autor:
Massimo Filippi, Maria A. Rocca
Publikováno v:
White Matter Diseases ISBN: 9783030386207
Neuromyelitis optica spectrum disorders (NMOSD) are a heterogeneous group of inflammatory, demyelinating and antibody-mediated diseases of the central nervous system (CNS). The anti-aquaporin-4-IgG (AQP4-IgG) seems to be the pathogenetic agent, being
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75e56c0834919c28bab3588c78dad8f3
https://doi.org/10.1007/978-3-030-38621-4_3
https://doi.org/10.1007/978-3-030-38621-4_3
Autor:
Alon Y. Mogilner
A 14-year-old female is referred to discuss deep brain stimulation surgery for idiopathic generalized dystonia. She is of Ashkenazi Jewish descent and presented in early childhood with dystonic movements of one leg, which later generalized. Multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcee7a7340027cb23dc40570b6171923
https://doi.org/10.1016/b978-0-12-817002-1.00012-2
https://doi.org/10.1016/b978-0-12-817002-1.00012-2
Autor:
Ana Catarina Franco, Filipa Falcão, Ana Rita Peralta, Miguel Coelho, Luísa Albuquerque, Tiago Teodoro, Carla Bentes, Linda Azevedo Kauppila
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Mov Disord Clin Pract
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Mov Disord Clin Pract
© 2019 International Parkinson and Movement Disorder Society
Glutamic acid decarboxylase (GAD) antibodies (ab) have been associated with rare disorders, such as Stiff-person syndrome, limbic encephalitis, cerebellar ataxia, and temporal lobe ep
Glutamic acid decarboxylase (GAD) antibodies (ab) have been associated with rare disorders, such as Stiff-person syndrome, limbic encephalitis, cerebellar ataxia, and temporal lobe ep
Autor:
Tania-Mihaela Idriceanu, Marc Sindou
Publikováno v:
Acta Neurochirurgica. 159:1707-1711
The authors present a case of a 42-year-old female admitted for disabling complex and atypical bilateral facial spasms associated with painful masticatory and motor ocular dystonic movements, difficult to fit in the definition of any known cranio-fac