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Gotowe bibliografie tematyczne / Dystonic movements

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Gotowa bibliografia na temat „Dystonic movements”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Dystonic movements"

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Honey, C. Michael, Armaan K. Malhotra, Maja Tarailo-Graovac, Clara D. M. van Karnebeek, Gabriella Horvath, and Adi Sulistyanto. "GNAO1 Mutation–Induced Pediatric Dystonic Storm Rescue With Pallidal Deep Brain Stimulation." Journal of Child Neurology 33, no. 6 (2018): 413–16. http://dx.doi.org/10.1177/0883073818756134.

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Dystonic storm or status dystonicus is a life-threatening hyperkinetic movement disorder with biochemical alterations due to the excessive muscle contractions. The medical management can require pediatric intensive care unit admission and a combination of medications while the underlying trigger is managed. Severe cases may require general anesthesia and paralytic agents with intubation and may relapse when these drugs are weaned. Deep brain stimulation of the globus pallidum has been reported to terminate dystonic storm in several pediatric cases. We present a 10-year-old boy with a de novo G

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Johans, Stephen J., Kevin N. Swong, Ryan C. Hofler, and Douglas E. Anderson. "A Stepwise Approach: Decreasing Infection in Deep Brain Stimulation for Childhood Dystonic Cerebral Palsy." Journal of Child Neurology 32, no. 10 (2017): 871–75. http://dx.doi.org/10.1177/0883073817713900.

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Dystonia is a movement disorder characterized by involuntary muscle contractions, which cause twisting movements or abnormal postures. Deep brain stimulation has been used to improve the quality of life for secondary dystonia caused by cerebral palsy. Despite being a viable treatment option for childhood dystonic cerebral palsy, deep brain stimulation is associated with a high rate of infection in children. The authors present a small series of patients with dystonic cerebral palsy who underwent a stepwise approach for bilateral globus pallidus interna deep brain stimulation placement in order

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Chu, Virginia Way Tong, Dagmar Sternad, and Terence David Sanger. "Healthy and dystonic children compensate for changes in motor variability." Journal of Neurophysiology 109, no. 8 (2013): 2169–78. http://dx.doi.org/10.1152/jn.00908.2012.

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Successful reaching requires that we plan movements to compensate for variability in motor output. Previous studies have shown that healthy adults optimally incorporate estimates of motor variability when planning a pointing task. Children with dystonia have increased variability compared with healthy children. It is not known whether they are able to compensate appropriately for the increased variability and whether this compensation leads to changes in reaching behavior. We examined healthy children and those with increased motor variability due to secondary dystonia. Using a simple virtual

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di Biase, Lazzaro, Alessandro Di Santo, Maria Letizia Caminiti, Pasquale Maria Pecoraro, Simona Paola Carbone, and Vincenzo Di Lazzaro. "Dystonia Diagnosis: Clinical Neurophysiology and Genetics." Journal of Clinical Medicine 11, no. 14 (2022): 4184. http://dx.doi.org/10.3390/jcm11144184.

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Dystonia diagnosis is based on clinical examination performed by a neurologist with expertise in movement disorders. Clues that indicate the diagnosis of a movement disorder such as dystonia are dystonic movements, dystonic postures, and three additional physical signs (mirror dystonia, overflow dystonia, and geste antagonists/sensory tricks). Despite advances in research, there is no diagnostic test with a high level of accuracy for the dystonia diagnosis. Clinical neurophysiology and genetics might support the clinician in the diagnostic process. Neurophysiology played a role in untangling d

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Mercan, F. N., E. Bayram, and M. C. Akbostanci. "A glance on dystonias, how to recognize and handle them." NATIONAL JOURNAL OF NEUROLOGY, no. 3 (January 8, 2019): 22–29. http://dx.doi.org/10.28942/nnj.v1i3.178.

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Dystonia refers to an involuntary, repetitive, sustained, painful and twisting movements of the affected body part. This movement disorder was first described in 1911 by Hermain Oppenheim, and many studies have been conducted to understand the mechanism, the diagnosis and the treatment of dystonia ever since. However, there are still many unexplained aspects of this phenomenon. Dystonia is diagnosed by clinical manifestations, and various classifications are recommended for the diagnosis and the treatment. Anatomic classification, which is based on the muscle groups involved, is the most helpf

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Mercan, F. N., E. Bayram, and M. C. Akbostanci. "A GLANCE ON DYSTONIAS, HOW TO RECOGNIZE AND HANDLE THEM." National Journal of Neurology 1, no. 03 (2013): 33–40. http://dx.doi.org/10.61788/njn.v1i13.05.

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Dystonia refers to an involuntary, repetitive, sustained, painful and twisting movements of the affected body part. This movement disorder was first described in 1911 by Hermain Oppenheim, and many studies have been conducted to understand the mechanism, the diagnosis and the treatment of dystonia ever since. However, there are still many unexplained aspects of this phenomenon. Dystonia is diagnosed by clinical manifestations, and various classifications are recommended for the diagnosis and the treatment. Anatomic classification, which is based on the muscle groups involved, is the most helpf

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Kowacs, Pedro A., Hélio A. Ghizoni Teive, Elcio J. Piovesan, Jorge A. Zavala, and Lineu C. Werneck. "Botulinum-A toxin in the treatment of painful post-stroke nocturnal paroxysmal dystonia triggered by periodic limb movements of sleep: case report." Arquivos de Neuro-Psiquiatria 64, no. 4 (2006): 1027–29. http://dx.doi.org/10.1590/s0004-282x2006000600028.

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INTRODUCTION: Sleep disorders presenting involuntary movements may be very annoying to patients, apart from their negative influence on sleep. OBJECTIVE: To report the use of botulinum type-A toxin (BoNT-A) to manage the case of a patient whose sleep was severely disrupted by episodes of dystonic posturing of the right lower limb triggered by periodic limb movements of sleep (PLMS). METHOD: A 79-year-old woman with mild post-stroke right hemiparesis presented with recurrent painful episodes of dystonia of the right lower limb, which disrupted her sleep. The dystonic episodes could also be volu

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Pranzatelli, Michael R. "Movement Disorders in Childhood." Pediatrics In Review 17, no. 11 (1996): 388–94. http://dx.doi.org/10.1542/pir.17.11.388.

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Clinical Aspects Dyskinesias are abnormal involuntary movements. The common dyskinesias include tics, chorea, tremor, dystonia, myoclonus, and hyperactivity (Table 1). Several other less common dyskinesias also are important to recognize. The diagnosis of the type of movement disorder is clinical. When the movements are episodic and not seen by the pediatrician, obtaining a home videotape is recommended. Most patients who have movement disorders, with the exception of tic disorders, should be referred to a neurologist, but it is important for the pediatrician to be able to identify them and to

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Umemura, Atsushi, Jurg L. Jaggi, Carol A. Dolinskas, Matthew B. Stern, and Gordon H. Baltuch. "Pallidal deep brain stimulation for longstanding severe generalized dystonia in Hallervorden—Spatz syndrome." Journal of Neurosurgery 100, no. 4 (2004): 706–9. http://dx.doi.org/10.3171/jns.2004.100.4.0706.

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✓ Generalized dystonia is one of the most disabling movement disorders. Ablative stereotactic surgery such as pallidotomy has been performed for medically refractory dystonia. Recently, deep brain stimulation (DBS) has appeared as an alternative to ablative procedures. Nevertheless, there have been few published reports detailing improvement in dystonia with DBS. This 36-year-old man with Hallervorden—Spatz syndrome suffered from intractable primary generalized dystonia for 28 years. He was completely dependent for activities of daily living and wheelchair bound because of continuous severe dy

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Godeiro-Junior, Clecio, Andre Carvalho Felício, Patrícia Maria de Carvalho Aguiar, Vanderci Borges, Sonia Maria Azevedo Silva, and Henrique Ballalai Ferraz. "Retrocollis, anterocollis or head tremor may predict the spreading of dystonic movements in primary cervical dystonia." Arquivos de Neuro-Psiquiatria 67, no. 2b (2009): 402–6. http://dx.doi.org/10.1590/s0004-282x2009000300006.

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BACKGROUND AND PURPOSE: Few studies have attempted to develop clinical predictors for cervical dystonia (CD) aiming at progression of the dystonic movement. METHOD: We retrospectively evaluated 73 patients with primary CD who underwent treatment with Botulinum toxin type-A (BTX-A). The patients were assembled in two groups according to the spread of dystonia during follow-up: spreading and non-spreading CD. We performed a binary logistic regression model using spreading of cervical dystonia as dependent variable aiming to find covariates which increase the risk of spreading. RESULTS: Our logis

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Rozprawy doktorskie na temat "Dystonic movements"

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Koelman, Johannes Henricus Theodorus Maria. "Dystonia reflexions on movement /." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2001. http://dare.uva.nl/document/84836.

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Chang, Florence. "Movement and postural control in dystonia." Thesis, University of Sydney, 2020. https://hdl.handle.net/2123/22982.

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Recently separate control systems for postural and movement control have been found in primates. Dystonia is a hyperkinetic movement disorder and its cause it not well understood. We have observed that dystonia patients have preserved fine movement control, but difficulty maintaining the appropriate and sustained posture that supports these movements. Postural control requires multiple modalities of sensory input such as cutaneous, proprioceptive, vestibular and visual stimuli. Through clinical observation, dystonia is improved by sensory alteration. Sensorimotor integration dysfunction has be

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Bleton, Jean-Pierre. "Les dystonies focales : leurs dysfonctionnements sensori-moteurs et leurs conséquences sur l'organisation du mouvement." Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4099.

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L’identification des muscles responsables des dystonies focales est un prérequis à l’instauration des traitements par toxine botulique et exercices correcteurs. A partir de deux dystonies apparemment dissemblables: la crampe de l’écrivain et la dystonie cervicale, nous avons montré que la réponse aux traitements est tributaire de la distribution des muscles impliqués. L’enregistrement des mouvements du segment tête-cou dans la dystonie cervicale , au moyen de capteurs inertiels 3-D, a montré qu’au mouvement volontaire de la tête, dans un plan, s’associent des mouvements non physiologiques dans

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Newman, Jeremy R. B. "Identifying and Assessing Risk Factors for Idiopathic Dystonia." Thesis, Griffith University, 2014. http://hdl.handle.net/10072/366155.

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Dystonia is a group of debilitating neurological movement disorders characterised by abnormal sustained or intermittent involuntary co-contraction of opposing muscle groups. While some forms of dystonia are caused by rare genetic mutations or acquired following a toxic or physical injury or other cause, the majority of cases arise with no clear aetiology. It is thought that these idiopathic dystonias manifest following a complex interaction between genetic susceptibility and non-genetic triggers. The inherited and idiopathic forms of dystonia share a number of symptomatic and physiological sim

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Lorentzos, Michelle Sarah. "The Psychiatry of Paediatric Movement Disorders." Thesis, The University of Sydney, 2019. http://hdl.handle.net/2123/20602.

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I compared the rate of psychiatric comorbidity in children with Non-tic movement disorders to children with tics and TS. In addition, this PhD explores whether children with Non-tic movement disorders have elevated rates of psychiatry compared to other hospital populations, including Emergency patients and other Neurology patients, as well as a healthy community control group. My hypothesis was that children with Non-tic movement disorders would have rates of psychiatric comorbidities that are similar to children with tics and TS.To examine this hypothesis, I recruited children between the age

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Zetterberg, Lena. "Multidimensional Aspects of Dystonia : Description and Physiotherapy Management." Doctoral thesis, Uppsala universitet, Institutionen för neurovetenskap, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-9417.

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<b>Aims:</b> The overall aim of this research was to increase the knowledge about dystonia by identifying factors that influence self-reported quality of life and health in this disorder and to determine what factors predict disability. A further aim was to develop an objective outcome measure for quantifying the movement dysfunction in cervical dystonia (CD) and evaluate effects of physiotherapy. <b>Methods:</b> A descriptive correlative design was adopted for study I (n=351), with a questionnaire covering physical activity, satisfaction with treatment, physiotherapy or not, and quality of li

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Vries, Paulien Maria de. "Cervical dystonia abnormal cerebral activation patterns related to preparation and execution of hand movement /." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2008. http://irs.ub.rig.nl/ppn/.

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Al, Ajia Moaz [Verfasser]. "The effect of GPi-DBS on automatic and controlled movement in dystonia / Moaz Al Ajia." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2021. http://d-nb.info/1241540624/34.

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Macintyre, Lucy. "An investigation of neuropsychological functioning in adults with primary focal dystonia : evidence for a deficit in extra-dimensional set shifting?" Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289344.

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Gonzalez, Martinez Maria Victoria. "Evaluation des réseaux neuronaux vecteurs de comportements par imagerie anatomique et fonctionnelle in vivo chez l'homme." Thesis, Montpellier 1, 2014. http://www.theses.fr/2014MON1T002.

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L'évolution des connaissances dans le domaine de la neurochirurgie fonctionnelle, la neuroradiologie et les études de traçage neuronal par virus neurotropes ont permis d'étudier les circuits sous-tendant l'expression clinique de plusieurs syndromes neurologiques. La stimulation cérébrale profonde (SCP) du globus pallidus interne (GPi) est une thérapie validée dans les syndromes dystono-dyskinétiques (SDD) isolés. L'extension des indications vers des SDD secondaires ou hérédo-dégénératifs nous confronte à la nécessité d'améliorer notre compréhension des mécanismes de réorganisation fonctionnell

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Książki na temat "Dystonic movements"

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National Institute of Neurological Disorders and Stroke (U.S.). Office of Scientific and Health Reports. The dystonias. U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health, 1996.

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Masaya, Segawa, ed. Hereditary progressive dystonia with marked diurnal fluctuation. Parthenon Pub. Group, 1993.

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Susan, Grube, and Patil Parag G, eds. Deep brain stimulation: A new life for people with Parkinson's, dystonia and essential tremor. Demos Health, 2012.

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Fletcher, Nicholas. Movement disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0926.

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Almost any neurological disorder can produce a disorder of movement but the ‘movement disorders’ include the akinetic rigid syndromes, hyperkinesias, and some tremors. It can sometimes seem, especially with the use of videotape recordings, that diagnosis of movement disorders is mainly a matter of correct visual recognition. Such an approach is not recommended and can lead to mistakes unless, as in other areas of medicine, the history is considered first and the physical signs second. Obvious examples include the family history in Huntington’s disease, developmental history in dystonic cerebra

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de Bie, Robertus M. A., and Susanne E. M. Ten Holter. A Tremor with an Abnormal Posture. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190607555.003.0018.

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Dystonic tremors are a commonly misdiagnosed group of primary tremor disorders, typically mistaken for Parkinson’s disease or essential tremor. Like most movement disorders, this is a clinical diagnosis, so the overlap in some features between all of these disorders can be confusing to less experienced and even more experienced physicians. A tremor in the presence of a dystonia is a dystonic tremor syndrome, regardless of the clinical features. Treatment of dystonic tremor can be challenging without the same gratifying response seen to levodopa in tremor associated with Parkinson’s disease or

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de Bie, Robertus M. A., and Susanne E. M. Ten Holter. Advanced Treatment for Dystonia. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190607555.003.0019.

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Deep-brain stimulation is a last resort for the management of dystonia or dystonic movement disorders when oral or injectable therapies do not provide adequate relief to allow an acceptable quality of life. The underlying pathogenesis of dystonia is less well understood than in Parkinson’s disease, in which deep-brain stimulation is generally expected to provide effective and long-lasting benefit. Furthermore, it is likely that dystonia represents a number of different basal ganglia pathologies. The response of dystonia to deep-brain stimulation is typically delayed for up to weeks or months f

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Williams, Jeri Yvonne, and David G. Standaert. Dystonia. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0011.

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Dystonia is a movement disorder characterized by sustained or intermittent muscle contractions. Classification of dystonia is based on age of onset, distribution of body parts affected, and underlying etiology. A large number of different genetic forms of dystonia have been discovered in recent years. Although these syndromes are important to recognize, the majority of dystonias encountered in clinical practice are of unknown cause. Therapy of dystonia includes medications, particularly anticholinergic drugs, use of botulinum toxins, and deep brain stimulation.

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Jinnah, H. A., Bettina Balint, and Victor S. C. Fung, eds. The Dystonias. Oxford University PressNew York, 2025. https://doi.org/10.1093/med/9780197631966.001.0001.

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Abstract The dystonias are a heterogeneous group of disorders characterized by excessive muscle contractions leading to abnormal postures and movements. The clinical manifestations of this broad group of disorders are quite varied. The dystonias may emerge at any age from infancy through late adulthood, they may affect muscles in nearly any region of the body, they may occur without other clinical problems, or they may be combined with other neurological or systemic disorders. There are many etiologies for dystonia, both acquired and inherited, although many are idiopathic. The clinical manife

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Jinnah, H. A., Cecilia N. Prudente, Samuel J. Rose, and Ellen J. Hess. The Neurobiology of Dystonia. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0010.

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The dystonias are a large group of disorders characterized by excessive muscle activity leading to abnormal movements. They are clinically diverse, affecting different parts of the body at all ages in both humans and other animals. They also are etiologically diverse, with causes that are either inherited due to specific dystonia-causing genes, or acquired because of nervous system injury or exposure to certain drugs or chemicals. Despite the clinical and etiological heterogeneity, there is an increasing appreciation that certain subgroups of dystonias share some biological abnormalities at th

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Nageshwaran, Sathiji, Heather C. Wilson, Anthony Dickenson, and David Ledingham. Hyperkinetic movement disorders. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199664368.003.0010.

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This chapter discusses the clinical features and evidence-based pharmacological management of tremor, dystonia (focal, generalized, and dopa-responsive dystonia), tics and Tourette’s syndrome, chorea (Huntington’s disease (HD) and Sydenham’s chorea), ballism and athetosis, myoclonus, and restless legs syndrome (RLS).

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Części książek na temat "Dystonic movements"

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Nirenberg, Melissa J., and Blair Ford. "Dystonic Storm." In Movement Disorder Emergencies. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-60761-835-5_9.

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Nirenberg, Melissa J., and Blair Ford. "Dystonic Storm." In Movement Disorder Emergencies. Humana Press, 2005. http://dx.doi.org/10.1385/1-59259-902-8:101.

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Del Sorbo, Francesca, and Alberto Albanese. "Dystonia." In Movement Disorders Curricula. Springer Vienna, 2017. http://dx.doi.org/10.1007/978-3-7091-1628-9_24.

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Shanker, Vicki, and Susan Bressman. "Dystonia." In Hyperkinetic Movement Disorders. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-60327-120-2_3.

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Frucht, Steven J., and Pichet Termsarasab. "Dystonia." In Movement Disorders Phenomenology. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-52573-5_12.

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Sherman, Rosalie, and K. Ray Chaudhuri. "Dystonia." In Handbook of Movement Disorders. Springer Healthcare Ltd., 2009. http://dx.doi.org/10.1007/978-1-908517-04-3_3.

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Sherman, Rosalie, and K. Ray Chaudhuri. "Dystonia." In Movement Disorders in Clinical Practice. Springer London, 2010. http://dx.doi.org/10.1007/978-1-84996-065-6_3.

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Tarsy, Daniel. "Dystonia." In Parkinson’s Disease and Movement Disorders. Humana Press, 2000. http://dx.doi.org/10.1007/978-1-59259-410-8_23.

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Frucht, Steven J., and Pichet Termsarasab. "Phenomenology of Dystonia." In Movement Disorders Phenomenology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-36975-0_9.

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Furukawa, Yoshiaki, Mark Guttman, Shinichiro Nakamura, and Stephen J. Kish. "Dopa-Responsive Dystonia." In Movement Disorder Emergencies. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-60761-835-5_24.

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Streszczenia konferencji na temat "Dystonic movements"

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Nakano, Bruno Eiji, Gabriel Flamarin Cavasana, Paula Carolina Grande Nakazato, et al. "Focal dystonia after an ischemic stroke: case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.769.

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Case presentation: A 77-year-old female patient, previously hypertensive, was admitted to the emergency room due to involuntary movements in the right upper limb onset one day ago with no other associated complaints. During neurological examination she presented hemiparesis and hypoesthesia in the right dimidium of the body besides involuntary movements in the ipsilateral hand. Skull magnetic resonance imaging evidences hyperintensity on T2/ FLAIR sequences in areas of periventricular and left parietal white matter in accordance to a previous ischemic event. Discussion: Dystonia is a movement

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Pereira, Camila Alves, Alana Strucker Barbosa, Vanessa de Freitas Moreira, et al. "Case report: motor neurone symptoms as initial clinical manifestation in a patient with Creutzfeldt-Jakob disease." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.590.

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Female, 54-year-old, began with weakness in her right hand and loss of dexterity. Four months after initial symptoms, patient developed sudden onset vertigo. She progressed with difficulties in coordination, dystonic posture and involuntary movements in her right arm. Family also reported insomnia and cognitive impairment. Ten days later, she had no recognition of family members, and developed myoclonia. After two weeks, progression of ataxia rendered her unable to walk and she also had urinary incontinence. Neurological examination revealed perseveration of speech, oculomotor apraxia, severe

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Paulo, Artur José Marques, Jeff Waugh, Joselisa Queirzos de Paiva, et al. "In vivo assessment of striatal compartments in patients with idiopathic upper limb dystonia." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.331.

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Introduction: The striatum is an essential hub in the motor system associated with dystonia and other movement disorders. The function of the striosomes and matrix in motor control is not clear. A recently developed method using diffusion tensor imaging (DTI) enables us to distinguish compartments of the striatum, namely matrixes-like and striosomes-like voxels. Objectives: To access striatal matrix and striosome compartments in patients with idiopathic upper limb dystonia using diffusion tensor imaging. Methods: We analyzed 3T magnetic resonance imaging (MRI) images from 26 patients with idio

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Abela, L., J. Häberle, K. Steindl, et al. "Severe Dystonic Movement Disorder and Developmental Encephalopathy Due to Hexokinase 1 Mutation." In Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1739687.

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Saito, Monalisa Moura, Dhyego Ferreira Moreira de Lacerda, Ana Claudia Marque Gouveia de Melo, Lucas Monteiro Barros Nunes, Luana Cristina Rodrigues de Oliveira Costa, and Eduarda Silvestre Ribeiro da Costa Gomes. "Neurodegeneration with cerebral iron accumulation: a case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.145.

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Introduction: NBIA is a rare disease, with a prevalence of 1/1,000,000.It is characterized by abnormal iron accumulation. Clinical findings may include progressive extrapyramidal disorders, involvement of the pyramidal, peripheral, autonomic nervous systems, superior cortical, visual and cerebellar functions. The diagnosis is made through the association of clinical findings and complementary exams. Currently, the treatment is only symptomatic, with no specific therapy. Case report: 5-year-old female, reporting involuntary movements and difficulty walking a day ago. Presented agitation and del

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Schöne-Bake, Jan-Christoph, Bernd Auber, Thomas Jack, and Hans Hartmann. "P 411. GNAO1-Associated Hyperkinetic-Dystonic Movement Disorder and Developmental Delay in a 14-Year-Old Girl." In Abstracts of the 44th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1675951.

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Santiago, Mayhara Rosany da Silva, Ana Caroline Paiva Simeão, Heloisy Maria Nunes Galvão, et al. "Atypical case of Wilson’s disease presenting with unusual neuroimage features." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.351.

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Introduction: Wilson’s disease (WD) is a rare autosomal recessive disorder resulting in hepatic and neurological symptoms. Uncommon presentations are prone to diagnostic and treatment delay. Objectives: Describe an atypical case of WD and improve clinicians awareness. Case report: A 19 years-old male presented to us with seizures and upper limb tremor in the past three years, evolving to torsion-like movements in limbs and trunk. He was unable to open his eyes and had severe dysphagia. There was no consanguinity, perinatal complications or neurodevelopmental delay. Examination revealed general

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Figueiredo, Camila Angelo Vidal de, Kaline dos Santos Kishishita Castro, and Sílvia Raimunda Costa Leite. "Therapeutic management of movement disorders present in Huntington’s Disease: a literature review." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.430.

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Background: Huntington’s Disease (HD) is a hereditary neurodegenerative genetic disease with motor, cognitive and behavioral repercussions that interferes in several areas of the patients’ lives. Therefore, to increase the quality of life for patients the therapeutic management of symptoms is necessary. Objective: to elucidate the main forms of treatment that reduces motor disorders present in HD. Methods: an integrative literature review was conducted using scientific articles published between 2016-2020 about this topic found in Pubmed and Google Scholar databases. Results: the chorea treatm

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Roark, Ryan. "Dystopia, Climate Change and Heritage Conservation in the Late Nineteenth Century." In The 39th Annual Conference of the Society of Architectural Historians Australia and New Zealand. SAHANZ, 2023. http://dx.doi.org/10.55939/a5037py0jq.

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The architectural conservation and restoration movements emerged in the Western world in the mid-nineteenth century, in part as a reaction to the acceleration of visible aging of buildings caused by the Industrial Revolution and associated changes in air quality. At the same time, Enlightenment ideals established at the end of the eighteenth century reinforced the relatively new idea that a building could have a single author and a fixed state. A new drive towards ‘restoration’ – the return of a building to a glorified singular past state – led William Morris in 1877 to establish the Society f

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Rocha, Maria Luísa, Amandra Gabriele Coelho Rodrigues Melo, Maria Eduarda Ramos Jubé Borges Lucas, et al. "Intraventricular baclofen for spasticity – a forgotten strategy?" In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.701.

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Introducion: Spasticity is persistent increased muscle resistance to joint movement. Treatments for this condition aim to prevent or minimize its evolution into severe movement restrictions. Among the therapeutic options are the use of oral medications or the surgical approach for continuous baclofen infusion, in which two forms of administration can be used: intraventricular or intrathecal. However, the intraventricular approach has been replaced by the intrathecal approach in most cases, making it necessary to investigate in the literature the possible reasons for such a change. Perhaps it i

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