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1

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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2

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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3

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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4

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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6

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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7

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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8

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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9

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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10

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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11

Seibler, Philip [Verfasser]. "Molecular studies of two genetic movement disorders : PRKRA-linked dystonia and PINK1-linked Parkinson disease / Philip Seibler." Lübeck : Zentrale Hochschulbibliothek Lübeck, 2012. http://d-nb.info/1024422062/34.

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12

Vanstone, Megan. "Identification, Validation and Characterization of the Mutation on Chromosome 18p which is Responsible for Causing Myoclonus-Dystonia." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23486.

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Myoclonus-Dystonia (MD) is an inherited, rare, autosomal dominant movement disorder characterized by quick, involuntary muscle jerking or twitching (myoclonus) and involuntary muscle contractions that cause twisting and pulling movements, resulting in abnormal postures (dystonia). The first MD locus was mapped to 7q21-q31 and called DYT11; this locus corresponds to the SGCE gene. Our group previously identified a second MD locus (DYT15) which maps to a 3.18 Mb region on 18p11. Two patients were chosen to undergo next-generation sequencing, which identified 2,292 shared novel variants within th
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13

Reis, Ana Filipa Moreira. "Distonias oromandibulares." Master's thesis, [s.n.], 2014. http://hdl.handle.net/10284/4602.

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Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Medicina Dentária<br>As distonias oromandibulares (DOM) são desordens neuromusculares raras que consistem em espasmos prolongados derivados de contrações dos músculos da cavidade oral e da mandíbula. Os músculos envolvidos podem ser os da mastigação, os da expressão facial ou até mesmo os da língua. Atualmente a fisiopatologia ainda não é clara e não existe tratamento que a elimine. Contudo, para a maioria das distonias focais, como é o caso da distonia
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14

James, Lisa. "“To shape God, Shape Self”: The Political Manipulation of the Human Body and Reclamation of Space in Octavia E. Butler’s The Parable of the Sower." Thesis, Malmö universitet, Fakulteten för kultur och samhälle (KS), 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-23673.

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This paper considers the role of the human body in Octavia E. Butler’s The Parable of theSower and the way it interacts with defined space to stage expressive forms of politicalopposition. Understanding the relationship between physical or metaphorical space and thecontradictions of the societies they encompass is crucial to deciphering Butler’s near-futuredystopia; a world where the problems of real-life Los Angeles and Southern California aredistorted into a gross carnivalesque of gender stereotypes, sociopolitical tensions, and vigilante warfare. This paper places a special emphasis on the
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15

Francesca, Magrinelli. "CLINICOGENETIC CORRELATIONS IN RARE COMPLEX MOVEMENT DISORDERS Focus on combined and complex dystonia phenotypes." Doctoral thesis, 2021. http://hdl.handle.net/11562/1052757.

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Movement disorders is relatively unique among neurology subspecialties in its reliance on clinical judgement to accurately define disease phenotypes which are often complex. Progress in genetics – particularly the advent of next-generation sequencing (NGS) – has enabled an unparalleled gene discovery and revealed unmatched intricacy of genotype-phenotype correlations in the field of movement disorders and neurodegeneration. “Deep phenotyping”, with detailed characterization and continual updating of movement disorder phenotypes, and the active involvement of movement disorder specialists in th
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16

Spröte, Christine Karin. "Pathophysiologische und therapeutische Bedeutung der a1- und a2-Untereinheiten des GABAA-Rezeptors für Dystonien: Untersuchungen im dtsz Hamstermodell." 2016. https://ul.qucosa.de/id/qucosa%3A15685.

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17

Tsang, Eric W. "The Functional Significance of Oscillatory Activities in the Basal Ganglia and Pedunculopontine Nucleus Region in Parkinson’s Disease and Dystonia." Thesis, 2012. http://hdl.handle.net/1807/32834.

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Parkinson’s disease (PD) and dystonia are movement disorders related to dysfunctions of basal ganglia (BG). Deep brain stimulation (DBS) of the subthalamic nucleus (STN) and internal globus pallidus (GPi) are treatments for PD and dystonia. Previous research indicated that abnormally elevated oscillatory activities at the theta (3-10 Hz) beta frequency bands (11-30 Hz) may be related to parkinsonian and dystonic motor symptoms but their precise roles are not well understood. Recently, DBS of the pedunculopontine nucleus region (PPNR) has been used to treat PD patients with postural and gait dy
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18

Mihai, Corina M. ""No" - Jose Saramago's subversive creativity from The History of the Siege of Lisbon to The Stone Raft: voyages into the idea of national identity." Thesis, 2009. http://hdl.handle.net/10539/6226.

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Abstract This study outlines a reading of Saramago’s novels as tracing a reflective itinerary into history, questioning the modalities informing a contemporary consciousness, thus acknowledging and re–configuring the past. Through an interpretation of these narratives as ‘voyages into the idea of identity’ it is shown that they reveal a symmetrical pattern tracing the Portuguese national saga from its foundation myth in The History of the Siege of Lisbon to contemporary images of identity in The Stone Raft. In light of this, the analysis examines the subversive narrative strategies employed w
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