Relevant bibliographies by topics / Paroxysmal dyskinesia

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Paroxysmal dyskinesia'

Author: Grafiati
Published: 18 April 2022
Last updated: 30 July 2025

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Journal articles on the topic "Paroxysmal dyskinesia"

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Lee, Suin, Jae Rim Kim, Young-Kyun Kim, et al. "Atypical Paroxysmal Kinesigenic Dyskinesia with Paroxysmal Exercise-induced Dyskinesia." Journal of the Korean Neurological Association 42, no. 1 (2024): 66–70. http://dx.doi.org/10.17340/jkna.2023.0069.

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Paroxysmal kinesigenic dyskinesia (PKD) is a diagnostic term for transient, involuntary abnormal movements triggered by sudden motions. The treatment for PKD differs from other paroxysmal dyskinesias, as it notably responds well to sodium channel blockers. We report a case of atypical PKD, coupled with paroxysmal exercise-induced dyskinesia (PED). Both PKD and PED in this patient showed a good response to oxcarbazepine. This case could be clinical evidence that paroxysmal dyskinesias could potentially be regarded as a spectrum disorder with overlapping features.
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Kim, N. L., and M. A. Yamin. "The case of paroxysmal kinesigenic dyskinesia: a long way from a symptom to the diagnosis." Almanac of Clinical Medicine 49, no. 3 (2021): 226–30. http://dx.doi.org/10.18786/2072-0505-2021-49-014.

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Paroxysmal kinesigenic dyskinesia belongs to the group of primary dyskinesias, which also includes paroxysmal non-kinesigenic dyskinesia and exercise-induced paroxysmal dyskinesia. Due to the rarity of this disease group, as well as to the existence of a wide spectrum of disorders associated with transient movement abnormalities, the diagnosis is often difficult. A thorough analysis of clinical presentation, objective registration of paroxysmal events (video-electroencephalography monitoring) is helpful in the diagnosis. The most common causes of paroxysmal kinesigenic dyskinesia are mutations
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Manso-Calderón, Raquel. "The spectrum of paroxysmal dyskinesias." Future Neurology 14, no. 3 (2019): FNL26. http://dx.doi.org/10.2217/fnl-2018-0047.

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Paroxysmal dyskinesias (PxD) comprise a group of heterogeneous syndromes characterized by recurrent attacks of mainly dystonia and/or chorea, without loss of consciousness. PxD have been classified according to their triggers and duration as paroxysmal kinesigenic dyskinesia, paroxysmal nonkinesigenic dyskinesia and paroxysmal exertion-induced dyskinesia. Of note, the spectrum of genetic and nongenetic conditions underlying PxD is continuously increasing, but not always a phenotype–etiology correlation exists. This creates a challenge in the diagnostic work-up, increased by the fact that most
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Bavdhankar, Koustubh P., and Pankaj A. Agarwal. "Paroxysmal Movement Disorders: An Update on Clinical approach, Pathophysiology and Genetic Underpinnings." Annals of Movement Disorders 8, no. 1 (2025): 14–36. https://doi.org/10.4103/aomd.aomd_115_24.

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Abstract Paroxysmal movement disorders (PxMDs) are a clinically, genetically, and pathophysiologically a diverse group of disorders, characterized by their sudden, short-lasting, episodic nature, onset in early childhood, reduced severity during adulthood, and often a normal neurological examination between episodes. PxMDs include paroxysmal dyskinesias (PxD), which present with sudden episodes of dystonia and chorea, and episodic ataxias (EA), which present with episodes of cerebellar dysfunction. PxDs can also be precipitated by secondary causes, including metabolic or immunological factors,
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Fishman, Paul S. "Paroxysmal dyskinesia." Current Treatment Options in Neurology 3, no. 6 (2001): 519–25. http://dx.doi.org/10.1007/s11940-001-0014-9.

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Škorvánek, Matej. "Paroxysmal dyskinesia." Neurologie pro praxi 24, no. 4 (2023): 248–52. http://dx.doi.org/10.36290/neu.2023.007.

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Hobson, Douglas E. "Paroxysmal kinesigenic dyskinesia sans dyskinesia or paroxysmal kinesigenic dysesthesia?" Movement Disorders 25, no. 9 (2010): 1305–6. http://dx.doi.org/10.1002/mds.23077.

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Alibhoy, AT, Subhashie Wijemanne, and Ranjanie Gamage. "Paroxysmal kinesigenic dyskinesia." Ceylon Medical Journal 51, no. 1 (2009): 36. http://dx.doi.org/10.4038/cmj.v51i1.1377.

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Millichap, J. Gordon. "Paroxysmal Nonkinesigenic Dyskinesia." Pediatric Neurology Briefs 20, no. 6 (2006): 46. http://dx.doi.org/10.15844/pedneurbriefs-20-6-7.

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Paucar, Martin, Helena Malmgren, and Per Svenningsson. "Paroxysmal Kinesigenic Dyskinesia." Tremor and Other Hyperkinetic Movements 7 (December 12, 2017): 529. http://dx.doi.org/10.5334/tohm.393.

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Dissertations / Theses on the topic "Paroxysmal dyskinesia"

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Du, Wei. "Role of KCNMA1 in the Pathogenesis of GEPD Syndrome." Cleveland State University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=csu1272045934.

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Méneret, Aurélie. "Génétique des mouvements anormaux : dyskinésies paroxystiques kinésigéniques et mouvements miroirs congénitaux." Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066587.

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L'objectif de mon travail a été d'étudier les bases génétiques de deux maladies du mouvement, les mouvements miroirs congénitaux (CMM) et les dyskinésies paroxystiques kinésigéniques (PKD). Nous avons tout d'abord mis en évidence le deuxième gène impliqué dans les CMM, RAD51, et commencé à explorer quelques hypothèses physiopathologiques. Nous avons ensuite recueilli les ADN de 26 cas index de CMM isolés, et montré que près de 50% d'entre eux avaient un variant possiblement pathogène dans RAD51 ou dans le premier gène de CMM décrit, DCC. Nous avons ensuite écarté l'implication d'un troisième g
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Almeida, Melanie Jesus. "Paroxysmal dyskinesia in dogs." Master's thesis, 2017. http://hdl.handle.net/10348/7708.

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Dissertação de Mestrado Integrado em Medicina Veterinária<br>As desordens de movimento, embora caracterizadas por apresentações dramáticas, são raramente reconhecidas e reportadas em medicina veterinária. A etiologia das desordens de movimento involuntário ainda não foi determinada e os sistemas de classificação permanecem uma controvérsia. Incluído nas desordens de movimento involuntário encontra-se a discinesia que é caracterizada por impedimento de movimentos voluntários. A discinesia é frequentemente considerada e denominada de paroxística uma vez que esta forma de movimento involuntário
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Hsu, Wan-Yu, and 徐婉瑜. "Altered Inhibitory Modulation of Motor and Somatosensory Cortices in Paroxysmal Kinesigenic Dyskinesia." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/35204824959403904535.

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博士<br>國立陽明大學<br>腦科學研究所<br>102<br>Paroxysmal kinesigenic dyskinesia (PKD) is a rare neurological disorder with dyskinetic movement triggered by sudden voluntary movements. The condition responds well to antiepileptic drugs (AEDs). However, little is known about the underlying mechanism of the disease. Previous studies have demonstrated dysfunction of thalamus or basal ganglia in patients with PKD. Corticospinal disinhibition was also reported. Since the dyskinetic movements in PKD patients are precipitated by voluntary movements, investigating changes in neural oscillatory activities related to
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Nian, Fang-Shin, and 粘芳馨. "Characterization of pathomechanisms of PRRT2 mutations involving Paroxysmal kinesigenic dyskinesia and its related neurological disorders." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/37e2mx.

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博士<br>國立陽明大學<br>分子醫學博士學位學程<br>107<br>Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene cause a wide spectrum of neurological diseases, including Paroxysmal Kinesigenic Dyskinesia (PKD) to mental retardation and epilepsy which implicated that PRRT2 might play an important role in the nervous system. Here, we reported that Prrt2 proteins are distributed widely in the brain and they are located at the pre- and post-synaptic membranes with a close spatial association with SNAP25 by synaptic membrane fractionation and immunostaining of the rat neurons. Using in utero electroporatio
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Bastos, Nádia Filipa Fernandes. "Discinesia paroxística em cães." Master's thesis, 2021. http://hdl.handle.net/10400.26/38170.

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A discinesia paroxística tem-se tornado cada vez mais reconhecida e estudada na Medicina Veterinária. É considerada uma doença do movimento e caracteriza-se por apresentar episódios de movimentos involuntários. Durante o episódio o animal permanece consciente, não se observa sinais do sistema nervoso autónomo e o comportamento pós ictal é normal. O mecanismo que suscita esta doença não é totalmente conhecido, porém alguns estudos consideram muito provável ser uma disfunção dos gânglios da base, que reflete uma alteração do funcionamento dos circuitos que contribuem para o controlo do movimento
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Books on the topic "Paroxysmal dyskinesia"

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Waln, Olga, and Joseph Jankovic. Paroxysmal Dyskinesias and Other Paroxysmal Movement Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0012.

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Paroxysmal dyskinesias are episodic, recurrent movement disorders characterized by attacks of dystonia, chorea, athetosis, ballism, or any combination of these hyperkinetic movements, with variable duration and frequency of the episodes and normal interictal neurological examination. Four main types of paroxysmal dyskinesias have been described: paroxysmal kinesigenic dyskinesia, paroxysmal nonkinesigenic dyskinesia, paroxysmal exercise-induced dyskinesia, and paroxysmal hypnogenic dyskinesia. The disorders are usually inherited in autosomal dominant fashion and have their onset in the first t
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Walsh, Richard A. “It Has to Be Functional!”. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190607555.003.0026.

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The paroxysmal dyskinesias are a heterogeneous group of rare movement disorders, characterized by the abrupt onset of involuntary hyperkinetic movements with or without trigger factors and of variable duration. Interictal periods are marked by relative normality, although there is evidence for an association between some genotypes and migraine, episodic ataxia, and seizure disorders. Three genes have been identified that are associated with the three most common syndromes; however, these do not account for some cases with an otherwise typical history. The clinical phenotype continues to evolve
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Myoclonus and Paroxysmal Dyskinesias (Advances in Neurology, Volumme 89). Lippincott Williams & Wilkins, 2002.

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Book chapters on the topic "Paroxysmal dyskinesia"

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Smilowska, Katarzyna, Roberto Erro, and Kailash P. Bhatia. "Paroxysmal Kinesigenic Dyskinesia." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_3.

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Gupta, Harsh Vardhan, Shyamal H. Mehta, and Kapil D. Sethi. "Acquired Paroxysmal Dyskinesia." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_6.

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Guduru, Zain, and Kapil D. Sethi. "Paroxysmal Non-kinesigenic Dyskinesia." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_4.

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Scannapieco, Sara, and Roberto Erro. "Paroxysmal Exercise-Induced Dyskinesia." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_5.

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Corradi, Anna Margherita, Pierluigi Valente, Caterina Michetti, and Fabio Benfenati. "Pathophysiology of Paroxysmal Dyskinesia." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_7.

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Palomar, Francisco J., and Pablo Mir. "Neurophysiology of Paroxysmal Dyskinesia." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_8.

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Brockmann, Knut, and Hendrik Rosewich. "Genetics of Paroxysmal Dyskinesia." In Movement Disorder Genetics. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17223-1_10.

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Erro, Roberto, Kapil D. Sethi, and Kailash P. Bhatia. "Paroxysmal Dyskinesia: Definitions and Clinical Approach." In Paroxysmal Movement Disorders. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53721-0_1.

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Guduru, Zain, and Kapil D. Sethi. "Treatment of Paroxysmal Nonkinesigenic Dyskinesia." In Current Clinical Neurology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-97897-0_72.

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Zis, Panagiotis, Davide Martino, and Tiziano Tamburini. "Paroxysmal Dyskinesias." In Movement Disorders Curricula. Springer Vienna, 2017. http://dx.doi.org/10.1007/978-3-7091-1628-9_32.

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Conference papers on the topic "Paroxysmal dyskinesia"

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Gomes, Hanid Fontes, Naiane Cristina Ferreira Mendes, Renata Beatriz Boechat Quadros, and Marlos Melo Martins. "Paroxysmal Kinesigenic Dyskinesia: when to Diagnose?" In SBN Conference 2022. Thieme Revinter Publicações Ltda., 2023. http://dx.doi.org/10.1055/s-0043-1774653.

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Dayasiri, MBKC, N. Weerapperuma, J. Wright, and G. Anand. "G53(P) Paroxysmal kinesigenic dyskinesia; a diagnostic challenge to the general paediatrician." In Royal College of Paediatrics and Child Health, Abstracts of the RCPCH Conference–Online, 25 September 2020–13 November 2020. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2020. http://dx.doi.org/10.1136/archdischild-2020-rcpch.39.

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Doummar, D., C. Dentel, V. Bouilleret, et al. "Biallelic PDE2A Mutations: A New Cause of Intellectual Disability with Paroxysmal Dyskinesia and/or Epilepsy." In Abstracts of the 47th Annual Meeting of the SENP (Société Européenne De Neurologie Pédiatrique). Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1685434.

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Leduc-Pessah, Heather, and Asif Doja. "Lamotrigine as a First-line Agent in the Management of Paroxysmal Kinesigenic Dyskinesia (P14-11.002)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000204255.

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Hermann, K., J. Johannsen, and J. Denecke. "Levetiracetam as a Therapeutic Option in the Treatment of MR1-Associated Paroxysmal Nonkinesigenic Dyskinesias in Children: A Case Report." In Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1739651.

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You might also be interested in the extended bibliographies on the topic 'Paroxysmal dyskinesia' for particular source types:
Journal articles
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