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Relevant bibliographies by topics / Choreoid movements

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Academic literature on the topic 'Choreoid movements'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Choreoid movements"

1

Biolsi, Brigitte, Laura Cif, Hassan El Fertit, Santiago Gil Robles, and Philippe Coubes. "Long-term follow-up of Huntington disease treated by bilateral deep brain stimulation of the internal globus pallidus." Journal of Neurosurgery 109, no. 1 (2008): 130–32. http://dx.doi.org/10.3171/jns/2008/109/7/0130.

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Deep brain stimulation is now accepted as a safe and efficient treatment for movement disorders including selected types of dystonia and dyskinesia. Very little, however, is known about its effect on other movement disorders, particularly for “choreic” movements. Huntington disease is a fatal autosomal-dominant neurodegenerative disorder characterized by movement disorders, progressive cognitive impairment, and psychiatric symptoms. Bilateral chronic stimulation of the internal globus pallidus was performed to control choreic movements in a 60-year-old man with a 10-year history of Huntington

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2

Szurhaj, William, Christine Daems‐Monpeurt, Haouaria Sediri, Alain Destée, and Philippe Derambure. "Ictal movement disorders and hypothalamic hamartoma." Epileptic Disorders 7, no. 1 (2005): 43–48. http://dx.doi.org/10.1684/j.1950-6945.2005.tb00099.x.

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We report the case of a woman presenting with unusual, symptomatic epilepsy related to a hypothalamic hamartoma, in the absence of mental retardation or precocious puberty. The seizures manifested themselves clinically as characteristic, paroxysmal movement disorders, such as choreic/ballistic movement. This type of phenomenon is rarely of epileptic origin: we thus suggest that the movement disorder observed here could be due to functional disorganization of the basal ganglia network by the epileptic discharge, causing loss of the inhibition of thalamic activity and thus allowing the occurrenc

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3

Sperotto, Roberto, Laura Ceccarelli, Yan Tereshko, Giovanni Merlino, Gian Luigi Gigli, and Mariarosaria Valente. "The Possible Precipitating Role of SARS-CoV-2 in a Case of Late-Onset Hemichorea Due to a Hyperosmolar Hyperglycemic State: Case Report and Brief Literature Review." Medicina 59, no. 11 (2023): 1949. http://dx.doi.org/10.3390/medicina59111949.

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Case report: An 83-year-old Italian female developed postural instability and gait disturbance associated with a concomitant hyperosmolar hyperglycemic state. Brain CT and MRI scans detected a lesion in the right putamen due to metabolic derangement. A month later, the patient started suffering from choreic movements along the left side of the body with brachio-crural distribution, approximately three weeks after SARS-CoV-2 infection. She was treated with tetrabenazine with complete resolution of the aberrant movements. Any attempt to reduce tetrabenazine caused a relapse of the symptoms. Disc

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Takeuchi, Toshiaki, Masafumi Harada, and Takao Mitsui. "Choreic movement in striatal infarction." Neurology: Clinical Practice 8, no. 2 (2018): 169–70. http://dx.doi.org/10.1212/cpj.0000000000000446.

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Takahashi, Toshiaki, Masashi Aoki, Takashi Imai, et al. "A case of dysferlinopathy presenting choreic movements." Movement Disorders 21, no. 9 (2006): 1513–15. http://dx.doi.org/10.1002/mds.21027.

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6

Ifergane, G., R. Masalha, and Y. O. Herishanu. "Transient Hemichorea/Hemiballismus Associated with New Onset Hyperglycemia." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 28, no. 4 (2001): 365–68. http://dx.doi.org/10.1017/s0317167100001608.

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Objective:To describe three patients suffering from transient hemichorea/hemiballismus associated with hyperglycemia, review previous reports and propose a possible pathophysiological explanation for this phenomenon.Results:Our original cases and previously reported ones reveal a uniform syndrome: mostly female patients (F/M ratio of 11/2), 50-80 years old, usually with no previous history of diabetes mellitus (9/13), develop choreic or ballistic movements on one side of the body over a period of hours. Serum glucose levels are elevated. In most of the patients, a lowering of the blood sugar l

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7

Lance, Eboni I., Martin Kronenbuerger, Julie S. Cohen, Orion Furmanski, Harvey S. Singer, and Ali Fatemi. "Successful treatment of choreo-athetotic movements in a patient with an EEF1A2 gene variant." SAGE Open Medical Case Reports 6 (January 2018): 2050313X1880762. http://dx.doi.org/10.1177/2050313x18807622.

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Pathogenic variants in EEF1A2, a gene encoding a eukaryotic translation elongation factor, have been previously reported in pediatric cases of epileptic encephalopathy and intellectual disability. We report a case of a 17-year-old male with a prior history of epilepsy, autism, intellectual disability, and the abrupt onset of choreo-athetotic movements. The patient was diagnosed with an EEF1A2 variant by whole exome sequencing. His movement disorder responded dramatically to treatment with tetrabenazine. To the best of our knowledge, this is the first report of successful treatment of a hyperki

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8

Delwaide, P. J., and J. Schoenen. "Hyperthyroidism as a cause of persistent choreic movements." Acta Neurologica Scandinavica 58, no. 5 (2009): 309–12. http://dx.doi.org/10.1111/j.1600-0404.1978.tb02892.x.

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Rana, Abdul Qayyum, Ambreen Nadeem, Muhammad Saad Yousuf, and Zakerabibi M. Kachhvi. "Late onset of atypical paroxysmal non-kinesigenic dyskinesia with remote history of Graves’ disease." Journal of Neurosciences in Rural Practice 04, no. 04 (2013): 449–50. http://dx.doi.org/10.4103/0976-3147.120226.

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ABSTRACTParoxysmal non-kinesigenic dyskinesia (PNKD) is a rare hyperkinetic movement disorder and falls under the category of paroxysmal movement disorders. In this condition, episodes are spontaneous, involuntary, and involve dystonic posturing with choreic and ballistic movements. Attacks last for minutes to hours and rarely occur more than once per day. Attacks are not typically triggered by sudden movement, but may be brought on by alcohol, caffeine, stress, fatigue, or chocolate. We report a patient with multiple atypical features of PNKD. She had a 7-year history of this condition with o

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Im, So-Hyang, Chang Wan Oh, O.-Ki Kwon, Byung-Kyu Cho, Young-Seob Chung, and Dae Hee Han. "Involuntary movement induced by cerebral ischemia: pathogenesis and surgical outcome." Journal of Neurosurgery 100, no. 5 (2004): 877–82. http://dx.doi.org/10.3171/jns.2004.100.5.0877.

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Object. Involuntary movement is an uncommon manifestation of a transient ischemic attack. It may be induced by cerebral hemodynamic insufficiency, which is associated with several cerebral ischemic diseases. The authors present three cases of limb shaking due to moyamoya disease (MMD) or radiation-induced middle cerebral artery stenosis, and three additional cases of choreic movement due to MMD. Neuroimaging studies and surgical outcomes in these patients were retrospectively analyzed to investigate the pathological mechanism underlying the symptoms and to provide guidance for the management o

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Book chapters on the topic "Choreoid movements"

1

"Section 5A Idiopathic choreic syndromes." In Marsden's Book of Movement Disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780192619112.010.0643.

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"Section 5B Symptomatic choreic syndromes." In Marsden's Book of Movement Disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780192619112.010.0693.

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Donaldson, Ivan, C. David Marsden, Susanne A. Schneider, and Kailash P. Bhatia. "Chapter 21 Other idiopathic choreic syndromes." In Marsden's Book of Movement Disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780192619112.003.0667.

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Shalash, Ali, Ferzana Amod, and José Fidel Baizabal-Carvallo. "Emergencies in tic and choreic disorders." In International Review of Movement Disorders. Elsevier, 2023. http://dx.doi.org/10.1016/bs.irmvd.2023.08.005.

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Donaldson, Ivan, C. David Marsden, Susanne A. Schneider, and Kailash P. Bhatia. "Chapter 24 Other symptomatic (secondary) choreic syndromes." In Marsden's Book of Movement Disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780192619112.003.0720.

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Donaldson, Ivan, C. David Marsden, Susanne A. Schneider, and Kailash P. Bhatia. "Chapter 49 Paroxysmal choreic, athetotic, or dystonic attacks." In Marsden's Book of Movement Disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780192619112.003.1156.

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Conference papers on the topic "Choreoid movements"

1

Chung, Gabriel, Bruno Pissolati Mattos Gonzaga, Darah Fontes da Silva Assunção, et al. "Acquired hemichorea secondary to hyponatremia: a case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.765.

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Introduction: Chorea is a movement disorder characterized by involuntary, random and irregular movements. In the emergency department, the most common causes of chorea are cerebrovascular disorders, but other conditions may also play an important role. The aim is to present a rare case of acquired hemichorea secondary to hyponatremia by reviewing the patient’s records. Case report: A 73-year-old female patient with a history of arterial hypertension, dyslipidemia, active smoking, and heart failure, taking enalapril, hydrochlorothiazide, furosemide and simvastatin, was admitted to the emergency

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Moura, Fernanda Maria Gonçalves de Sousa, Bruno Rezende Trindade Borges, Davi Vargas Freitas Teixeira, and Roberta Arb Saba Rodrigues Pinto. "Phenytoin-induced Chorea: a case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.392.

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A 67-years-old woman, with no significant medical history, presents herself at Hospital do Servidor Público do Estado de São Paulo after a seizure episode following two weeks of a moderate heat trauma at home. At initial evaluation, no neurological deficit was found, but computed tomography showed a mild subdural hemorrhage in the left frontal area that was promptly drained. The patient was discharged with oral phenytoin 100 mg each eight hours. After thirty days, the patient returns to the hospital reporting the progressive onset of involuntary abnormal movements of upper limbs and head, asso

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Guerra, Leonardo Cortez, Alessandra Luiza Lara Poloni, and Marcela Maria Mattos Almeida. "Multidisciplinary Care in Huntington’s Disease: Case Report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.463.

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Context: Huntington’s disease (HD) is a degenerative neurological disorder with autosomal dominant inheritance resulting from the loss of GABAergic neurons in the striatum. The prevalence of HD is 10.6 to 13.7 individuals per 100,000 in the Western population. Case report: DRO is a 57- year-old female admitted to a Long-Term Care Facility in 2018 due to the diagnosis of Huntington’s Disease (HD) four years ago. The patient presented right-side hemiplegia, choreic movements in the upper extremities, postural instability, dysarthria, visual hallucinations, behavioral changes, alert and communica

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