| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Kazuya Yoshid. Movement disorders of the stomatognathic system: A blind spot between dentistry and medicine. Dental and medical problems. vol 61. issue 4. 2024-09-03. PMID:39223990. |
movement disorders of the stomatognathic system include oromandibular dystonia (omd), oral dyskinesia, sleep/awake bruxism, functional (psychogenic) stomatognathic movement disorders (fsmds), tremors, and hemimasticatory spasm (hms). |
2024-09-03 |
2024-09-05 |
Not clear |
| Davide Mei, Elena Parrini, Claudia Bianchini, Maria Luisa Ricci, Renzo Guerrin. Autism and mild epilepsy associated with a de novo missense pathogenic variant in the GTPase effector domain of DNM1. American journal of medical genetics. Part C, Seminars in medical genetics. 2023-05-03. PMID:37132416. |
pathogenic variants in the dnm1 gene are associated with intractable epilepsy, often manifested as infantile spasms at onset, developmental delay, and a movement disorder, and are located in the gtpase and middle domains of the protein. |
2023-05-03 |
2023-08-14 |
Not clear |
| Frederike L Harms, Deike Weiss, Jasmin Lisfeld, Malik Alawi, Kerstin Kutsch. A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a. Neurogenetics. 2023-04-11. PMID:37039969. |
dnm1 developmental and epileptic encephalopathy (dee) is characterized by severe to profound intellectual disability, hypotonia, movement disorder, and refractory epilepsy, typically presenting with infantile spasms. |
2023-04-11 |
2023-08-14 |
mouse |
| Tao Li, Zhuo Feng, Chunli Song, Zhanhua Lian. Hemifacial spasm is not affected by state of consciousness: a case report. European journal of medical research. vol 26. issue 1. 2021-12-12. PMID:34876223. |
hemifacial spasm (hfs) is a movement disorder caused by mechanical compression of the facial nerve after it has left the brainstem and is characterized by brief or sustained twitching of the muscles innervated by that nerve. |
2021-12-12 |
2023-08-13 |
Not clear |
| Suma Gn, Adrita Na. Management of Oromandibular Dystonia: A Case Report and Literature Update. Case reports in dentistry. vol 2017. 2020-10-01. PMID:28706744. |
oromandibular dystonia (omd) is a movement disorder characterized by involuntary, paroxysmal, and patterned muscle contractions of varying severity resulting in sustained spasms of masticatory muscles, affecting the jaws, tongue, face, and pharynx. |
2020-10-01 |
2023-08-13 |
Not clear |
| Anas S Al Dehaila. Paroxysmal dystonia as an initial presentation of multiple sclerosis posing a diagnostic challenge. Neurosciences (Riyadh, Saudi Arabia). vol 24. issue 3. 2020-01-03. PMID:31380825. |
paroxysmal dystonia (pd), also known as painful tonic spasm (pts), is a relatively less common but well-recognized movement disorder in multiple sclerosis (ms). |
2020-01-03 |
2023-08-13 |
Not clear |
| Jesse D Lawrence, Andrew M Frederickson, Yue-Fang Chang, Patricia M Weiss, Peter C Gerszten, Raymond F Sekul. An investigation into quality of life improvement in patients undergoing microvascular decompression for hemifacial spasm. Journal of neurosurgery. vol 128. issue 1. 2019-09-12. PMID:28186450. |
objective hemifacial spasm (hfs) is a movement disorder characterized by involuntary spasms of the facial muscles, and it can negatively impact quality of life (qol). |
2019-09-12 |
2023-08-13 |
Not clear |
| Young Goo Kim, Na Young Jung, MinSoo Kim, Won Seok Chang, Hyun Ho Jung, Jin Woo Chan. Benefits of microvascular decompression on social anxiety disorder and health-related quality of life in patients with hemifacial spasm. Acta neurochirurgica. vol 158. issue 7. 2017-09-08. PMID:27155866. |
hemifacial spasm (hfs), an involuntary movement disorder characterized by unilateral spasms of the muscles innervated by the facial nerve, is likely to cause social anxiety disorder due to its significant facial disfigurement and may have a significant influence on a patient's health-related quality of life (hrqol). |
2017-09-08 |
2023-08-13 |
Not clear |
| Corina Roman-Filip, Aurelian Ungureanu, Mihaela Cernuşcă-Miţar. Painful tonic spasms and brainstem involvement in a patient with neuromyelitis optica spectrum disorder. Neurologia i neurochirurgia polska. vol 50. issue 1. 2016-06-16. PMID:26851692. |
painful tonic spasms have been described as movement disorders associated with multiple sclerosis, but a growing number of reports describe them in cases of nmo. |
2016-06-16 |
2023-08-13 |
Not clear |
| Daniela Privitera, Valeria Corti, Massimo Alessio, Maria Antonietta Volontè, Antonietta Volontè, Vito Lampasona, Giancarlo Comi, Gianvito Martino, Diego Franciotta, Roberto Furlan, Raffaella Fazi. Proteomic identification of aldolase A as an autoantibody target in patients with atypical movement disorders. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 34. issue 3. 2013-09-04. PMID:22391679. |
we tried to identify the target/s of autoantibodies to basal ganglia neurons found in a patient with hyperkinetic movement disorders (hmd) characterized by rapid, rhythmic involuntary movements or spasms in both face and neck. |
2013-09-04 |
2023-08-12 |
mouse |
| Canan Doğanli, Hans C Beck, Angeles B Ribera, Claus Oxvig, Karin Lykke-Hartman. α3Na+/K+-ATPase deficiency causes brain ventricle dilation and abrupt embryonic motility in zebrafish. The Journal of biological chemistry. vol 288. issue 13. 2013-05-30. PMID:23400780. |
mutations in the na(+)/k(+)-atpase α3 subunit gene (atp1a3) cause rapid-onset dystonia-parkinsonism, a rare movement disorder characterized by sudden onset of dystonic spasms and slow movements. |
2013-05-30 |
2023-08-12 |
zebrafish |
| Monika Rudzińska, Magdalena Wójcik, Michalina Malec, Natalia Grabska, Michał Szubiga, Marcin Hartel, Andrzej Szczudli. Factors affecting the quality of life in hemifacial spasm patients. Neurologia i neurochirurgia polska. vol 46. issue 2. 2012-07-03. PMID:22581593. |
hemifacial spasm (hfs), a movement disorder manifested by unilateral spasms of the muscles innervated by the facial nerve, interferes with social life in about 90% of patients, causing social isolation and depression and having a significant impact on the quality of life. |
2012-07-03 |
2023-08-12 |
Not clear |
| Pernille Bøttger, Zuzanna Tracz, Anders Heuck, Poul Nissen, Marina Romero-Ramos, Karin Lykke-Hartman. Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain. The Journal of comparative neurology. vol 519. issue 2. 2011-03-18. PMID:21165980. |
mutations in the atp1a3 gene cause rapid-onset of dystonia parkinsonism (rdp), a rare movement disorder characterized by sudden onset of dystonic spasms and slowness of movement. |
2011-03-18 |
2023-08-12 |
mouse |
| Karine Poirier, Monika Eisermann, Isabelle Caubel, Anna Kaminska, Sylviane Peudonnier, Nathalie Boddaert, Yoann Saillour, Olivier Dulac, Isabelle Souville, Chérif Beldjord, Karine Lascelles, Perrine Plouin, Jamel Chelly, Nadia Bahi-Buisso. Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsy. Epilepsy research. vol 80. issue 2-3. 2008-12-12. PMID:18468866. |
this combination of early infantile spasms followed by a complex movement disorder contributes further to extent the pleiotropy of the arx-linked "interneuronopathy" and should lead the clinician to arx mutation screening. |
2008-12-12 |
2023-08-12 |
Not clear |
| Duangjai Kasantikul, Buranee Kanchanatawa. Antipsychotic-induced tardive movement disorders: a series of twelve cases. Journal of the Medical Association of Thailand = Chotmaihet thangphaet. vol 90. issue 1. 2007-08-27. PMID:17621754. |
prolonged use of antipsychotic drugs (ap) with or without sudden withdrawal as well as high dosage of ap (at least 3 months) may result in a variety of movement disorders such as classical tardive dyskinesia (tongue rolling, lip pouting, trunkal choreiform movements), tardive myoclonus (sudden, brief involuntary jerking), tardive dystonia (tongue protrusion, torticollis, scoliosis, jaw spasm, bruxism, abnormal trunkal posture, or "pisa syndrome", strong contraction of arm and leg). |
2007-08-27 |
2023-08-12 |
Not clear |
| A Brashear, G K Mulholland, Q H Zheng, M R Farlow, E R Siemers, G D Hutchin. PET imaging of the pre-synaptic dopamine uptake sites in rapid-onset dystonia-parkinsonism (RDP). Movement disorders : official journal of the Movement Disorder Society. vol 14. issue 1. 1999-04-01. PMID:9918356. |
rapid-onset dystonia-parkinsonism (rdp) is a genetic movement disorder characterized by abrupt onset over hours to days of bradykinesia, postural instability, dysphagia, dysarthria, and severe dystonic spasms with decreased levels of the dopamine metabolite, homovanillic acid (hva), in cerebrospinal fluid (csf). |
1999-04-01 |
2023-08-12 |
Not clear |
| P Brown, N P Quinn, D Barnes, D R Wren, C D Marsde. Spinal rigidity following acute myelitis. Movement disorders : official journal of the Movement Disorder Society. vol 12. issue 6. 1998-02-10. PMID:9399237. |
this patient is similar to those recently reported as having stiffness and spasms of the legs due to a possible chronic spinal interneuronitis and provides further evidence that this kind of movement disorder may be caused by spinal cord pathology. |
1998-02-10 |
2023-08-12 |
Not clear |