Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1990 1
1997 1
2002 1
2008 1
2010 1
2011 2
2012 1
2013 1
2014 3
2015 3
2016 2
2017 3
2018 1
2019 1
2020 1
2021 1
2022 3
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

24 results

Results by year

Filters applied: . Clear all
Page 1
Chorea.
Stimming EF, Bega D. Stimming EF, et al. Continuum (Minneap Minn). 2022 Oct 1;28(5):1379-1408. doi: 10.1212/CON.0000000000001169. Continuum (Minneap Minn). 2022. PMID: 36222771 Review.
Once it has been determined that the patient has chorea, the investigation into determining an etiology can begin. Factors such as age of onset, time course, family history, unique clinical features, and imaging and laboratory findings can guide the diagnosis. ...
Once it has been determined that the patient has chorea, the investigation into determining an etiology can begin. Factors such as age of on …
Tardive dyskinesia.
Casey DE. Casey DE. West J Med. 1990 Nov;153(5):535-41. West J Med. 1990. PMID: 1979705 Free PMC article. Review.
Clinical Reasoning: A Teenage Girl With Progressive Hyperkinetic Movements, Seizures, and Encephalopathy.
Khamis S, Mitakidou MR, Champion M, Goyal S, Jones RL, Siddiqui A, Sabanathan S, Hedderly T, Lin JP, Jungbluth H, Papandreou A. Khamis S, et al. Neurology. 2023 Jan 3;100(1):30-37. doi: 10.1212/WNL.0000000000201385. Epub 2022 Sep 21. Neurology. 2023. PMID: 36130841 Free PMC article.
Nevertheless, clinical awareness and timely diagnosis are paramount to facilitate appropriate prognostication, counseling, and management.This report describes a case of a teenage girl who had presented at 14 months with a protracted illness manifesting as gastrointestinal …
Nevertheless, clinical awareness and timely diagnosis are paramount to facilitate appropriate prognostication, counseling, and manage …
Quantitative analysis of hyperkinetic seizures and correlation with seizure onset zone.
Fayerstein J, McGonigal A, Pizzo F, Bonini F, Lagarde S, Braquet A, Trébuchon A, Carron R, Scavarda D, Julia S, Lambert I, Giusiano B, Bartolomei F. Fayerstein J, et al. Epilepsia. 2020 May;61(5):1019-1026. doi: 10.1111/epi.16510. Epub 2020 May 7. Epilepsia. 2020. PMID: 32378738
SIGNIFICANCE: We propose a first attempt to quantify clinical patterns of HKS. The HSS may help to predict SOZ localization according to three main groups of hyperkinetic seizures....
SIGNIFICANCE: We propose a first attempt to quantify clinical patterns of HKS. The HSS may help to predict SOZ localization according …
Hyperglycemic hemichorea due to diabetic striatopathy: case-based review.
Tsalta-Mladenov ME, Georgieva DK, Andonova SP. Tsalta-Mladenov ME, et al. Curr Med Res Opin. 2022 Mar;38(3):365-369. doi: 10.1080/03007995.2021.2015159. Epub 2021 Dec 14. Curr Med Res Opin. 2022. PMID: 34873977 Review.
The patient was managed with Insulin and Haloperidol as the symptoms entirely resolved on the tenth day. In conclusion (DS) is a condition with a good prognosis and reversible clinical and neuroimaging findings after a prompt diagnosis and management. ...
The patient was managed with Insulin and Haloperidol as the symptoms entirely resolved on the tenth day. In conclusion (DS) is a condition w …
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Gorman KM, Meyer E, Grozeva D, Spinelli E, McTague A, Sanchis-Juan A, Carss KJ, Bryant E, Reich A, Schneider AL, Pressler RM, Simpson MA, Debelle GD, Wassmer E, Morton J, Sieciechowicz D, Jan-Kamsteeg E, Paciorkowski AR, King MD, Cross JH, Poduri A, Mefford HC, Scheffer IE, Haack TB, McCullagh G; Deciphering Developmental Disorders Study; UK10K Consortium; NIHR BioResource; Millichap JJ, Carvill GL, Clayton-Smith J, Maher ER, Raymond FL, Kurian MA. Gorman KM, et al. Am J Hum Genet. 2019 May 2;104(5):948-956. doi: 10.1016/j.ajhg.2019.03.005. Epub 2019 Apr 11. Am J Hum Genet. 2019. PMID: 30982612 Free PMC article.
CACNA1B encodes the pore-forming subunit of the pre-synaptic neuronal voltage-gated calcium channel Ca(v)2.2/N-type, crucial for SNARE-mediated neurotransmission, particularly in the early postnatal period. Bi-allelic loss-of-function variants in CACNA1B are predicted to c …
CACNA1B encodes the pore-forming subunit of the pre-synaptic neuronal voltage-gated calcium channel Ca(v)2.2/N-type, crucial for SNARE-media …
GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.
Ohba C, Shiina M, Tohyama J, Haginoya K, Lerman-Sagie T, Okamoto N, Blumkin L, Lev D, Mukaida S, Nozaki F, Uematsu M, Onuma A, Kodera H, Nakashima M, Tsurusaki Y, Miyake N, Tanaka F, Kato M, Ogata K, Saitsu H, Matsumoto N. Ohba C, et al. Epilepsia. 2015 Jun;56(6):841-8. doi: 10.1111/epi.12987. Epub 2015 Apr 10. Epilepsia. 2015. PMID: 25864721 Free article.
Three mutations were located in the transmembrane domain (3/4, 75%), and one in the extracellular loop near transmembrane helix 1. All the mutations were predicted to impair the function of the NMDA receptor. SIGNIFICANCE: Clinical features of de novo GRIN1 mutations inclu …
Three mutations were located in the transmembrane domain (3/4, 75%), and one in the extracellular loop near transmembrane helix 1. All the m …
The improvement of motor symptoms in Huntington's disease during cariprazine treatment.
Csehi R, Molnar V, Fedor M, Zsumbera V, Palasti A, Acsai K, Grosz Z, Nemeth G, Molnar MJ. Csehi R, et al. Orphanet J Rare Dis. 2023 Dec 1;18(1):375. doi: 10.1186/s13023-023-02930-z. Orphanet J Rare Dis. 2023. PMID: 38041194 Free PMC article.
Such a biphasic change potentially explains the alterations in motor symptoms: increased dopamine-production induces hyperkinetic movements early in the disease course, while depleted dopamine storage leads to hypokinetic symptoms in the advanced phase. Dopamine D2-D3 part …
Such a biphasic change potentially explains the alterations in motor symptoms: increased dopamine-production induces hyperkinetic movements …
Safety of Converting From Tetrabenazine to Deutetrabenazine for the Treatment of Chorea.
Frank S, Stamler D, Kayson E, Claassen DO, Colcher A, Davis C, Duker A, Eberly S, Elmer L, Furr-Stimming E, Gudesblatt M, Hunter C, Jankovic J, Kostyk SK, Kumar R, Loy C, Mallonee W, Oakes D, Scott BL, Sung V, Goldstein J, Vaughan C, Testa CM; Huntington Study Group/Alternatives for Reducing Chorea in Huntington Disease Investigators. Frank S, et al. JAMA Neurol. 2017 Aug 1;74(8):977-982. doi: 10.1001/jamaneurol.2017.1352. JAMA Neurol. 2017. PMID: 28692723 Free PMC article.
Motor Retraining (MoRe) for Functional Movement Disorders: Outcomes From a 1-Week Multidisciplinary Rehabilitation Program.
Jacob AE, Kaelin DL, Roach AR, Ziegler CH, LaFaver K. Jacob AE, et al. PM R. 2018 Nov;10(11):1164-1172. doi: 10.1016/j.pmrj.2018.05.011. Epub 2018 May 18. PM R. 2018. PMID: 29783067
These disorders are commonly seen in neurologic practice, and prognosis is often poor. No consensus treatment guidelines have been established; however, the role of physical therapy in addition to psychotherapy has increasingly been recognized. ...OBJECTIVE: To assess outc …
These disorders are commonly seen in neurologic practice, and prognosis is often poor. No consensus treatment guidelines have been es …
24 results