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

Year Number of Results
1988 1
1991 2
1992 1
1993 6
1994 1
1995 2
1996 3
1997 3
2000 8
2001 2
2002 6
2003 9
2004 4
2005 2
2006 4
2007 5
2008 6
2009 5
2010 7
2011 15
2012 4
2013 6
2014 16
2015 10
2016 12
2017 16
2018 14
2019 10
2020 21
2021 15
2022 16
2023 14
2024 9

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221 results

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Page 1
Autoimmune encephalitis: proposed best practice recommendations for diagnosis and acute management.
Abboud H, Probasco JC, Irani S, Ances B, Benavides DR, Bradshaw M, Christo PP, Dale RC, Fernandez-Fournier M, Flanagan EP, Gadoth A, George P, Grebenciucova E, Jammoul A, Lee ST, Li Y, Matiello M, Morse AM, Rae-Grant A, Rojas G, Rossman I, Schmitt S, Venkatesan A, Vernino S, Pittock SJ, Titulaer MJ; Autoimmune Encephalitis Alliance Clinicians Network. Abboud H, et al. J Neurol Neurosurg Psychiatry. 2021 Jul;92(7):757-768. doi: 10.1136/jnnp-2020-325300. Epub 2021 Mar 1. J Neurol Neurosurg Psychiatry. 2021. PMID: 33649022 Free PMC article. Review.
Corticosteroids alone or combined with other agents (intravenous IG or plasmapheresis) were selected as a first-line therapy by 84% of responders for patients with a general presentation, 74% for patients presenting with faciobrachial dystonic seizures, 63% for NMDAR-IgG e …
Corticosteroids alone or combined with other agents (intravenous IG or plasmapheresis) were selected as a first-line therapy by 84% of respo …
Neuropathology and emerging biomarkers in corticobasal syndrome.
Koga S, Josephs KA, Aiba I, Yoshida M, Dickson DW. Koga S, et al. J Neurol Neurosurg Psychiatry. 2022 Jun 13;93(9):919-29. doi: 10.1136/jnnp-2021-328586. Online ahead of print. J Neurol Neurosurg Psychiatry. 2022. PMID: 35697501 Free PMC article. Review.
Corticobasal syndrome (CBS) is a clinical syndrome characterised by progressive asymmetric limb rigidity and apraxia with dystonia, myoclonus, cortical sensory loss and alien limb phenomenon. ...Genetic mutations associated with CBS, including GRN and MAPT, are also review …
Corticobasal syndrome (CBS) is a clinical syndrome characterised by progressive asymmetric limb rigidity and apraxia with dystonia, m …
DYT-GNAL.
Deutschländer AB, Wszolek ZK. Deutschländer AB, et al. 2019 Jan 3. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2019 Jan 3. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 30605297 Free Books & Documents. Review.
Tremor reported in DYT-GNAL may be dystonic (i.e., occurring in a body part that shows at least minimal signs of dystonia) and may precede or follow the onset of dystonia. ...Treatment of depression and anxiety, commonly associated with cervical dystonia …
Tremor reported in DYT-GNAL may be dystonic (i.e., occurring in a body part that shows at least minimal signs of dystonia) and …
SERAC1 Deficiency.
Wortmann SB, de Brouwer APM, Wevers RA, Morava E. Wortmann SB, et al. 2014 Apr 17 [updated 2020 Jul 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2014 Apr 17 [updated 2020 Jul 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 24741715 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: The phenotypic spectrum of SERAC1 deficiency comprises MEGD(H)EL syndrome (3-methylglutaconic aciduria with deafness-dystonia, [hepatopathy], encephalopathy, and Leigh-like syndrome), juvenile-onset complicated hereditary spastic paraplegia (in 1 …
CLINICAL CHARACTERISTICS: The phenotypic spectrum of SERAC1 deficiency comprises MEGD(H)EL syndrome (3-methylglutaconic aciduria with deafne …
Torticollis.
Cunha B, Tadi P, Bragg BN. Cunha B, et al. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 30969679 Free Books & Documents.
The most frequent and common cases seem to be related to dysfunctions in the local neuromuscular mechanisms (focal dystonia). Cervical dystonia is among the most common focal dystonias in adults, causing a tetanus contraction of the sternocleidomastoid and/or trapez …
The most frequent and common cases seem to be related to dysfunctions in the local neuromuscular mechanisms (focal dystonia). Cervica …
Speech-induced action myoclonus.
Simpson HD, Duffy JR, Stierwalt JAG, Ahlskog JE, Hassan A. Simpson HD, et al. Parkinsonism Relat Disord. 2022 May;98:41-46. doi: 10.1016/j.parkreldis.2022.04.002. Epub 2022 Apr 14. Parkinsonism Relat Disord. 2022. PMID: 35468498 Review.
Diagnostic aids included modulation with different speech tasks and speaking rates, and surface electrophysiology which confirmed craniofacial myoclonus induced by speaking tasks (three cases). Previous misdiagnosis included functional, dystonic, neuromuscular junction pat …
Diagnostic aids included modulation with different speech tasks and speaking rates, and surface electrophysiology which confirmed craniofaci …
Extrapyramidal Symptoms.
D'Souza RS, Hooten WM. D'Souza RS, et al. 2023 Jul 31. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jul 31. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 30475568 Free Books & Documents.
Extrapyramidal side effects (EPS), commonly referred to as drug-induced movement disorders are among the most common adverse drug effects patients experience from dopamine-receptor blocking agents. ...A variety of movement phenotypes has since been described along the EPS …
Extrapyramidal side effects (EPS), commonly referred to as drug-induced movement disorders are among the most common adverse drug eff …
Sex differences in movement disorders.
Turcano P, Savica R. Turcano P, et al. Handb Clin Neurol. 2020;175:275-282. doi: 10.1016/B978-0-444-64123-6.00019-9. Handb Clin Neurol. 2020. PMID: 33008531 Review.
Movement disorders including Parkinson's disease, dementia with Lewy body, Huntington's disease, Tourette's syndrome, and dystonia among others display significant clinical differences between sexes, with structural differences in the dopaminergic pathways between m …
Movement disorders including Parkinson's disease, dementia with Lewy body, Huntington's disease, Tourette's syndrome, and dystonia …
Best Practices in the Clinical Management of Progressive Supranuclear Palsy and Corticobasal Syndrome: A Consensus Statement of the CurePSP Centers of Care.
Bluett B, Pantelyat AY, Litvan I, Ali F, Apetauerova D, Bega D, Bloom L, Bower J, Boxer AL, Dale ML, Dhall R, Duquette A, Fernandez HH, Fleisher JE, Grossman M, Howell M, Kerwin DR, Leegwater-Kim J, Lepage C, Ljubenkov PA, Mancini M, McFarland NR, Moretti P, Myrick E, Patel P, Plummer LS, Rodriguez-Porcel F, Rojas J, Sidiropoulos C, Sklerov M, Sokol LL, Tuite PJ, VandeVrede L, Wilhelm J, Wills AA, Xie T, Golbe LI. Bluett B, et al. Front Neurol. 2021 Jul 1;12:694872. doi: 10.3389/fneur.2021.694872. eCollection 2021. Front Neurol. 2021. PMID: 34276544 Free PMC article. Review.
CBS presents with prominent and usually asymmetric dystonia, apraxia, myoclonus, pyramidal signs, and cortical sensory loss. ...The authors hope that this publication will serve as a convenient guide for all clinicians caring for patients with PSP and CBS and that it will …
CBS presents with prominent and usually asymmetric dystonia, apraxia, myoclonus, pyramidal signs, and cortical sensory loss. ...The a …
Niemann-Pick Disease Type C.
Patterson M. Patterson M. 2000 Jan 26 [updated 2020 Dec 10]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Jan 26 [updated 2020 Dec 10]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301473 Free Books & Documents. Review.
The youngest children may present with hypotonia and developmental delay, with the subsequent emergence of ataxia, dysarthria, dysphagia, and, in some individuals, epileptic seizures, dystonia, and gelastic cataplexy. Although cognitive impairment may be subtle at first, i …
The youngest children may present with hypotonia and developmental delay, with the subsequent emergence of ataxia, dysarthria, dysphagia, an …
221 results