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

Year Number of Results
2002 1
2004 2
2007 1
2010 1
2017 3
2018 2
2019 2
2020 2
2021 2
2022 1
2023 2
2024 2

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18 results

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Page 1
Treatable inherited rare movement disorders.
Jinnah HA, Albanese A, Bhatia KP, Cardoso F, Da Prat G, de Koning TJ, Espay AJ, Fung V, Garcia-Ruiz PJ, Gershanik O, Jankovic J, Kaji R, Kotschet K, Marras C, Miyasaki JM, Morgante F, Munchau A, Pal PK, Rodriguez Oroz MC, Rodríguez-Violante M, Schöls L, Stamelou M, Tijssen M, Uribe Roca C, de la Cerda A, Gatto EM; International Parkinson's Disease Movement Disorders Society Task Force on Rare Movement Disorders. Jinnah HA, et al. Among authors: uribe roca c. Mov Disord. 2018 Jan;33(1):21-35. doi: 10.1002/mds.27140. Epub 2017 Sep 1. Mov Disord. 2018. PMID: 28861905 Free PMC article. Review.
Alcohol-Sensitive Generalized Dystonia.
Micheli F, Uribe-Roca C, Saenz-Farret M. Micheli F, et al. Among authors: uribe roca c. Clin Neuropharmacol. 2017 Jan/Feb;40(1):48-49. doi: 10.1097/WNF.0000000000000199. Clin Neuropharmacol. 2017. PMID: 27941525
[Stiff person syndrome associated with thymoma].
Perri M, Pellegrini D, Uribe Roca C, Gonzalez F, Buero A, Chimondeguy D, Bruetman JE. Perri M, et al. Among authors: uribe roca c. Medicina (B Aires). 2023;83(4):626-630. Medicina (B Aires). 2023. PMID: 37582138 Free article. Spanish.
Ischemic stroke of the "hand knob area": A case series and literature review.
Finkelsteyn AM, Saucedo MA, Miquelini LA, Chertcoff A, Bandeo L, Pacha S, León Cejas L, Uribe Roca C, Fernández Pardal M, Reisin R, Bonardo P. Finkelsteyn AM, et al. Among authors: uribe roca c. J Clin Neurosci. 2019 Jul;65:100-105. doi: 10.1016/j.jocn.2019.03.025. Epub 2019 Mar 22. J Clin Neurosci. 2019. PMID: 30910548 Review.
[Trident sign in spinal cord neurosarcoidosis].
Bala M, Saucedo M, Bandeo L, Chertcoff A, Uribe-Roca C, Bonardo P, Fernández-Pardal M, Miquelini L, Méndez J, Reisin R. Bala M, et al. Among authors: uribe roca c. Rev Neurol. 2020 Mar 1;70(5):193-194. doi: 10.33588/rn.7005.2019180. Rev Neurol. 2020. PMID: 32100280 Free article. Spanish.
Worldwide barriers to genetic testing for movement disorders.
Gatto EM, Walker RH, Gonzalez C, Cesarini M, Cossu G, Stephen CD, Balint B, Rodríguez-Violante M, Jankovic J, Morgante F, Jinnah HA; Rare Movement Disorders Study Group of the International Parkinson Disease, Movement Disorders Society. Gatto EM, et al. Eur J Neurol. 2021 Jun;28(6):1901-1909. doi: 10.1111/ene.14826. Epub 2021 Apr 9. Eur J Neurol. 2021. PMID: 33730413
Mystery Case: A 78-year-old man with a gait disorder.
Saucedo M, Chertcoff A, Bandeo L, León Cejas L, Uribe Roca C, Bonardo P, Fernandez Pardal M, Torino R, Mendez J, Reisin R. Saucedo M, et al. Among authors: uribe roca c. Neurology. 2019 Jul 30;93(5):223-227. doi: 10.1212/WNL.0000000000007865. Neurology. 2019. PMID: 31358671 No abstract available.
Non-convulsive status epilepticus as the initial manifestation in a family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
González F, Bala M, Saucedo M, Bandeo L, Pacio G, Chertcoff A, De Francesco L, León Cejas L, Pacha MS, Uribe Roca C, Martínez O, Fernández Pardal M, Reisin R, Bonardo P. González F, et al. Among authors: uribe roca c. Neurologia (Engl Ed). 2023 Mar;38(2):82-86. doi: 10.1016/j.nrleng.2020.04.031. Epub 2022 Nov 17. Neurologia (Engl Ed). 2023. PMID: 36402400 Free article.
18 results