These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
179 related articles for article (PubMed ID: 36396537)
1. A novel clinicopathologic entity causing rapidly progressive cerebellar ataxia? Koga S; Ali S; Baker MC; Wierenga KJ; Dompenciel M; Dickson DW; Wszolek ZK Parkinsonism Relat Disord; 2022 Dec; 105():149-153. PubMed ID: 36396537 [TBL] [Abstract][Full Text] [Related]
2. [Cortical Cerebellar Atrophy and Idiopathic Cerebellar Ataxia: Nomenclature and Diagnostic Approach]. Yoshida K Brain Nerve; 2020 Sep; 72(9):923-930. PubMed ID: 32934181 [TBL] [Abstract][Full Text] [Related]
3. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders. Berciano J; García A; Infante J Handb Clin Neurol; 2013; 115():907-32. PubMed ID: 23931821 [TBL] [Abstract][Full Text] [Related]
4. The Diagnosis and Natural History of Multiple System Atrophy, Cerebellar Type. Lin DJ; Hermann KL; Schmahmann JD Cerebellum; 2016 Dec; 15(6):663-679. PubMed ID: 26467153 [TBL] [Abstract][Full Text] [Related]
5. Idiopathic cerebellar ataxia (IDCA): Diagnostic criteria and clinical analyses of 63 Japanese patients. Yoshida K; Kuwabara S; Nakamura K; Abe R; Matsushima A; Beppu M; Yamanaka Y; Takahashi Y; Sasaki H; Mizusawa H; J Neurol Sci; 2018 Jan; 384():30-35. PubMed ID: 29249373 [TBL] [Abstract][Full Text] [Related]
6. Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study. Bogdan T; Wirth T; Iosif A; Schalk A; Montaut S; Bonnard C; Carre G; Lagha-Boukbiza O; Reschwein C; Albugues E; Demuth S; Landsberger H; Einsiedler M; Parratte T; Nguyen A; Lamy F; Durand H; Fahrer P; Voulleminot P; Bigaut K; Chanson JB; Nicolas G; Chelly J; Cazeneuve C; Koenig M; Bund C; Namer IJ; Kremer S; Calmels N; Tranchant C; Anheim M J Neurol; 2022 Dec; 269(12):6354-6365. PubMed ID: 35869996 [TBL] [Abstract][Full Text] [Related]
7. Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work. Gebus O; Montaut S; Monga B; Wirth T; Cheraud C; Alves Do Rego C; Zinchenko I; Carré G; Hamdaoui M; Hautecloque G; Nguyen-Them L; Lannes B; Chanson JB; Lagha-Boukbiza O; Fleury MC; Devys D; Nicolas G; Rudolf G; Bereau M; Mallaret M; Renaud M; Acquaviva C; Koenig M; Koob M; Kremer S; Namer IJ; Cazeneuve C; Echaniz-Laguna A; Tranchant C; Anheim M J Neurol; 2017 Jun; 264(6):1118-1126. PubMed ID: 28478596 [TBL] [Abstract][Full Text] [Related]
8. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea. Fox SH; Nieves A; Bergeron C; Lang AE Mov Disord; 2003 Dec; 18(12):1550-4. PubMed ID: 14673899 [TBL] [Abstract][Full Text] [Related]
9. Differentiation Between Multiple System Atrophy and Other Spinocerebellar Degenerations Using Diffusion Kurtosis Imaging. Ito K; Ohtsuka C; Yoshioka K; Maeda T; Yokosawa S; Mori F; Matsuda T; Terayama Y; Sasaki M Acad Radiol; 2019 Nov; 26(11):e333-e339. PubMed ID: 30658931 [TBL] [Abstract][Full Text] [Related]
10. Clonidine GH stimulation test to differentiate MSA from idiopathic late onset cerebellar ataxia: a prospective, controlled study. Bonnard C; Wirth T; Gebus O; Fahrer P; Montaut S; Robelin L; Tuzin N; Tranchant C; Anheim M J Neurol; 2020 Mar; 267(3):855-859. PubMed ID: 32034477 [TBL] [Abstract][Full Text] [Related]
11. Degenerative and acquired sporadic adult onset ataxia. Lieto M; Roca A; Santorelli FM; Fico T; De Michele G; Bellofatto M; Saccà F; De Michele G; Filla A Neurol Sci; 2019 Jul; 40(7):1335-1342. PubMed ID: 30927137 [TBL] [Abstract][Full Text] [Related]
12. Characterization of Cerebellar Atrophy and Resting State Functional Connectivity Patterns in Sporadic Adult-Onset Ataxia of Unknown Etiology (SAOA). Jiang X; Faber J; Giordano I; Machts J; Kindler C; Dudesek A; Speck O; Kamm C; Düzel E; Jessen F; Spottke A; Vielhaber S; Boecker H; Klockgether T; Scheef L Cerebellum; 2019 Oct; 18(5):873-881. PubMed ID: 31422550 [TBL] [Abstract][Full Text] [Related]
13. Pure cerebellar ataxia due to bi-allelic PRDX3 variants including recurring p.Asp202Asn. Efthymiou S; Novis LE; Koutsis G; Koniari C; Maroofian R; Turchetti V; Velonakis G; Vasconcellos LF; Raskin S; Srinivasan VM; Pagnamenta AT; Arun YB; Kinhal UV; Gowda VK; Teive HAG; Houlden H Ann Clin Transl Neurol; 2023 Oct; 10(10):1910-1916. PubMed ID: 37553803 [TBL] [Abstract][Full Text] [Related]
14. [Neuropathology of Cerebellar Cortical Atrophy]. Koga S Brain Nerve; 2020 Sep; 72(9):939-946. PubMed ID: 32934183 [TBL] [Abstract][Full Text] [Related]
15. [Spinocerebellar ataxia type 8 in Russian patients]. Nuzhnyi EP; Abramycheva NY; Chkhartishvili IA; Protopopova AO; Fedotova EY; Illarioshkin SN Zh Nevrol Psikhiatr Im S S Korsakova; 2022; 122(8):106-111. PubMed ID: 36036411 [TBL] [Abstract][Full Text] [Related]
16. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea]. Iwabuchi K; Nakazawa Y; Akai J; Yagishita S; Amano N No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439 [TBL] [Abstract][Full Text] [Related]
17. A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in Childhood. Ferrera G; Izzo R; Ghezzi D; Nanetti L; Lamantea E; Ardissone A Neuropediatrics; 2024 Apr; 55(2):135-139. PubMed ID: 37935417 [TBL] [Abstract][Full Text] [Related]
20. Magnetic resonance and nuclear medicine imaging in ataxias. Mascalchi M; Vella A Handb Clin Neurol; 2012; 103():85-110. PubMed ID: 21827882 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]