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

Year Number of Results
1967 2
1968 2
1969 2
1970 1
1971 1
1976 2
1978 2
1979 1
1981 3
1982 3
1983 1
1984 6
1985 4
1986 9
1987 9
1988 7
1989 7
1990 10
1991 10
1992 13
1993 15
1994 16
1995 21
1996 14
1997 19
1998 22
1999 25
2000 21
2001 20
2002 15
2003 24
2004 24
2005 19
2006 8
2007 18
2008 23
2009 18
2010 19
2011 22
2012 32
2013 24
2014 29
2015 25
2016 29
2017 37
2018 53
2019 39
2020 33
2021 38
2022 40
2023 38
2024 12

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804 results

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Page 1
Multiple system atrophy.
Poewe W, Stankovic I, Halliday G, Meissner WG, Wenning GK, Pellecchia MT, Seppi K, Palma JA, Kaufmann H. Poewe W, et al. Nat Rev Dis Primers. 2022 Aug 25;8(1):56. doi: 10.1038/s41572-022-00382-6. Nat Rev Dis Primers. 2022. PMID: 36008429 Review.
Multiple system atrophy (MSA) is a rare neurodegenerative disease that is characterized by neuronal loss and gliosis in multiple areas of the central nervous system including striatonigral, olivopontocerebellar and central autonomic structures. ...A firm clinical diagnosis …
Multiple system atrophy (MSA) is a rare neurodegenerative disease that is characterized by neuronal loss and gliosis in multiple area …
Ciliopathies and the Kidney: A Review.
McConnachie DJ, Stow JL, Mallett AJ. McConnachie DJ, et al. Am J Kidney Dis. 2021 Mar;77(3):410-419. doi: 10.1053/j.ajkd.2020.08.012. Epub 2020 Oct 9. Am J Kidney Dis. 2021. PMID: 33039432 Free article. Review.
Immune-mediated Cerebellar Ataxias: Practical Guidelines and Therapeutic Challenges.
Mitoma H, Manto M, Hampe CS. Mitoma H, et al. Curr Neuropharmacol. 2019;17(1):33-58. doi: 10.2174/1570159X16666180917105033. Curr Neuropharmacol. 2019. PMID: 30221603 Free PMC article. Review.
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia (GA), paraneoplastic cerebellar degenerations (PCDs), antiglutamate decarboxylase 65 (GAD) antibody-associated cerebellar ataxia, pos …
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia (GA), p …
Evaluation of Cerebellar Ataxic Patients.
Radmard S, Zesiewicz TA, Kuo SH. Radmard S, et al. Neurol Clin. 2023 Feb;41(1):21-44. doi: 10.1016/j.ncl.2022.05.002. Epub 2022 Aug 31. Neurol Clin. 2023. PMID: 36400556 Free PMC article. Review.
Cerebellar ataxia results from damage to the cerebellum and presents as movement incoordination and variability, gait impairment, and slurred speech. ...Symptomatic and potential disease-modifying therapies may benefit patients with cerebellar ataxia....
Cerebellar ataxia results from damage to the cerebellum and presents as movement incoordination and variability, gait impairme
Multiple system atrophy.
Goh YY, Saunders E, Pavey S, Rushton E, Quinn N, Houlden H, Chelban V. Goh YY, et al. Pract Neurol. 2023 Jun;23(3):208-221. doi: 10.1136/pn-2020-002797. Epub 2023 Mar 16. Pract Neurol. 2023. PMID: 36927875 Free PMC article. Review.
This is a practical guide to diagnosing and managing multiple system atrophy (MSA). We explain the newly published Movement Disorders Society Consensus Diagnostic Criteria, which include new 'Clinically Established MSA' and 'Possible Prodromal MSA' categories, hopefully re …
This is a practical guide to diagnosing and managing multiple system atrophy (MSA). We explain the newly published Movement Disorders …
A Diagnostic Approach to Spastic ataxia Syndromes.
Pedroso JL, Vale TC, França Junior MC, Kauffman MA, Teive H, Barsottini OGP, Munhoz RP. Pedroso JL, et al. Cerebellum. 2022 Dec;21(6):1073-1084. doi: 10.1007/s12311-021-01345-5. Epub 2021 Nov 15. Cerebellum. 2022. PMID: 34782953 Review.
Spastic ataxia is characterized by the combination of cerebellar ataxia with spasticity and other pyramidal features. It is the hallmark of some hereditary ataxias, but it can also occur in some spastic paraplegias and acquired conditions. ...
Spastic ataxia is characterized by the combination of cerebellar ataxia with spasticity and other pyramidal features. It is the hallm …
The Differential Diagnosis and Treatment of Atypical Parkinsonism.
Levin J, Kurz A, Arzberger T, Giese A, Höglinger GU. Levin J, et al. Dtsch Arztebl Int. 2016 Feb 5;113(5):61-9. doi: 10.3238/arztebl.2016.0061. Dtsch Arztebl Int. 2016. PMID: 26900156 Free PMC article. Review.
BACKGROUND: Aside from idiopathic Parkinson syndrome (Parkinson's disease), there are a number of other, so-called atypical parkinsonian syndromes: dementia with Lewy bodies (DLB), multiple system atrophy (MSA), progressive supranuclear palsy (PSP), and corticobasal degene …
BACKGROUND: Aside from idiopathic Parkinson syndrome (Parkinson's disease), there are a number of other, so-called atypical parkinsonian syn …
Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Pathophysiology and Clinical Implications.
Cabal-Herrera AM, Tassanakijpanich N, Salcedo-Arellano MJ, Hagerman RJ. Cabal-Herrera AM, et al. Int J Mol Sci. 2020 Jun 20;21(12):4391. doi: 10.3390/ijms21124391. Int J Mol Sci. 2020. PMID: 32575683 Free PMC article. Review.
The clinical features usually begin in the 60 s with an action or intention tremor followed by cerebellar ataxia, although 20% have only ataxia. MRI features include brain atrophy and white matter disease, especially in the middle cerebellar peduncles, perive …
The clinical features usually begin in the 60 s with an action or intention tremor followed by cerebellar ataxia, although 20% have o …
Phenytoin - An anti-seizure drug: Overview of its chemistry, pharmacology and toxicology.
Patocka J, Wu Q, Nepovimova E, Kuca K. Patocka J, et al. Food Chem Toxicol. 2020 Aug;142:111393. doi: 10.1016/j.fct.2020.111393. Epub 2020 May 4. Food Chem Toxicol. 2020. PMID: 32376339 Review.
The side effects on human health associated with phenytoin use are thoroughly described. In particular, DRESS syndrome and cerebellar atrophy are addressed. This review will help in further understanding the benefits phenytoin use in the treatment of epilepsy....
The side effects on human health associated with phenytoin use are thoroughly described. In particular, DRESS syndrome and cerebellar
X-linked ataxias.
Zanni G, Bertini E. Zanni G, et al. Handb Clin Neurol. 2018;155:175-189. doi: 10.1016/B978-0-444-64189-2.00011-1. Handb Clin Neurol. 2018. PMID: 29891057 Review.
X-linked cerebellar ataxias (XLCA) are an expanding group of genetically heterogeneous and clinically variable conditions characterized by cerebellar dysgenesis (hypoplasia, atrophy, or dysplasia) caused by gene mutations or genomic imbalances on the X chromo …
X-linked cerebellar ataxias (XLCA) are an expanding group of genetically heterogeneous and clinically variable conditions characteriz …
804 results