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

Year Number of Results
1973 1
1980 1
1983 1
1985 1
1987 1
1988 1
1990 2
1991 3
1992 1
1993 2
1994 6
1995 1
1996 2
1997 9
1998 1
1999 3
2000 5
2001 2
2003 3
2004 4
2005 1
2007 2
2008 1
2009 2
2010 3
2011 2
2012 3
2014 1
2015 1
2016 2
2017 3
2018 1
2019 1
2022 1
2023 1

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71 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 …
[Neuro-Langerhans cell histiocytosis].
Le Guennec L, Martin-Duverneuil N, Mokhtari K, Santiago-Ribeiro M, Bayen E, Del Cul A, Delgadillo D, Kas A, Courtillot C, Haroche J, Cohen F, Donadieu J, Hoang-Xuan K, Idbaih A. Le Guennec L, et al. Presse Med. 2017 Jan;46(1):79-84. doi: 10.1016/j.lpm.2016.09.014. Epub 2016 Nov 2. Presse Med. 2017. PMID: 27816346 Review. French.
Degenerative neuro-LCH, accounting for 45% of cases, is usually revealed, mostly in children, by: (i) a cerebellar syndrome, (ii) a pyramidal syndrome, (iii) a pseubulbar palsy, and/or (iv) cognitive disorders. ...Pathological analysis of degenerative neuro-LCH lesions hav …
Degenerative neuro-LCH, accounting for 45% of cases, is usually revealed, mostly in children, by: (i) a cerebellar syndrome, (ii) a p …
Multiple system atrophy.
Wenning GK, Colosimo C, Geser F, Poewe W. Wenning GK, et al. Lancet Neurol. 2004 Feb;3(2):93-103. doi: 10.1016/s1474-4422(03)00662-8. Lancet Neurol. 2004. PMID: 14747001 Review.
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder characterised clinically by any combination of parkinsonian, autonomic, cerebellar, or pyramidal signs and pathologically by cell loss, gliosis, and glial cytoplasmic inclusions in several CNS st …
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder characterised clinically by any combination of parkinsonian, autonomi …
The spinocerebellar ataxias.
Gilman S. Gilman S. Clin Neuropharmacol. 2000 Nov-Dec;23(6):296-303. doi: 10.1097/00002826-200011000-00002. Clin Neuropharmacol. 2000. PMID: 11575863 Review.
The spinocerebellar ataxias (SCAs) are diseases characterized by the progressive degeneration and subsequent loss of neurons accompanied by reactive gliosis, degeneration of fibers from the deteriorating neurons, and clinical symptoms reflecting the locations of the lost n …
The spinocerebellar ataxias (SCAs) are diseases characterized by the progressive degeneration and subsequent loss of neurons accompanied by …
Congenital Zika virus infection: a neuropathological review.
Chimelli L, Avvad-Portari E. Chimelli L, et al. Childs Nerv Syst. 2018 Jan;34(1):95-99. doi: 10.1007/s00381-017-3651-3. Epub 2017 Nov 22. Childs Nerv Syst. 2018. PMID: 29167994 Review.
Histologically, there is extensive destruction of the hemispheric parenchyma, calcifications, various disturbances of neuronal migration, reactive gliosis, microglial hyperplasia and occasional perivascular cuffs of lymphocytes, also in the meninges. Hypoplastic lesions se …
Histologically, there is extensive destruction of the hemispheric parenchyma, calcifications, various disturbances of neuronal migration, re …
Progressive supranuclear palsy: what do we know about it?
Long L, Cai XD, Wei XB, Liao JC, Xu YQ, Gao HM, Chen XH, Wang Q. Long L, et al. Curr Med Chem. 2015;22(10):1182-93. doi: 10.2174/0929867322666150302170552. Curr Med Chem. 2015. PMID: 25732053 Review.
Progressive supranuclear palsy (PSP) is a progressive tauopathy characterized by supranuclear ophthalmoplegia, pseudobulbar palsy, dysarthria, axial rigidity, frontal lobe dysfunction, and dementia. The typical pathology includes neuronal loss, gliosis and microtubule-asso …
Progressive supranuclear palsy (PSP) is a progressive tauopathy characterized by supranuclear ophthalmoplegia, pseudobulbar palsy, dysarthri …
Infectious acute hemicerebellitis.
García-Cazorla A, Oliván JA, Pancho C, Sans A, Boix C, Campistol J. García-Cazorla A, et al. J Child Neurol. 2004 May;19(5):390-2. doi: 10.1177/088307380401900514. J Child Neurol. 2004. PMID: 15224713 Review.
Forty-five days later, a second MRI disclosed signs of hemiatrophy and cortical gliosis. The clinical outcome was favorable, with only a slight lack of motor coordination in the involved hand remaining. ...We underline the need to consider this rare entity in asymmetric …
Forty-five days later, a second MRI disclosed signs of hemiatrophy and cortical gliosis. The clinical outcome was favorable, with onl …
Pathomechanisms of cognitive impairment in progressive supranuclear palsy.
Jellinger KA. Jellinger KA. J Neural Transm (Vienna). 2023 Apr;130(4):481-493. doi: 10.1007/s00702-023-02613-w. Epub 2023 Mar 2. J Neural Transm (Vienna). 2023. PMID: 36862189 Review.
This four-repeat tauopathy is morphologically featured by accumulation of tau protein in neurons and glia causing neuronal loss and gliosis in the extrapyramidal system associated with cortical atrophy and white matter lesions. ...Showing longitudinal decline, it has been …
This four-repeat tauopathy is morphologically featured by accumulation of tau protein in neurons and glia causing neuronal loss and glios …
Essential tremor--neurodegenerative or nondegenerative disease towards a working definition of ET.
Deuschl G, Elble R. Deuschl G, et al. Mov Disord. 2009 Oct 30;24(14):2033-41. doi: 10.1002/mds.22755. Mov Disord. 2009. PMID: 19750493 Review.
Essential tremor (ET) is a syndrome of tremor in posture and movement, but recent studies have revealed additional cerebellar motor disturbances, cognitive disturbances, personality changes, hearing loss, and olfactory deficits. ...We propose the alternative hypothesis tha …
Essential tremor (ET) is a syndrome of tremor in posture and movement, but recent studies have revealed additional cerebellar motor d …
Neuropathology of Gerstmann-Sträussler-Scheinker disease.
Bugiani O, Giaccone G, Piccardo P, Morbin M, Tagliavini F, Ghetti B. Bugiani O, et al. Microsc Res Tech. 2000 Jul 1;50(1):10-5. doi: 10.1002/1097-0029(20000701)50:1<10::AID-JEMT3>3.0.CO;2-6. Microsc Res Tech. 2000. PMID: 10871543 Review.
Gerstmann-Straussler-Scheinker disease is a familial neurodegeneration characterized clinically by adult-onset ataxia, postural abnormalities, and cognitive decline, and pathologically by amyloid deposits mostly localized in the cerebral and cerebellar cortices and the bas …
Gerstmann-Straussler-Scheinker disease is a familial neurodegeneration characterized clinically by adult-onset ataxia, postural abnormalitie …
71 results