Detalhe da pesquisa
1.
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low-power view findings.
Neuropathology
; 42(5): 379-393, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35859519
2.
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
Brain
; 131(Pt 3): 772-84, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18079167
3.
Was the ataxia of Pierre Marie Machado-Joseph disease?: A reappraisal based on the last autopsy case from la Salpêtrière Hospital.
Arch Neurol
; 61(5): 784-90, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15148161
4.
[Pathology of hereditary spastic paraplegia: SPG 11 and related disorders].
No To Shinkei
; 55(9): 748-54, 2003 Sep.
Artigo
em Japonês
| MEDLINE | ID: mdl-14571836
5.
Attenuated nuclear shrinkage in neurons with nuclear aggregates--a morphometric study on pontine neurons of Machado-Joseph disease brains.
Exp Neurol
; 178(1): 124-8, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12460614
6.
Reversible conformational change of tau2 epitope on exposure to detergent in glial cytoplasmic inclusions of multiple system atrophy.
Acta Neuropathol
; 105(5): 508-14, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12677452
7.
PML nuclear bodies and neuronal intranuclear inclusion in polyglutamine diseases.
Neurobiol Dis
; 13(3): 230-7, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12901837