Detalhe da pesquisa
1.
A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: consideration of the pathology of post-polio syndrome.
Neuropathology
; 33(1): 93-101, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22672529
2.
[Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder].
Rinsho Shinkeigaku
; 63(10): 650-655, 2023 Oct 25.
Artigo
em Japonês
| MEDLINE | ID: mdl-37779024
3.
[Neuropsychological and regional cerebral blood flow of posterior parietal area features in patients with Parkinson's disease with mild cognitive impairment].
Rinsho Shinkeigaku
; 62(7): 532-540, 2022 Jul 29.
Artigo
em Japonês
| MEDLINE | ID: mdl-35753785
4.
Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.
Neurol Genet
; 8(5): e200030, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36176336
5.
Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism.
BMC Neurol
; 11: 72, 2011 Jun 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-21682904
6.
Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length.
Mov Disord
; 25(11): 1694-700, 2010 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20589872
7.
[An apraxia of eyelid closure in association with frontal lobe atrophy in a patient with amyotrophic lateral sclerosis].
Rinsho Shinkeigaku
; 47(5): 226-30, 2007 May.
Artigo
em Japonês
| MEDLINE | ID: mdl-17585605
8.
[Two cases of generalized tetanus presenting with dysphagia as an initial symptom].
No To Shinkei
; 55(11): 973-6, 2003 Nov.
Artigo
em Japonês
| MEDLINE | ID: mdl-14727538
9.
Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a family.
J Neurol Sci
; 372: 128-130, 2017 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28017198