Detalhe da pesquisa
1.
Clinical uses of Bupropion in patients with Parkinson's disease and comorbid depressive or neuropsychiatric symptoms: a scoping review.
BMC Neurol
; 22(1): 169, 2022 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35513785
2.
Neurofilament light chain serum levels reflect disease severity in MOG-Ab associated disorders.
J Neurol Neurosurg Psychiatry
; 90(11): 1293-1296, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30952681
3.
Listeria Meningoencephalitis in a Patient With Rheumatoid Arthritis on Anti-Interleukin 6 Receptor Antibody Tocilizumab.
J Clin Rheumatol
; 21(6): 330, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26267715
4.
Design and Operation of the Lombardy Parkinson's Disease Network.
Front Neurol
; 11: 573, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32670185
5.
Anti-myelin oligodendrocyte glycoprotein antibodies: Magnetic resonance imaging findings in a case series and a literature review.
Neuroradiol J
; 31(1): 69-82, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28379073
6.
Stereotypic behaviours in frontotemporal dementia and progressive supranuclear palsy.
Cortex
; 109: 272-278, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30399478
7.
Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patients.
J Neurol
; 254(11): 1538-46, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17934876
8.
The relevance of gender in Parkinson's disease: a review.
J Neurol
; 264(8): 1583-1607, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28054129
9.
Unusual primary central nervous system lymphoma location involving the fourth ventricle and hypothalamus.
Neuroradiol J
; 28(2): 120-5, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25923685
10.
Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Arch Neurol
; 61(5): 727-33, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15148151
11.
Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) gene.
Neuromuscul Disord
; 14(11): 723-6, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15482956