Detalhe da pesquisa
1.
Early Detection of Cardiac Amyloidosis in Transthyretin Mutation Carriers.
Int Heart J
; 63(1): 168-175, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35095067
2.
SIRT1 decelerates morphological processing of oligodendrocyte cell lines and regulates the expression of cytoskeleton-related oligodendrocyte proteins.
Biochem Biophys Res Commun
; 546: 7-14, 2021 03 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33556638
3.
Abrupt Onset of Cardiac Tamponade in Sarcoidosis.
Int Heart J
; 62(5): 1176-1181, 2021 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34544983
4.
Fingolimod induces BAFF and expands circulating transitional B cells without activating memory B cells and plasma cells in multiple sclerosis.
Clin Immunol
; 187: 95-101, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29079163
5.
Latitude and HLA-DRB1*04:05 independently influence disease severity in Japanese multiple sclerosis: a cross-sectional study.
J Neuroinflammation
; 13(1): 239, 2016 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27599848
6.
A case presenting electrophysiological and immunological characteristics of Fisher syndrome and Lambert-Eaton myasthenic syndrome.
Muscle Nerve
; 63(3): E16-E18, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33290573
7.
Latitude and HLA-DRB1 alleles independently affect the emergence of cerebrospinal fluid IgG abnormality in multiple sclerosis.
Mult Scler
; 21(9): 1112-20, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25583844
8.
A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case.
BMC Neurol
; 15: 13, 2015 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25886484
9.
A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis.
Tohoku J Exp Med
; 235(4): 305-10, 2015 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25843429
10.
[Clinical characteristics of seizure-predominant autoimmune encephalitis and utility of anti-neuronal antibody scores for early treatment].
Rinsho Shinkeigaku
; 64(4): 272-279, 2024 Apr 24.
Artigo
em Japonês
| MEDLINE | ID: mdl-38508734
11.
The Movement Disorder Society Criteria: Its Clinical Usefulness in Multiple System Atrophy.
Intern Med
; 2024 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38494718
12.
3-[(2,4-Dimethoxy)benzylidene]-anabaseine dihydrochloride protects against 6-hydroxydopamine-induced parkinsonian neurodegeneration through α7 nicotinic acetylcholine receptor stimulation in rats.
J Neurosci Res
; 91(3): 462-71, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23239187
13.
Transthyretin Variant Amyloidosis with a TTR A97D (p.A117D) Mutation Manifesting Remarkable Asymmetric Neuropathy.
Intern Med
; 62(15): 2261-2266, 2023 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36543209
14.
Cerebral Tuberculoma Diagnosed by Nested Polymerase Chain Reaction of a Formalin-fixed Paraffin-embedded Brain Biopsy Sample.
Intern Med
; 62(12): 1827-1833, 2023 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328574
15.
Activation of SIRT1 promotes membrane resealing via cortactin.
Sci Rep
; 12(1): 15328, 2022 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36097021
16.
Anti-signal Recognition Particle Antibody-positive Immune-mediated Myopathy after mRNA-1273 SARS-CoV-2 Vaccination.
Intern Med
; 61(23): 3605-3609, 2022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36104199
17.
Ubiquitin-dependent rapid degradation conceals a cell-protective function of cytoplasmic SIRT3 against oxidative stress.
J Biochem
; 171(2): 201-213, 2022 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34718606
18.
Induction of manganese superoxide dismutase by nuclear translocation and activation of SIRT1 promotes cell survival in chronic heart failure.
J Biol Chem
; 285(11): 8375-82, 2010 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20089851
19.
Histone deacetylase SIRT1 modulates neuronal differentiation by its nuclear translocation.
Proc Natl Acad Sci U S A
; 105(40): 15599-604, 2008 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-18829436
20.
[A case of Charcot-Marie-Tooth disease type 2Z caused by MORC2 S87L mutation mimicking spinal muscular atrophy].
Rinsho Shinkeigaku
; 61(4): 262-264, 2021 Apr 21.
Artigo
em Japonês
| MEDLINE | ID: mdl-33762496