Detalhe da pesquisa
1.
Concomitant Cerebral Venous Thrombosis and Intracranial Hemorrhages in Presentation of a Patient with Secondary Polycythemia: A Case Report.
Am J Case Rep
; 24: e941507, 2023 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37838828
2.
Postacute-Stroke Management Problems in Home Care Service: A Qualitative Single-Centered Study in Yogyakarta, Indonesia.
J Neurosci Rural Pract
; 13(1): 50-59, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-35110920
3.
Progressive Worsening of Neurological Manifestations in HIV-Associated Opportunistic Central Nervous System (CNS) Infection Patients After COVID-19 Vaccinations: A Possible Co-Incidence Causality.
Am J Case Rep
; 23: e936257, 2022 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35610955
4.
Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy.
Genes (Basel)
; 13(2)2022 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35205250
5.
Clinical characterizations of three adults with genetically confirmed spinal muscular atrophy: a case series.
J Med Case Rep
; 16(1): 435, 2022 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36376972
6.
Dried Blood Spot Screening System for Spinal Muscular Atrophy with Allele-Specific Polymerase Chain Reaction and Melting Peak Analysis.
Genet Test Mol Biomarkers
; 25(4): 293-301, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33877896
7.
Centella asiatica Prevents Increase of Hippocampal Tumor Necrosis Factor-α Independently of Its Effect on Brain-Derived Neurotrophic Factor in Rat Model of Chronic Stress.
Biomed Res Int
; 2019: 2649281, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30956976
8.
Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.
Brain Dev
; 40(8): 670-677, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29580671
9.
New, Improved Version of the mCOP-PCR Screening System for Detection of Spinal Muscular Atrophy Gene (SMN1) Deletion.
Kobe J Med Sci
; 63(2): E37-E40, 2017 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29434172
10.
SMA mutations in SMN Tudor and C-terminal domains destabilize the protein.
Brain Dev
; 39(7): 606-612, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28366534
11.
Gender Effects on the Clinical Phenotype in Japanese Patients with Spinal Muscular Atrophy.
Kobe J Med Sci
; 63(2): E41-E44, 2017 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29434173
12.
SMA Diagnosis: Detection of SMN1 Deletion with Real-Time mCOP-PCR System Using Fresh Blood DNA.
Kobe J Med Sci
; 63(3): E80-E83, 2017 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29434179
13.
Spinal muscular atrophy carriers with two SMN1 copies.
Brain Dev
; 39(10): 851-860, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28676237
14.
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNA.
Brain Dev
; 39(9): 774-782, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28522225
15.
Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2.
Hum Genome Var
; 3: 16040, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27917293
16.
Salbutamol inhibits ubiquitin-mediated survival motor neuron protein degradation in spinal muscular atrophy cells.
Biochem Biophys Rep
; 4: 351-356, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29124224
17.
Two Japanese Patients With SMA Type 1 Suggest that Axonal-SMN May Not Modify the Disease Severity.
Pediatr Neurol
; 52(6): 638-41, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25838041
18.
SMA screening system using dried blood spots on filter paper: application of COP-PCR to the SMN1 deletion test.
Kobe J Med Sci
; 60(4): E78-85, 2015 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25791416
19.
Attention Deficit/Hyperactivity Disorder (ADHD): age related change of completion time and error rates of Stroop test.
Kobe J Med Sci
; 61(1): E19-26, 2015 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25868610