Detalhe da pesquisa
1.
Prevalence and clinical characteristics of Sarcopenia in older adult patients with stable chronic obstructive pulmonary disease: a cross-sectional and follow-up study.
BMC Pulm Med
; 24(1): 219, 2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38698380
2.
Effects of a new respiratory muscle training device in community-dwelling elderly men: an open-label, randomized, non-inferiority trial.
BMC Geriatr
; 22(1): 155, 2022 02 24.
Artigo
Inglês
| MEDLINE | ID: mdl-35209851
3.
Gold Standard? Method of Citric Acid Solution Swallowing Test as a Screening Test for Patients with Tracheostomy.
Dysphagia
; 37(3): 533-539, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33905045
4.
Development of a questionnaire to identify ocular torticollis.
Eur J Pediatr
; 180(2): 561-567, 2021 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32979091
5.
Multi-Odor Discrimination by Rat Sniffing for Potential Monitoring of Lung Cancer and Diabetes.
Sensors (Basel)
; 21(11)2021 May 26.
Artigo
Inglês
| MEDLINE | ID: mdl-34073351
6.
Olfactory Detection of Toluene by Detection Rats for Potential Screening of Lung Cancer.
Sensors (Basel)
; 21(9)2021 Apr 23.
Artigo
Inglês
| MEDLINE | ID: mdl-33922694
7.
The feasibility of quantitative parameters of lymphoscintigraphy without significant dermal backflow for the evaluation of lymphedema in post-operative patients with breast cancer.
Eur J Nucl Med Mol Imaging
; 47(5): 1094-1102, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31734782
8.
Effects of Traction on Interpretation of Lumbar Bone Mineral Density in Patients with Duchenne Muscular Dystrophy: A New Measurement Method and Diagnostic Criteria Based on Comparison of Dual-Energy X-Ray Absorptiometry and Quantitative Computed Tomography.
J Clin Densitom
; 23(1): 53-62, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-30143440
9.
Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis.
Hum Mutat
; 40(8): 1115-1126, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31264822
10.
Neural Compensatory Response During Complex Cognitive Function Tasks in Mild Cognitive Impairment: A Near-Infrared Spectroscopy Study.
Neural Plast
; 2019: 7845104, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31320893
11.
GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.
Ann Neurol
; 82(3): 466-478, 2017 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-28856709
12.
Portable low-power thermal cycler with dual thin-film Pt heaters for a polymeric PCR chip.
Biomed Microdevices
; 20(1): 14, 2018 01 29.
Artigo
Inglês
| MEDLINE | ID: mdl-29376193
13.
Evaluation of Early Left Ventricular Dysfunction in Patients with Duchenne Muscular Dystrophy Using Two-Dimensional Speckle Tracking Echocardiography and Tissue Doppler Imaging.
Pediatr Cardiol
; 39(8): 1614-1619, 2018 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-30003298
14.
Revisiting respiratory muscle strength and pulmonary function in spinal cord injury: The effect of body positions.
Neuro Endocrinol Lett
; 39(3): 189-195, 2018 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-30431744
15.
A novel sensor-based assessment of lower limb spasticity in children with cerebral palsy.
J Neuroeng Rehabil
; 15(1): 45, 2018 06 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29866177
16.
Crystal structures of two forms of the Acanthamoeba polyphaga mimivirus Rab GTPase.
Arch Virol
; 162(11): 3407-3416, 2017 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-28779233
17.
Improved sensing characteristics of dual-gate transistor sensor using silicon nanowire arrays defined by nanoimprint lithography.
Sci Technol Adv Mater
; 18(1): 17-25, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28179955
18.
Protocol for a prospective observational study of conventional treatment and traditional Korean medicine combination treatment for children with cerebral palsy.
BMC Complement Altern Med
; 16: 172, 2016 Jun 08.
Artigo
Inglês
| MEDLINE | ID: mdl-27267182
19.
A study of the development of the Korean version of PedsQL(TM) 3.0 cerebral palsy module and reliability and validity.
J Phys Ther Sci
; 28(7): 2132-9, 2016 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-27512282
20.
Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations.
J Hum Genet
; 60(4): 213-5, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25608830