Detalhe da pesquisa
1.
Development of a 3D Relative Motion Method for Human-Robot Interaction Assessment.
Sensors (Basel)
; 22(6)2022 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35336593
2.
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane.
Hum Mol Genet
; 23(10): 2551-68, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24363064
3.
Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment.
Am J Hum Genet
; 91(5): 883-9, 2012 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23122587
4.
Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss.
Am J Hum Genet
; 88(5): 621-7, 2011 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21549336
5.
A methodology to implement a closed-loop feedback-feedforward level control in a laboratory-scale flotation bank using peristaltic pumps.
MethodsX
; 10: 102081, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36896313
6.
Robotically Aided Method to Characterise the Soft Tissue Interaction with Wearable Robots.
IEEE Int Conf Rehabil Robot
; 2023: 1-6, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37941219
7.
Biomechanical Effects of Adding an Ankle Soft Actuation in a Unilateral Exoskeleton.
Biosensors (Basel)
; 12(10)2022 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36291010
8.
Guía de práctica clínica mexicana para el diagnóstico y tratamiento de las dislipidemias y enfermedad cardiovascular aterosclerótica.
Arch Cardiol Mex
; 92(Supl): 1-62, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35275904
9.
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Hum Mutat
; 32(7): 825-34, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21520338
10.
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment.
Hum Mol Genet
; 18(16): 3075-89, 2009 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19477959
11.
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA.
Proc Natl Acad Sci U S A
; 105(47): 18608-13, 2008 Nov 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-19017801
12.
The Actuation System of the Ankle Exoskeleton T-FLEX: First Use Experimental Validation in People with Stroke.
Brain Sci
; 11(4)2021 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33805216
13.
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.
Hum Genet
; 128(4): 411-9, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20668882
14.
Experimental model for removal of snake venom via hemoperfusion in rats.
J Vet Emerg Crit Care (San Antonio)
; 30(3): 286-294, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32112523
15.
New pharmacological insights of Galactia glaucescens.
Nat Prod Res
; 33(16): 2389-2393, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29488401
16.
A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy.
Hum Mutat
; 29(6): 823-31, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18381613
17.
A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.
Eur J Hum Genet
; 16(8): 888-96, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18285825
18.
A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression.
Hum Genet
; 123(1): 41-53, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18030493
19.
A Spanish sporadic case of deafness-dystonia (Mohr-Tranebjaerg) syndrome with a novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexes.
Neuromuscul Disord
; 18(12): 979-81, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18952432
20.
Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.
J Assoc Res Otolaryngol
; 9(2): 202-14, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18452040