Detalhe da pesquisa
1.
Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations.
Proc Natl Acad Sci U S A;
121(18): e2310283121, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38669183
2.
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning.
Am J Hum Genet;
109(2): 270-281, 2022 02 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35063063
3.
Rare variant association analyses reveal the significant contribution of carbohydrate metabolic disturbance in severe adolescent idiopathic scoliosis.
J Med Genet;
2024 May 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38724173
4.
Can the Sterilization Protocol Be Improved to Enhance the Healing of Allograft Tendons? An In Vivo Study in Rabbit Tendons.
Clin Orthop Relat Res;
482(6): 1074-1086, 2024 Jun 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38427791
5.
Ten-year trends in surgical management of 1207 congenital scoliosis.
Eur Spine J;
32(7): 2533-2540, 2023 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37160441
6.
Unsuspected severe tracheal stenosis and tracheomalacia after correction surgery for congenital scoliosis: A case report.
Paediatr Anaesth;
33(2): 167-169, 2023 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36217730
7.
Correlation between supine flexibility and postoperative correction in adolescent idiopathic scoliosis.
BMC Musculoskelet Disord;
24(1): 126, 2023 Feb 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36793065
8.
The incidence and interrelationship of hemivertebra and concomitant cardiac abnormalities in congenital scoliosis.
BMC Musculoskelet Disord;
24(1): 621, 2023 Jul 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37525123
9.
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS).
J Med Genet;
58(1): 41-47, 2021 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32381727
10.
A Review of the Methods on Cobb Angle Measurements for Spinal Curvature.
Sensors (Basel);
22(9)2022 Apr 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35590951
11.
Cross-sectional analysis of associated anomalies and vertebral anomaly location in 1289 surgical congenital scoliosis.
Eur Spine J;
30(12): 3577-3584, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34235574
12.
Risk factors for blood transfusion in adolescent patients with scoliosis undergoing scoliosis surgery: a study of 722 cases in a single center.
BMC Musculoskelet Disord;
22(1): 13, 2021 Jan 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33402158
13.
Older fusion-surgery age in congenital scoliosis patients is a risk factor for extended length of stay, more estimated blood loss, longer fused segments and higher medical costs: a retrospective study.
BMC Musculoskelet Disord;
22(1): 779, 2021 Sep 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34511086
14.
The effect of pedicle subtraction osteotomy for the correction of severe Scheuermann thoracolumbar kyphosis on sagittal spinopelvic alignment.
BMC Musculoskelet Disord;
22(1): 165, 2021 Feb 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33568117
15.
Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosis.
BMC Musculoskelet Disord;
22(1): 483, 2021 May 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34034738
16.
Cross-sectional analysis and trend of vertebral and associated anomalies in Chinese congenital scoliosis population: a retrospective study of one thousand, two hundred and eighty nine surgical cases from 2010 to 2019.
Int Orthop;
45(8): 2049-2059, 2021 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34059967
17.
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.
Hum Mutat;
41(1): 182-195, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31471994
18.
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.
BMC Med Genet;
21(1): 115, 2020 05 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32460719
19.
Identification of novel FBN1 variations implicated in congenital scoliosis.
J Hum Genet;
65(3): 221-230, 2020 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31827250
20.
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome.
BMC Musculoskelet Disord;
21(1): 220, 2020 Apr 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32278351