Detalhe da pesquisa
1.
Cannabidiol Exerts Sedative and Hypnotic Effects in Normal and Insomnia Model Mice Through Activation of 5-HT1A Receptor.
Neurochem Res;
49(5): 1150-1165, 2024 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38296858
2.
[Quality evaluation of salt-fired Eucommiae Cortex based on HPLC fingerprint, multi-component content determination, and chemometrics].
Zhongguo Zhong Yao Za Zhi;
49(1): 141-150, 2024 Jan.
Artigo
em Zh
| MEDLINE
| ID: mdl-38403347
3.
Histopathologic features and molecular genetic landscape of HER2-amplified endometrial carcinomas.
Mod Pathol;
35(7): 962-971, 2022 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34972830
4.
Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms.
J Med Genet;
58(7): 465-474, 2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32737134
5.
[Psychological and behavioral problems in children and adolescents during the coronavirus disease 2019 epidemic: a Scoping review]. / æ°åå ç¶ç æ¯èºçæµè¡æé´å¿ç«¥åéå°å¹´çå¿çè¡ä¸ºé®é¢ï¼Scoping综述.
Zhongguo Dang Dai Er Ke Za Zhi;
24(7): 728-735, 2022 Jul 15.
Artigo
em Zh
| MEDLINE
| ID: mdl-35894185
6.
AI detection of mild COVID-19 pneumonia from chest CT scans.
Eur Radiol;
31(9): 7192-7201, 2021 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33738595
7.
The significance of enhancer of zeste homolog 2 (EZH2) expression in spindle cell lesions of the breast.
Pathol Int;
71(6): 415-419, 2021 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33730427
8.
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.
J Med Genet;
55(5): 298-306, 2018 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29453195
9.
Tumor budding in colorectal carcinoma: An institutional interobserver reliability and prognostic study of colorectal adenocarcinoma cases.
Ann Diagn Pathol;
43: 151420, 2019 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31731034
10.
Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.
Neural Plast;
2017: 3192090, 2017.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28695016
11.
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.
Hum Mol Genet;
22(14): 2941-7, 2013 Jul 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23535823
12.
Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss.
Am J Med Genet A;
167A(10): 2357-65, 2015 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26079994
13.
Treatment strategies for huge central neurocytomas.
J Huazhong Univ Sci Technolog Med Sci;
35(1): 105-110, 2015 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25673202
14.
[Analysis of infection status and pathogenic features of human metapneumovirus among children in Hangzhou between year 2009 and 2011].
Zhonghua Yu Fang Yi Xue Za Zhi;
47(1): 31-4, 2013 Jan.
Artigo
em Zh
| MEDLINE
| ID: mdl-23601519
15.
Endovascular embolization for basal ganglia and thalamic arteriovenous malformations.
Front Neurol;
14: 1244782, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38020631
16.
Development and Validation of a Deep Learning Predictive Model Combining Clinical and Radiomic Features for Short-Term Postoperative Facial Nerve Function in Acoustic Neuroma Patients.
Curr Med Sci;
43(2): 336-343, 2023 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37059936
17.
Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations.
Medicine (Baltimore);
102(7): e33000, 2023 Feb 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36800592
18.
A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4.
Mol Genet Genomic Med;
11(3): e2103, 2023 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36373990
19.
[Systematic review and Meta-analysis on the auriculotherapy in treatment of insomnia].
Zhongguo Zhen Jiu;
42(10): 1184-94, 2022 Oct 12.
Artigo
em Zh
| MEDLINE
| ID: mdl-37199212
20.
Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss.
Front Genet;
13: 825082, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35711932