Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Longxia, Wang"'
Publikováno v:
International Journal of Hyperthermia, Vol 40, Iss 1 (2023)
AbstractObjectives To investigate the pattern of change over time and predictors for metastasis in indeterminate lymph nodes (LNs) among patients with thyroid cancer post-ablation.Methods We enrolled patients who developed new cervical LNs after papi
Externí odkaz:
https://doaj.org/article/5ad080cc30c94d2e8bf0a8817baad46f
Publikováno v:
Advanced Ultrasound in Diagnosis and Therapy, Vol 6, Iss 1, Pp 7-13 (2022)
Objective: To compare the etiologies and adverse outcomes of pregnancies with short fetal femur length (FL) categorized based on relative proportion and percentile placement. Methods: Fetuses (n = 254) with short FL measured by ultrasound were classi
Externí odkaz:
https://doaj.org/article/02feb2891d744815891c923dda0c3a3f
Autor:
Jianan Li, Yixin Chen, Minyu Zhang, Peifang Zhang, Kunlun He, Fengqin Yan, Jingbo Li, Hong Xu, Daniel Burkhoff, Yukun Luo, Longxia Wang, Qiuyang Li
Publikováno v:
Cancers, Vol 14, Iss 21, p 5291 (2022)
Appropriate clinical management of adnexal masses requires a detailed diagnosis. We retrospectively collected ultrasound images of 1559 cases from the first Center of Chinese PLA General Hospital and developed a fully automatic deep learning (DL) mod
Externí odkaz:
https://doaj.org/article/d6732909572749c181a5eb9536afef4c
Autor:
Xinyue Zhang, Yanqin You, Xiaoxiao Xie, Hong Xu, Honghui Zhou, Yuanmei Lei, Pei Sun, Yuanguang Meng, Longxia Wang, Yanping Lu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 12, Pp n/a-n/a (2020)
Abstract Background Skeletal ciliopathies are a group of clinically and genetically heterogeneous disorders with the spectrum of severity spanning from relatively mild to prenatally lethal. The aim of our study was to identify pathogenic mutations in
Externí odkaz:
https://doaj.org/article/751e50f4a36543bea2db11051f342921
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Skeletal disorders, which have great genotypic and phenotypic varieties, are a considerable challenge to differentiate these diseases and provide a definitive prenatal diagnosis or pre‐implantation. The present study aims to ide
Externí odkaz:
https://doaj.org/article/d59268a53a2247bfbc3a3997c2bf191c
Publikováno v:
Cellular and Molecular Biology. 68:15-23
The study focused on the performance of ultrasound imaging in detecting fetal spinal deformities. First, the double emulsification method and the carbodiimide method were used to prepare the target Au-loaded nanorod phase-change nano-level contrast a
Publikováno v:
International Journal of Biological Sciences, Vol 7, Iss 5, Pp 600-606 (2011)
Angiogenesis is a critical factor in tumor growth and metastasis, and microvessel density (MVD) was an important parameter for assessing vessels in tumors. However, radiologic assessment of tumor vascularity is not yet well established. In our study,
Externí odkaz:
https://doaj.org/article/5a72d80e75364bc082972444566908f4
Autor:
H. Xu, Yuan Ren, Zhiying Gao, Qingdong Zhao, Honghui Zhou, Rui Song, Pei Sun, Manli Zhang, Xinyue Zhang, Longxia Wang, Yanping Lu, Xiaoxiao Xie, Yuanguang Meng, Yanqin You
Publikováno v:
Prenatal diagnosisREFERENCES. 41(11)
Objective To investigate the genetic etiology of skeletal dysplasia in highly selected fetuses during the first and second trimesters using deep phenotyping and exome sequencing (ES). Method Fetuses with short femurs were identified using the establi
Publikováno v:
Ann Transl Med
Background Genetic mutations in genes related to the production, migration, or differentiation of cortical neurons can result in malformations of cortical development (MCDs). However, a large number of MCD-related pathogenetic mutations remain unknow
Autor:
H. Xu, Yuanmei Lei, Yuanguang Meng, Xiaoxiao Xie, Yanping Lu, Honghui Zhou, Xinyue Zhang, Longxia Wang, Pei Sun, Yanqin You
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Skeletal ciliopathies are a group of clinically and genetically heterogeneous disorders with the spectrum of severity spanning from relatively mild to prenatally lethal. The aim of our study was to identify pathogenic mutations in a Chines