Results 41 to 50 of about 52,798 (289)

Risk Factors for Testicular Atrophy in Children With Testicular Torsion Following Emergent Orchiopexy

Frontiers in Pediatrics, 2020
Objective: To analyze the risk factors for testicular atrophy (TA) in children with testicular torsion (TT) following emergent orchiopexy.Methods: Clinical data of patients with TT undergoing orchiopexy were retrospectively reviewed, including age at ...
Xiao-Mao Tian, Xiao-Mao Tian, Xiao-Mao Tian, Xiao-Hui Tan, Xiao-Hui Tan, Qin-Lin Shi, Qin-Lin Shi, Qin-Lin Shi, Sheng Wen, Sheng Wen, Peng Lu, Peng Lu, Xing Liu, Xing Liu, Xing Liu, Xu-Liang Li, Xu-Liang Li, Da-Wei He, Da-Wei He, Da-Wei He, Tao Lin, Tao Lin, Tao Lin, Guang-Hui Wei, Guang-Hui Wei, Guang-Hui Wei   +25 more
doaj   +1 more source

Paternal Circadian Disruption Impairs Offspring Cognition via Sperm microRNAs

Advanced Science, EarlyView.
Paternal circadian disruption remodels the sperm small RNA payload, elevating miR‐92a‐3p/miR‐25‐3p levels and perturbing early embryonic gene regulatory programs. Microinjection experiments and single‐embryo transcriptomics reveal sex‐specific developmental vulnerabilities, ultimately impairing offspring hippocampal synaptic plasticity and cognition ...
Kexin Zou, Sisi Luo, Binliang Tang, Zhiqiang Liu, Yuchuan Zhou, Yicong Meng, Zhengmu Wu, Zheng Sun, Weihui Shi, Jianzhong Sheng, Chuanjin Yu, Zhenhua Li, Siyi Wei, Mo Zhang, Yujie Luo, Jing Yan, Xueyun Qin, Jiahang Mo, Chengliang Zhou, Jinsong Li, Hefeng Huang, Yifu Ding, Guolian Ding   +22 more
wiley   +1 more source

NQO1‐Mediated Anoikis Resistance and Immune Evasion Define a High‐Risk Multi‐Omic Subtype for Precision Management of T1 High‐Grade Bladder Cancer

Advanced Science, EarlyView.
Multi‐omic profiling of T1 high‐grade bladder cancer identifies a high‐risk subtype (T1HG1) driven by NQO1, which couples anoikis resistance with immune evasion. NQO1 orchestrates macrophage–T cell crosstalk suppression via CXCL9 modulation. Pharmacological NQO1 inhibition with skullcapflavone II enhances cisplatin efficacy, representing a promising ...
Bin Guo, Chunru Xu, Shufan Fu, Qiang Cheng, Juan Li, Linkuo Shang, Gaojie Li, Yang Yang, Ying Wang, Yanqing Gong, Shengwei Xiong, Jian Fan, Changwei Yuan, Mei Zhang, Yifan Zuo, Elena Papaleo, Yue Shi, Yuan Liang, Xuesong Li, Hongzhao Li, Weimin Ci   +20 more
wiley   +1 more source

Urogenital Myiasis Caused by Psychoda Albipennis: A Case Report

, 2015
Urogenital myiasis is one of the parasitic diseases of the urinary system. We report a case of urogenital myiasis caused by Psychoda albipennis in a 64-year-old male patient.
Ömer Kutlu, Ali Ertan Okatan, Ersagun Karagüzel, Kurtuluş Buruk, Güner Kemal Özgür   +4 more
core   +1 more source

Design, Control, and Clinical Applications of Magnetic Actuation Systems: Challenges and Opportunities

Advanced Intelligent Systems, Volume 7, Issue 3, March 2025.
This review aims to provide a broad understanding for interdisciplinary researchers in engineering and clinical applications. It addresses the development and control of magnetic actuation systems (MASs) in clinical surgeries and their revolutionary effects in multiple clinical applications.
Yingxin Huo, Lidong Yang, Tiantian Xu, Dong Sun   +3 more
wiley   +1 more source

Analysis of the correlation between clinical phenotypes of mitochondrial encephalomyopathy with lactic academia and stroke-like episodes and the heteroplasmy of m.3243A>G mutation

Chinese Journal of Contemporary Neurology and Neurosurgery
Objective To retrospectively analyze the heteroplasmy levels of the m.3243A>G mutation in peripheral blood, urinary epithelial cell and oral epithelial cell from patients with mitochondrial encephalopathy with lactic academia and stroke-like episodes ...
WEN Li-min, LI Ran, ZHU Yuan, WANG Lin, LIU An-jie, LIU Hui, XIA Min   +6 more
doaj   +1 more source

Telocytes of the male urogenital system: Interrelationships, possible functions, and pathological implications

, 2021
The male urogenital system is composed of the reproductive system and the urinary tract; they have an interconnected embryonic development and share one of their anatomical components, the urethra.
Bruno Domingos Azevedo Sanches, Góes, Rejane Maira [UNESP], Juliana Dos Santos Maldarine, Maldarine, Juliana Dos Santos, Guilherme Henrique Tamarindo, Dos Santos, Vitória Alário [UNESP], Sebastião Roberto Taboga, Alana Della Torre Da Silva, Rejane Maira Góes, Vitória Alário Dos Santos, Da Silva, Alana Della Torre [UNESP], Taboga, Sebastião Roberto [UNESP], Carvalho, Hernandes F., Sanches, Bruno Domingos Azevedo, Tamarindo, Guilherme Henrique, Hernandes F. Carvalho   +15 more
core   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli, Giulia Bruna Marchetti, Maria Iascone, Maria Grazia Patricelli, Sara Giangiobbe, Gabriella Cinzia Pozzobon, Miriam Nella Savini, Fabio Giglio, Alessandro Aiuti, Paola Carrera, Francesca Ferrua, Angela Peron   +11 more
wiley   +1 more source

Von Recklinghausen's disease with urogenital manifestation

International Brazilian Journal of Urology, 2005
Neurofibromatosis or Von Recklinghausen's disease is a rare disease that affects the urogenital system in its visceral form. We report on one case where the patient had a recurring mass located in the vesicouterine space that caused irritative urinary ...
Thiago F. Nunes, Renato P. Costa, Fabio C. Navarro   +2 more
doaj   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy, Jesse Richards, Brooke R. Sweeney, Seema Kumar, Katie E. Queen, Joshua Zaritsky, Carl H. Cramer, Elias I. Traboulsi, Brittni A. Scruggs, Erica E. Davis, Ekaterina Keifer, Emma McGibbon, Timothy Ogden, Bendert De Graaf, Tonia Hymers, Elizabeth Forsythe, Philip Beales   +16 more
wiley   +1 more source