Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yaowang, Zhao"'
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Children with hypospadias are at risk of serious physical and mental health problems, including abnormal urination, sexual dysfunction, and infertility. The sole available treatment is the surgical restoration of genital appearanc
Externí odkaz:
https://doaj.org/article/bb506947e3704f36a4d7049e7dad1e84
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
The incidence of urolithiasis (UL) in children has been increasing. Although the pathogenesis of pediatric UL is controversial and remains unclear, multiple monogenic causes of UL have been identified. We aim to investigate the prevalence of inherite
Externí odkaz:
https://doaj.org/article/756cdc46ad8748809df9ce1484e1cc13
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundCystinuria is a rare genetic disorder characterized by defective renal reabsorption of cystine, ornithine, arginine, and lysine. The increased urinary excretion of cystine results in the development of cystine urolithiasis (CU). The mutated
Externí odkaz:
https://doaj.org/article/9fe3ce9c8b1f4ed6b5c705a30986efc4
Autor:
Xiulan Lu, Weijian Chen, Liping Li, Xinyuan Zhu, Caizhi Huang, Saijun Liu, Yongjia Yang, Yaowang Zhao
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
Primary hyperoxaluria type 1 (PH1) is a rare metabolic disorder characterized by a defect in the liver-specific peroxisomal enzyme alanine-glyoxylate and serine-pyruvate aminotransferase (AGT). This disorder results in hyperoxaluria, recurrent urolit
Externí odkaz:
https://doaj.org/article/18a657f3c89246cba19b60a706da4e51
Publikováno v:
Archivos Españoles de Urología; 2023, Vol. 76 Issue 9, p666-673, 8p
Autor:
Yong Li, Zhen-Jian Zhuo, Haiyan Zhou, Jiabin Liu, Zan Liu, Jiao Zhang, Jiwen Cheng, Suhong Li, Haixia Zhou, Rong Zhou, Jing He, Yaowang Zhao
Publikováno v:
Aging. 11:2369-2377
Neuroblastoma is the most frequently diagnosed neural tumor of childhood. Abnormal function of the long intergenic non-coding RNA (lincRNA) LINC00673 has been implicated in various human malignancies. Genome-wide association studies revealed the LINC
Publikováno v:
Experimental and Therapeutic Medicine.
The aim of the present case report was to investigate the clinical features, pathological examination and treatment of eosinophilic cystitis (EC) in children. Two cases of EC were reported and reviewed from January 2016 to March 2017. Case 1 (male; 6
Autor:
Xiulan, Lu, Weijian, Chen, Liping, Li, Xinyuan, Zhu, Caizhi, Huang, Saijun, Liu, Yongjia, Yang, Yaowang, Zhao
Publikováno v:
Frontiers in Pharmacology
Primary hyperoxaluria type 1 (PH1) is a rare metabolic disorder characterized by a defect in the liver-specific peroxisomal enzyme alanine-glyoxylate and serine-pyruvate aminotransferase (AGT). This disorder results in hyperoxaluria, recurrent urolit
Publikováno v:
Experimental and Therapeutic Medicine
The aim of this study was to determine the clinical characteristics and diagnosis of severe, acute urolithiasis in infants and toddlers, caused by melamine contamination in infant formula milk. The clinical data of 28 patients were collected and anal
Publikováno v:
Diagnostic Pathology
Background Extra-adrenal paraganglioma of the retroperitoneum with metastasis to the vertebra is very rare. To our knowledge this is the first report of this kind of disease in the literature. Case presentation Here, we present an oroginal case of pa