Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Luya Ruan"'
Publikováno v:
Renal Failure, Vol 44, Iss 1, Pp 1840-1849 (2022)
Objective Early diagnosis of diabetic kidney disease (DKD) has long been a complex problem. This study aimed to analyze the metabolomic characteristics of plasma extracellular vesicles (EVs) at different stages of DKD in order to evaluate the metabol
Externí odkaz:
https://doaj.org/article/02ea6abf1d7b4328b8c63024707fa5d2
Publikováno v:
Journal of International Medical Research, Vol 47 (2019)
Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome. We herein report a rare case of TIO in a 58-year-old Chinese man who presented with a large lump in the right palm. Clinical, biochemical, and radiological assessments were performed
Externí odkaz:
https://doaj.org/article/0e3d61f270fc486fad8f8f3b3f5f355a
Autor:
Meng-Te Shi, Luya Ruan, You-Jin Pan, Yanying Qian, Yao-Xin Zhu, Zhijuan Dai, Jian Jin, Chaoming Wu
Publikováno v:
Drug Design, Development and Therapy.
Yan-Ying Qian, Zhi-Juan Dai, Lu-Ya Ruan, You-Jin Pan, Jian Jin, Meng-Te Shi, Yao-Xin Zhu, Chao-Ming WuDepartment of Endocrinology, The Second Affiliated Hospital and Yuying Children’s Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7252417f21a77eec2c1d5da6bff25a67
https://www.dovepress.com/low-dose-adefovir-dipivoxil-induced-hypophosphatemia-osteomalacia-in-f-peer-reviewed-article-DDDT
https://www.dovepress.com/low-dose-adefovir-dipivoxil-induced-hypophosphatemia-osteomalacia-in-f-peer-reviewed-article-DDDT
Publikováno v:
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology. 35(9)
Silver-Russell syndrome (SRS) is a heterogeneous disorder characterized by severe intrauterine and postnatal growth retardation and typical dysmorphic features including body asymmetry, relative macrocephaly, protruding forehead, and feeding difficul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc8e9f924b3218238fdb135d014fbc82
https://pubmed.ncbi.nlm.nih.gov/30905204
https://pubmed.ncbi.nlm.nih.gov/30905204
Publikováno v:
The Journal of International Medical Research
Journal of International Medical Research, Vol 47 (2019)
Journal of International Medical Research, Vol 47 (2019)
Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome. We herein report a rare case of TIO in a 58-year-old Chinese man who presented with a large lump in the right palm. Clinical, biochemical, and radiological assessments were performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b5fda0925d4ee59ce275a8126074f6a
https://pubmed.ncbi.nlm.nih.gov/30859855
https://pubmed.ncbi.nlm.nih.gov/30859855
Publikováno v:
Molecular Oncology
Non-small-cell lung carcinoma (NSCLC) accounts for the majority of lung cancer deaths, and thus there is a clinical need to understand the molecular mechanisms underlying this malignancy. Tumor-initiating cells (TICs) have been accepted to be closely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8d7ec1bc6019cfc1766671d00ca7015
http://europepmc.org/articles/PMC7718952
http://europepmc.org/articles/PMC7718952
Publikováno v:
International Journal of Diabetes in Developing Countries. 35:588-592
Maternally inherited diabetes and deafness (MIDD) is a rare form of diabetes with a maternal transmission and sensorineural hearing loss. Neuroradiological abnormality manifestations have been relatively rarely reported in MIDD patients. In this repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11f122b0e67faa0edb0db464865878ee
https://doi.org/10.1007/s13410-015-0384-2
https://doi.org/10.1007/s13410-015-0384-2
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 33(5)
To detect potential mutation in a pedigree affected with congenital nephrogenic diabetes insipidus (NDI).Clinical data of a male patient affected with NDI was collected. Genomic DNA was extracted from peripheral blood samples from the patient and fiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b0f892a6384e2c262a41b0587bd6882
https://pubmed.ncbi.nlm.nih.gov/27577218
https://pubmed.ncbi.nlm.nih.gov/27577218