Zobrazeno 1 - 9
of 9
pro vyhledávání: '"YeFeng Dai"'
Publikováno v:
Hereditas, Vol 161, Iss 1, Pp 1-6 (2024)
Abstract SOLAMEN syndrome is a rare, recently recognized congenital syndrome that is characterized by progressive and hypertrophic diseases involving multiple systems, including segmental overgrowth, lipomatosis, arteriovenous malformation (AVM) and
Externí odkaz:
https://doaj.org/article/cfe5e22539ef4e90ae939206d5e0a0d6
Publikováno v:
Hereditas, Vol 158, Iss 1, Pp 1-5 (2021)
Abstract LEOPARD syndrome (OMIM #151,100) caused by a germline PTPN11 mutation are characterized as multisystemic anomalies and variable marked phenotypes such as multiple lentigines and cafe´-au-lait spots, electrocardiographic conduction abnormali
Externí odkaz:
https://doaj.org/article/e60f6527bba64073be9bbc7eb57961e8
Autor:
Fan Gao, Dongyao Guan, Gangliang Wang, Luting Zhang, Junmin He, Wenqiao Lv, Xiaofeng Zhang, Weifeng Tao, YeFeng Dai, Song Xu, Yeqi Chen, Bin Lu
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Background: In recent years, gallstones have become a major condition affecting people’s health. Cholecystectomy remains an effective treatment method, but it has large risk factors. It is well known that the hepatoenteric axis plays a key role in
Externí odkaz:
https://doaj.org/article/658b783a128846268182f300a7a7a7c6
Publikováno v:
Clinical and experimental dermatologyReferences. 47(12)
Background Congenital melanocytic naevi (CMN) are known to be associated with mosaic NRAS or BRAF variants. However, the exact correlations of the allele load of mosaic variants in CMN with phenotypic characteristics have not been determined. Aim To
Publikováno v:
Zhejiang Da Xue Xue Bao Yi Xue Ban
OBJECTIVE: To improve the method of vermillion flap and orbicularis oris bundle anastomosis in repair of transverse facial cleft. METHODS: Based on the precise fixed point, the modified vermillion flap was designed slender at the new corner of the up
Autor:
Xufei Zhao, Yefeng Dai
The aim of the present study was to examine the combined efficacy of simvastatin and kallistatin treatment for pediatric burn sepsis. A total of 72 pediatric patients with burn sepsis were recruited and randomly divided into 3 groups, receiving simva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01552be83ae775a06009dafbfd612758
https://europepmc.org/articles/PMC5867412/
https://europepmc.org/articles/PMC5867412/
Publikováno v:
Vaccine. 35(48 Pt)
Kasabach-Merritt phenomenon (KMP) is a rare potentially life-threatening consumptive coagulopathy characterized by thrombocytopenia and hypofibrinogenemia occurring associated with the vascular tumors kaposiform hemangioendothelioma (KHE) and tufted
Publikováno v:
Sensors and Materials. 30:1977
Publikováno v:
Sensors & Materials; 2018, Vol. 30 Issue 9, p1977-1987, 11p