Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Wen-Ze Wang"'
Autor:
Qian Lu, Xiu-Yu Shi, Yang-Yang Wang, Meng-Na Zhang, Wen-Ze Wang, Jing Wang, Qiu-Hong Wang, Hui-Min Chen, Li-Ping Zou
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-5 (2020)
Abstract Objective Tuberous sclerosis complex (TSC) is a rare autosomal dominant genetic disease with many manifestations, and it involves any organ. In this study, we report a TSC patient with new type skin lesions. Methods A 7-month-old TSC boy wit
Externí odkaz:
https://doaj.org/article/122867552ebb4dc5ab14e55391136941
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 22, Pp 2686-2690 (2017)
Background: Overexpression and constitutive activation of signal transducer and activator of transcription (STAT) 3 have been suggested in the tumorigenesis of many human cancers, including multiple carcinomas, melanoma, and lymphoma. The diagnosis o
Externí odkaz:
https://doaj.org/article/965ed81ed5444dfc863e10d67551263c
Publikováno v:
Clinical Otolaryngology. 46:175-180
OBJECTIVES Laryngeal dysplasia (LD) is a precancerous lesion of the larynx. In this study, the laryngeal tissue of patients with laryngeal dysplasia was taken as the research object, and the aetiology of reflux was analysed. METHOD Patients with lary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f5b481a6c105fc151c86d623b8119af
https://doi.org/10.1111/coa.13638
https://doi.org/10.1111/coa.13638
Autor:
Qian Lu, Xiu-Yu Shi, Yang-Yang Wang, Meng-Na Zhang, Wen-Ze Wang, Jing Wang, Qiu-Hong Wang, Hui-Min Chen, Li-Ping Zou
Objective Tuberous sclerosis complex (TSC) is a rare autosomal dominant genetic disease and has many manifestations involves virtually any organ. In this study, we report a TSC patient with new type skin lesions. Methods The 7-month-old patient had c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::294721fdd3a2d35a54d42d82e277efd7
https://doi.org/10.21203/rs.3.rs-16982/v1
https://doi.org/10.21203/rs.3.rs-16982/v1
Autor:
Li-Ping Zou, Xiu-Yu Shi, Jing Wang, Yang-Yang Wang, Qiu-Hong Wang, Wen-Ze Wang, Qian Lu, Hui-Min Chen, Meng-Na Zhang
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-5 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-5 (2020)
Objective Tuberous sclerosis complex (TSC) is a rare autosomal dominant genetic disease with many manifestations, and it involves any organ. In this study, we report a TSC patient with new type skin lesions. Methods A 7-month-old TSC boy with multipl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a62e00933e80ed1029e5b81afba257f
https://pubmed.ncbi.nlm.nih.gov/32532290
https://pubmed.ncbi.nlm.nih.gov/32532290
Publikováno v:
Chinese Medical Journal
Chinese Medical Journal, Vol 130, Iss 22, Pp 2686-2690 (2017)
Chinese Medical Journal, Vol 130, Iss 22, Pp 2686-2690 (2017)
Background: Overexpression and constitutive activation of signal transducer and activator of transcription (STAT) 3 have been suggested in the tumorigenesis of many human cancers, including multiple carcinomas, melanoma, and lymphoma. The diagnosis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f846f029d5dd8bbfd18a64d9cc2a94
https://doi.org/10.4103/0366-6999.218016
https://doi.org/10.4103/0366-6999.218016
Autor:
Atsushi Ishii, Shinichi Hirose, Yuko Tomonoh, Xiu-Yu Shi, Norimichi Higurashi, Wen-Ze Wang, Sunao Kaneko, Hirokazu Kurahashi
Publikováno v:
Brain and Development. 38:40-46
Objective Evaluation of the efficacy of antiepileptic drugs (AEDs) used in the treatment of Dravet syndrome (DS) with different genotypes. Methods Patients with DS were recruited from different tertiary hospitals. Using a direct sequencing method and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b8b222587c29efcb4403de9b0c5a24f
https://doi.org/10.1016/j.braindev.2015.06.008
https://doi.org/10.1016/j.braindev.2015.06.008
Publikováno v:
Medicine
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is a multisystem hereditary disease characterized by formation of cysts in the ductal organs. Renal pelvis malignancy in ADPKD is very rare and sporadically reported in the previous l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91af09af149954703ae355771eb3f982
https://pubmed.ncbi.nlm.nih.gov/27537592
https://pubmed.ncbi.nlm.nih.gov/27537592
Autor:
Wen-Ze Wang, Xiao-Ping Wei
Publikováno v:
Computational Materials Science. 50:2253-2256
Based on the first-principle calculations within density functional theory of electronic structure, we propose that the CuHg 2 Ti-type intermetallic ternary compound Mn 2 ZnCa is strong candidate for half-metallic (HM) antiferromagnet (AFM), the HM-A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b7135b9f187488c8cb75fd3d9012356
https://doi.org/10.1016/j.commatsci.2011.02.039
https://doi.org/10.1016/j.commatsci.2011.02.039
Publikováno v:
Acta neurologica Belgica. 116(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcaece3ef2a6e113a64caa8e1b7b630e
https://pubmed.ncbi.nlm.nih.gov/26085379
https://pubmed.ncbi.nlm.nih.gov/26085379