Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Jihong Hao"'
Autor:
Chaoxin Tao, Min Zhao, Xiaohui Zhang, Jihong Hao, Qiuyue Huo, Jie Sun, Jiangtao Xing, Yuna Zhang, Jianhong Zhao, Huaipeng Huang
Publikováno v:
BMC Infectious Diseases, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Niemann-Pick Disease type C is a fatal autosomal recessive lipid storage disorder caused by NPC1 or NPC2 gene mutations and characterized by progressive, disabling neurological deterioration and hepatosplenomegaly. Herein, we iden
Externí odkaz:
https://doaj.org/article/5a4380d4ce4a43f7b6d392b830351422
Publikováno v:
Turkish Journal of Hematology, Vol 40, Iss 3, Pp 216-219 (2023)
Externí odkaz:
https://doaj.org/article/79f56a9826714880acea53130a1349ba
Autor:
Zhirong Li, Ning Dong, Jihong Hao, Zirou Ouyang, Cuixin Qiang, Ying Yang, Chaoyi Mi, Yanan Niu, Jing Yang, Baojiang Wen, Liwei Wang, Shaodan Zhang, Jianhong Zhao
Publikováno v:
Gut Pathogens, Vol 15, Iss 1, Pp 1-12 (2023)
Abstract Background Clostridioides difficile (C. difficile) is the major pathogen causing antibiotic-associated diarrhea. There are a variety of symptoms associated with C. difficile infection (CDI) in adults, including self-limiting diarrhea, pseudo
Externí odkaz:
https://doaj.org/article/e7b757bfd3244fa5a41e99f9d89ed4fd
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Wiskott–Aldrich syndrome (WAS) is a rare X-linked immunodeficiency disorder caused by abnormal expression of the WAS protein (WASp) due to mutations in the WAS gene, and is generally characterized by microthrombocytopenia, eczem
Externí odkaz:
https://doaj.org/article/442ecb69184e4cc5a6a1ce3c82909c25
Publikováno v:
Turkish Journal of Hematology, Vol 40, Iss 3, Pp 202-203 (2023)
Externí odkaz:
https://doaj.org/article/4edb7104965b499c9e9d2024ed69992f
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Wiskott-Aldrich syndrome (WAS) is a rare X-linked immunodeficiency disorder caused by abnormal expression of Wiskott-Aldrich syndrome protein due to WAS gene mutation, which is generally characterized by microthrombocytopenia, eczema, recurrent infec
Externí odkaz:
https://doaj.org/article/7a07868f0ebd453ebbf074b0ceef8dd4
Publikováno v:
Clinical laboratory. 67(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea48f4174afefdd115edd22a4c0f46bb
https://pubmed.ncbi.nlm.nih.gov/34910433
https://pubmed.ncbi.nlm.nih.gov/34910433
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 59:e398-e400
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f65df3f0035c97432d83fb2d4801328
https://doi.org/10.1515/cclm-2021-0205
https://doi.org/10.1515/cclm-2021-0205
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics, Vol 9 (2021)
Wiskott-Aldrich syndrome (WAS) is a rare X-linked immunodeficiency disorder caused by abnormal expression of Wiskott-Aldrich syndrome protein due to WAS gene mutation, which is generally characterized by microthrombocytopenia, eczema, recurrent infec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f11c764ad99f64aa582e419f64c4d8ed
http://europepmc.org/articles/PMC8295588
http://europepmc.org/articles/PMC8295588
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:156-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cff83889a03cce23192fefbe601b9da6
https://doi.org/10.1097/mph.0000000000002062
https://doi.org/10.1097/mph.0000000000002062