Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Shao-Hua Bi"'
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Familial hemophagocytic lymphohistiocytosis type 2 (FHL2) is a rare genetic disorder presenting with fever, hepatosplenomegaly, and pancytopenia secondary to perforin-1 (PRF1) mutation. FLH2 has been described in Chinese but usually presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b22b579ae43c3fda7c2884e827558a
http://europepmc.org/articles/PMC8316947
http://europepmc.org/articles/PMC8316947
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Kasabach–Merritt syndrome (KMS) is characterized by large hemangiomas and persistent thrombocytopenia, which may result in visceral hemorrhage and disseminated intravascular coagulation. This study aimed to evaluate the value of transar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baffb6feab1fe27b871417ca4ec4cb1b
https://pubmed.ncbi.nlm.nih.gov/35795336
https://pubmed.ncbi.nlm.nih.gov/35795336
Autor:
Chao Zhu, Yong-Li Zhang, Ru-Jeng Teng, Jian Zhang, Chao Wang, Shao-Hua Bi, Juan Wang, Hong Zheng, Li-Ying Dai, Yu Liu, Qiao Jiang, Liang-Liang Jiang, Li-Li Wang, Guang-Hui Liu
Publikováno v:
World Journal of Clinical Cases
Background Anti-D antibody is not the common cause of Rh-isoimmunization in Chinese neonatal jaundice. Recent change in national population policy has followed by an increase in Rh-isoimmunization related hemolytic disease of the newborn (HDN). Unfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c9376a84237fd13be31a4e0e53425bc
https://doi.org/10.12998/wjcc.v7.i20.3202
https://doi.org/10.12998/wjcc.v7.i20.3202