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
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
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