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pro vyhledávání: '"Babak Ghavami"'
Autor:
Setila Dalili, Nasrin Sedighi Pirsaraei, Ameneh Sharifi, Alireza Pouryousef, Fatemeh Aghaee, Reza Bayat, Babak Ghavami, Bahareh Rabbani, Nejat Mahdieh
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101136- (2024)
Background: FBPase deficiency as an autosomal recessive disorder is due pathogenic variants in the FBP1 gene. It usually presents with hyperlactic acidemia and hypoglycaemia starting from early childhood. Here, genotypes and phenotypes of all reporte
Externí odkaz:
https://doaj.org/article/bda67eb6aa4f4c328371f0492c64b07d
Publikováno v:
Interactive CardioVascular and Thoracic Surgery. 15:23-27
Bleeding diathesis and allogenic transfusion after complex heart surgery, such as heart valve surgery, may result in complications such as transfusion reaction, viral infection, postoperative infection, haemodynamic disturbance, prolonged stay in the