[Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis]. [PDF]
Lu YF +6 more
europepmc +1 more source
[Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes]. [PDF]
Guo YL +6 more
europepmc +1 more source
[Clinical and genetic characteristics of 14 children with sodium taurocholate co-transporting polypeptide deficiency]. [PDF]
Ma RX +7 more
europepmc +1 more source
[Analysis of familial intrahepatic cholestasis caused by ubiquitin-specific peptidase 53 gene mutation]. [PDF]
Wang H, Zheng X, Yu MM, Yu ZD, Wang YS.
europepmc +1 more source
[<b>"</b>Triple-hit<b>"</b> pathogenic mechanism of Leber hereditary optic neuropathy]. [PDF]
Wang K, Li S, Zhang Y, Guan M.
europepmc +1 more source
[Association between auditory processing and behavioral problems in preschool children with developmental language disorder]. [PDF]
Dong T +9 more
europepmc +1 more source
[Duchenne muscular dystrophy-associated cardiomyopathy: advances in diagnosis and management]. [PDF]
Gu J, Liu YH, Hong SQ.
europepmc +1 more source
[Dynamic assessment of upper airway in obstructive sleep apnea patients with a focus on drug-induced sleep endoscopy]. [PDF]
Duan F, Zhang S, DU Y, Li T, Yan Y.
europepmc +1 more source
[Electroacupuncture ameliorates cognitive impairment and suppresses TLR4/MyD88/NF-κB pathway-mediated astrocyte activation in rats with vascular dementia]. [PDF]
Gao J +6 more
europepmc +1 more source

