Results 111 to 117 of about 1,655 (117)

[Towards precision diagnosis and treatment: interpretation of the ten highlights of the expert consensus on the diagnosis and treatment of hereditary hyperbilirubinemia (version 2025)]. [PDF]

Zhonghua Gan Zang Bing Za Zhi
Hou W, Duan ZP, Zheng SJ.
europepmc   +1 more source

[Two cases of Coffin-Siris syndrome type 3 caused by de novoSMARCB1 gene mutations]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi
Jin Y, Li MQ, Yang YL.
europepmc   +1 more source

[Risk factors for white matter damage in preterm infants with necrotizing enterocolitis]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi
Xu X, Wang SR, Zhang P, Cheng GQ.
europepmc   +1 more source

[C1q-neutralizing antibodies improves postpartum depressive-like behaviors in mice by regulating the C1q/C3 pathway]. [PDF]

Nan Fang Yi Ke Da Xue Xue Bao
Sun Y, Xu X, Zhuo X, Cai H, Wang Y.
europepmc   +1 more source