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Articles by Z. Liao
Hippocampal adult-born granule cells drive network activity in a mouse model of chronic temporal lobe epilepsy
Abstract Temporal lobe epilepsy (TLE) is characterized by recurrent seizures driven by synchronous neuronal activity. The reorganization of the dentate gyrus (DG) in TLE may create pathological conduction pathways for synchronous discharges in the temporal lobe, though critical microcircuit-level detail is missing from this pathophysiological intuition. In particular, the relative contribution of adult-born (abGC) and mature (mGC) granule cells to epileptiform network events remains unknown.
Risk of second malignant neoplasms in women and girls with germ cell tumors
Background While an elevated risk of second malignant neoplasms (SMNs) has been observed in men treated for germ cell tumors (GCTs), risk of SMNs have not been quantified in adult women or in girls treated for GCTs. Patients and methods One-year survivors of primary GCTs diagnosed between January 1980 and December 2012 were identified from Surveillance, Epidemiology, and End Results (SEER 9) registries. Risk of SMNs was calculated using SEER*Stat.
269P Transarterial ethanol ablation combined with transarterial chemoembolization for hepatocellular carcinoma with portal vein tumor thrombus
269P Transarterial ethanol ablation combined with transarterial chemoembolization for hepatocellular carcinoma with portal vein tumor thrombus B. Yang and Z. Liao Abdominal Oncology, West China Hospital, Huaxi, Sichuan University, Chengdu, China Background: Portal vein tumor thrombus (PVTT) can be detected in 30-62% of patients with Hepatocellular Carcinoma (HCC). HCC with PVTT is considered to have an extremely poor prognosis.
Risk of Second Malignant Neoplasms in Women and Girls with Germ Cell Tumors
While an elevated risk of second malignant neoplasms (SMNs) has been observed in men treated for germ cell tumors (GCTs), risk of SMNs have not been quantified in adult women nor in girls treated for GCTs. One-year survivors of primary GCTs diagnosed between January 1980 and December 2012 were identified from Surveillance, Epidemiology, and End Results registries (SEER 9). Risk of SMNs were calculated using SEER*Stat. Among 1,507 patients, a total of 47 SMNs were identified.
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