Hao Yu

[Foscarnet sodium for treatment in patients with severe chronic hepatitis B].

A novel gene, optrA, that confers transferable resistance to oxazolidinones and phenicols and its presence in Enterococcus faecalis and Enterococcus faecium of human and animal origin.

Prognostic significance of neutrophil-to-lymphocyte ratio in prostate cancer: evidence from 16,266 patients.

Prognostic value of platelet to lymphocyte ratio in non-small cell lung cancer: evidence from 3,430 patients.

Overexpression of AKR1C3 significantly enhances human prostate cancer cells resistance to radiation.

Prognostic significance of osteopontin expression in gastric cancer: a meta-analysis.

Elevated Platelet to Lymphocyte Ratio Is Associated with Poor Survival Outcomes in Patients with Colorectal Cancer.

Autophagy in long propriospinal neurons is activated after spinal cord injury in adult rats.

Atorvastatin prolongs the lifespan of radiation‑induced reactive oxygen species in PC-3 prostate cancer cells to enhance the cell killing effect.

CD4 Lymphocyte Enumeration and Hemoglobin Assessment Aid for Priority Decisions: A Multisite Evaluation of the BD FACSPresto System.

Restoring electrical connection using a conductive biomaterial provides a new therapeutic strategy for rats with spinal cord injury.

Correction: Overexpression of AKR1C3 significantly enhances human prostate cancer cells resistance to radiation.

Surgical treatment in children with intractable epilepsy after viral encephalitis.

Postoperative seizure and developmental outcomes of children with hemimegalencephaly and drug-resistant epilepsy.

A de novo variant of POLR3B causes demyelinating Charcot-Marie-Tooth disease in a Chinese patient: a case report.

Identification of an IDO1-based immune classifier for survival prediction of upper tract urothelial carcinoma.

Subtotal hemispherotomy for intractable lesional hemispheric epilepsy without hemiparesis in children.

Lesional Intractable Epileptic Spasms in Children: Electroclinical Localization and Postoperative Outcomes.

Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis.

Cerebral small-vessel disease at high altitude: A comparison of patients from plateau and plain.

Disconnection Surgery in Pediatric Epilepsy: A Single Center's Experience With 185 Cases.

Long-term seizure and developmental outcomes of epilepsy surgery in children under 3 years old: A single-center study of 113 patients.

Epilepsy Outcome and Pathology Analysis for Ganglioglioma: A Series of 51 Pediatric Patients.

Enhanced focal cortical dysplasia detection in pediatric frontal lobe epilepsy with asymmetric radiomic and morphological features.

Surgical treatment for drug-resistant epilepsy due to early brain injury in children.

Microenvironment-Responsive Hydrogel Reduces Seizures After Traumatic Brain Injury in Juvenile Rats by Reducing Oxidative Stress and Hippocampal Inflammation.

Noninvasive microvascular imaging in newborn rats using high-frequency ultrafast ultrasound.

Establishment of a normal control model of children's brain 18-fluorodeoxyglucose positron emission tomography and analysis of the changing pattern in patients aged 0-14 years.

A novel GJA8 mutation (p.V44A) causing autosomal dominant congenital cataract.

Na⁺-Ca²⁺ exchanger mediates ChR2-induced [Ca²⁺]i elevation in astrocytes.

A molecular roadmap for induced multi-lineage trans-differentiation of fibroblasts by chemical combinations.

Clinical features and outcome in patients with osseomuscular type of Wilson's disease.

A molecular roadmap for induced multi-lineage trans-differentiation of fibroblasts by chemical combinations.

A molecular roadmap for induced multi-lineage trans-differentiation of fibroblasts by chemical combinations.

A Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient.

Phase III study of dulanermin (recombinant human tumor necrosis factor-related apoptosis-inducing ligand/Apo2 ligand) combined with vinorelbine and cisplatin in patients with advanced non-small-cell lung cancer.

Famitinib versus placebo in the treatment of refractory metastatic colorectal cancer: a multicenter, randomized, double-blinded, placebo-controlled, phase II clinical trial.

Cardiotoxicity of 5-fluorouracil and capecitabine in Chinese patients: a prospective study.

Machine perfusion for liver transplantation: A concise review of clinical trials.

Contribution of intragenic deletions to mutation spectrum in Chinese patients with Wilson's disease and possible mechanism underlying ATP7B gross deletions.

A cephalometric study in patients with Wilson's disease.

Presynaptic Endosomal Cathepsin D Regulates the Biogenesis of GABAergic Synaptic Vesicles.

Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease.

Clinical features and outcome of Wilson's disease with generalized epilepsy in Chinese patients.

Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson's Disease.

Immune checkpoint-related serum proteins and genetic variants predict outcomes of localized prostate cancer, a cohort study.

Patients' preferences for health insurance coverage of new technologies for treating chronic diseases in China: a discrete choice experiment.

Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy.

Spermatorrhea in a Chinese patient with temporal lobe epilepsy: a case report.

Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.

Clinical and genetic characteristics of Chinese patients with reducing body myopathy.

Morvan syndrome associated with LGI1 antibody: a case report.

The global burden of nasopharyngeal carcinoma from 2009 to 2019: an observational study based on the Global Burden of Disease Study 2019.

Protocol for a pharmacogenomic study on individualised antipsychotic drug treatment for patients with schizophrenia.

A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia.

Novel bi-allelic HPDL variants cause hereditary spastic paraplegia in a Chinese patient.

Chronic Diseases as a Predictor for Severity and Mortality of COVID-19: A Systematic Review With Cumulative Meta-Analysis.

Assessment of the satisfaction with public health insurance programs by patients with chronic diseases in China: a structural equation modeling approach.

Discovery of new genetic loci for male sexual orientation in Han population.

Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy.

Author Correction: Discovery of new genetic loci for male sexual orientation in Han population.

Radiofrequency Ablation of Parathyroid Glands to Treat a Patient With Hypercalcemia Caused by a Novel Inactivating Mutation in .

Validation of a three-dimensional printed dry lab pancreaticojejunostomy model in surgical assessment: a cross-sectional study.

Comprehensive profiling of the TRIpartite motif family to identify pivot genes in hepatocellular carcinoma.

Prognostic and biological role of the N-Myc downstream-regulated gene family in hepatocellular carcinoma.

A Novel Variant Identified in a Chinese Patient: Case Report and Review of the Literature.

Sustained-Release Ivabradine Hemisulfate in Patients With Systolic Heart Failure.

Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhage.

Chinese expert consensus on organ protection of transplantation (2022 edition).

Early Efficacy of Antipsychotic Medications at Week 2 Predicts Subsequent Responses at Week 6 in a Large-scale Randomized Controlled Trial.

Prognostic implications of necroptosis-related long noncoding RNA signatures in muscle-invasive bladder cancer.

A powerful antitumor "trident": the combination of radio-, immuno- and anti-angiogenesis therapy based on mesoporous silica single coated gold nanoparticles.

Association Between Serum Neurofilament Light Chain and Neurochemistry Deficits in Patients with Spinocerebellar Ataxia Type 3.

STC2 activates PRMT5 to induce radioresistance through DNA damage repair and ferroptosis pathways in esophageal squamous cell carcinoma.

Using health technology assessment to inform insurance reimbursement of high technology medicines in China: an example of cancer immunotherapy.

Efficacy and safety of a bolus of half-dose r-SAK prior to primary PCI in ST-elevation myocardial infarction: Rationale and design of the OPTIMA-6 trial.

A Dual-Targeted Metal-Organic Framework Based Nanoplatform for the Treatment of Rheumatoid Arthritis by Restoring the Macrophage Niche.

Envonalkib versus crizotinib for treatment-naive ALK-positive non-small cell lung cancer: a randomized, multicenter, open-label, phase III trial.

Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.

Single Bolus r-SAK Before Primary PCI for ST-Segment-Elevation Myocardial Infarction.

Radiotherapy-Induced Astrocyte Senescence Promotes an Immunosuppressive Microenvironment in Glioblastoma to Facilitate Tumor Regrowth.

Sensitive and rapid identification of pathogens by droplet digital PCR in a cohort of septic patients: a prospective diagnostic study.

Injectable hydrogel encapsulating siMMP13 with anti-ROS and anti-apoptotic functions for osteoarthritis treatment.

Animal models and related techniques for dentin study.

Clinical Features and Novel Pathogenic Variants of Chinese Patients With McLeod Syndrome and Chorea-Acanthocytosis.

Sequential Release HydroLipo System for STING Gene Epigenetic Reprogramming and Immune Activation in Glioblastoma.

Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia.

Establishing a prognostic scoring system and exploring prognostic value of examined lymph node numbers for stage I non-small cell lung cancer: a retrospective study of Surveillance, Epidemiology, and End Results (SEER) database and a Chinese cohort.

A Multicenter Study of Hereditary Transthyretin Amyloidosis in China.

Research trends on spinal muscular atrophy from 1995 to 2023: A bibliometric analysis.