Hao Yu

Hao Yu

Pediatric Epilepsy Center, Peking University First Hospital

Affiliated withPeking University First HospitalZhejiang University School of Medicine

Research Area

MedicineBiology

Biography

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JoVE Journal Publications

ArticleTotal : 2
Year
Frontal Disconnection for Treating Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) in the Frontal Lobe
Publication title
2024
2025

Other Publications

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

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology| PubMed ID: 17125606

2006
2015
2016
2016
2016
2016
2016
2016
2017
2017
2019
2020
2020
2021
2021
2022
2022
2022
2023
2023
2023
2024
2023
2023
2024
2024
2024
2024
2014
2015
2017
2017
2017
2017
2017
2018
2017
2018
Machine perfusion for liver transplantation: A concise review of clinical trials.

Hepatobiliary & pancreatic diseases international : HBPD INT| PubMed ID: 30352672

2018
2019
A cephalometric study in patients with Wilson's disease.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia| PubMed ID: 31229425

2019
2019
2019
2020
Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson's Disease.

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association| PubMed ID: 32485301

2021
2021
2020
2021
Spermatorrhea in a Chinese patient with temporal lobe epilepsy: a case report.

The Journal of international medical research| PubMed ID: 33445995

2021
2021
2021
2021
The global burden of nasopharyngeal carcinoma from 2009 to 2019: an observational study based on the Global Burden of Disease Study 2019.

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery| PubMed ID: 34146150

2022
2021
A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia.

Journal of genetics and genomics = Yi chuan xue bao| PubMed ID: 34384721

2021
2021
2021
2021
2021
2021
2021
2021
2022
2022
2022
2022
Sustained-Release Ivabradine Hemisulfate in Patients With Systolic Heart Failure.

Journal of the American College of Cardiology| PubMed ID: 35926931

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

Hepatobiliary & pancreatic diseases international : HBPD INT| PubMed ID: 36376226

2022
2023
2022
2023
2024
2023
2023
2023
2023
2023
2024
Single Bolus r-SAK Before Primary PCI for ST-Segment-Elevation Myocardial Infarction.

Circulation. Cardiovascular interventions| PubMed ID: 38258563

2024
2024
2024
2024
2025
2024
Sequential Release HydroLipo System for STING Gene Epigenetic Reprogramming and Immune Activation in Glioblastoma.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)| PubMed ID: 39661716

2025
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia.

Journal of genetics and genomics = Yi chuan xue bao| PubMed ID: 39814172

2025
2025
2025
2025