Y. Liu

ORCID: 0000-0002-9787-9749
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About
Contact & Profiles
Research Areas
  • Stroke Rehabilitation and Recovery
  • Neurogenetic and Muscular Disorders Research
  • Hereditary Neurological Disorders
  • Occupational Therapy Practice and Research
  • Art Therapy and Mental Health
  • Amyotrophic Lateral Sclerosis Research
  • Adolescent and Pediatric Healthcare
  • Medical Research and Treatments
  • Voice and Speech Disorders

Hebei Medical University
2014-2025

Second Hospital of Hebei Medical University
2025

Southwest Medical University
2024

In the context of continuous deepening social aging, an increasing number patients are suffering from upper limb dysfunction, and rehabilitation treatment for patients' motor ability has become a major concern. This paper commences with emergence robot comprehensively summarizes analyzes research progress both domestically internationally. Upper robots can be classified into different categories based on diverse classification methods. Based feedback approaches, they divided system machine...

10.54254/2755-2721/2025.21205 article EN cc-by Applied and Computational Engineering 2025-02-27

Rationale: Kartagener syndrome is a rare respiratory disorder caused by genetic mutation that often combines abnormal manifestations of multiple systems. By discussing this case, we will be able to further deepen our understanding and improve the diagnosis rate disease reduce its misdiagnosis rate. Patient concerns: A 62-year-old Chinese man had history bronchiectasis for 5 years developed small amount hemoptysis days before admission. Diagnoses: Peripheral blood tests indicated primary...

10.1097/md9.0000000000000361 article EN Medicine Case Reports and Study Protocols 2025-04-01

Background The epidemiology, diagnosis, and treatment of motor neuron disease (MND) in Chinese patients are ill known. Methods A registered study 461 MND was conducted across 10 facilities 7 cities from February 2009 to March 2010. Results Patients were classified as amyotrophic lateral sclerosis (ALS) (84.4%), progressive bulbar palsy (PBP) (4.1%), muscular atrophy (PMA) (10.4%), or primary (PLS) (0.9%). predominant men (men/women; 1.6:1.0). Mean onset age 52.6 years, with the highest...

10.1111/ane.12240 article EN Acta Neurologica Scandinavica 2014-04-01
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