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Keyword [paraplegia]
Result: 21 - 40 | Page: 2 of 5
21. Study On Spinal Cord Injury And Treatment Effect Among Inpatients With Paraplegia
22. Mutation Analysis Of The Candidate Genes Of A Novel Subtype Of Hereditary Spastic Paraplegia
23. Anatomic And Clinical Study On Treatment Of The Burst Fractrue Of Upper Thoracic Vertebras With Paralysis Through The "U" Fenestration Approach In The Sternal Manubrium
24. The Research About The Efficacy Adopting L6 Transposition To Reconstruct The Function Of Sciatic Nerve
25. Mutation Analysis Of The Spastin Gene In Chinese Patients With Hereditary Spastic Paraplegia Disease
26. The Research On Gene Mutation Analysis Of SPG4 And SPG3A In Hereditary Spastic Paraplegia Patients
27. A Case Of Aortic Dissection Presenting With Paraplegia
28. Gene Sequence Analysis Of Hereditary Spastic Paraplegia Pedigree PLP1
29. The Related Research Of Different Days Of Anti-tuberculosis Before Surgery To Spinal Tuberculosis With Paraplegia Patients
30. Research On Clinical Features And Mitochondrial DNA Mutation Analysis Of Hereditary Spastic Paraplegia Type 4 (SPG4) Patients
31. Clinical Features And Mutation Analysis Of The Spastin Gene In A Hereditary Spastic Paraplegia Family
32. Features Of Magnetic Resonance Imaging In Hereditary Spastic Paraplegia Due To Spastin Mutation And Reep1 Mutation
33. Study On Muscle Morphology And Activity Under Functional Electrical Stimulation Based On Ultrasound Image Analysis
34. The DWI,~1H-MRS And ASL Study Of SCA3/MJD And SPG4
35. Research Of Coverage Of Left Subclavian Artery In Thoracic Endovascular Aortic Repair
36. Investigation Of SLC33A1Gene Function And Its Role In Hereditary Spastic Paraplegia Using Zebrafish Model
37. Mutation Analysis Of Infectious And Hereditary Diseases Using Next-generation Sequencing
38. Clinicai And Genetic Analysis Of Patients With Kennedy’s Disease And Hereditary Spastic Paraplegia
39. Effect Of Pnf And Comprehensive Rehabilitation Therapy For Patients With Paraplegia Of Thoracic And Waist Segment Spinal Cord Injury
40. Exome Sequencing Identifies Novel Compound Heterozygous Mutations In SPG11That Cause Autosomal Recessive Hereditary Spastic Paraplegia
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