38 results on '"Nam, Soo‐Hyun"'
Search Results
2. An on-demand bioresorbable neurostimulator
3. Identification and clinical characterization of Charcot-Marie-Tooth disease type 1C patients with LITAF p.G112S mutation
4. Self‐Powered Electrical Bandage Based on Body‐Coupled Energy Harvesting.
5. Different Influence of Negative and Positive Spillover between Work and Life on Depression in a Longitudinal Study
6. Experiences of restrictive interventions in psychiatric health care from the perspectives of patients and health care professionals: Meta‐synthesis of qualitative evidence.
7. Compound Heterozygous Mutations of SACS in a Korean Cohort Study of Charcot-Marie-Tooth Disease Concurrent Cerebellar Ataxia and Spasticity.
8. Morc2a variants cause hydroxyl radical-mediated neuropathy and are rescued by restoring GHKL ATPase.
9. Intraepineurial fat quantification and cross-sectional area analysis of the sciatic nerve using MRI in Charcot-Marie-Tooth disease type 1A patients
10. Alanyl-tRNA synthetase 1 (AARS1) gene mutation in a family with intermediate Charcot-Marie-Tooth neuropathy
11. BAG3 mutation in a patient with atypical phenotypes of myofibrillar myopathy and Charcot–Marie–Tooth disease
12. Serum CXCL13 reflects local B-cell mediated inflammatory demyelinating peripheral neuropathy
13. Psychometric Evaluation of the Korean Version of the Perceived Costs and Benefits Scale for Sexual Intercourse.
14. Neural cell adhesion molecule 1 is a cellular target engaged plasma biomarker in demyelinating Charcot–Marie–Tooth disease.
15. Axonal Charcot‐Marie‐Tooth neuropathy concurrent with distal and proximal weakness by translational elongation of the 3′ UTR in NEFH
16. How Mothers' Problematic Smartphone Use Affects Adolescents' Problematic Smartphone Use: Mediating Roles of Time Mothers Spend with Adolescents and Adolescents' Self-Esteem.
17. PINK1 and Parkin Ameliorate the Loss of Motor Activity and Mitochondrial Dysfunction Induced by Peripheral Neuropathy-Associated HSPB8 Mutants in Drosophila Models.
18. INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis.
19. Ser135Phe mutation in HSPB1 (HSP27) from Charcot–Marie–Tooth disease type 2F families
20. DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease
21. Effect of Meaning-in-Life Interventions for Advanced Cancer Patients: A Systematic Review and Meta-Analysis.
22. Lack of Interventional Studies on Suicide Prevention among Healthcare Workers: Research Gap Revealed in a Systematic Review.
23. Multifaceted Work-to-Life Negative Spillover and Depressive Symptoms among Working Women: The Moderating Effect of Social Activities Satisfaction.
24. Genetic and Clinical Studies of Peripheral Neuropathies with Three Small Heat Shock Protein Gene Variants in Korea.
25. Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study.
26. HDAC6 Inhibition Corrects Electrophysiological and Axonal Transport Deficits in a Human Stem Cell‐Based Model of Charcot‐Marie‐Tooth Disease (Type 2D).
27. Phenotypic heterogeneity in patients with NEFL‐related Charcot–Marie–Tooth disease.
28. Prenatal diagnosis of congenital heart disease: Trends in pregnancy termination rate, and perinatal and 1-year infant mortalities in Korea between 1994 and 2005
29. Genetic and clinical spectrums in Korean Charcot‐Marie‐Tooth disease patients with myelin protein zero mutations.
30. A novel histone deacetylase 6 inhibitor improves myelination of Schwann cells in a model of Charcot-Marie-Tooth disease type 1A.
31. p75 and neural cell adhesion molecule 1 can identify pathologic Schwann cells in peripheral neuropathies.
32. Association of miR-149 polymorphism with onset age and severity in Charcot–Marie–Tooth disease type 1A.
33. Replication studies of MIR149 association in Charcot–Marie–Tooth disease type 1A in a European population - response.
34. A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.
35. SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3.
36. Comparison of the Mental Health Impact of COVID-19 on Vulnerable and Non-Vulnerable Groups: A Systematic Review and Meta-Analysis of Observational Studies.
37. Clinical and Neuroimaging Features in Charcot–Marie–Tooth Patients with GNB4 Mutations.
38. Human HSPB1 mutation recapitulates features of distal hereditary motor neuropathy (dHMN) in Drosophila.
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