147 results on '"Perić S"'
Search Results
2. Prospective analysis of gait characteristics in chronic inflammatory demyelinating polyradiculoneuropathy
3. Non-native tree species : strategies for sustainable management in Europe
4. Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen
5. MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study
6. Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions
7. Genetic testing of individuals with pre‐senile cataract identifies patients with myotonic dystrophy type 2
8. Cardiac autonomic control in patients with myasthenia gravis and thymoma
9. Duglasul verde (Pseudotsuga menziesii var. menziesii (Mirb.) Franco) în Ocolul silvic Călimănești: o utilizare de succes pe termen lung.
10. P277 Long-term safety, tolerability, and efficacy of Efgartigimod in patients with Generalized Myasthenia Gravis: concluding analyses from the ADAPT+ study
11. Validation of Serbian version of the disease-specific myasthenia gravis questionnaire
12. P.212 TREAT-NMD Myotonic dystrophy (DM) Global Registry Network: An update in 2022
13. P.211 TREAT-NMD myotonic dystrophy Global Registry Network: Providing data in congenital myotonic dystrophy to support FDA regulatory decision making
14. P.213 TREAT-NMD myotonic dystrophy global registry network: An international collaboration in myotonic dystrophy type 2
15. VP.54 Amifampridine safety and efficacy in spinal muscular atrophy ambulatory patients: a randomized placebo-controlled, crossover, phase 2 trial
16. Applicative Monitoring of Vehicles Engine Oil
17. Switchgear Reliability and Principles of Design
18. Basophilic peripheral nerve inclusions in a patient with L144F SOD1 amyotrophic lateral sclerosis
19. Detection of TRIM32 variants associated with LGMD2H in a large cohort of patients with unexplained limb-girdle weakness
20. Ocular surface disease in pseudoexfoliation syndrome
21. Video head impulse test findings in patients with Charcot-Marie-tooth disease 1A
22. Longitudinal gait analysis in patients with chronic inflammatory demyelinating polyradiculoneuropathy
23. phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia
24. Risk factors for malnutrition among hospitalized gastroenterological patients
25. Assessment of the neuropathic component in a chronic low back pain syndrome
26. A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort
27. Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations
28. Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking
29. Sliding mode control based on orthogonal models
30. Validation of Serbian version of the disease-specific myasthenia gravis questionnaire
31. Effects of immunotherapy in mild Guillain-Barre Syndrome
32. Quality of life in patients with Limb-Girdle muscular dystrophies
33. Metabolic syndrome in myotonic dystrophy type 2
34. P.152 - Detection of TRIM32 variants associated with LGMD2H in a large cohort of patients with unexplained limb-girdle weakness
35. P.138 - Two novel mutations in the FHL1 gene extending the phenotypic spectrum
36. OD12 - Detection of TRIM32 variants associated with LGMD2H in a large cohort of patients with unexplained limb-girdle weakness
37. Immunization in inflammatory bowel diseases: Recommendations on vaccines administration
38. The small man in the book of the essays 'Some Things' by Borislav Radović
39. Neuropathic pain as independent predictor of worse quality of life in patients with diabetic neuropathy
40. Laboratorijska dijagnostika uzročnika koji se mogu koristiti u bioterorističke svrhe
41. N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome
42. The judiciary system and the social care system policy on contractual capacity: Overview of research conducted in the City of Belgrade
43. P.81 - A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort
44. P.64 - Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations
45. The Fate of Patients with Intermittent Claudication in the 21st Century Revisited – Results from the CAVASIC Study
46. Validation of Serbian version of the disease-specific myasthenia gravis questionnaire
47. Ultra‐selective lowpass linear‐phase FIR filter function
48. Destiny of a beautiful foreigner in the universe of Banjane: Character of Sarah in a novel by Petar Sarić
49. SMN1 copy number as a modifying factor of survival in Serbian patients with sporadic amyotrophic lateral sclerosis
50. The influence of atmospheric conditions on the migration of diesel fuel spilled in soil
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