238 results on '"Zidar J"'
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2. Auditory neuropathy is asymptomatic in one of two forms of autosomal dominant axonal Charcot-Marie-Tooth disease linked to 8P21 chromosome
3. Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
4. Using ANN on EEG signals to predict working memory task response
5. Identification of Gripping-Force Control from Electroencephalographic Signals
6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)
7. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)
8. Clinical neurophysiological assessment of spasticity
9. A PRELIMINARY ANNOTATED BIBLIOGRAPHY OF INFORMATION HANDLING ACTIVITIES IN BIOLOGY
10. The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features
11. Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele
12. Spatio-temporal dynamics of cortical activity during reaching preparation: P1540
13. Irish cardiac society: Proceedings of annual general meeting held 1st November, 1997
14. Functional changes of the cortical motor system in hereditary spastic paraparesis
15. Exploring the Control of Reaching by Using EEG-fMRI with a Haptic Device
16. ALS and FTLD: two faces of TDP-43 proteinopathy
17. Clinical Conference Proceedings: 15th Biennial International Andreas Gruentzig Society Meeting
18. Sleep-wake rhythm development in infants suffering apparent life threatening event (ALTE): P153
19. Subclinical auditory neuropathy in one of two forms of Charcot–Marie–Tooth disease linked to CMT2E locus
20. Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family
21. Irish cardiac society
22. Actigraphic assessment of sleep–wake rhythm during the first 6 months of life
23. Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia
24. Wide prefrontal and sensory-motor network involvement in the preparation of the choice in comparison to the simple reaching
25. Correlations between clinical, electrophysiological and genetic findings in hereditary motor and sensory neuropathy type I (HMSN I)
26. CTG repeat analysis in lymphocytes, muscles and fibroblasts in patients with myotonic dystrophy
27. Evolutionary associations between host traits and parasite load: insights from Lake Tanganyika cichlids
28. ID 274 – Separating idea from the action: A standardized low-resolution brain electromagnetic tomography (sLORETA) study
29. ID 339 – Increases and decreases of power of EEG mu rhythm in patients with amyotrophic lateral sclerosis
30. The spectrum of limb-girdle muscular dystrophy in Slovenia defined by molecular genetic analysis
31. Clinical, molecular and genetic features of calpainopathy in Slovenia
32. I-3. Heterogeneity and atypical phenotypes in patients with facioscapulohumeral muscular dystrophy
33. CRITICAL ILLNESS MYOPATHY IN PATIENTS WITH CENTRAL NERVOUS SYSTEM DISORDERS
34. Using ANN on EEG signals to predict working memory task response
35. Identification of Gripping-Force Control from Electroencephalographic Signals
36. P89: Do higher proximal ulnar nerve compound muscle action potentials result from higher conduction velocities of axons mediating the second of its two negative peaks?
37. P45: Event related desynchronisation/synchronisation (ERD/ERS) in the actual and imagined reaching movements
38. Identification of calpain deficient patients in Slovenia by Western Blotting
39. 11-year clinical follow-up of a patient with dysferlinopathy-report on the first diagnosed slovenian case
40. Scent of the enemy: behavioural responses to predator faecal odour in the fowl
41. W11.4 Relationship between cortical fMRI activity and functional measures in amyotrophic lateral sclerosis
42. Current husbandry of red pandas (Ailurus fulgens) in zoos
43. Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele
44. P36-18 Scalp topography of sniffing-related cortical potentials
45. G.P.15.10 Patients with facioscapulohumeral muscular dystrophy-like phenotype not linked to 4q35
46. PHP013 Sleep-wake rhythm development in infants with an apparent life threatening event
47. Information processes in the motor system: approach with transcranial magnetic stimulation
48. Relation of CTG expansion and clinical variables to electrocardiogram conduction abnormalities and sudden death in patients with myotonic dystrophy
49. Using ANN on EEG signals to predict working memory task response.
50. Identification of Gripping-Force Control from Electroencephalographic Signals.
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