32 results on '"Battini R."'
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2. Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy
3. Reliability of the North Star Ambulatory Assessment in a multicentric setting
4. P.148Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53
5. Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions
6. Revised North Star ambulatory assessment for young boys with Duchenne muscular dystrophy
7. The 24-month performance of upper limb (PUL) scale: Changes and steroids correlation in DMD
8. Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy
9. Registries versus tertiary care centers: How do we measure standards of care in Duchenne muscular dystrophy?
10. T.P.4
11. T.P.10
12. Muscle MRI in FHL1-linked reducing body myopathy
13. P.332 - Revised North Star ambulatory assessment for young boys with Duchenne muscular dystrophy
14. P.333 - The 24-month performance of upper limb (PUL) scale: Changes and steroids correlation in DMD
15. Registries versus tertiary care centers: How do we measure standards of care in Duchenne muscular dystrophy?
16. P.2.3 Assessment of Upper Limb function in DMD patients: Comparison with normative data
17. P.2.7 6min walk test 12month changes in DMD: Correlation with genotype
18. P.9.15 Centronuclear myopathies: The experience of Italian Network for congenital myopathies
19. S.P.4 Functional changes in Duchenne muscular dystrophy: A 24month longitudinal cohort study
20. P1.57 Neuropsychological profiles in children with Duchenne muscular dystrophy compared to dyslexic population
21. M.P.2.01 Reliability of the north star ambulatory assessment in a multicentric setting
22. G.O.2 Proteomic identification of the LIM domain protein FHL1 as the gene-product mutated in reducing body myopathy
23. The Hammersmith functional score correlates with the SMN2 copy number: A multicentric study
24. Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric study
25. Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study
26. T.P.10: 6 min walk test and Performance of Upper Limb in ambulant DMD boys
27. T.P.4: Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36 month changes
28. P.2.7 6 min walk test 12 month changes in DMD: Correlation with genotype
29. S.P.4 Functional changes in Duchenne muscular dystrophy: A 24 month longitudinal cohort study
30. P3.2 Novel mutation of TRPV4 in congenital distal SMA with vocal cord paralysis
31. 250P Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey.
32. N.P.2 01 Spinal muscular atrophy: correlation between the number of SMN2 genes and functional ability
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