32 results on '"Shy, Rosemary"'
Search Results
2. Association of Body Mass Index With Disease Progression in Children With Charcot-Marie-Tooth Disease
3. A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores
4. Natural history of Charcot‐Marie‐Tooth disease during childhood
5. The Charcot-Marie-Tooth Functional Outcome Measure (CMT-FOM)
6. Disease Progression in Charcot–Marie–Tooth Disease Related to MPZ Mutations: A Longitudinal Study.
7. Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease
8. Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth Disease
9. Genotype–phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene
10. Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study
11. Development, reliability and validity of the Charcot-Marie-Tooth disease Pediatric Scale (CMTPedS)
12. Transitioning outcome measures: relationship between the CMTPedS and CMTNSv2 in children, adolescents, and young adults with Charcot-Marie-Tooth disease
13. Symmetry of foot alignment and ankle flexibility in paediatric Charcot-Marie-Tooth disease
14. Validation of the Charcot–Marie–Tooth Disease Pediatric Scale as an Outcome Measure of Disability
15. Validation of the Italian version of the Charcot‐Marie‐Tooth disease Pediatric Scale
16. 50 Years Ago in The Journal of Pediatrics: SPEECH PROBLEMS IN CHILDREN
17. Stoichiometric Alteration of PMP22 Protein Determines the Phenotype of Hereditary Neuropathy With Liability to Pressure Palsies
18. Dysphonia
19. Commentary
20. Phenotypic clustering in MPZ mutations
21. Erratum to: Development and validation of the Charcot-Marie-Tooth Disease Infant Scale
22. Development and validation of the Charcot-Marie-Tooth Disease Infant Scale
23. Balance impairment in pediatric charcot-marie-tooth disease.
24. Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS.
25. The Charcot-Marie-Tooth (CMT) Infant Scale: A Pilot Study Testing the Ability of the Scale To Monitor Disease Progression in Infant and Children Younger Than Three Years Old (S26.006)
26. Development, reliability and validity of the Charcot‐Marie‐Tooth disease Pediatric Scale (CMTPedS)
27. Tinea corporis and tinea capitis.
28. Development and validation of the CMT infant scale
29. Optimizing the clinical trial responsiveness of the CMT pediatric scale
30. Validation of the Charcot-Marie-Tooth Pediatric Scale as an Outcome Measure of Disability
31. Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
32. Diagnosis: cystic fibrosis.
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