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2. A reference human induced pluripotent stem cell line for large-scale collaborative studies.

3. Probability of independent walking and wheeled mobility in individuals with cerebral palsy

6. Parents' Perspectives of Using a Therapeutic Listening Program with Their Children with Sensory Processing Difficulties: A Qualitative Study

8. Microglia produce the amyloidogenic ABri peptide in familial British dementia

9. Is there evidence for a relationship between cognitive impairment and fatigue after acquired brain injury: a systematic review and meta-analysis.

12. A reference human induced pluripotent stem cell line for collaborative studies

13. Kinematic Measures of Imitation Fidelity in Primary School Children

14. Occupational Therapy Students' Attitudes towards Individuals with Disabilities: A Comparison between Australia, Taiwan, the United Kingdom, and the United States

15. Postural asymmetries, pain, and ability to change position of children with cerebral palsy in sitting and supine : a cross-sectional study

16. Relationship between scoliosis, windswept hips and contractures with pain and asymmetries in sitting and supine in 2450 children with cerebral palsy

18. A reference induced pluripotent stem cell line for large-scale collaborative studies

22. Relationship between scoliosis, windswept hips and contractures with pain and asymmetries in sitting and supine in 2450 children with cerebral palsy

23. Familial Alzheimer’s Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis

27. Premature neuronal differentiation in familial Alzheimer’s disease human stem cells in vitro and in postmortem brain tissue

32. Haploinsufficiency of progranulin causes cell type specific impairments in PINK1/Parkin mitophagy.

35. Physical risk factors influencing wheeled mobility in children with cerebral palsy : a cross-sectional study

38. Contributors List

48. Establishing best practice in seating assessment for children with physical disabilities using qualitative methodologies.

49. Familial Alzheimer’s Disease Mutations in PSEN1Lead to Premature Human Stem Cell Neurogenesis

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