25 results on '"Koto, Yuta"'
Search Results
2. Development and evaluation of a patient-reported outcome measure specific for Gaucher disease with or without neurological symptoms in Japan
3. Experiences of patients with metachromatic leukodystrophy, adrenoleukodystrophy, or Krabbe disease and their family members: a qualitative systematic review
4. Correction: Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan
5. Impact on physical, social, and family functioning of patients with metachromatic leukodystrophy and their family members in Japan: A qualitative study
6. Burden of caregivers of patients with neuronopathic and non-neuronopathic Gaucher disease in Japan: A survey-based study
7. Experiences of patients and their family members with metachromatic leukodystrophy, adrenoleukodystrophy, and Krabbe disease: a qualitative systematic review protocol
8. Development and validation of a disease-specific quality of life scale for adult patients with Fabry disease in Japan
9. Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan
10. Experiences of patients with lysosomal storage disorders who are receiving enzyme-replacement therapy and the experiences of their family members: a qualitative systematic review
11. Supporters' experiences of sensory characteristics of children with profound intellectual and multiple disabilities in after‐school daycare centres: A qualitative study
12. Experiences of patients with lysosomal storage disorders treated with enzyme replacement therapy: a qualitative systematic review protocol
13. Assessing the impact on caregivers burden for patients with Gaucher disease in Japan
14. Qualitative analysis of patient characters, interviews on the burden of neuronopathic Gaucher disease in Japan
15. Development and evaluation of Gaucher disease-specific patient reported outcome measurement in Japan
16. Experiences of patients and their family members with metachromatic leukodystrophy, adrenoleukodystrophy, and Krabbe disease: a qualitative systematic review protocol
17. Translation of quality of life scale for pediatric patients with Fabry disease in Japan
18. Additional file 1 of Development and validation of a disease-specific quality of life scale for adult patients with Fabry disease in Japan
19. Additional file 1 of Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan
20. Experiences of patients with lysosomal storage disorders who are receiving enzyme-replacement therapy and the experiences of their family members: a qualitative systematic review
21. Assessment of Characteristics of Imaging Biomarkers for Quantifying Anterior Cingulate Cortex Changes: A Twin Study of Middle- to Advanced-Aged Populations in East Asia.
22. Prevalence of patients with lysosomal storage disorders and peroxisomal disorders: A nationwide survey in Japan
23. Experiences of patients with lysosomal storage disorders treated with enzyme replacement therapy: a qualitative systematic review protocol.
24. Experiences of siblings of children with profound intellectual and multiple disabilities: a qualitative systematic review protocol.
25. Experiences of patients with metachromatic leukodystrophy, adrenoleukodystrophy, or Krabbe disease and the experiences of their family members: a qualitative systematic review.
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