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Development and evaluation of a patient-reported outcome measure specific for Gaucher disease with or without neurological symptoms in Japan

Abstract Background Patients with Gaucher disease (GD), a rare lysosomal storage disorder, have reduced health-related quality of life (HRQOL). A patient-reported outcome measure (PROM) for HRQOL developed for type 1 GD (GD1) is not appropriate for patients with neuronopathic GD (nGD) types 2 (GD2)...

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Bibliografski detalji
Glavni autori: Aya Narita, Yuta Koto, Shinichi Noto, Masafumi Okada, Midori Ono, Terumi Baba, Rieko Sagara, Norio Sakai
Format: Artigo
Jezik:Inglês
Izdano: BMC 2024-01-01
Serija:Orphanet Journal of Rare Diseases
Teme:
Online pristup:https://doi.org/10.1186/s13023-023-02996-9
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