Quality of life and psychological functioning of pediatric and young adult patients with Gaucher disease, type 1-Reference-Cited by-同舟云学术

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Quality of life and psychological functioning of pediatric and young adult patients with Gaucher disease, type 1

Published:2020-03-03 Issue:5 Volume:182 Page:1130-1142
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Alioto Andrea G.¹^ORCID,Gomez Rowena²,Moses James²,Paternostro Jennifer³,Packman Seymour⁴,Packman Wendy²

Affiliation:

1. Department of NeurologyUniversity of California, Davis Walnut Creek California USA

2. Department of Clinical PsychologyPalo Alto University Palo Alto California USA

3. Department of PediatricsUniversity of Iowa Iowa City Iowa USA

4. Department of PediatricsUniversity of California, San Francisco San Francisco California USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61533

Reference38 articles.

1. Newborn Screening for Lysosomal Storage Disorders—Continuing Education Posttest

2. Childhood chronic conditions and health-related quality of life: Findings from a large population-based study

3. Chronic Illness and Developmental Vulnerability at School Entry

4. Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease

5. The Psychosocial Impact of Fabry Disease on Pediatric Patients

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of patient-reported outcomes measures (PROMs) and patient-reported experiences measures (PREMs) in Gaucher disease in Spain;Medicina Clínica;2024-08

2. Measuring health related quality of life (HRQoL) in Lysosomal Storage Disorders (LSDs): a rapid scoping review of available tools and domains;Orphanet Journal of Rare Diseases;2024-07-04

3. Women with Gaucher Disease;Biomedicines;2024-03-05

4. Development and evaluation of a patient-reported outcome measure specific for Gaucher disease with or without neurological symptoms in Japan;Orphanet Journal of Rare Diseases;2024-01-05

5. Burden of caregivers of patients with neuronopathic and non-neuronopathic Gaucher disease in Japan: A survey-based study;Molecular Genetics and Metabolism Reports;2023-09

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