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Rosemarie Felder-Puig

Researcher at Boston Children's Hospital

Publications -  16
Citations -  759

Rosemarie Felder-Puig is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Quality of life (healthcare) & Population. The author has an hindex of 9, co-authored 14 publications receiving 717 citations.

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Validation of the German version of the Pediatric Quality of Life InventoryTM (PedsQLTM) in childhood cancer patients off treatment and children with epilepsy

TL;DR: The results of translating the original US generic core instrument and the cancer module into German and testing the German PedsQLTM in samples of paediatric patients who have been treated for cancer or epilepsy seem to be equivalent to the original version.
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Quality of life and psychosocial adjustment of young patients after treatment of bone cancer.

TL;DR: The aim of this study was to collect information about the psychosocial situation of young patients after multimodality therapy for bone cancer.
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Health-related quality of life of pediatric patients receiving allogeneic stem cell or bone marrow transplantation: results of a longitudinal, multi-center study

TL;DR: The results of a 5-year longitudinal prospective study about the health-related quality of life (HRQL) of pediatric patients receiving allogeneic bone marrow or stem cell transplantation (BMT) are described, with an average positive evolution.
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Using a children's book to prepare children and parents for elective ENT surgery: results of a randomized clinical trial.

TL;DR: It was found that mothers who received the preparation book exhibited less self-reported state anxiety prior to the operation compared to mothers who did not, and children of the experimental group showed less distress in 4 of 11 feeling states.
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Quality of life in long-term childhood cancer survivors and the relation of late effects and subjective well-being

TL;DR: The results of the present study may be helpful in planning an appropriate multidisciplinary, long-term follow-up of childhood cancer survivors.