Výsledky vyhledávání - "I. Asseiceira"

Change in Nutrient and Dietary Intake in European Children with Cystic Fibrosis after a 6-Month Intervention with a Self-Management mHealth Tool

Autor: Hettie M. Janssens, Mieke Boon, María Roca, Luísa Pereira, Jessie M. Hulst, Joaquim Calvo-Lerma, Sandra Woodcock, Anna Bulfamante, L. Zazzeron, I. Asseiceira, I. Claes, Etna Masip, Carla Colombo, Carmen Ribes-Koninckx, Saioa Vicente, Victoria Fornés, Kris De Boeck, María Garriga, Bo van Schijndel

Publikováno v: Nutrients
Volume 13
Issue 6
Nutrients, Vol 13, Iss 1801, p 1801 (2021)
Nutrients, 13(6):1801. Multidisciplinary Digital Publishing Institute (MDPI)
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname

Cystic Fibrosis (CF) is a life-long genetic disease, causing increased energy needs and a healthy diet with a specific nutrient distribution. Nutritional status is an indicator of disease prognosis and survival. This study aimed at assessing the effe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28379401960c41bdae0fc6bc9b9f5521
https://lirias.kuleuven.be/handle/20.500.12942/693507

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Clinical evaluation of an evidence-based method based on food characteristics to adjust pancreatic enzyme supplements dose in cystic fibrosis

Publikováno v: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Journal of Cystic Fibrosis, 20(5), e33-e39. Elsevier

[EN] Background: Patients with cystic fibrosis (CF) and pancreatic insufficiency need pancreatic enzyme replacement therapy (PERT) for dietary lipids digestion. There is limited evidence for recommending the adequate PERT dose for every meal, and con

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed60a6387d7a9f09ac77d354493156c
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=13535

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Use of a mobile application for self-management of pancreatic enzyme replacement therapy is associated with improved gastro-intestinal related quality of life in children with Cystic Fibrosis

Publikováno v: Journal of Cystic Fibrosis, 19(4), 562-568. Elsevier
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname

Background: Most patients with cystic fibrosis (CF) suffer from pancreatic insufficiency (PI), leading to fat malabsorption, malnutrition, abdominal discomfort and impaired growth. Pancreatic enzyme replacement therapy (PERT) is effective, but eviden

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94106794aa0d92a677112abe2a63b688
https://pure.eur.nl/en/publications/af11e923-bc32-4b67-a9df-2f1cc8e918c5

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The Relative Contribution of Food Groups to Macronutrient Intake in Children with Cystic Fibrosis: A European Multicenter Assessment

Publikováno v: JOURNAL OF THE ACADEMY OF NUTRITION AND DIETETICS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of the Academy of Nutrition and Dietetics
Journal of the Academy of Nutrition and Dietetics, 119(8), 1305-1319. Elsevier Inc.

Background Optimal nutrition for children with cystic fibrosis (CF) improves prognosis and survival, but an increased caloric intake recommendation for this population raises concerns about the nutrient profile of their diets. Objective Our aim was t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::099bafc0390f870822d479ed8ed2c49b
https://pubmed.ncbi.nlm.nih.gov/31655721

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WS12.6 MyCyFAPP project: validation of the PEDsQL GI symptom scale to evaluate gastro-intestinal symptoms in children with cystic fibrosis

Publikováno v: Journal of Cystic Fibrosis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ff1b1d8b579a4669675ceb8db84ac89

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Optimisation of children z-score calculation based on new statistical techniques

Autor: Peter Witters, Kris De Boeck, Mieke Boon, I. Asseiceira, Antonio Martinez-Millana, Carlos Fernandez-Llatas, Carmen Ribes-Koninckx, Jessie M. Hulst, Joaquin Calvo-Lerma, Vicente Traver, Ignacio Basagoiti

Publikováno v: PLoS ONE, Vol 13, Iss 12, p e0208362 (2018)
PLOS ONE
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
PLoS ONE
Plos One
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
PLoS One (online), 13(12):e0208362. Public Library of Science

[EN] Background Expressing anthropometric parameters (height, weight, BMI) as z-score is a key principle in the clinical assessment of children and adolescents. The Centre for Disease Control and Prevention (CDC) growth charts and the CDC-LMS method

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb62c9fde6969bde82f8d77c0b45646c
https://doaj.org/article/2d3d2e58cd0b4954a7258bbf2cdf3f42

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