Výsledky vyhledávání

Initial investigation of associations between feeding practices, eating behaviours, and weight status in Vietnamese children using modified questionnaires

Autor: S K, Ayre, E, Jansen, D, Gallegos, C Q, Tran, D N, Do, S, Nambiar

Publikováno v: Obesity Research & Clinical Practice. 16:301-306

This cross-sectional study aims to extend the preliminary validation of the Feeding Practices and Structure Questionnaire (FPSQ) and Children's Eating Behaviour Questionnaire (CEBQ) in the Vietnamese context by examining associations between maternal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fbfdb793aaa3ac33400c9962ef0d204
https://doi.org/10.1016/j.orcp.2022.07.002

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Preliminary exploration of the use of the Children’s Eating Behaviour Questionnaire (CEBQ) and Feeding Practices and Structure Questionnaire (FPSQ) in Vietnamese mothers

Autor: Danielle Gallegos, D. N. Do, Smita Nambiar, C. Q. Tran, Elena Jansen, S. Ayre

Publikováno v: European Journal of Clinical Nutrition. 76:442-449

Objective This preliminary pilot study aims to explore the use of the Feeding Practices and Structure Questionnaire (FPSQ) and Children's Eating Behaviour Question (CEBQ) in a sample of Vietnamese mothers. Subjects/methods Cross-sectional data from t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e415b9843ad113d7b3f5bff4c7d81da7
https://doi.org/10.1038/s41430-021-00947-w

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Preliminary exploration of the use of the Children's Eating Behaviour Questionnaire (CEBQ) and Feeding Practices and Structure Questionnaire (FPSQ) in Vietnamese mothers

Autor: S, Ayre, D, Gallegos, S, Nambiar, C Q, Tran, D N, Do, E, Jansen

Publikováno v: European journal of clinical nutrition. 76(3)

This preliminary pilot study aims to explore the use of the Feeding Practices and Structure Questionnaire (FPSQ) and Children's Eating Behaviour Question (CEBQ) in a sample of Vietnamese mothers.Cross-sectional data from the FPSQ and CEBQ were collec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::96fbeea403789d55bd70145812f02ab7
https://pubmed.ncbi.nlm.nih.gov/34302134

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Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

Autor: R E, Amir, I B, Van den Veyver, R, Schultz, D M, Malicki, C Q, Tran, E J, Dahle, A, Philippi, L, Timar, A K, Percy, K J, Motil, O, Lichtarge, E O, Smith, D G, Glaze, H Y, Zoghbi

Publikováno v: Annals of neurology. 47(5)

We screened 71 sporadic and 7 familial Rett syndrome (RTT) patients for MECP2 mutations by direct sequencing and determined the pattern of X chromosome inactivation (XCI) in 39 RTT patients. We identified 23 different disease-causing MECP2 mutations

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::13364c0be929d2307da04ad01167f981
https://pubmed.ncbi.nlm.nih.gov/10805343

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