Zobrazeno 1 - 10
of 28
pro vyhledávání: '"F.M. Hollander"'
Autor:
E.A. van de Graaf, F.M. Hollander-Kraaijeveld, Harry G.M. Heijerman, A.S. van Lanen, N.M. de Roos
Publikováno v:
Journal of Cystic Fibrosis, 19(6), 975-980
Journal of Cystic Fibrosis 19 (2020) 6
Journal of Cystic Fibrosis 19 (2020) 6
REE and REE/kg FFM significantly decrease after lung transplantation in CF patients. Prediction equations for energy requirement are inaccurate until a year after LTx. Measuring REE by indirect calorimetry is advised in CF patients before and until o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f4e22cbfe5ff4ba7f9eb66b24d5be93
https://research.wur.nl/en/publications/resting-energy-expenditure-in-cystic-fibrosis-patients-decreases-
https://research.wur.nl/en/publications/resting-energy-expenditure-in-cystic-fibrosis-patients-decreases-
Autor:
E.A. van de Graaf, M. Burghard, N.M. de Roos, Harry G.M. Heijerman, Y. Lindeman, F.M. Hollander-Kraaijeveld
Publikováno v:
Journal of Cystic Fibrosis, 19(1), 153-158
Journal of Cystic Fibrosis 19 (2020) 1
Journal of Cystic Fibrosis 19 (2020) 1
Background: Nutritional status affects pulmonary function in cystic fibrosis (CF) patients and can be monitored by using bioelectrical impedance analysis (BIA). BIA measurements are commonly performed in the fasting state, which is burdensome for pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89940965138f45d2912c0583113eefc3
https://research.wur.nl/en/publications/non-fasting-bioelectrical-impedance-analysis-in-cystic-fibrosis-i
https://research.wur.nl/en/publications/non-fasting-bioelectrical-impedance-analysis-in-cystic-fibrosis-i
Publikováno v:
Journal of Cystic Fibrosis. 19:S16-S17
Autor:
S Sophie Ghijsen, H.G.M. Heijerman, Erik H. J. Hulzebos, M. Burghard, K. van der Ent, Tim Takken, Gitte Berkers, K. Winter-de Groot, F.M. Hollander-Kraaijeveld
Publikováno v:
Journal of Cystic Fibrosis. 18:S157-S158
Publikováno v:
Current Opinion in Pulmonary Medicine, 23(6), 556. Lippincott Williams and Wilkins
Current Opinion in Pulmonary Medicine, 23(6), 556-561
Current Opinion in Pulmonary Medicine 23 (2017) 6
Current Opinion in Pulmonary Medicine, 23(6), 556-561
Current Opinion in Pulmonary Medicine 23 (2017) 6
PURPOSE OF REVIEW: Cystic fibrosis (CF) is a progressive genetic disease that affects multiple organ systems. Therapy is directed to maintain and optimize nutritional status and pulmonary function, as these are key factors in survival. In this review
Autor:
Ed A. van de Graaf, Ferdinand Teding van Berkhout, F.M. Hollander, Gerdien Belle-van Meerkerk, Nicole M. de Roos, Harry G.M. Heijerman
Publikováno v:
Journal of the Academy of Nutrition and Dietetics, 117(11), 1808-1815
Journal of the Academy of Nutrition and Dietetics, 117(11), 1808. Elsevier USA
Journal of the Academy of Nutrition and Dietetics 117 (2017) 11
Journal of the Academy of Nutrition and Dietetics, 117(11), 1808. Elsevier USA
Journal of the Academy of Nutrition and Dietetics 117 (2017) 11
BACKGROUND: Enteral tube feeding (ETF) is widely used in patients with cystic fibrosis (CF) and end-stage lung disease, but previous studies have been limited to investigating whether ETF improves outcomes in patients with moderately or mildly impair
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9961662f0b7532e3deff7bcf08b3487a
https://research.wur.nl/en/publications/body-weight-and-body-mass-index-in-patients-with-end-stage-cystic
https://research.wur.nl/en/publications/body-weight-and-body-mass-index-in-patients-with-end-stage-cystic
Publikováno v:
Journal of Cystic Fibrosis. 18:S154
Publikováno v:
Journal of Cystic Fibrosis. 17:S114
Autor:
E.A. van de Graaf, F. Teding van Berkhout, N.M. de Roos, F.M. Hollander, G. Belle-van Meerkerk
Publikováno v:
Journal of Cystic Fibrosis. 16:S149
Autor:
Gerdien Belle-van Meerkerk, Nicole M. de Roos, Ed A. van de Graaf, Annemieke Kok, F.M. Hollander
Publikováno v:
Nutrition in Clinical Practice, 32(1), 116-121
Nutrition in Clinical Practice, 32(1), 116. SAGE Publications Ltd
Nutrition in Clinical Practice 32 (2017) 1
Nutrition in Clinical Practice, 32(1), 116. SAGE Publications Ltd
Nutrition in Clinical Practice 32 (2017) 1
Background: Resting energy expenditure (REE) is increased in patients with cystic fibrosis (CF) with end-stage lung disease due to chronic inflammation and pulmonary infections. After lung transplantation (LTx), energy expenditure is expected to be l