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ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic fibrosis
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Ultra-processed food intake does not correlate with pediatric MASLD in the National Health and Nutrition Examination Survey
(2024) -
- Journal Article
- A1
- open access
Glycemic indices at night measured by CGM are predictive for a lower pulmonary function in adults but not in children with cystic fibrosis
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- Journal Article
- A1
- open access
Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis
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Vitamine D voor kinderen in Vlaanderen
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Effect of 18 months elexacaftor-tezacaftor-ivacaftor on body mass index and glycemic control in adults with cystic fibrosis
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Abnormale glucosetolerantie bij personen met mucoviscidose
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- Journal Article
- A1
- open access
Urinary sodium/creatinine ratio is a predictor for fractional sodium excretion and related to age in patients with cystic fibrosis
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Working towards an optimal nutritional status in people with cystic fibrosis
(2022) -
The effect of an intensive residential rehabilitation program on body composition in patients with cystic fibrosis
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Evaluation of sodium status in patients with cystic fibrosis
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Long-term use of tube feeding in children with cystic fibrosis : results from two Belgian CF centers
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Sodiumstatus in patients with cystic fibrosis : how to monitor based on urine sample?
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Sodium status and replacement in children and adults living with cystic fibrosis : a narrative review
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- Journal Article
- A1
- open access
Acid-base disturbances in dehydrated patients with cystic fibrosis : four case reports with review of literature
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The nutritional status in CF : being certain about the uncertainties
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Long-term experience with tube feeding in children with cystic fibrosis in two Belgian CF Centers : preliminary results
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Body composition measured by BIA of tube-fed cystic fibrosis patients compared to age-sex matched controls
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The effect of enteral tube feeding in cystic fibrosis : a registry based study
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Impact of tube feeding (TF) on pulmonary function in children and adults with cystic fibrosis
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Evaluation of HbA1c and OGTT-results after a first abnormal OGTT
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Single centre long-term experience with tube feeding in children with cystic fibrosis
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Characteristics at baseline of tube-fed cystic fibrosis (CF) patients with matched controls : a registry study
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The impact of tube feeding in children and adults with cystic fibrosis
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Clinical effects of probiotics in cystic fibrosis patients : a systematic review
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Position paper: Koolhydraatarme voeding bij diabetes type 2
(2017) -
ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis
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Highlights of the ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants and children with cystic fibrosis
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- Journal Article
- A2
- open access
Diagnosis of pancreatic insufficiency in cystic fibrosis : a practical approach
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Daily physical activity and peripheral muscle force in adults with cystic fibrosis compared with controls
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The use of enteral nutrition in Belgian CF centers : a pilot study
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Preliminary results : should patients with cystic fibrosis count their fat-intake?
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Gastro-intestinal manifestations in cystic fibrosis patients
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How are pancreatic enzymes distributed over mealtimes and meal types?
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Influencing factors of skeletal muscle weakness in adults with cystic fibrosis
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Intake of pancreatic enzymes : consistent with the guidelines?
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Skeletal muscle strength measurements in adult CF patients compared to controls
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Nutrition and pancreatic enzyme intake in patients with cystic fibrosis with distal intestinal obstruction syndrome
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Mucoviscidosegerelateerde diabetes mellitus
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No evidence for a provoking role of nutritinal factors in distal intestinal obstruction syndrome
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- Conference Paper
- C3
- open access
No evidence for a provoking role of nutritional factors in distal intestinal obstruction syndrome
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Relation between fatty acid composition and clinical status or genotype in cystic fibrosis patients
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An assessment of validity in entrepreneurship research
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Relation between fatty acid composition and clinical status/genotype in CF?
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Serum zinc concentrations of the CF population above the age of 4 years: a cross sectional evaluation
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Vitamin D binding protein in cystic fibrosis patients in relation to serum vitamin D
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No evidence for provoking rule of nutritional factors in distal intestinal obstruction syndrome (DIOS)
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sun exposure rather than oral supplements determines vitamin D levels (VDSL) in cystic fibrosis
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clinical Effect of zinc supplements in cystic fibrosis patients
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Dietary habits related to bone disease in cystic fibrosis patients
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An assessment of validity in small business and entrepreneurship research
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No evidence for provoking role of nutritional factors in distal intestinal obstruction syndrome (DIOS)
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Observations on compatibility between Bulinus truncatus and Schistosoma haematobium in the Senegal River Basin.
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Failure of mebendazole in treatment of human hookworm infections in the southern region of Mali.
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Circulating anodic and cathodic antigen in serum and urine of mixed Schistosoma haematobium and S-mansoni infections in Office du Niger, Mali.
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Ankle bracing in running: the effect of a Push(r) type medium ankle brace upon movements of the foot and ankle during the stance phase
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The effects of isolation on the mechanics of the human heel pad.
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Comparison of the circulating anodic antigen-detection assay and urine filtration in Schistosoma-haematobium infections in Mali.
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Schistosoma and geohelminth infections in Mali, West Africa.
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THE MECHANICAL-PROPERTIES OF THE HUMAN HEEL PAD - A PARADOX RESOLVED.
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Schistosomiasis in Dogon Country, Mali - identification and prevalence of the species responsible for infection in the local-community.
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Studies on transmission and schistosome interactions in Senegal, Mali and Zambia.
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The Mechanical Characteristics of the Human Heel Pad during foot strike in running - An in vivo cineradiographic study.