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Nutrition in patients with cystic fibrosis: a European Consensus

Journal of cystic fibrosis, 2002-06, Vol.1 (2), p.51-75

2002

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Sunlight is an important determinant of vitamin D serum concentrations in cystic fibrosis

European journal of clinical nutrition, 2011-05, Vol.65 (5), p.574-579

2011

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EPS3.5 Probiotics in cystic fibrosis (CF) patients: a double blind cross-over study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S42-S42

2017

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ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis

Clinical nutrition (Edinburgh, Scotland), 2016-06, Vol.35 (3), p.557-577

2016

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Oral DHA supplementation in ΔF508 homozygous cystic fibrosis patients

Prostaglandins, leukotrienes and essential fatty acids, 2008-02, Vol.78 (2), p.109-115

2008

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Effect of Zinc Supplements in Cystic Fibrosis Patients

Annals of nutrition and metabolism, 2008-01, Vol.52 (2), p.152-156

2008

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Pre-emptive transjugular intrahepatic porto-systemic shunt (TIPSS) for portal hypertension from cystic fibrosis liver disease: 1 year evaluation

Journal of cystic fibrosis, 2010, Vol.9, p.S81-S81

2010

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The Forecast for Tomorrow is Not Only Based on the Weather of Today

Journal of pediatric gastroenterology and nutrition, 2002-10, Vol.35 (4), p.470-471

Robberecht, E.

2002

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The Forecast for Tomorrow is Not Only Based on the Weather of Today

Journal of pediatric gastroenterology and nutrition, 2002-10, Vol.35 (4), p.470-471

Robberecht, E.

2002

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Serum zinc concentrations in cystic fibrosis patients aged above 4 years: a cross-sectional evaluation

Biological trace element research, 2007-10, Vol.119 (1), p.19-26

2007

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The role of acceptance in psychological functioning in adolescents with cystic fibrosis: A preliminary study

Psychology & health, 2008-07, Vol.23 (5), p.629-638

2008

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Serum zinc in patients with cystic fibrosis at diagnosis and after one year of therapy

Biological trace element research, 2006-09, Vol.112 (3), p.205-211

2006

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Can quantitative ultrasound replace bone mineral assessment by DXA or pQCT in patients with cystic fibrosis?

Bone (New York, N.Y.), 2009-07, Vol.45, p.S73-S74

2009

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Quantitative ultrasound results at the fore-arm are independent of anthropometry in children and adolescents with cystic fibrosis

Bone (New York, N.Y.), 2007-06, Vol.40 (6), p.S37-S38

2007

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Successful liver transplantation for argininosuccinate lyase deficiency (ASLD)

Journal of inherited metabolic disease, 2006-02, Vol.29 (1), p.184-185

2006

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Fatty acid status in patients with CF-related liver disease

Journal of cystic fibrosis, 2008-06, Vol.7, p.S80-S80

2008

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Clinical effect of long term oral DHA supplementation in cystic fibrosis patients

Journal of cystic fibrosis, 2008-06, Vol.7, p.S93-S93

2008

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Cystic fibrosis presenting as diabetes insipidus unresponsive to desmopressin

Acta gastro-enterologica belgica, 2007-07, Vol.70 (3), p.300-301

2007

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Highlights of the ESPEN‐ESPGHAN‐ECFS Guidelines on Nutrition Care for Infants and Children With Cystic Fibrosis

Journal of pediatric gastroenterology and nutrition, 2016-12, Vol.63 (6), p.671-675

2016

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Docosahexaenoic acid trials in cystic fibrosis: A review of the rationale behind the clinical trials

Journal of cystic fibrosis, 2005-03, Vol.4 (1), p.27-34

2005

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339 The role of acceptance in adolescents with cystic fibrosis

Journal of cystic fibrosis, 2007, Vol.6, p.S83-S83

2007

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238 Relation between fatty acid (FA) composition and clinical status/genotype in CF?

Journal of cystic fibrosis, 2007, Vol.6, p.S59-S59

2007

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236 Serum zinc concentrations of the CF population above the age of 4 years: a cross-sectional evaluation

Journal of cystic fibrosis, 2007, Vol.6, p.S58-S58

2007

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Hypocalcaemic seizures : sign of intestinal disease ?

Acta gastro-enterologica belgica, 2007-04, Vol.70 (2), p.243-244

2007

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Defining DIOS and constipation in cystic fibrosis: a multicenter study on the incidence characteristics and treatment of DIOS

Journal of cystic fibrosis, 2008-06, Vol.7, p.S79-S79

2008

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Nutrition in patients with cystic fibrosis: a European Consensus

Sunlight is an important determinant of vitamin D serum concentrations in cystic fibrosis

EPS3.5 Probiotics in cystic fibrosis (CF) patients: a double blind cross-over study

ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis

Oral DHA supplementation in ΔF508 homozygous cystic fibrosis patients

Effect of Zinc Supplements in Cystic Fibrosis Patients

Pre-emptive transjugular intrahepatic porto-systemic shunt (TIPSS) for portal hypertension from cystic fibrosis liver disease: 1 year evaluation

The Forecast for Tomorrow is Not Only Based on the Weather of Today

The Forecast for Tomorrow is Not Only Based on the Weather of Today

Serum zinc concentrations in cystic fibrosis patients aged above 4 years: a cross-sectional evaluation

The role of acceptance in psychological functioning in adolescents with cystic fibrosis: A preliminary study

Serum zinc in patients with cystic fibrosis at diagnosis and after one year of therapy

Can quantitative ultrasound replace bone mineral assessment by DXA or pQCT in patients with cystic fibrosis?

Quantitative ultrasound results at the fore-arm are independent of anthropometry in children and adolescents with cystic fibrosis

Successful liver transplantation for argininosuccinate lyase deficiency (ASLD)

Fatty acid status in patients with CF-related liver disease

Clinical effect of long term oral DHA supplementation in cystic fibrosis patients

Cystic fibrosis presenting as diabetes insipidus unresponsive to desmopressin

Highlights of the ESPEN‐ESPGHAN‐ECFS Guidelines on Nutrition Care for Infants and Children With Cystic Fibrosis

Docosahexaenoic acid trials in cystic fibrosis: A review of the rationale behind the clinical trials

339 The role of acceptance in adolescents with cystic fibrosis

238 Relation between fatty acid (FA) composition and clinical status/genotype in CF?

236 Serum zinc concentrations of the CF population above the age of 4 years: a cross-sectional evaluation

Hypocalcaemic seizures : sign of intestinal disease ?

Defining DIOS and constipation in cystic fibrosis: a multicenter study on the incidence characteristics and treatment of DIOS

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