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1
Phosphatidylcholine and Iysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S
Phosphatidylcholine and Iysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S
AH Chen | Cadmus journal ser | 2005
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2
Short-term protein intake and stimulation of protein synthesis in stunted children with cystic fibrosis
Short-term protein intake and stimulation of protein synthesis in stunted children with cystic fibrosis
VGM Geukers | Cadmus journal ser | 2005
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3
Comarison of the use of body mass index percentiles and percentage of ideal body weight to screen for malnutrition in children with cystic fibrosis
Comarison of the use of body mass index percentiles and percentage of ideal body weight to screen for malnutrition in children with cystic fibrosis
Z Zhang | Cadmus journal ser | 2004
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4
Antioxidant deficiency in cystic fibrosis, when is the right time to take action?
Antioxidant deficiency in cystic fibrosis, when is the right time to take action?
EI Back | Cadmus journal ser | 2004
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5
Lutein, zeaxanthin, macular pigment, and viaual function in adult cystic fibrosis patients
Lutein, zeaxanthin, macular pigment, and viaual function in adult cystic fibrosis patients
C Schupp | Cadmus journal ser | 2004
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6
Efficiency of calcium absorption is not compromised in clinically stable prepubertal and pubertal girls with cystic fibrosis
Efficiency of calcium absorption is not compromised in clinically stable prepubertal and pubertal girls with cystic fibrosis
KJ Schulze | Cadmus journal ser | 2003
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7
Improved antioxidant and fatty acid status of patients with cystic fibrosis after antioxidant supplementation is linked to improved lung function
Improved antioxidant and fatty acid status of patients with cystic fibrosis after antioxidant supplementation is linked to improved lung function
LG Wood | Cadmus journal ser | 2003
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8
Prevalence of vitamin K deficiency in cystic fibrosis
Prevalence of vitamin K deficiency in cystic fibrosis
M Rashid | Cadmus journal ser | 1999
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9
Energy and protein metabolism : Energy expenditure and substrate utilization in adults with cystic fibrosis and diabetes mellitus
Energy and protein metabolism : Energy expenditure and substrate utilization in adults with cystic fibrosis and diabetes mellitus
S.A. Ward | Cadmus journal ser | 1999
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10
Digestion : Fat malabsorption in cystic fibrosis patients receiving enzyme replacement therapy is due to impaired intestinal uptake of long-chain fat
Digestion : Fat malabsorption in cystic fibrosis patients receiving enzyme replacement therapy is due to impaired intestinal uptake of long-chain fat
M. Kalivianakis | Cadmus journal ser | 1999
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