Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis.
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Background and EpidemiologyEarly glucose abnormalities in cystic fibrosis are preceded by poor weight gain.Early attained weight and length predict growth faltering better than velocity measures in infants with CF.Growth and pulmonary outcomes during the first 2 y of life of breastfed and formula-fed infants diagnosed with cystic fibrosis through the Wisconsin Routine Newborn Screening ProgramRelationships among health-related quality of life, pulmonary health, and newborn screening for cystic fibrosis[Factors impacting the growth and nutritional status of cystic fibrosis patients younger than 10 years of age who did not undergo neonatal screening].Comparison of WHO and CDC growth charts in predicting pulmonary outcomes in cystic fibrosisNutritional outcomes following gastrostomy in children with cystic fibrosis.Genetic modifiers of nutritional status in cystic fibrosisPubertal Height Growth and Adult Height in Cystic Fibrosis After Newborn Screening.Pubertal height velocity and associations with prepubertal and adult heights in cystic fibrosisEarly Life Growth Trajectories in Cystic Fibrosis are Associated with Pulmonary Function at Age 6 YearsRisk factors for the progression of cystic fibrosis lung disease throughout childhood.Update in cystic fibrosis 2009.Nutritional considerations in patients with cystic fibrosis.Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life.Cystic fibrosis related diabetes (CFRD)--the end stage of progressive insulin deficiency.Staphylococcus aureus in early cystic fibrosis lung disease.Cystic fibrosis newborn screening: a model for neuromuscular disease screening?Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?Socioeconomic status and health outcomes: cystic fibrosis as a model.Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter Study.Early life growth patterns persist for 12 years and impact pulmonary outcomes in cystic fibrosis.Early diagnosis from newborn screening maximises survival in severe cystic fibrosis.
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P2860
Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis.
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article científic
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bilimsel makale
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scientific article published on February 2009
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vetenskaplig artikel
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videnskabelig artikel
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name
Recovery of birth weight z sco ...... children with cystic fibrosis.
@en
Recovery of birth weight z sco ...... children with cystic fibrosis.
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type
label
Recovery of birth weight z sco ...... children with cystic fibrosis.
@en
Recovery of birth weight z sco ...... children with cystic fibrosis.
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prefLabel
Recovery of birth weight z sco ...... children with cystic fibrosis.
@en
Recovery of birth weight z sco ...... children with cystic fibrosis.
@nl
P2093
P2860
P921
P356
P1433
P1476
Recovery of birth weight z sco ...... children with cystic fibrosis.
@en
P2093
Huichuan J Lai
Philip M Farrell
Suzanne M Shoff
Wisconsin Cystic Fibrosis Neonatal Screening Group
P2860
P304
P356
10.1542/PEDS.2007-3089
P407
P577
2009-02-01T00:00:00Z