Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The adolescent growth spurt in children with cystic fibrosis.

Annals of human biology - 1 Jan 2000

Byard P J

Abstract excerpt

The adolescent spurt in 230 children with cystic fibrosis (CF) treated at the Cleveland CF centre in northeastern Ohio was compared to that found in normal children from the Fels Longitudinal Growth Study in southwestern Ohio. The Preece-Baines Model 1 (PB1) growth equation was applied to longitudinal height data from both samples to describe a large number of data points for each child in terms of a few...

Topics

Adolescent
Child
Cystic Fibrosis
Female
Genotype
Growth
Humans
Longitudinal Studies
Lung
Male
Reference Values

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8060112
DOI: 10.1080/03014469400003242

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-8060112-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

The adolescent growth spurt in children with cystic fibrosis.PMID 8060112Read ↗

Growth trajectories in Pediatric Cystic Fibrosis Population on Elexacaftor-Tezacaftor-Ivacaftor: Real-Life DataSemantic proximity Read ↗

Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis.Semantic proximity Read ↗

Growth and nutritional status in children and adolescents with cystic fibrosis.Semantic proximity Read ↗

Growth in prepubertal children with cystic fibrosis, homozygous for the Delta F508 mutation.Semantic proximity Read ↗

Increased rate of lung function decline in Australian adolescents with cystic fibrosis.Semantic proximity Read ↗

Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection.Semantic proximity Read ↗

Delayed puberty in girls with cystic fibrosis despite good clinical status.Semantic proximity Read ↗

Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.