Recombinant growth hormone therapy for cystic fibrosis in children and young adults (Q24202203)

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Alexandra L Haagensen

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Ben Carter

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Brian W Houston

Cochrane Database of Systematic Reviews

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language of work or name

English

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publication date

2013

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published in

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volume

6

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page(s)

CD008901

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cites work

Recombinant growth hormone therapy for cystic fibrosis in children and young adults

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Quantitating the effect of cystic fibrosis on linear growth by mathematical modelling of longitudinal growth curves

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Effect of growth hormone on exercise tolerance in children with cystic fibrosis.

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Effect of growth hormone therapy on nitric oxide formation in cystic fibrosis patients

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Anabolic effects of growth hormone treatment in young children with cystic fibrosis.

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Effects of glutamine and recombinant human growth hormone on protein metabolism in prepubertal children with cystic fibrosis

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Effects of megestrol acetate on weight gain, body composition, and pulmonary function in patients with cystic fibrosis

21 January 2018

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Growth hormone improves weight velocity and height velocity in prepubertal children with cystic fibrosis

21 January 2018

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Effect of insulinlike growth factor-1 treatment in children with cystic fibrosis

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Incidence of diabetes mellitus and impaired glucose tolerance in children and adolescents receiving growth-hormone treatment.

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Evaluation of body mass index percentiles for assessment of malnutrition in children with cystic fibrosis.

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Growth hormone decreases protein catabolism in children with cystic fibrosis

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Nutritional Rehabilitation in Cystic Fibrosis

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Growth hormone normalizes pubertal onset in children with cystic fibrosis

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Anabolic effect of biosynthetic growth hormone in cystic fibrosis patients

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Growth hormone treatment improves growth and clinical status in prepubertal children with cystic fibrosis: results of a multicenter randomized controlled trial

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Dinucleotide repeat in the insulin-like growth factor-I gene is not related to risk of colorectal adenoma

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12 December 2020

Prospective evaluation of growth, nutritional status, and body composition in children with cystic fibrosis

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Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis

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