𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Role of progestational agents in the treatment of undernourished patients with cystic fibrosis

✍ Scribed by Dana G. Kissner


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
52 KB
Volume
29
Category
Article
ISSN
8755-6863

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Quality of life in patients with cystic
✍ Wietze de Jong; Adrian A. Kaptein; Cees P. van der Schans; Gregor P. M. Mannes; πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 56 KB πŸ‘ 2 views

The majority of patients with cystic fibrosis (CF) will grow into adulthood. Despite this improvement in survival, the disease is progressive, especially with respect to the decline in pulmonary function, which in turn may have an impact on a patient's quality of life. In this study we evaluated the

Treatment of anorexia and weight loss wi
✍ Samya Z. Nasr; Martin E. Hurwitz; Randall W. Brown; Mahmoud Elghoroury; David Ro πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 22 KB πŸ‘ 1 views

Four patients with severe cystic fibrosis lung disease, anorexia and weight loss, received Megestrol Acetate (MA), as an appetite stimulant. The initial dose was 400-800 mg daily and was continued for 6-15 months. Appetite was improved, with significant weight gain in all patients and an increase in

Is the spectrum of mutations in Indian p
✍ Kabra, Madhulika ;Kabra, S.K. ;Ghosh, Manju ;Khanna, Aarti ;Arora, Sadhana ;Meno πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 165 KB

The suggested incidence of cystic fibrosis (CF) in Asian migrants (Indians and Pakistanis) in the United Kingdom is about 1 in 10,000 to 12,000 [Goodchild et al., 1974]. There are no large studies on CF in Asian Indians. The disorder is thought to be rare and most studies from the Asian subcontinent

Improved survival in the Danish center-t
✍ Birgitte Frederiksen; Susanne Lanng; Christian Koch; Niels HΓΈlby πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 493 KB πŸ‘ 1 views

We report survival data for Danish center-treated cystic fibrosis (CF) patients, covering the period 1974-1 993 and using cross-sectional cumulative survival probability based on annual age-specific mortality rates. Analyses by age and by years after diagnosis were made. No significant differences w