✦ LIBER ✦

Self-hypnosis for patients with cystic fibrosis

✍ Scribed by Ran D. Anbar

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 31 KB
Volume: 30
Category: Article
ISSN: 8755-6863
DOI: 10.1002/1099-0496(200012)30:6<461::aid-ppul4>3.0.co;2-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Quality of life in patients with cystic

Quality of life in patients with cystic fibrosis

✍ Wietze de Jong; Adrian A. Kaptein; Cees P. van der Schans; Gregor P. M. Mannes; 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 56 KB 👁 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

Cystic fibrosis: A guide for patient and

Cystic fibrosis: A guide for patient and family

✍ Mary M. Kontos 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 18 KB

Left ventricular perfusion deficit in pa

Left ventricular perfusion deficit in patients with cystic fibrosis

✍ Daniel De Wolf; P. Franken; A. Piepsz; I. Dab 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 37 KB 👁 1 views

Left ventricular failure is not considered an important feature in cystic fibrosis (CF), but abnormalities of left ventricular function have been reported. Except for a few cases of heart failure in neonates with CF, there is no evidence of a primary disorder of the myocardium in patients with CF. S

Upregulation of RANTES in nasal polyps f

Upregulation of RANTES in nasal polyps from patients with cystic fibrosis

✍ Victor I. Scapa; Vijay R. Ramakrishnan; Pamela A. Mudd; Todd T. Kingdom 📂 Article 📅 2011 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 160 KB

Missense mutations in the cystic fibrosi

Missense mutations in the cystic fibrosis gene in adult patients with asthma

✍ Conxi Lázaro; Rafael de Cid; Jordi Sunyer; Joan Soriano; Javier Giménez; Mónica 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 293 KB 👁 1 views

Asthma is a complex genetic disorder that affects 5% of adults and 10% of children worldwide. The complete characterization of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified missense mutations in 15% of 144 unrelated adult patients with asthma, but in none of 41 subje

Decreased concentration of exhaled nitri

Decreased concentration of exhaled nitric oxide (NO) in patients with cystic fibrosis

✍ H. Grasemann; E. Michler; M. Wallot; F. Ratjen 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 56 KB 👁 1 views

Nitric oxide (NO) is produced by various cell types in the human respiratory tract. Endogenously produced nitric oxide is detectable in the exhaled air of healthy individuals. Exhaled NO has been shown to be increased in airway inflammation, most probably due to cytokine-mediated activation of NO sy