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Literature DB >> 5785189

Ventilatory function in infants with cystic fibrosis. Physiological assessment of halation therapy.

P D Phelan, M Gracey, H E Williams, C M Anderson.

Abstract

Entities: Disease Species

Mesh：

Substances：
Anti-Bacterial Agents

Year: 1969 PMID： 5785189 PMCID： PMC2020304 DOI： 10.1136/adc.44.235.393

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

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19 in total

1. IMPROVED TECHNIQUE FOR ESTIMATING PLEURAL PRESSURE FROM ESOPHAGEAL BALLOONS.

Authors: J MILIC-EMILI; J MEAD; J M TURNER; E M GLAUSER
Journal: J Appl Physiol Date: 1964-03 Impact factor: 3.531

2. 'Sweat test' results in normal persons of different ages compared with families with fibrocystic disease of the pancreas.

Authors: C M ANDERSON; M FREEMAN
Journal: Arch Dis Child Date: 1960-12 Impact factor: 3.791

3. Importance of particle size in aerosol therapy.

Authors: F W LOVEJOY; H CONSTANTINE; L DAUTREBANDE
Journal: Proc Soc Exp Biol Med Date: 1960-04

4. Pulmonary function in cystic fibrosis of the pancreas.

Authors: J R WEST; S M LEVIN; P A DI SANT'AGNESE
Journal: Pediatrics Date: 1954-02 Impact factor: 7.124

5. The respiratory rate and ventilation in the newborn baby.

Authors: K W CROSS
Journal: J Physiol Date: 1949-09 Impact factor: 5.182

6. Obstructive disease of the airways in cystic fibrosis.

Authors: R B Mellins; O R Levin; R H Ingram; A P Fishman
Journal: Pediatrics Date: 1968-03 Impact factor: 7.124

7. Observations in cystic fibrosis of the pancreas. 3. Pulmonary lesions.

Authors: J R Esterly; E H Oppenheimer
Journal: Johns Hopkins Med J Date: 1968-02

8. Evaluation of a prophylactic and therapeutic program for patients with cystic fibrosis.

Authors: C F Doershuk; L W Matthews; A S Tucker; S Spector
Journal: Pediatrics Date: 1965-11 Impact factor: 7.124

9. Mist tent therapy of the obstructive pulmonary lesion of cystic fibrosis.

Authors: L W Matthews; C F Doershuk; S Spector
Journal: Pediatrics Date: 1967-02 Impact factor: 7.124

10. Studies of respiratory physiology in children. II. Lung volumes and mechanics of respiration in 64 patients with cystic fibrosis of the pancreas.

Authors: C D COOK; P J HELLIESEN; L KULCZYCKI; H BARRIE; L FRIEDLANDER; S AGATHON; G B HARRIS; H SHWACHMAN
Journal: Pediatrics Date: 1959-08 Impact factor: 7.124

19 in total

1. Respiratory function after repair of congenital diaphragmatic hernia.

Authors: L I Landau; P D Phelan; G L Gillam; E Coombs; H R Noblett
Journal: Arch Dis Child Date: 1977-04 Impact factor: 3.791

2. Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints.

Authors: Stephanie D Davis; Margaret Rosenfeld; Gwendolyn S Kerby; Lyndia Brumback; Margaret H Kloster; James D Acton; Andrew A Colin; Carol K Conrad; Meeghan A Hart; Peter W Hiatt; Peter J Mogayzel; Robin C Johnson; Stephanie L Wilcox; Robert G Castile
Journal: Am J Respir Crit Care Med Date: 2010-07-09 Impact factor: 21.405

Review 7. Aerosol therapy in cystic fibrosis.

Authors: M B Mearns
Journal: Arch Dis Child Date: 1970-10 Impact factor: 3.791

Ventilatory function in infants with cystic fibrosis. Physiological assessment of halation therapy.

1. IMPROVED TECHNIQUE FOR ESTIMATING PLEURAL PRESSURE FROM ESOPHAGEAL BALLOONS.

2. 'Sweat test' results in normal persons of different ages compared with families with fibrocystic disease of the pancreas.

3. Importance of particle size in aerosol therapy.

4. Pulmonary function in cystic fibrosis of the pancreas.

5. The respiratory rate and ventilation in the newborn baby.

6. Obstructive disease of the airways in cystic fibrosis.

7. Observations in cystic fibrosis of the pancreas. 3. Pulmonary lesions.

8. Evaluation of a prophylactic and therapeutic program for patients with cystic fibrosis.

9. Mist tent therapy of the obstructive pulmonary lesion of cystic fibrosis.

10. Studies of respiratory physiology in children. II. Lung volumes and mechanics of respiration in 64 patients with cystic fibrosis of the pancreas.

1. Respiratory function after repair of congenital diaphragmatic hernia.

2. Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints.

3. Good outcome after prolonged ventilation in an infant with cystic fibrosis.

4. Management of the chest in cystic fibrosis.

5. Lung function in infants with cystic fibrosis.

6. Influence of mist tent therapy on sputum viscosity and water content in cystic fibrosis.

Review 7. Aerosol therapy in cystic fibrosis.

Review 8. Monitoring early inflammation in CF. Infant pulmonary function testing.

9. Early airway infection, inflammation, and lung function in cystic fibrosis.

10. Serial lung function studies in cystic fibrosis in the first 5 years of life.