Professor, Pediatrics, University of Minnesota Medical School
Pediatric Pulmonology
Dr. Warren J. Warwick, MD
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Warren Warwick practices Pediatric Pulmonology. He researched medicine at University of Minnesota Medical School. University of Minnesota Medical School is ranked 40/10 in Research/PrimaryCare. Doctor Warren J. Warwick, MD is a published doctor and has 99 publications published. The lastest was: 'Chest calipers for measurement of the thoracic index.'
Publications
- High-frequency and low-frequency chest compression: effects on lung water secretion, mucus transport, heart rate, and blood pressure using a trapezoidal source pressur...
- A simulation tool to study high-frequency chest compression energy transfer mechanisms and waveforms for pulmonary disease applications.
- The trapezoid waveform high frequency chest compression therapy increases water secretion by the cystic fibrosis respiratory epithelium.
- Detecting changes in respiratory patterns in high frequency chest compression therapy by single-channel blind source separation.
- Free-knot spline model for analysis of pulmonary function.
- Induced respiratory system modeling by high frequency chest compression using lumped system identification method.
- Waveforms of high-frequency chest compression systems change with jacket, body.
- The comparison of three high-frequency chest compression devices.
- High frequency chest compression effects on cardio-respiratory interaction.
- High frequency chest compression effects heart rate variability.
- Two models of high frequency chest compression therapy: interaction of jacket pressure and mouth airflow.
- Different frequencies should be prescribed for different high frequency chest compression machines.
- Comparison of expectorated sputum after manual chest physical therapy and high-frequency chest compression.
- High-frequency chest compression: effect of the third generation compression waveform.
- Surgical experience in patients with cystic fibrosis: a 25-year perspective.
- Linkage between the loci for cystic fibrosis and paraoxonase.
- Bronchoscopy and lavage in management of pulmonary complications of cystic fibrosis.
- Alcohol, drugs and AIDS-related risks: results from a prospective study.
- Pediatric lung and heart-lung transplantation at the University of Minnesota.
- MEASLES VIRUS VACCINATION.
- Editorial: Heredity vs. environment.
- Amyloidosis as a complication of cystic fibrosis.
- Secondary (AA) amyloidosis in cystic fibrosis. A report of three cases.
- Modeled velocity of airflow in the airways during various respiratory patterns.
- Serum fatty acid profiles in cystic fibrosis patients and their parents.
- High-strength pancreatic enzymes.
- Cystic fibrosis-associated colitis and fibrosing colonopathy.
- Cooperative study comparing three methods of performing sweat tests to diagnose cystic fibrosis.
- Undiagnosed patients with cystic fibrosis.
- Pulmonary function in healthy Minnesota children. Forced expiratory flow volume studies.
- Ascertainment of CF in Minnesota.
- Clindamycin therapy of staphylococcal pulmonary infections in patients with cystic fibrosis.
- Axonal dystrophy in the gracile nucleus in congenital biliary atresia and cystic fibrosis (mucoviscidosis): beneficial effect of vitamin E therapy.
- Comparison of two forms of enteric-coated pancrelipase In six teenagers with cystic fibrosis.
- Erythrocyte indices in cystic fibrosis.
- Cystic fibrosis and meconium ileus.
- Mechanisms of mucous transport.
- Cystic fibrosis: mutations at more than one locus?
- Dietary supplements in cystic fibrosis.
- Sweat chloride assay for cystic fibrosis. Using pilocarpine iontophoresis stimulation, filter paper collection and cotlove chloridometer analysis.
- Life table studies of mortality.
- Cystic fibrosis: nature and prognosis.
- The involvement of the labial mucous salivary gland in patients with cystic fibrosis. II. The heterozygote state.
- Cystic fibrosis sweat test for newborns.
- A fluorometric micro method for serum tocopherol.
- Planning perfect children.
- Annotation on life.
- Early diagnosis of cystic fibrosis.
- Respiratory complications of cystic fibrosis. Prevention.
- Cystic fibrosis. A new challenge to internal medicine.
- How cystic fibrosis can be confused with chronic bronchitis and bronchial asthma.
- Chronic respiratory disease in children.
- Pneumothorax in cystic fibrosis.
- The unborn patient.
- Phenylketonuria and the practice of medicine.
- A fluorometric micromethod for serum vitamins A and E.
- A fluorometric micromethod for liver vitamin A.
- A fluorometric micromethod for serum vitamin A.
- The prognosis for children with cystic fibrosis based on reasoned approaches to therapy: past, present, and future.
- Sweat chloride analysis by chloride ion-specific electrode method using heat stimulation.
- Cystic fibrosis detection clinic program in Minnesota.
- A fluorometric micro method for fat tocopherol.
- Cystic fibrosis presenting with severe hemorrhage due to vitamin K malabsorption: a report of three cases.
- Editorials. Family practice and specialty practice.
- A universal chart for the chronological graphing of any anatomical, biochemical or physiological parameters that have a normal or log-normal distribution.
- Multinodular hemangiomatosis of the liver in infancy.
- Water vapour pressure in expired air.
- Red cell glutathione and glutathione reductase in cystic fibrosis.
- Cancer risk among patients with cystic fibrosis.
- The long-term effect of high-frequency chest compression therapy on pulmonary complications of cystic fibrosis.
- The impact of home monitoring and daily diary recording on patient status in cystic fibrosis.
- Clinical observations on the biliary system in cystic fibrosis.
- Letter: Serum glutathione reductase and cystic fibrosis.
- Survival patterns in cyctic fibrosis.
- Letter: The end-expiratory to arterial carbon dioxide tension ratio in acute pulmonary embolism.
- Insulin iontophoresis in cystic fibrosis.
- Chest calipers for measurement of the thoracic index.
- Pulmonary function in healthy Minnesota children.
- Reassessment of the diagnostic value of the vectorcardiogram in cystic fibrosis (correlation with clinical score, pulmonary function tests and echocardiogram).
- Estimation of fraction of perfused lung.
- Absorption of vitamin A in patients with cystic fibrosis. Absorption is best with emulsified vitamin A alcohol.
- An improved assay method for serum vitamins A and E using fluorometry.
- Measurement of chloride in sweat with the chloride-selective electrode.
- Measurement of total lung capacity by a roentgenography-planimetry method in children 4-16 years of age.
- Open thoracotomy and pleural abrasion in the treatment of spontaneous pneumothorax in cystic fibrosis.
- The incidence of cystic fibrosis in Caucasian populations.
- Measurement of chloride in sweat by use of a selective electrode and strip-chart recorder.
- Doubling time alpha-aminoisobutyrate transport and calcium exchange in cultured fibroblasts from cystic fibrosis and control subjects.
- Cystic fibrosis. An expanding challenge for internal medicine.
- Comparison of the errors due to the use of gauze and the use of filter paper in the gravimetric chloride titration sweat test.
- Comparison of the chloride electrode and gravimetric chloride titration sweat tests.
- Gallbladder disease in cystic fibrosis.
- Spine deformities and cystic fibrosis.
- Frequency of the delta Phe508 mutation and correlation with XV.2c/KM-19 haplotypes in an American population of cystic fibrosis patients: results of a collaborative st...
- Reduction of sputum Pseudomonas aeruginosa density by antibiotics improves lung function in cystic fibrosis more than do bronchodilators and chest physiotherapy alone.
- High-frequency chest compression system to aid in clearance of mucus from the lung.
- Thoracic duct opacification for CT scanning.
- Operative therapy of gallbladder disease in patients with cystic fibrosis.
Schools
University of Mn Med Sch
Doctors Specialties
- Pulmonology
- Pediatric Pulmonology
Accepted Insurances
Education
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University of Minnesota at Fairview -
University of Minnesota Medical School
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