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Results: 1-14 |
Results: 14
PROTEINASE-FREE MYELOPEROXIDASE INCREASES AIRWAY EPITHELIAL PERMEABILITY IN A WHOLE TRACHEA MODEL
Authors: REGELMANN WE SCHNEIDER LA FAHRENKRUG SC GRAY BH JOHNSON S HERRON JM CLAWSON CC CLAWSON DJ WANGENSTEEN OD
Citation: We. Regelmann et al., PROTEINASE-FREE MYELOPEROXIDASE INCREASES AIRWAY EPITHELIAL PERMEABILITY IN A WHOLE TRACHEA MODEL, Pediatric pulmonology, 24(1), 1997, pp. 29-34
TO THE EDITOR - ASPERGILLUS ORGANISMS IN PATIENTS WITH CYSTIC-FIBROSIS - REPLY
Authors: MILLA CE REGELMANN WE
Citation: Ce. Milla et We. Regelmann, TO THE EDITOR - ASPERGILLUS ORGANISMS IN PATIENTS WITH CYSTIC-FIBROSIS - REPLY, Pediatric pulmonology, 23(4), 1997, pp. 318-318
PCR RIBOTYPING AND ENDONUCLEASE SUBTYPING IN THE EPIDEMIOLOGY OF BURKHOLDERIA-CEPACIO INFECTION
Authors: SHREVE MR JOHNSON SJ MILLA CE WIELINSKI CL REGELMANN WE
Citation: Mr. Shreve et al., PCR RIBOTYPING AND ENDONUCLEASE SUBTYPING IN THE EPIDEMIOLOGY OF BURKHOLDERIA-CEPACIO INFECTION, American journal of respiratory and critical care medicine, 155(3), 1997, pp. 984-989
EFFECT OF EOSINOPHIL PEROXIDASE ON AIRWAY EPITHELIAL PERMEABILITY IN THE GUINEA-PIG
Authors: BROTTMAN GM REGELMANN WE SLUNGAARD A WANGENSTEEN OD
Citation: Gm. Brottman et al., EFFECT OF EOSINOPHIL PEROXIDASE ON AIRWAY EPITHELIAL PERMEABILITY IN THE GUINEA-PIG, Pediatric pulmonology, 21(3), 1996, pp. 159-166
CLINICAL-SIGNIFICANCE OF THE RECOVERY OF ASPERGILLUS SPECIES FROM THERESPIRATORY SECRETIONS OF CYSTIC-FIBROSIS PATIENTS
Authors: MILLA CE WIELINSKI CL REGELMANN WE
Citation: Ce. Milla et al., CLINICAL-SIGNIFICANCE OF THE RECOVERY OF ASPERGILLUS SPECIES FROM THERESPIRATORY SECRETIONS OF CYSTIC-FIBROSIS PATIENTS, Pediatric pulmonology, 21(1), 1996, pp. 6-10
SPUTUM PEROXIDASE-ACTIVITY CORRELATES WITH THE SEVERITY OF LUNG-DISEASE IN CYSTIC-FIBROSIS
Authors: REGELMANN WE SIEFFERMAN CM HERRON JM ELLIOTT GR CLAWSON CC GRAY BH
Citation: We. Regelmann et al., SPUTUM PEROXIDASE-ACTIVITY CORRELATES WITH THE SEVERITY OF LUNG-DISEASE IN CYSTIC-FIBROSIS, Pediatric pulmonology, 19(1), 1995, pp. 1-9
DEVELOPMENT OF A NOVEL METHOD TO STUDY INTRAPHAGOCYTIC BACTERIAL KILLING
Authors: MILLA CE REGELMANN WE
Citation: Ce. Milla et We. Regelmann, DEVELOPMENT OF A NOVEL METHOD TO STUDY INTRAPHAGOCYTIC BACTERIAL KILLING, Pediatric research, 37(4), 1995, pp. 184-184
DELIVERY OF OXYGEN TO CHILDREN WITH LOWER RESPIRATORY-TRACT INFECTION
Authors: REGELMANN WE
Citation: We. Regelmann, DELIVERY OF OXYGEN TO CHILDREN WITH LOWER RESPIRATORY-TRACT INFECTION, The Journal of pediatrics, 127(3), 1995, pp. 427-428
ELASTIN DEGRADATION AND ITS INHIBITION BY CYSTIC-FIBROSIS BRONCHOALVEOLAR LAVAGE
Authors: REGELMANN AG GRAY BH HASEMAN JR REGELMANN WE
Citation: Ag. Regelmann et al., ELASTIN DEGRADATION AND ITS INHIBITION BY CYSTIC-FIBROSIS BRONCHOALVEOLAR LAVAGE, Pediatric research, 35(4), 1994, pp. 10000397-10000397
DIAGNOSING THE CAUSE OF RECURRENT AND PERSISTENT PNEUMONIA IN CHILDREN
Authors: REGELMANN WE
Citation: We. Regelmann, DIAGNOSING THE CAUSE OF RECURRENT AND PERSISTENT PNEUMONIA IN CHILDREN, Pediatric annals, 22(9), 1993, pp. 561
PROGNOSTIC IMPLICATIONS OF INITIAL OROPHARYNGEAL BACTERIAL-FLORA IN PATIENTS WITH CYSTIC-FIBROSIS DIAGNOSED BEFORE THE AGE OF 2 YEARS
Authors: HUDSON VL WIELINSKI CL REGELMANN WE
Citation: Vl. Hudson et al., PROGNOSTIC IMPLICATIONS OF INITIAL OROPHARYNGEAL BACTERIAL-FLORA IN PATIENTS WITH CYSTIC-FIBROSIS DIAGNOSED BEFORE THE AGE OF 2 YEARS, The Journal of pediatrics, 122(6), 1993, pp. 854-860
USE OF A NEGATIVE-PRESSURE TECHNIQUE ON TRANSBRONCHIAL BIOPSY SPECIMENS IN LUNG-TRANSPLANT RECIPIENTS
Authors: PRYOR M REGELMANN WE JESSURUN J WARWICK WJ
Citation: M. Pryor et al., USE OF A NEGATIVE-PRESSURE TECHNIQUE ON TRANSBRONCHIAL BIOPSY SPECIMENS IN LUNG-TRANSPLANT RECIPIENTS, The American review of respiratory disease, 147(4), 1993, pp. 338-338
COMPARISON OF THE DECLINE IN PULMONARY-FUNCTION IN DECEASED CYSTIC-FIBROSIS (CF) PATIENTS HOMOZYGOUS FOR THE DELTA-F508 MUTATION VERSUS COMPOUND HETEROZYGOTES FOR THE DELTA-F508 MUTATION
Authors: MILLA CE WIELINSKI C REGELMANN WE
Citation: Ce. Milla et al., COMPARISON OF THE DECLINE IN PULMONARY-FUNCTION IN DECEASED CYSTIC-FIBROSIS (CF) PATIENTS HOMOZYGOUS FOR THE DELTA-F508 MUTATION VERSUS COMPOUND HETEROZYGOTES FOR THE DELTA-F508 MUTATION, The American review of respiratory disease, 147(4), 1993, pp. 464-464
THE DISTRIBUTION OF THE DELTA-F508 MUTATION IN A GROUP OF DECEASED CYSTIC-FIBROSIS (CF) PATIENTS
Authors: MILLA CE REGELMANN WE WIELINSKI C
Citation: Ce. Milla et al., THE DISTRIBUTION OF THE DELTA-F508 MUTATION IN A GROUP OF DECEASED CYSTIC-FIBROSIS (CF) PATIENTS, The American review of respiratory disease, 147(4), 1993, pp. 579-579
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