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A G Davidson

Showing results (41-50 of 85) with videos related to

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Archives of Disease in Childhood|January 1, 1973
Muscular performance in cystic fibrosis patients and its relation to vitamin EC W Darby, A G Davidson, I D Desai
Journal of Clinical Pathology|May 1, 1995
Selective media for isolation of Burkholderia (Pseudomonas) cepacia from the respiratory secretions of patients with cystic fibrosisN Cimolai, C Trombley, A G Davidson, et al.
The Journal of Pediatrics|June 8, 2001
Long-term comparative trial of positive expiratory pressure versus oscillating positive expiratory pressure (flutter) physiotherapy in the treatment of cystic fibrosisP M McIlwaine, L T Wong, D Peacock, et al.
Biochemical and Biophysical Research Communications|June 29, 1978
Anti-plasmin (alpha2-macroglobulin) activity of plasma from cystic fibrosis patientsH Choy, D A Applegarth, A G Davidson, et al.
Lancet (London, England)|December 15, 1973
Letter: Carcinoembryonic antigen in cystic fibrosisA G Davidson, E K Mincey, S Israels, et al.
Pediatric Research|May 1, 1984
Abnormal anion exchange mechanism operates in the sweat glands of cystic fibrosis patientsD A Applegarth, A G Davidson, P Sorenson, et al.
Canadian Medical Association Journal|March 22, 1975
Letter: Screening for hereditary metabolic diseaseD F Hardwick, D A Applegarth, A G Davidson, et al.
Bone Marrow Transplantation|August 1, 1994
Bone marrow transplantation in Gaucher's disease: effect of mixed chimeric stateK W Chan, L T Wong, D Applegarth, et al.
The American Journal of Gastroenterology|November 1, 1993
Barrett's esophagus in children with cystic fibrosis: not a coincidental associationE Hassall, D M Israel, A G Davidson, et al.
The Journal of Pediatrics|June 1, 1989
Communicability of Pseudomonas infections in patients with cystic fibrosisD P Speert, A G Davidson, L T Wong, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Archives of Disease in Childhood|January 1, 1973
Muscular performance in cystic fibrosis patients and its relation to vitamin EC W Darby, A G Davidson, I D Desai
Journal of Clinical Pathology|May 1, 1995
Selective media for isolation of Burkholderia (Pseudomonas) cepacia from the respiratory secretions of patients with cystic fibrosisN Cimolai, C Trombley, A G Davidson, et al.
The Journal of Pediatrics|June 8, 2001
Long-term comparative trial of positive expiratory pressure versus oscillating positive expiratory pressure (flutter) physiotherapy in the treatment of cystic fibrosisP M McIlwaine, L T Wong, D Peacock, et al.
Biochemical and Biophysical Research Communications|June 29, 1978
Anti-plasmin (alpha2-macroglobulin) activity of plasma from cystic fibrosis patientsH Choy, D A Applegarth, A G Davidson, et al.
Lancet (London, England)|December 15, 1973
Letter: Carcinoembryonic antigen in cystic fibrosisA G Davidson, E K Mincey, S Israels, et al.
Pediatric Research|May 1, 1984
Abnormal anion exchange mechanism operates in the sweat glands of cystic fibrosis patientsD A Applegarth, A G Davidson, P Sorenson, et al.
Canadian Medical Association Journal|March 22, 1975
Letter: Screening for hereditary metabolic diseaseD F Hardwick, D A Applegarth, A G Davidson, et al.
Bone Marrow Transplantation|August 1, 1994
Bone marrow transplantation in Gaucher's disease: effect of mixed chimeric stateK W Chan, L T Wong, D Applegarth, et al.
The American Journal of Gastroenterology|November 1, 1993
Barrett's esophagus in children with cystic fibrosis: not a coincidental associationE Hassall, D M Israel, A G Davidson, et al.
The Journal of Pediatrics|June 1, 1989
Communicability of Pseudomonas infections in patients with cystic fibrosisD P Speert, A G Davidson, L T Wong, et al.
Pageof 9