Alexander Spock, M.D.
Affiliations: | Pediatric Pulmonary and Gastroenterology | Duke Medical School, Durham, NC, United States |
Website:
http://www.clementsfuneralservice.com/sitemaker/sites/Clemen1/obit.cgi?user=1428338SpockGoogle:
"Alexander Spock"Bio:
(1929 - 2014)
Children
Sign in to add traineeSalman Mroueh | fellowship/program director | 1985-1988 | Duke Medical School |
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Publications
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Highsmith WE, Friedman KJ, Burch LH, et al. (2005) A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides. Clinical Genetics. 68: 88-90 |
Spock A. (2005) Fifty-year perspective of "cystic fibrosis of the pancreas". Pediatric Radiology. 35: 735-8 |
Tucker JA, Spock A, Spicer SS, et al. (2003) Inspissation of pancreatic zymogen material in cystic fibrosis. Ultrastructural Pathology. 27: 323-35 |
Thompson RJ, Gustafson KE, Gil KM, et al. (1999) Change in the Psychological Adjustment of Children with Cystic Fibrosis or Sickle Cell Disease and Their Mothers Journal of Clinical Psychology in Medical Settings. 6: 373-392 |
Spock A. (1997) Pulmonary alveolar proteinosis. Pediatrics. 99: 756 |
Potts SB, Roggli VL, Spock A. (1995) Immunohistologic quantification of Pseudomonas aeruginosa in the tracheobronchial tree from patients with cystic fibrosis. Pediatric Pathology & Laboratory Medicine : Journal of the Society For Pediatric Pathology, Affiliated With the International Paediatric Pathology Association. 15: 707-21 |
Mroueh S, Spock A. (1994) Allergic bronchopulmonary aspergillosis in patients with cystic fibrosis. Chest. 105: 32-6 |
Thompson RJ, Gustafson KE, George LK, et al. (1994) Change over a 12-month period in the psychological adjustment of children and adolescents with cystic fibrosis. Journal of Pediatric Psychology. 19: 189-203 |
Thompson RJ, Gil KM, Gustafson KE, et al. (1994) Stability and change in the psychological adjustment of mothers of children and adolescents with cystic fibrosis and sickle cell disease. Journal of Pediatric Psychology. 19: 171-88 |
Highsmith WE, Burch LH, Zhou Z, et al. (1994) A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations. The New England Journal of Medicine. 331: 974-80 |