RandyLChilcoteDO

PubMed

• Comparison of long-term outcome of children and adolescents with disseminated non-lymphoblastic non-Hodgkin lymphoma treated with COMP or daunomycin-COMP: A report fro...
  Sposto, R., Meadows, A. T., Chilcote, R. R., Steinherz, P. G., Kjeldsberg, C., Kadin, M. E., Krailo, M. D., Termuhlen, A. M., Morse, M., Siegel, S. E.> ;Med Pediatr Oncol. 2001 Nov
• Mediastinal germ cell tumor in a child with precocious puberty and Klinefelter syndrome.
  Bebb, G. G., Grannis, F. W., Paz, I. B., Slovak, M. L., Chilcote, R.> ;Ann Thorac Surg. 1998 Aug
• Primary lymphoepithelioma-like carcinoma of the lung in a child. Report of an Epstein-Barr virus-related neoplasm.
  Curcio, L. D., Cohen, J. S., Grannis, F. W., Paz, I. B., Chilcote, R., Weiss, L. M.> ;Chest. 1997 Jan
• Primary mediastinal large cell lymphoma in children: a report from the Childrens Cancer Group.
  Piira, T., Perkins, S. L., Anderson, J. R., Meadows, A. T., Chilcote, R. R., Kadin, M., Kjeldsberg, C. R.> ;Pediatr Pathol Lab Med. 1995 Jul 01
• Long-term follow-up of patients treated with COMP or LSA2L2 therapy for childhood non-Hodgkin's lymphoma: a report of CCG-551 from the Childrens Cancer Group.
  Anderson, J. R., Jenkin, R. D., Wilson, J. F., Kjeldsberg, C. R., Sposto, R., Chilcote, R. R., Coccia, P. F., Exelby, P. R., Siegel, S., Meadows, A. T.> ;J Clin Oncol. 1993 Jun
• Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines.
  Diaz, M. O., Ziemin, S., Le Beau, M. M., Pitha, P., Smith, S. D., Chilcote, R. R., Rowley, J. D.> ;Proc Natl Acad Sci U S A. 1988 Jul
• Similar efficacy of 6 and 18 months of therapy with four drugs (COMP) for localized non-Hodgkin's lymphoma of children: a report from the Childrens Cancer Study Group.
  Meadows, A. T., Sposto, R., Jenkin, R. D., Kersey, J. H., Chilcote, R. R., Siegel, S. E., Coccia, P. F., Rosenstock, J., Pringle, K. C., Stolar, C. J.> ;J Clin Oncol. 1989 Jan
• Demonstration of the deletion of a copy of the ankyrin gene in a patient with hereditary spherocytosis by in situ hybridization.
  Tse, W. T., Menninger, J. C., Ward, D. C., Chilcote, R. R., John, K. M., Lux, S. E., Forget, B. G.> ;Trans Assoc Am Physicians. 1990
• Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
  Lux, S. E., Tse, W. T., Menninger, J. C., John, K. M., Harris, P., Shalev, O., Chilcote, R. R., Marchesi, S. L., Watkins, P. C., Bennett, V.> ;Nature. 1990 Jun 21
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