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D A Reardon

Showing results (1-10 of 21) with videos related to

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The American Journal of Pediatric Hematology/Oncology|January 1, 1991
Virus-associated hemophagocytic syndrome following bone marrow transplantationD A Reardon, R Roskos, C A Hanson, et al.
Genomics|June 20, 1998
Chromosomal localization of the human smoothened gene (SMOH) to 7q32. 3 by fluorescence in situ hybridization and radiation hybrid mappingJ E Sublett, R E Entrekin, A T Look, et al.
Blood|July 15, 1992
Detection of circulating donor white blood cells in patients receiving multiple transfusionsP T Adams, R D Davenport, D A Reardon, et al.
Cancer|March 1, 1994
Lineage switch in Philadelphia chromosome-positive acute lymphoblastic leukemiaD A Reardon, C A Hanson, M S Roth, et al.
Neurology|March 29, 2007
Neurofibromatosis type 2S Sathornsumetee, A DesJardins, D A Reardon, et al.
The British Journal of Radiology|October 21, 2010
Prognostic significance of parameters derived from co-registered 18F-fluorodeoxyglucose PET and contrast-enhanced MRI in patients with high-grade gliomaM J Paldino, T Z Wong, D A Reardon, et al.
Pediatric Neurosurgery|August 15, 2000
Multiple genomic alterations including N-myc amplification in a primary large cell medulloblastomaD A Reardon, J J Jenkins, J E Sublett, et al.
Pediatric Neurosurgery|April 15, 1999
High-grade pediatric spinal cord tumorsT E Merchant, D Nguyen, S J Thompson, et al.
AJNR. American Journal of Neuroradiology|April 28, 2022
Radiomics-Based Machine Learning for Outcome Prediction in a Multicenter Phase II Study of Programmed Death-Ligand 1 Inhibition Immunotherapy for GlioblastomaE George, E Flagg, K Chang, et al.
Genes, Chromosomes & Cancer|August 19, 1999
Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymomaD A Reardon, R E Entrekin, J Sublett, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
The American Journal of Pediatric Hematology/Oncology|January 1, 1991
Virus-associated hemophagocytic syndrome following bone marrow transplantationD A Reardon, R Roskos, C A Hanson, et al.
Genomics|June 20, 1998
Chromosomal localization of the human smoothened gene (SMOH) to 7q32. 3 by fluorescence in situ hybridization and radiation hybrid mappingJ E Sublett, R E Entrekin, A T Look, et al.
Blood|July 15, 1992
Detection of circulating donor white blood cells in patients receiving multiple transfusionsP T Adams, R D Davenport, D A Reardon, et al.
Cancer|March 1, 1994
Lineage switch in Philadelphia chromosome-positive acute lymphoblastic leukemiaD A Reardon, C A Hanson, M S Roth, et al.
Neurology|March 29, 2007
Neurofibromatosis type 2S Sathornsumetee, A DesJardins, D A Reardon, et al.
The British Journal of Radiology|October 21, 2010
Prognostic significance of parameters derived from co-registered 18F-fluorodeoxyglucose PET and contrast-enhanced MRI in patients with high-grade gliomaM J Paldino, T Z Wong, D A Reardon, et al.
Pediatric Neurosurgery|August 15, 2000
Multiple genomic alterations including N-myc amplification in a primary large cell medulloblastomaD A Reardon, J J Jenkins, J E Sublett, et al.
Pediatric Neurosurgery|April 15, 1999
High-grade pediatric spinal cord tumorsT E Merchant, D Nguyen, S J Thompson, et al.
AJNR. American Journal of Neuroradiology|April 28, 2022
Radiomics-Based Machine Learning for Outcome Prediction in a Multicenter Phase II Study of Programmed Death-Ligand 1 Inhibition Immunotherapy for GlioblastomaE George, E Flagg, K Chang, et al.
Genes, Chromosomes & Cancer|August 19, 1999
Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymomaD A Reardon, R E Entrekin, J Sublett, et al.
Pageof 3