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Dieter Harms

Showing results (1-10 of 38) with videos related to

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The American Journal of Surgical Pathology|December 23, 2004
Juvenile xanthogranuloma in childhood and adolescence: a clinicopathologic study of 129 patients from the kiel pediatric tumor registryDirk Janssen, Dieter Harms
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 15, 2002
Induction of drug resistance in human rhabdomyosarcoma cell lines is associated with increased maturation: possible explanation for differentiation in recurrences?Ivo Leuschner, Thomas Heuer, Dieter Harms
Virchows Archiv : an International Journal of Pathology|May 23, 2006
Genetic clonality is a feature unifying nephroblastomas regardless of the variety of morphological subtypesBarbara Guertl, Ivo Leuschner, Dieter Harms, et al.
The American Journal of Surgical Pathology|April 27, 2007
Clonality in juvenile xanthogranulomaDirk Janssen, Regina Fölster-Holst, Dieter Harms, et al.
The Journal of Reproductive Medicine|July 30, 2005
Ovarian sex cord-stromal tumors in children and adolescentsDominik T Schneider, Gabriele Calaminus, Dieter Harms, et al.
Medical and Pediatric Oncology|January 29, 2002
Synchronous detection of a pulmonary papillary adenoma and lung metastases in a patient with osteosarcoma in relapseAndrea Neusuess, Alexander Claviez, Thomas Schroeter, et al.
Virchows Archiv : an International Journal of Pathology|August 12, 2003
Ovarian sex cord-stromal tumors--a clinicopathological study of 72 cases from the Kiel Pediatric Tumor RegistryDominik T Schneider, Ute Jänig, Gabriele Calaminus, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 8, 2003
p53 and mdm-2 expression in Rhabdomyosarcoma of childhood and adolescence: clinicopathologic study by the Kiel Pediatric Tumor Registry and the German Cooperative Soft Tissue Sarcoma StudyIvo Leuschner, Inken Langhans, Regina Schmitz, et al.
The American Journal of Pathology|February 25, 2003
Full-length telomerase reverse transcriptase messenger RNA is an independent prognostic factor in neuroblastomaMatthias Krams, Barbara Hero, Frank Berthold, et al.
Oncogene|January 16, 2004
Expression of the c-kit receptor characterizes a subset of neuroblastomas with favorable prognosisMatthias Krams, Reza Parwaresch, Bence Sipos, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
The American Journal of Surgical Pathology|December 23, 2004
Juvenile xanthogranuloma in childhood and adolescence: a clinicopathologic study of 129 patients from the kiel pediatric tumor registryDirk Janssen, Dieter Harms
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 15, 2002
Induction of drug resistance in human rhabdomyosarcoma cell lines is associated with increased maturation: possible explanation for differentiation in recurrences?Ivo Leuschner, Thomas Heuer, Dieter Harms
Virchows Archiv : an International Journal of Pathology|May 23, 2006
Genetic clonality is a feature unifying nephroblastomas regardless of the variety of morphological subtypesBarbara Guertl, Ivo Leuschner, Dieter Harms, et al.
The American Journal of Surgical Pathology|April 27, 2007
Clonality in juvenile xanthogranulomaDirk Janssen, Regina Fölster-Holst, Dieter Harms, et al.
The Journal of Reproductive Medicine|July 30, 2005
Ovarian sex cord-stromal tumors in children and adolescentsDominik T Schneider, Gabriele Calaminus, Dieter Harms, et al.
Medical and Pediatric Oncology|January 29, 2002
Synchronous detection of a pulmonary papillary adenoma and lung metastases in a patient with osteosarcoma in relapseAndrea Neusuess, Alexander Claviez, Thomas Schroeter, et al.
Virchows Archiv : an International Journal of Pathology|August 12, 2003
Ovarian sex cord-stromal tumors--a clinicopathological study of 72 cases from the Kiel Pediatric Tumor RegistryDominik T Schneider, Ute Jänig, Gabriele Calaminus, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 8, 2003
p53 and mdm-2 expression in Rhabdomyosarcoma of childhood and adolescence: clinicopathologic study by the Kiel Pediatric Tumor Registry and the German Cooperative Soft Tissue Sarcoma StudyIvo Leuschner, Inken Langhans, Regina Schmitz, et al.
The American Journal of Pathology|February 25, 2003
Full-length telomerase reverse transcriptase messenger RNA is an independent prognostic factor in neuroblastomaMatthias Krams, Barbara Hero, Frank Berthold, et al.
Oncogene|January 16, 2004
Expression of the c-kit receptor characterizes a subset of neuroblastomas with favorable prognosisMatthias Krams, Reza Parwaresch, Bence Sipos, et al.
Pageof 4