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Ivo Leuschner

Showing results (41-50 of 137) with videos related to

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The Journal of Pathology. Clinical Research|November 1, 2017
TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasiaJenny Wegert, Christian Vokuhl, Barbara Ziegler, et al.
Experimental Cell Research|September 25, 2012
Differential expression of miRNAs in rhabdomyosarcoma and malignant rhabdoid tumorSorin Armeanu-Ebinger, Delia Herrmann, Michael Bonin, et al.
Archives of Gynecology and Obstetrics|May 26, 2011
Diagnosis and management of an unilateral giant fibroadenoma of the breast in pregnancyThorsten Heilmann, Ivo Leuschner, Felix Hilpert, et al.
Archives of Gynecology and Obstetrics|August 8, 2007
Congenital diaphragmatic hernia, etiology and management, a 10-year analysis of a single centerCornelia Beck, Ozkan Alkasi, Werner Nikischin, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 13, 2014
Nephroblastomas show low expression of microR-204 and high expression of its target, the oncogenic transcription factor MEIS1Karin Koller, Martin Pichler, Karin Koch, et al.
Surgical Oncology|March 24, 2010
Vascular encasement as element of risk stratification in abdominal neuroblastomaSteven W Warmann, Guido Seitz, Juergen F Schaefer, et al.
Cancer Genetics|September 29, 2014
Synchronous congenital malignant rhabdoid tumor of the orbit and atypical teratoid/rhabdoid tumor--feasibility and efficacy of multimodal therapy in a long-term survivorAngela Seeringer, Harald Reinhard, Martin Hasselblatt, et al.
Oncotarget|July 9, 2016
CNS germinomas are characterized by global demethylation, chromosomal instability and mutational activation of the Kit-, Ras/Raf/Erk- and Akt-pathwaysSimone Laura Schulte, Andreas Waha, Barbara Steiger, et al.
Annals of Surgery|November 10, 2016
Outcome, Treatment, and Treatment Failures in Patients Suffering Localized Embryonal Paratesticular Rhabdomyosarcoma: Results From the "Cooperative Weichteilsarkom Studiengruppe" Trials CWS-86, -91, -96, and -2002PGuido Seitz, Jörg Fuchs, Peter Martus, et al.
Pediatric Blood & Cancer|January 24, 2009
Does the time-point of relapse influence outcome in pediatric rhabdomyosarcomas?Adrian C Mattke, Emily J Bailey, Andreas Schuck, et al.
Pageof 14

Showing results (41-50 of 137) with videos related to

Sort By:
Pageof 14
The Journal of Pathology. Clinical Research|November 1, 2017
TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasiaJenny Wegert, Christian Vokuhl, Barbara Ziegler, et al.
Experimental Cell Research|September 25, 2012
Differential expression of miRNAs in rhabdomyosarcoma and malignant rhabdoid tumorSorin Armeanu-Ebinger, Delia Herrmann, Michael Bonin, et al.
Archives of Gynecology and Obstetrics|May 26, 2011
Diagnosis and management of an unilateral giant fibroadenoma of the breast in pregnancyThorsten Heilmann, Ivo Leuschner, Felix Hilpert, et al.
Archives of Gynecology and Obstetrics|August 8, 2007
Congenital diaphragmatic hernia, etiology and management, a 10-year analysis of a single centerCornelia Beck, Ozkan Alkasi, Werner Nikischin, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 13, 2014
Nephroblastomas show low expression of microR-204 and high expression of its target, the oncogenic transcription factor MEIS1Karin Koller, Martin Pichler, Karin Koch, et al.
Surgical Oncology|March 24, 2010
Vascular encasement as element of risk stratification in abdominal neuroblastomaSteven W Warmann, Guido Seitz, Juergen F Schaefer, et al.
Cancer Genetics|September 29, 2014
Synchronous congenital malignant rhabdoid tumor of the orbit and atypical teratoid/rhabdoid tumor--feasibility and efficacy of multimodal therapy in a long-term survivorAngela Seeringer, Harald Reinhard, Martin Hasselblatt, et al.
Oncotarget|July 9, 2016
CNS germinomas are characterized by global demethylation, chromosomal instability and mutational activation of the Kit-, Ras/Raf/Erk- and Akt-pathwaysSimone Laura Schulte, Andreas Waha, Barbara Steiger, et al.
Annals of Surgery|November 10, 2016
Outcome, Treatment, and Treatment Failures in Patients Suffering Localized Embryonal Paratesticular Rhabdomyosarcoma: Results From the "Cooperative Weichteilsarkom Studiengruppe" Trials CWS-86, -91, -96, and -2002PGuido Seitz, Jörg Fuchs, Peter Martus, et al.
Pediatric Blood & Cancer|January 24, 2009
Does the time-point of relapse influence outcome in pediatric rhabdomyosarcomas?Adrian C Mattke, Emily J Bailey, Andreas Schuck, et al.
Pageof 14