Search research articles
Contact Us
Filters
Showing results (51-60 of 127) with videos related to
Page
of 13
Sort By:
Acta Neuropathologica
|
December 2, 2022
Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohorts
Martin Mynarek, Denise Obrecht, Martin Sill, et al.
Clinical Sarcoma Research
|
May 10, 2017
Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases
Christian Koelsche, Daniel Schrimpf, Lars Tharun, et al.
Acta Neuropathologica
|
July 11, 2014
Integrated DNA methylation and copy-number profiling identify three clinically and biologically relevant groups of anaplastic glioma
Benedikt Wiestler, David Capper, Martin Sill, et al.
Journal of Neuro-Oncology
|
February 22, 2022
Clinical and molecular characterization of isolated M1 disease in pediatric medulloblastoma: experience from the German HIT-MED studies
Denise Obrecht, Martin Mynarek, Christian Hagel, et al.
Neuro-Oncology
|
June 5, 2024
Risk factors for domain-specific neurocognitive outcome in pediatric survivors of a brain tumor in the posterior fossa-Results of the HIT 2000 trial
Martin Mynarek, Anne Rossius, Anika Guiard, et al.
Acta Neuropathologica
|
December 17, 2013
Embryonal tumor with abundant neuropil and true rosettes (ETANTR), ependymoblastoma, and medulloepithelioma share molecular similarity and comprise a single clinicopathological entity
Andrey Korshunov, Dominik Sturm, Marina Ryzhova, et al.
Acta Neuropathologica
|
May 6, 2017
Meningiomas induced by low-dose radiation carry structural variants of NF2 and a distinct mutational signature
Felix Sahm, Umut H Toprak, Daniel Hübschmann, et al.
Neuro-Oncology
|
January 30, 2023
Risk prediction in early childhood sonic hedgehog medulloblastoma treated with radiation-avoiding chemotherapy: Evidence for more than 2 subgroups
Svenja Tonn, Andrey Korshunov, Denise Obrecht, et al.
Acta Neuropathologica
|
March 14, 2025
Constitutional variants in PTEN: a frequent finding in patients with papillary tumors of the pineal region subtype B (PTPR-B) associated with isolated loss of chromosome 10
Steffen Hirsch, Ramin Rahmanzade, Kerstin Grund, et al.
Brain Pathology (Zurich, Switzerland)
|
November 18, 2014
Melanotic tumors of the nervous system are characterized by distinct mutational, chromosomal and epigenomic profiles
Christian Koelsche, Volker Hovestadt, David T W Jones, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 127) with videos related to
Sort By:
Page
of 13
Acta Neuropathologica
|
December 2, 2022
Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohorts
Martin Mynarek, Denise Obrecht, Martin Sill, et al.
Clinical Sarcoma Research
|
May 10, 2017
Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases
Christian Koelsche, Daniel Schrimpf, Lars Tharun, et al.
Acta Neuropathologica
|
July 11, 2014
Integrated DNA methylation and copy-number profiling identify three clinically and biologically relevant groups of anaplastic glioma
Benedikt Wiestler, David Capper, Martin Sill, et al.
Journal of Neuro-Oncology
|
February 22, 2022
Clinical and molecular characterization of isolated M1 disease in pediatric medulloblastoma: experience from the German HIT-MED studies
Denise Obrecht, Martin Mynarek, Christian Hagel, et al.
Neuro-Oncology
|
June 5, 2024
Risk factors for domain-specific neurocognitive outcome in pediatric survivors of a brain tumor in the posterior fossa-Results of the HIT 2000 trial
Martin Mynarek, Anne Rossius, Anika Guiard, et al.
Acta Neuropathologica
|
December 17, 2013
Embryonal tumor with abundant neuropil and true rosettes (ETANTR), ependymoblastoma, and medulloepithelioma share molecular similarity and comprise a single clinicopathological entity
Andrey Korshunov, Dominik Sturm, Marina Ryzhova, et al.
Acta Neuropathologica
|
May 6, 2017
Meningiomas induced by low-dose radiation carry structural variants of NF2 and a distinct mutational signature
Felix Sahm, Umut H Toprak, Daniel Hübschmann, et al.
Neuro-Oncology
|
January 30, 2023
Risk prediction in early childhood sonic hedgehog medulloblastoma treated with radiation-avoiding chemotherapy: Evidence for more than 2 subgroups
Svenja Tonn, Andrey Korshunov, Denise Obrecht, et al.
Acta Neuropathologica
|
March 14, 2025
Constitutional variants in PTEN: a frequent finding in patients with papillary tumors of the pineal region subtype B (PTPR-B) associated with isolated loss of chromosome 10
Steffen Hirsch, Ramin Rahmanzade, Kerstin Grund, et al.
Brain Pathology (Zurich, Switzerland)
|
November 18, 2014
Melanotic tumors of the nervous system are characterized by distinct mutational, chromosomal and epigenomic profiles
Christian Koelsche, Volker Hovestadt, David T W Jones, et al.
Page
of 13