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Acta Neuropathologica
|
December 17, 2020
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases
Dörthe Holdhof, Pascal D Johann, Michael Spohn, 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.
Cancer Gene Therapy
|
June 8, 2024
Proteomic profiling reveals ACSS2 facilitating metabolic support in acute myeloid leukemia
Liliana H Mochmann, Denise Treue, Michael Bockmayr, et al.
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.
Neuro-Oncology
|
August 22, 2024
Distinct relapse pattern across molecular ependymoma types
Denise Obrecht-Sturm, Melanie Schoof, Alicia Eckhardt, 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.
Neuro-Oncology
|
April 5, 2022
Comprehensive profiling of myxopapillary ependymomas identifies a distinct molecular subtype with relapsing disease
Michael Bockmayr, Kim Harnisch, Lara C Pohl, et al.
Acta Neuropathologica
|
September 14, 2020
Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity
Leonille Schweizer, Felix Thierfelder, Christian Thomas, et al.
Acta Neuropathologica
|
June 11, 2025
Outcome-associated factors in a molecularly defined cohort of central neurocytoma
Maja Krech, Amos Muench, Daniel Teichmann, et al.
Acta Neuropathologica
|
January 24, 2024
Transcriptomic and epigenetic dissection of spinal ependymoma (SP-EPN) identifies clinically relevant subtypes enriched for tumors with and without NF2 mutation
Sina Neyazi, Erika Yamazawa, Karoline Hack, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 51) with videos related to
Sort By:
Page
of 6
Acta Neuropathologica
|
December 17, 2020
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases
Dörthe Holdhof, Pascal D Johann, Michael Spohn, 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.
Cancer Gene Therapy
|
June 8, 2024
Proteomic profiling reveals ACSS2 facilitating metabolic support in acute myeloid leukemia
Liliana H Mochmann, Denise Treue, Michael Bockmayr, et al.
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.
Neuro-Oncology
|
August 22, 2024
Distinct relapse pattern across molecular ependymoma types
Denise Obrecht-Sturm, Melanie Schoof, Alicia Eckhardt, 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.
Neuro-Oncology
|
April 5, 2022
Comprehensive profiling of myxopapillary ependymomas identifies a distinct molecular subtype with relapsing disease
Michael Bockmayr, Kim Harnisch, Lara C Pohl, et al.
Acta Neuropathologica
|
September 14, 2020
Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity
Leonille Schweizer, Felix Thierfelder, Christian Thomas, et al.
Acta Neuropathologica
|
June 11, 2025
Outcome-associated factors in a molecularly defined cohort of central neurocytoma
Maja Krech, Amos Muench, Daniel Teichmann, et al.
Acta Neuropathologica
|
January 24, 2024
Transcriptomic and epigenetic dissection of spinal ependymoma (SP-EPN) identifies clinically relevant subtypes enriched for tumors with and without NF2 mutation
Sina Neyazi, Erika Yamazawa, Karoline Hack, et al.
Page
of 6