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European Journal of Cancer (Oxford, England : 1990)
|
September 24, 2019
A tailored molecular profiling programme for children with cancer to identify clinically actionable genetic alterations
Sally L George, Elisa Izquierdo, James Campbell, et al.
Acta Neuropathologica
|
May 21, 2014
Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations
Leanne de Kock, Nelly Sabbaghian, François Plourde, et al.
Epilepsia
|
May 5, 2021
Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial
Ingmar Blümcke, Roland Coras, Robyn M Busch, et al.
Human Molecular Genetics
|
September 6, 2022
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
Athina Ververi, Sara Zagaglia, Lara Menzies, et al.
Radiology
|
April 19, 2022
MRI Radiogenomics of Pediatric Medulloblastoma: A Multicenter Study
Michael Zhang, Samuel W Wong, Jason N Wright, et al.
Cancer Discovery
|
November 5, 2021
DIPG Harbors Alterations Targetable by MEK Inhibitors, with Acquired Resistance Mechanisms Overcome by Combinatorial Inhibition
Elisa Izquierdo, Diana M Carvalho, Alan Mackay, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 10, 2025
The spectrum of IDH- and H3-wildtype high-grade glioma subgroups occurring across teenage and young adult patient populations
Rita Pereira, Alan Mackay, Yura Grabovska, et al.
Neuro-Oncology
|
May 19, 2026
Tempered Optimism: Advances in the Precision Medicine Era for Pediatric Low-Grade Glioma
Chelsea Kotch, Sebastien Perreault, Phoebe Power, et al.
Acta Neuropathologica
|
March 16, 2018
Tumour compartment transcriptomics demonstrates the activation of inflammatory and odontogenic programmes in human adamantinomatous craniopharyngioma and identifies the MAPK/ERK pathway as a novel therapeutic target
John R Apps, Gabriela Carreno, Jose Mario Gonzalez-Meljem, et al.
Nature Communications
|
May 28, 2016
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia
Karin Tuschl, Esther Meyer, Leonardo E Valdivia, et al.
Page
of 35
Search research articles
Search
Showing results (321-330 of 348) with videos related to
Sort By:
Page
of 35
European Journal of Cancer (Oxford, England : 1990)
|
September 24, 2019
A tailored molecular profiling programme for children with cancer to identify clinically actionable genetic alterations
Sally L George, Elisa Izquierdo, James Campbell, et al.
Acta Neuropathologica
|
May 21, 2014
Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations
Leanne de Kock, Nelly Sabbaghian, François Plourde, et al.
Epilepsia
|
May 5, 2021
Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial
Ingmar Blümcke, Roland Coras, Robyn M Busch, et al.
Human Molecular Genetics
|
September 6, 2022
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
Athina Ververi, Sara Zagaglia, Lara Menzies, et al.
Radiology
|
April 19, 2022
MRI Radiogenomics of Pediatric Medulloblastoma: A Multicenter Study
Michael Zhang, Samuel W Wong, Jason N Wright, et al.
Cancer Discovery
|
November 5, 2021
DIPG Harbors Alterations Targetable by MEK Inhibitors, with Acquired Resistance Mechanisms Overcome by Combinatorial Inhibition
Elisa Izquierdo, Diana M Carvalho, Alan Mackay, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 10, 2025
The spectrum of IDH- and H3-wildtype high-grade glioma subgroups occurring across teenage and young adult patient populations
Rita Pereira, Alan Mackay, Yura Grabovska, et al.
Neuro-Oncology
|
May 19, 2026
Tempered Optimism: Advances in the Precision Medicine Era for Pediatric Low-Grade Glioma
Chelsea Kotch, Sebastien Perreault, Phoebe Power, et al.
Acta Neuropathologica
|
March 16, 2018
Tumour compartment transcriptomics demonstrates the activation of inflammatory and odontogenic programmes in human adamantinomatous craniopharyngioma and identifies the MAPK/ERK pathway as a novel therapeutic target
John R Apps, Gabriela Carreno, Jose Mario Gonzalez-Meljem, et al.
Nature Communications
|
May 28, 2016
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia
Karin Tuschl, Esther Meyer, Leonardo E Valdivia, et al.
Page
of 35