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mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis

Acta neuropathologica, 2013-08, Vol.126 (2), p.207-218

2013

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Tissue metabolite profiles for the characterisation of paediatric cerebellar tumours

Scientific reports, 2018-08, Vol.8 (1), p.11992-10, Article 11992

2018

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Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene

Neuromuscular disorders : NMD, 2013-05, Vol.23 (5), p.391-398

2013

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Multi-omic approach identifies hypoxic tumor-associated myeloid cells that drive immunobiology of high-risk pediatric ependymoma

iScience, 2023-09, Vol.26 (9), p.107585, Article 107585

2023

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Approach to the post-mortem investigation of neurodegenerative diseases: from diagnosis to research

Diagnostic histopathology (Oxford, England : 2008), 2011-05, Vol.17 (5), p.211-216

2011

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Astrovirus VA1/HMO-C: An Increasingly Recognized Neurotropic Pathogen in Immunocompromised Patients

Clinical infectious diseases, 2015-03, Vol.60 (6), p.881-888

2015

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Disproportionate Expression of ATM in Cerebellar Cortex During Human Neurodevelopment

Cerebellum (London, England), 2024-04, Vol.23 (2), p.502-511

2024

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Untargeted Metabolomic Characterization of Glioblastoma Intra-Tumor Heterogeneity Using OrbiSIMS

Analytical chemistry (Washington), 2023-04, Vol.95 (14), p.5994-6001

2023

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A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups

Pediatric blood & cancer, 2020-09, Vol.67 (9), p.e28426-n/a

2020

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EPN-09KETOLYTIC AND GLYCOLYTIC ENZYMATIC EXPRESSION IN PAEDIATRIC EPENDYMOMAS: IMPLICATION FOR KETOGENIC DIET THERAPY

Neuro-oncology (Charlottesville, Va.), 2016-06, Vol.18 (suppl 3), p.iii32.1-iii32

2016

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SIOP Ependymoma I: Final results, long-term follow-up, and molecular analysis of the trial cohort-A BIOMECA Consortium Study

Neuro-oncology (Charlottesville, Va.), 2022-06, Vol.24 (6), p.936-948

2022

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A case series of Diffuse Glioneuronal Tumours with Oligodendroglioma‐like features and Nuclear Clusters (DGONC)

Neuropathology and applied neurobiology, 2021-04, Vol.47 (3), p.464-467

2021

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Spatially resolved transcriptomic profiles reveal unique defining molecular features of infiltrative 5ALA-metabolizing cells associated with glioblastoma recurrence

Genome medicine, 2023-07, Vol.15 (1), p.48-34, Article 48

2023

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Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study

Neuro-oncology (Charlottesville, Va.), 2023-10, Vol.25 (10), p.1871-1882

2023

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Continued 26S proteasome dysfunction in mouse brain cortical neurons impairs autophagy and the Keap1-Nrf2 oxidative defence pathway

Cell death & disease, 2017-01, Vol.8 (1), p.e2531-e2531

2017

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Review: Neuropathological features of unexplained sudden unexpected death in infancy: current evidence and controversies

Neuropathology and applied neurobiology, 2014-06, Vol.40 (4), p.364-384

2014

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Pale body-like inclusion formation and neurodegeneration following depletion of 26S proteasomes in mouse brain neurones are independent of α-synuclein

PloS one, 2013, Vol.8 (1), p.e54711-e54711

2013

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Brain weight in sudden unexpected death in infancy: experience from a large single-centre cohort

Neuropathology and applied neurobiology, 2016-06, Vol.42 (4), p.344-351

2016

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Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRI

Acta neuropathologica, 2012-03, Vol.123 (3), p.453-456

2012

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Tubular aggregates caused by serine active site containing 1 (SERAC1) mutations in a patient with a mitochondrial encephalopathy

Neuropathology and applied neurobiology, 2015-04, Vol.41 (3), p.399-402

2015

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Characterization of a population of neural progenitor cells in the infant hippocampus

Neuropathology and applied neurobiology, 2014-08, Vol.40 (5), p.544-550

2014

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Genetic heterogeneity for SMARCB1, H3F3A and BRAF in a malignant childhood brain tumour: genetic-pathological correlation

Neuropathology and applied neurobiology, 2015-10, Vol.41 (6), p.832-836

2015

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Challenges for the functional diffusion map in pediatric brain tumors

Neuro-oncology (Charlottesville, Va.), 2014-03, Vol.16 (3), p.449-456

2014

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Atypical progressive multifocal leukoencephalopathy associated with an unusual JC polyomavirus mutation

Archives of neurology (Chicago), 2009-08, Vol.66 (8), p.1021

2009

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The Neuropathology of Progressive Multiple Sclerosis

Progressive Multiple Sclerosis, 2017, p.49-69

2017

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mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis

Tissue metabolite profiles for the characterisation of paediatric cerebellar tumours

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene

Multi-omic approach identifies hypoxic tumor-associated myeloid cells that drive immunobiology of high-risk pediatric ependymoma

Approach to the post-mortem investigation of neurodegenerative diseases: from diagnosis to research

Astrovirus VA1/HMO-C: An Increasingly Recognized Neurotropic Pathogen in Immunocompromised Patients

Disproportionate Expression of ATM in Cerebellar Cortex During Human Neurodevelopment

Untargeted Metabolomic Characterization of Glioblastoma Intra-Tumor Heterogeneity Using OrbiSIMS

A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups

EPN-09KETOLYTIC AND GLYCOLYTIC ENZYMATIC EXPRESSION IN PAEDIATRIC EPENDYMOMAS: IMPLICATION FOR KETOGENIC DIET THERAPY

SIOP Ependymoma I: Final results, long-term follow-up, and molecular analysis of the trial cohort-A BIOMECA Consortium Study

A case series of Diffuse Glioneuronal Tumours with Oligodendroglioma‐like features and Nuclear Clusters (DGONC)

Spatially resolved transcriptomic profiles reveal unique defining molecular features of infiltrative 5ALA-metabolizing cells associated with glioblastoma recurrence

Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study

Continued 26S proteasome dysfunction in mouse brain cortical neurons impairs autophagy and the Keap1-Nrf2 oxidative defence pathway

Review: Neuropathological features of unexplained sudden unexpected death in infancy: current evidence and controversies

Pale body-like inclusion formation and neurodegeneration following depletion of 26S proteasomes in mouse brain neurones are independent of α-synuclein

Brain weight in sudden unexpected death in infancy: experience from a large single-centre cohort

Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRI

Tubular aggregates caused by serine active site containing 1 (SERAC1) mutations in a patient with a mitochondrial encephalopathy

Characterization of a population of neural progenitor cells in the infant hippocampus

Genetic heterogeneity for SMARCB1, H3F3A and BRAF in a malignant childhood brain tumour: genetic-pathological correlation

Challenges for the functional diffusion map in pediatric brain tumors

Atypical progressive multifocal leukoencephalopathy associated with an unusual JC polyomavirus mutation

The Neuropathology of Progressive Multiple Sclerosis

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