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Invited Review: The spectrum of neuropathology in COVID‐19

Neuropathology and applied neurobiology, 2021-02, Vol.47 (1), p.3-16

2021

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RYR1 mutations are a common cause of congenital myopathies with central nuclei

Annals of neurology, 2010-11, Vol.68 (5), p.717-726

2010

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British Neuropathological Society and International Society of Forensic Radiology and Imaging expert consensus statement for post mortem neurological imaging

Neuropathology and applied neurobiology, 2018-12, Vol.44 (7), p.663-672

2018

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Unusual neuropathological features and increased brain aluminium in a resident of Camelford, UK

Neuropathology and applied neurobiology, 2017-10, Vol.43 (6), p.537-541

2017

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Cortical selective vulnerability in motor neuron disease: a morphometric study

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1237-1251

2004

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Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS inclusions

Neuropathology and applied neurobiology, 2013-08, Vol.39 (5), p.553-561

2013

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Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

Neuropathology and applied neurobiology, 2004-08, Vol.30 (4), p.369-373

2004

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Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2565-2581

2011

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Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium

Neuropathology and applied neurobiology, 2013-02, Vol.39 (2), p.166-178

2013

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Has the survival of patients with glioblastoma changed over the years?

British journal of cancer, 2016-01, Vol.114 (2), p.146-150

2016

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Traumatic axonal damage in the brain can be detected using β-APP immunohistochemistry within 35 min after head injury to human adults

Neuropathology and applied neurobiology, 2007-04, Vol.33 (2), p.226-237

2007

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Changes in the expression of genes related to neuroinflammation over the course of sporadic Alzheimer’s disease progression: CX3CL1, TREM2, and PPARγ

Journal of Neural Transmission, 2015-07, Vol.122 (7), p.1069-1076

2015

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Subacute necrotising encephalomyelopathy (Leigh's disease; Leigh syndrome)

Journal of neurology, neurosurgery and psychiatry, 2015-04, Vol.86 (4), p.363-365

2015

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Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation

Journal of neurology, neurosurgery and psychiatry, 2009-11, Vol.80 (11), p.1297-1298

2009

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Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates

Acta neuropathologica, 2020-04, Vol.139 (4), p.717-734

2020

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Control tissue in brain banking: the importance of thorough neuropathological assessment

Journal of Neural Transmission, 2015-07, Vol.122 (7), p.949-956

2015

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ATRX immunohistochemistry can help refine 'not elsewhere classified' categorisation for grade II/III gliomas

British journal of neurosurgery, 2019-09, Vol.33 (5), p.536-540

2019

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Has the survival of patients with glioblastoma changed over the years?

British journal of cancer, 2016-06, Vol.114 (12), p.e20-e20

2016

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The glial precursor proteoglycan, NG2, is expressed on tumour neovasculature by vascular pericytes in human malignant brain tumours

Neuropathology and applied neurobiology, 2002-10, Vol.28 (5), p.367-380

2002

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Intracranial laterally based supratentorial neurenteric cyst

British journal of radiology, 2004-11, Vol.77 (923), p.963-965

2004

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Pilocytic astrocytoma of the adult--clinical features, radiological features and management

British journal of neurosurgery, 2004-12, Vol.18 (6), p.613-616

2004

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Papillary glioneuronal tumour: a review of the literature with two illustrative cases

British journal of neurosurgery, 2013-06, Vol.27 (3), p.401-404

2013

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Ubiquitin-only intraneuronal inclusion in the substantia nigra is a characteristic feature of motor neurone disease with dementia

Neuropathology and applied neurobiology, 2002-04, Vol.28 (2), p.120-128

2002

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Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples

The Lancet (British edition), 1999-01, Vol.353 (9148), p.183-189

1999

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P46 THE KI-67 LABELLING INDEX WITH MAXIMALLY SELECTED CUT-OFFS IS BETTER AT PREDICTING RECURRENCE THAN THE WHO GRADING SYSTEM OF MENINGIOMAS

Neuro-oncology (Charlottesville, Va.), 2014-10, Vol.16 (suppl 6), p.vi7-vi7

2014

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Invited Review: The spectrum of neuropathology in COVID‐19

RYR1 mutations are a common cause of congenital myopathies with central nuclei

British Neuropathological Society and International Society of Forensic Radiology and Imaging expert consensus statement for post mortem neurological imaging

Unusual neuropathological features and increased brain aluminium in a resident of Camelford, UK

Cortical selective vulnerability in motor neuron disease: a morphometric study

Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS inclusions

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium

Has the survival of patients with glioblastoma changed over the years?

Traumatic axonal damage in the brain can be detected using β-APP immunohistochemistry within 35 min after head injury to human adults

Changes in the expression of genes related to neuroinflammation over the course of sporadic Alzheimer’s disease progression: CX3CL1, TREM2, and PPARγ

Subacute necrotising encephalomyelopathy (Leigh's disease; Leigh syndrome)

Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation

Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates

Control tissue in brain banking: the importance of thorough neuropathological assessment

ATRX immunohistochemistry can help refine 'not elsewhere classified' categorisation for grade II/III gliomas

Has the survival of patients with glioblastoma changed over the years?

The glial precursor proteoglycan, NG2, is expressed on tumour neovasculature by vascular pericytes in human malignant brain tumours

Intracranial laterally based supratentorial neurenteric cyst

Pilocytic astrocytoma of the adult--clinical features, radiological features and management

Papillary glioneuronal tumour: a review of the literature with two illustrative cases

Ubiquitin-only intraneuronal inclusion in the substantia nigra is a characteristic feature of motor neurone disease with dementia

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples

P46 THE KI-67 LABELLING INDEX WITH MAXIMALLY SELECTED CUT-OFFS IS BETTER AT PREDICTING RECURRENCE THAN THE WHO GRADING SYSTEM OF MENINGIOMAS

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