about
Myotubular myopathy. Case report and review of the literatureRecessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy.Chordoid glioma: ten years of a low-grade tumor with high morbidityAssessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe ConsortiumSensory, psychological, and metabolic dysfunction in HIV-associated peripheral neuropathy: A cross-sectional deep profiling study.MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle.Control tissue in brain banking: the importance of thorough neuropathological assessment.Is it worth pursuing surgery for epilepsy in patients with normal neuroimaging?Neurological picture. Devastating calcinosis in a patient with adult onset myositis.EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy.Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgiaProstate-derived sterile 20-like kinases (PSKs/TAOKs) phosphorylate tau protein and are activated in tangle-bearing neurons in Alzheimer disease.Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy.Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe ConsortiumFatal granulomatous amoebic meningoencephalitis due to Balamuthia mandrillaris.Giant cystic intracranial chondroma of the falx with review of literature.MR diffusion histology and micro-tractography reveal mesoscale features of the human cerebellum.Primary glioblastoma with oligodendroglial differentiation has better clinical outcome but no difference in common biological markers compared with other types of glioblastoma.Giant cell tumour and central giant cell reparative granuloma of the skull: do these represent ends of a spectrum? A case report and literature review.Two cases of multinodular and vacuolating neuronal tumourDiffuse form of dysembryoplastic neuroepithelial tumour: the histological and immunohistochemical features of a distinct entity showing transition to dysembryoplastic neuroepithelial tumour and ganglioglioma.Spontaneous epidural spinal haematoma in children caused by vascular malformations.Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium.Gliomatosis cerebri type 1 with extensive involvement of the spinal cord and BRAF V600E mutation.Chondromyxoid fibroma of the skull base invading the occipitocervical junction: report of a unique case and discussion.Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG).Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium.Rare case of cerebral MALToma presenting with stroke-like symptoms and seizuresSimulated surgical-type cerebral biopsies from post-mortem brains allows accurate neuropathological diagnoses in the majority of neurodegenerative disease groupsPronounced response of papillary craniopharyngioma to treatment with vemurafenib, a BRAF inhibitor.Macrophages in human immunodeficiency virus-associated kidney diseases.A 72-year-old woman with right frontal extra-axial mass.Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency.Myxopapillary ependymoma of the cerebellopontine angle: retrograde metastasis or primary tumour?Assessment of the degree of asymmetry of pathological features in neurodegenerative diseases. What is the significance for brain banks?Single Pulse Electrical Stimulation Identifies Epileptogenicity in a Case With Subcortical Nodular Heterotopia and MRI Negative Epilepsy.Comment on "The geometric structure of the brain fiber pathways".The need to unify neuropathological assessments of vascular alterations in the ageing brain: multicentre survey by the BrainNet Europe consortium.Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium.Staging/typing of Lewy body related alpha-synuclein pathology: a study of the BrainNet Europe Consortium.
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-2533-4758
@en
name
Istvan Bodi
@ast
Istvan Bodi
@en
Istvan Bodi
@es
Istvan Bodi
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type
label
Istvan Bodi
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Istvan Bodi
@en
Istvan Bodi
@es
Istvan Bodi
@nl
prefLabel
Istvan Bodi
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Istvan Bodi
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Istvan Bodi
@es
Istvan Bodi
@nl
P106
P1153
55367947400
P31
P496
0000-0002-2533-4758