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Distribution, characterization and clinical significance of microglia in glioneuronal tumours from patients with chronic intractable epilepsy

Neuropathology and applied neurobiology, 2005-06, Vol.31 (3), p.280-291

2005

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Chronic activation of anti‐oxidant pathways and iron accumulation in epileptogenic malformations

Neuropathology and applied neurobiology, 2020-10, Vol.46 (6), p.546-563

2020

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A neuropathological study of two autopsy cases of syndromic hemimegalencephaly

Neuropathology and applied neurobiology, 2007-08, Vol.33 (4), p.455-470

2007

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Expression of microRNAs miR21, miR146a, and miR155 in tuberous sclerosis complex cortical tubers and their regulation in human astrocytes and SEGA-derived cell cultures

Glia, 2016-06, Vol.64 (6), p.1066-1082

2016

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Calcinosis in juvenile dermatomyositis: a possible role for the vitamin K-dependent protein matrix Gla protein

Rheumatology (Oxford, England), 2008-03, Vol.47 (3), p.267-271

2008

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Increased matrix metalloproteinases expression in tuberous sclerosis complex: modulation by microRNA 146a and 147b in vitro

Neuropathology and applied neurobiology, 2020-02, Vol.46 (2), p.142-159

2020

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Promoter-Specific Hypomethylation Correlates with IL-1β Overexpression in Tuberous Sclerosis Complex (TSC)

Journal of molecular neuroscience, 2016-08, Vol.59 (4), p.464-470

2016

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Expression of neurodegenerative disease-related proteins and caspase-3 in glioneuronal tumours

Neuropathology and applied neurobiology, 2015-02, Vol.41 (2), p.e1-e15

2015

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Immunohistochemical localization of vascular endothelial growth factor receptors-1, -2 and -3 in human spinal cord: altered expression in amyotrophic lateral sclerosis

Neuropathology and applied neurobiology, 2004-08, Vol.30 (4), p.351-359

2004

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Activation of toll-like receptor, RAGE and HMGB1 signalling in malformations of cortical development

Brain (London, England : 1878), 2011-04, Vol.134 (Pt 4), p.1015-1032

2011

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Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours

Neuropathology and applied neurobiology, 2015-10, Vol.41 (6), p.743-755

2015

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Peroneal nerve compression by fibrous histiocytoma

Journal of neurology, 2000-01, Vol.247 (1), p.68-69

2000

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P07.19 Fractal structure on gadolineum-enhanced MRI scans correlates with oxidative metabolism and VEGF expression in glioblastoma

Neuro-oncology (Charlottesville, Va.), 2016-10, Vol.18 (suppl_4), p.iv38-iv38

2016

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P01.09 Epilepsy associates with decreased HIF1-α/STAT5B and SRF signaling in glioblastoma

Neuro-oncology (Charlottesville, Va.), 2016-10, Vol.18 (suppl_4), p.iv20-iv20

2016

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P01.10 Effects of valproic acid on NF-κB signaling in glioblastoma

Neuro-oncology (Charlottesville, Va.), 2016-10, Vol.18 (suppl_4), p.iv20-iv20

2016

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O9.06 PROGNOSTIC RELEVANCE AND ONCOGENIC CORRELATES OF EPILEPSY IN GLIOBLASTOMA PATIENTS

Neuro-oncology (Charlottesville, Va.), 2014-09, Vol.16 (suppl 2), p.ii21-ii21

2014

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Hepatic GVHD after HLA‐haploidentical bone marrow transplantation in children with severe combined immunodeficiency: the effect of ursodeoxycholic acid

British journal of haematology, 1997-03, Vol.96 (4), p.776-780

1997

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Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON

American journal of medical genetics. Part A, 2006-07, Vol.140A (13), p.1478-1481

2006

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Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON: Split hand foot malformation

American journal of medical genetics. Part A, 2006, Vol.140 (13), p.1478-1481

2006

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Peroneal nerve compression by fibrous histiocytoma

Journal of neurology, 2000, Vol.247 (1), p.68-69

2000

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Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON

American journal of medical genetics. Part A, 2006, Vol.140 (13), p.1478-1481

2006

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Predominance of Nonatherosclerotic Internal Elastic Lamina Calcification in the Intracranial Internal Carotid Artery

Stroke (1970), 2016-01, Vol.47 (1), p.221-223

2016

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Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex

Neuropathology, 2008-12, Vol.28 (6), p.577-590

2008

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Distribution, characterization and clinical significance of microglia in glioneuronal tumours from patients with chronic intractable epilepsy

Chronic activation of anti‐oxidant pathways and iron accumulation in epileptogenic malformations

A neuropathological study of two autopsy cases of syndromic hemimegalencephaly

Expression of microRNAs miR21, miR146a, and miR155 in tuberous sclerosis complex cortical tubers and their regulation in human astrocytes and SEGA-derived cell cultures

Calcinosis in juvenile dermatomyositis: a possible role for the vitamin K-dependent protein matrix Gla protein

Increased matrix metalloproteinases expression in tuberous sclerosis complex: modulation by microRNA 146a and 147b in vitro

Promoter-Specific Hypomethylation Correlates with IL-1β Overexpression in Tuberous Sclerosis Complex (TSC)

Expression of neurodegenerative disease-related proteins and caspase-3 in glioneuronal tumours

Immunohistochemical localization of vascular endothelial growth factor receptors-1, -2 and -3 in human spinal cord: altered expression in amyotrophic lateral sclerosis

Activation of toll-like receptor, RAGE and HMGB1 signalling in malformations of cortical development

Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours

Peroneal nerve compression by fibrous histiocytoma

P07.19 Fractal structure on gadolineum-enhanced MRI scans correlates with oxidative metabolism and VEGF expression in glioblastoma

P01.09 Epilepsy associates with decreased HIF1-α/STAT5B and SRF signaling in glioblastoma

P01.10 Effects of valproic acid on NF-κB signaling in glioblastoma

O9.06 PROGNOSTIC RELEVANCE AND ONCOGENIC CORRELATES OF EPILEPSY IN GLIOBLASTOMA PATIENTS

Hepatic GVHD after HLA‐haploidentical bone marrow transplantation in children with severe combined immunodeficiency: the effect of ursodeoxycholic acid

Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON

Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON: Split hand foot malformation

Peroneal nerve compression by fibrous histiocytoma

Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON

Predominance of Nonatherosclerotic Internal Elastic Lamina Calcification in the Intracranial Internal Carotid Artery

Distinct DNA Methylation Patterns of Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex

Dysregulation of the MMP/TIMP Proteolytic System in Subependymal Giant Cell Astrocytomas in Patients With Tuberous Sclerosis Complex: Modulation of MMP by MicroRNA-320d In Vitro

Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex

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