The contribution of systemic inflammation to neurodegeneration in protein misfolding diseases : P1
Transsynaptic mechanisms of neuronal impairments in Alzheimer's Disease : P4
Mitochondria fusion/fission in the balance of alzheimer disease : S1-2
Biological diversity of TSE agents: the strain typing puzzle : S2-1
Neuropathology of animal Prion diseases: toxic effects of PrPd, relationships with strain and clinical disease : S2-2
Variably protease-sensitive prionopathy: update on this novel human prion disease : S2-3
Neuropathological concepts in typing of human non-transmissible dementias : S2-4
Genetic, biochemical and neuroimaging markers in preclinical and clinical Alzheimer's disease - current state and future perspectives : S2-5
MGMT promoter methylation testing - clinical significance, assays and pitfalls : S3-2
Significance of IDH1/2 mutation testing as biomarker : S3-3
Multiple sclerosis: new insights from pathology : S4-1
Emerging epidemic viral Encephalitis : S4-4
Muscular dystrophies: an update on pathology and diagnosis : S5-1
Protein aggregate myopathies : S5-3
Neuropathology in developmental disorders : S6-1
New insights in the pathomechanisms of acquired perinatal brain damage : S6-3
Classification and grading of CNS tumors: a historical perspective : W1-1
Detection of anaplastic foci in diffusely infiltrating gliomas with non-significant contrast- enhancement : W1-2
Grading: which tumors? : W1-3
Evaluating the pathology diagnosis of primary brain tumors in the context of clinical trials : W1-4
TDP-43 regulates its mRNA levels through a negative feedback loop : W2-1
TDP-43 in FTD and ALS : W2-2
FUS in FTD and ALS : W2-3
Stem cells as tools for functional studies: the example of huntingtin in Huntington's Disease : W3-2
Brain tumour typing: integration of neuropathology and genetics : W4-1
Nerve Biopsy: requirements for diagnosis and clinical value : W4-2
Brain biopsy in dementia - clinical indications and diagnostic approach : W4-4
How to revive the dead brain: Proteomics/Metabolomics : W6-1
Microarrays on archival paraffin embedded brain tissue : W6-2
Cell specific gene expression in the diseased brain : W6-3
Resurrection of autoreactive immune cells : W6-4
Bridging clinic and neuropathology in Focal Cortical Dysplasia : W7-2
Focal cortical dysplasia associated with an epileptogenic pathology : W7-3
Mild malformation of cortical development (mMCD) in the epileptic brain : W7-4
Molecular pathology of Abeta peptides in Alzheimer's disease : W8-1
Molecular imaging approaches in Alzheimer's Disease : W8-3
Neuropathology after AD vaccination: implications for pathogenesis : W8-4
Neuropathology: the struggle for training and recognition : W9-3
Perspectives for the future development of neuropathology and the ISN : W9-4
Capzb2 is specifically increased in the hippocampi of patients diagnosed with mid-stage non-familial Alzheimer's disease : Po1-1
Immunohistochemical and ultrastructural study of neuronal cytoplasmic inclusion bodies in SCA8 : Po1-2
Alpha synuclein, beta amyloid and hyperphosphorylated tau aggregation after mitochondrial complex I impairment : Po1-3
Possible alteration of mitochondrial traffic in hippocampal cell cultures during protein aggregation related to neurodegeneration : Po1-4
Exosome secretion bypasses lysosomal storage of cholesterol in Niemann-Pick type C disease : Po1-5
Alpha7 nicotinic receptor activation modulates toxic tau in the neuroblastoma sh-sy5y cell line. An interesting tool to study the molecular mecanisms in Alzheimer Disease : Po1-6
Alpha2-adrenergic receptor distribution and density within the nucleus tractus solitarii of normotensive and hypertensive rats during development : Po1-7
Cellular localization of Sphingosine-1-Phosphate receptor 1 expression in the human central nervous system : Po1-8
Methylmercury causes oxidative stress through its post-transcriptional effect on antioxidant selenoenzymes : Po1-9
Cytosolic amyloids derived from human nested genes with regard to the Alzheimer's disease pathogenesis : Po1-10
A new antibody raised against CD2 may be a novel marker of glial differentiation : Po1-11
Protection of neural precursor cells by Notoginsenoside R1 against Glutamate neurotoxicity : Po1-12
Autophagy is a common feature of human brain tumors : Po1-13
An immunohistochemical study of NMDA receptors in human cerebellum and hippocampus : Po1-14
Histological analysis of S-form local anesthetics ropivacaine and levobupivacaine compared with other local anesthetics : Po2-1
Friedreich's ataxia: abnormal distribution of iron, copper, and zinc in the dentate nucleus : Po2-2
Development of a new DNA vaccine for Alzheimer disease targeting Abeta species and amyloiditogenic peptides in the brain : Po3-1
Immune complexes impair elimination of solutes from the brain: implications for immunotherapy in Alzheimer's disease : Po3-2
Immunopositivity for ESCRT-III subunit CHMP2B in granulovacuolar degeneration of neurons in the Alzheimer's disease hippocampus : Po3-3
An autopsy case of familial Alzheimer's disease with an L381V substitution in the presenilin 1 gene : Po3-4
Cortical microinfarcts are related to cerebral amyloid angiopathy rather than to senile plaques or neurofibrillary tangles : Po3-5
Granulovacuolar degenerations are associated with tau pathology : Po3-6
Aβ induces endothelin-1 production by SH-SY5Y neuroblastoma cells : Po3-7
The distribution and expression of picalm in Alzheimer's disease : Po3-8
Brainstem tauopathy with progressive bulbar paralysis - a case presentation and analysis : Po3-9
Abundant Abeta deposition in a patient with CADASIL : Po3-10
Prevalence and pathology of dementia disorders in the oldest-old : Po3-11
High but not low levels of soluble Abeta-aggregates induce dendritic degeneration in APP-transgenic mouse models and distinguish AD cases from nondemented elderly individuals : Po3-12
Secretagogin expression in the human olfactory bulb in Alzheimer's disease : Po3-13
Genetic associations with the pattern of amyloid beta-protein pathology point to subtypes of sporadic Alzheimer's disease : Po3-14
Parieto-Occipital lobe atrophy, cotton wool plaques, and corticospinal tract degeneration associated with I229F mutation in the Presenilin 1 gene : Po3-15
Proteomic analysis of prefrontal cortical and hippocampal synaptosomes isolated from cerebral vascular hypoperfusion rats before cognitive decline : Po3-16
Association of Alzheimer disease pathologies with abnormal lipid metabolism : Po3-17
Changes of some oxidative stress markers in the serum of patients with mild cognitive impairment and Alzheimer's disease : Po3-18
Familial Alzheimer disease associated with the A673V APP recessive mutation presents a distinctive neuropathological phenotype : Po3-19
Attenuation of amyloid beta deposits, inflammatory cells and proinflammatory cytokines in MIF-knockout APPPS1 mice : Po3-20
There are significant correlations in Alzheimer brains between NFT and SP lesions and BBB associated vasoregulatory and transport proteins : Po3-21
CD163: a marker of alternative microglial activation in Alzheimer's disease : Po3-22
Details of neuropathology in Arctic Alzheimer's disease : Po3-23
Clinicoradiologic and pathological studies on the relationship between Binswanger's disease and idiopathic NPH: does the pathogenesis of the two diseases overlap? : Po4-1
Do specific MRI features of Binswanger's disease also reveal cognitive / motor impairments and the corresponding neuropathology? The Vienna Trans-Danube Aging (VITA) study : Po4-2
Leukoencephalopathy with progressive dementia : Po4-3
Pure argyrophilic grains dementia showing low perfusion of parietal lobe : Po4-4
Cytoplasmic TDP-43 accumulation is related to nuclear transport dysfunction in frontotemporal lobar degeneration and motor neuron disease : Po4-5
Frontotemporal lobar degeneration with FUS-positive inclusions : Po4-6
Amyloid independent neurofibrillary tangles in brain malformation of young adult and/or elderly patients : Po4-7
Post-mortem findings in 60 cases of fronto-temporal dementia : Po4-8
Is a synaptic cortical alpha-synuclein pathology detectable in Parkinson's disease and Parkinson's disease dementia? : Po4-9
Tauopathy with intronic 10 + 14 splice site tau gene mutation mimicking Perry syndrome : Po5-1
Early-stage progressive supranuclear palsy with degenerative lesions confined to the subthalamic nucleus and substantia nigra : Po5-2
Smad ubiquitination regulatory factor-2 in progressive supranuclear palsy : Po5-3
ESCRT pathway is involved in the formation of Lewy body and Glial cytoplasmic inclusion : Po5-4
Selective nuclear shrinkage of oligodendrocytes lacking glial cytoplasmic inclusions in multiple system atrophy: A three-dimensional volumetric study : Po5-5
Neuropathological Imaging and Long Term Follow-up Outcome in Dysequilibrium of Unknown Cause in Older People : Po5-6
Immunocytochemical localization of histone deacetylase 6 in neurodegenerative disorders : Po5-7
Existence of pre-synaptic proteinase K-resistant alpha-synuclein in human Lewy body disease and A53T alpha-synuclein transgenic mice : Po5-8
D-cycloserine and amantadine reverse recognition deficits in MPTP-induced Parkinson's disease mice mode : Po5-9
Effects of D-cycloserine on the behavioral changes and neurodegeneration in MPTP-induced Parkinson's disease animal model : Po5-10
Effects of exercise and systemic chronic nicotine in a rat model of Parkinson's disease : Po5-11
Pathological Correlates of Visual Hallucinations in Parkinson's disease : Po5-12
Oligodendrocyte precursor cells do not contain pathological inclusions in multiple system atrophy or progressive supranuclear palsy : Po5-13
Disequilibrium in MSA phenotype distribution between populations: genetics or environment? : Po5-14
Analysis of epicardial fat tissue as a potential tool for in vivo evaluation of autonomic nervous tissue in premotor Parkinson's disease (PD): a pilot study in cardiac surgery : Po5-15
Pergolide attenuates memory impairment and oxidative stress induced by a 6-hydroxydopamine model of Parkinson's disease : Po5-16
Conditional expression of mutant A30P alpha-synuclein in the olfactory bulb of transgenic mice: implications for early stage of Parkinson's disease : Po5-17
Progression of hippocampal involvement in amyotrophic lateral sclerosis: distinction from Alzheimer disease : Po6-1
An autopsy case of familial amyotrophic lateral sclerosis with Gly93Ser mutation in Cu/Zn superoxide dismutase : Po6-2
A case of multiple system atrophy combined with amyotrophic lateral sclerosis : Po6-3
Adenoviral Expression of TDP-43 and FUS Genes in Adult Rat Motoneurons in vivo : Po6-4
FUS pathology in patients with motor neuron disease : Po6-5
Neuropathology of facial onset sensory and motor neuronopathy (fosmn syndrome) : Po6-6
An immunohistochemical study on basophilic inclusions of adult-onset atypical motor neuron disease : Po6-7
Distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions in sporadic amyotrophic lateral sclerosis : Po6-8
TARDBP mutations, amyotrophic lateral sclerosis and alternative splicing in human fibroblasts : Po6-9
Relationship between Bunina bodies and TDP-43 inclusions in spinal anterior horn in amyotrophic lateral sclerosis : Po6-10
An autopsy case of amyotrophic lateral sclerosis showing an upper-motor predominant form with frontotemporal lobar degeneration : Po6-11
Familial TDP proteinopathy with ALS presentation: characteristic clinical and pathological features : Po6-12
Mutant VAPB transgenic mice linked to amyotrophic lateral sclerosis type-8 develop TDP-43 pathology : Po6-13
Involvement of the endosomal-lysosomal system in motor neuron disease : Po6-14
Clinical and neuropathologic investigation of a family with ALS associated with mutated optineurin : Po6-15
ALS of Guam: neuropathological reevaluation in comparison with the parkinsonism-dementia complex, frontotemporal lober degeneration and classic ALS : Po6-16
Progranulin immunoreactivity of the spinal cord in amyotrophic lateral sclerosis : Po6-17
FUS pathology and FUS mutations characterize juvenile ALS with basophilic inclusions : Po6-18
Analysis of the mode of photoreceptor cell death in the Ataxia and Male Sterility (AMS) mouse, a Nna1 mutant : Po7-1
Involvement of Onuf's nucleus in Machado-Joseph disease : Po7-2
An aged patient with spinocerebellar ataxia type 2: an autopsy case report with review of the literature : Po7-3
SCA31: A new SCA identified in Japan showing peculiar pathology of Purkinje cells : Po7-4
Neuropathological characteristics of spinal cord in dentatorubral-pallidoluysian atrophy (DRPLA) : Po7-5
Ultrastructural characteristics of Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies or prion diseases : Po8-1
Detection of common RNA in the plasma of patients with sporadic Crutzfeldt-Jakob disease, Gerstmann-Straussler Schenker disease, and brain disorders other than transmissible spongiform encephalopathies : Po8-2
Clinicopathologic characteristics of V180I Creutzfeldt-Jakob disease in Japan : Po8-3
Effect of therapeutic drugs on prion protein polymerization in a prion-infected cell line : Po8-4
Detection of prion-protein oligomers by single molecule fluorescence imaging : Po8-5
Localized metal dysregulation in prion disease-infected brains : Po8-6
Hirano body - rich subtypes of sporadic CJD: a morphological marker of rare variants? : Po8-7
Plasma proteome changes in mice affected by neurodegeneration : Po8-8
Prion-induced changes in the urinary protein profile of mice : Po8-9
Expansion of the BSE surrogate biomarker inventory : Po8-10
Transcriptional profiling of microRNAs and messenger RNAs reveals gene regulatory circuits involved in neurodegeneration : Po8-11
Systemic surveys of an expanded inventory of TSE associated biomarkers : Po8-12
Neuropathological changes correlate temporally but not spatially with selected neuromodulatory responses in natural scrapie : Po8-13
Deposition of multiple proteins in the brain: experience in a community-based cohort : Po9-1
Disruption of neuron-glia interaction at the paranodal junctions in myelinated nerves causes the axonal degeneration and cell death : Po9-2
Withdrawn : Po9-3
An autopsy case of Hallervorden-Spatz syndrome with abundant neurofibrillary tangles : Po9-4
Methylmercury induces neuropathological changes with tau hyperphosphorylation mainly through the activation of c-jun-N-terminal kinase pathway in the cerebral cortex, but not in the hippocampus of the mouse brain : Po9-5
An autopsy case of adult-onset Leukoencephalopathy with vanishing white matter (VWM) : Po9-6
Immunohistochemical study of microglia in the Nasu-Hakola diseased brain : Po9-7
Nodular bilateral amygdala degeneration in dementing disorders : Po9-8
Neuropathological changes in the spinal cords of centenarians : Po9-9
Loss of layer Pre-alpha entorhinal neurons in Huntington disease : Po9-10
Capillary CAA and perivascular Abeta-deposition : Po9-11
Neuroinflammation in the frontal cortex of patients with late-life depression : Po9-12
The carboxy-terminal fragment of α1A-calcium channel behavior underlies SCA6 neurodenegeration : Po9-13
Neuropathological diversity of corticobasal degeneration (CBD) in 23 autopsied cases : Po9-14
Cerebral amyloid angiopathy, neurodegeneration, and dementia in a population-based study on very elderly Finns (Vantaa 85+) : Po9-15
Simultaneous evaluation of neuronal degeneration and regeneration in experimental traumatic brain injury : Po9-16
TAR-DNA binding protein-43 and alterations in the hippocampus : Po9-17
Correlation of taupathy and alpha-synucleinopathy with tissue lesioning in neurodegeneration with brain iron accumulation (NBIA) : Po9-18
Establishment of Japanese brain bank network for neuroscience research : Po9-19
The neurodegenerative process of the mouse trigeminal motor nucleus after nerve injury : Po9-20
Microarray analysis of the astrocyte transcriptome in the ageing brain: relationship to Alzheimer's pathology and ApoE genotype : Po9-21
TP53 mutation analysis of malignant peripheral nerve sheath tumors : Po10-1
Grading of astrocytomas: role of immunohistochemical markers : Po10-2
Oligodendroglial neoplasms with ganglioglioma-like maturation: a diagnostic pitfall : Po10-3
Clinicopathological and immunohistochemical profile of meningiomas : Po10-4
Isocitrate dehydrogenase 1 mutations are adverse prognostic markers in gangliogliomas : Po10-5
INI1 immunohistochemical expression in glioblastoma: correlation with MGMT gene promoter methylation and patient survival : Po10-6
Histological characterization of low-grade diffuse astrocytomas : Po10-7
HIF-1α, VEGF, PRL 3 and MMP-9 in Gliomas: an MR correlation : Po10-8
Histological characterization of human glioblastomas : Po10-9
Immunohistochemical findings of intraparenchymatous metastases of the central nervous system : Po10-10
Histological types of primary central nervous system tumors associated to topography, age, gender and immunohistochemical features : Po10-11
Differential diagnosis of low grade astrocytoma and reactive gliosis - immunostaining for peripheral benzodiazepine receptors may provide additional tool : Po10-12
Diagnostic methods in primary central nervous system lymphomas (PCNSL) : Po10-13
Development of myofibroblastic sarcoma in meningioma: a new variant of ‘metaplastic’ meningioma : Po10-14
Epigenetic inactivation of the candidate tumor suppressor gene RRP22 on 22q12.2 by means of promoter hypermethylation and histone modifications in diffusely infiltrating human gliomas : Po10-15
Correlation of parameters derived from DCE-MRI with histopathologic features in Glioblastomas : Po10-16
The expanding histopathological spectrum of tanycytic ependymoma: Report of two cases : Po10-17
A case of intramedullary mixed germ cell tumor in the cervical spine proceeded by twenty-seven years ago intracranial pure germinoma : Po10-18
Integrative immunohistochemical analysis in glioblastoma multiforme : Po10-19
Expression of ZIC family genes in meningiomas and other brain tumors : Po10-20
Epigenetic regulation of microRNA expression in glioma cells : Po10-21
Central neurocytomas: a French multicenter clinicopathologic study of 93 cases : Po10-22
Unusual presentations of central nervous system non-hodgkin and hodgkin lymphoma: a clinicopathologic review of four tumours from Tan Tock Seng Hospital, Singapore : Po10-23
Glutamate transporters in diagnostic neurooncology : Po10-24
Activated leukocyte cell adhesion molecule expression in neuroepithelial neoplasms is dependent on tumor type : Po10-25
Cell lines derived from low-grade gliomas by hTERT-mediated immortalization : Po10-26
Sellar paraganglioma mimicking pituitary macroadenoma. Report of a case : Po10-27
Extraventricular neurocytomas: A morphological and histogenetic consideration - A study of six cases : Po10-28
Improved outcome of glioblastoma patients, a population-based study by the Austrian Brain Tumor Registry : Po10-29
Evaluating the role of TPPP/p25 in oligodendrogliomas : Po10-30
Hypoxia in the 3-D glioblastoma-derived neurospheres: luck or bug? : Po10-31
Fluorescence in situ hybridization (FISH) for 1p/19q in oligodendrogliomas - The need for consensus criteria and uniform guidelines : Po10-32
Clinicopathological investigation of tight junction-associated proteins in human brain tumors : Po10-33
CD133 Immunohistochemisty in Glioblastoma - Identification of tumor stem cells or a matter of coincidence? : Po10-34
P-gP and MRP immunostaining in gliomas - does the expression of P-gP and MRP correlate with chemosensitivity in glioma cell cultures? : Po10-35
Glioneuronal tumor of the fourth ventricle associated with neurofibromatosis type 1 : Po10-36
The role of ARF-BP1 in primary intracranial germ cell tumors : Po10-37
Nodal regulates cell metabolism through HIF-1a in glioma cells : Po10-38
Metastatic meningioma to small intestine : Po10-39
Expression of ER- β and steroid receptor co-regulators (AIB-1, TIF-2, PELP-1) in gliomas and correlation with clinical outcomes : Po10-40
The mitogen activated protein kinases (MAPKs) p38, p44/42 and JNK are markers of tumor progression in gliomas : Po10-41
The Gli code in gliomas: Correlation of expression of Gli 1, 2 & 3 with histology, SHH, PTCH and stemness markers : Po10-42
Glioblastomas in Indian population: Analysis of genetic alterations and correlation with age : Po10-43
Papillary glioneuronal tumour in unusual intraventricular localization : Po10-44
Angiogenesis proteome: a comparison between physiological angiogenesis and angiogenesis in Glioblastoma : Po10-45
Protein and gene expression of vascular endothelial growth factor in intracranial meningiomas with brain edema : Po10-46
Molecular analysis of TP53, IDH-1/IDH-2, β -catenin and c-myc/N-myc status in 12 cases of supratentorial PNET (s-PNET) in adults : Po10-47
A GBM proliferative compartment with aggressive oncogenic signature can be identified by the expression of NG2 : Po10-48
Preserved DARPP-32 expression in gliomas is associated with favorable disease parameters : Po10-49
Clinicopathological and immunohistochemical studies of metastatic brain tumors : Po10-50
Neuropilin-1 mRNA expression in intracranial meningeomas with brain edema : Po10-51
A rapid, user-friendly approach for distinguishing between partial and complete 1p/19q losses in gliomas : Po10-52
Cell signalling pathway in diffuse astrocytic tumors. Correlation between 4E-BP1 factor and histological grading : Po10-53
A high-throughput in vivo screen in Drosophila melanogaster reveals LOX/LOXL as mediator of PDGFR-associated gliomagenesis : Po10-54
Preliminary study of the methylation status of MGMT gene promoter in glioblastoma - hopefully a first step toward ‘personalized’ treatment of gliomas : Po10-55
GNAQ mutation analysis might be useful in distinguishing between primary melanocytic lesions of the CNS and melanotic schwannomas : Po10-56
Pituitary adenomas: a series of 270 cases : Po10-57
Neurofibromatosis type 1 and rosette-forming glioneuronal tumor : Po10-58
Immunohistochemical study of neural stem, precursor and mature cells in different astrocytoma grades : Po10-59
Role of eIF3 in glioblastoma : Po10-60
Oligodendroglial tumor classification: phenotype vs genetic signature : Po10-61
Preoperative diffusion imaging-derived data in prediction of glioma grades : Po10-62
Comprehensive molecular analysis of oligodendroglial tumors. merging genomic, transcriptomic and metabolomic data : Po10-63
Alpha-internexin - a useful marker in the differential diagnosis of oligodendroglial tumors : Po10-64
Lipoastrocytoma: case report : Po10-65
Grading of brain gliomas based on the synchrotron radiation x-ray fluorescence and discriminant analysis : Po10-66
Differential immunohistochemical expression of beta-catenin and nestin in endothelial cells of low grade versus high grade gliomas : Po10-67
Are fibrous bodies in sparsely granulated somatotroph pituitary adenomas aggresomes? : Po10-68
Peptidyl Argine Deiminase 2 (PADI2) on 1p36.13 is a candidate tumour suppressor gene frequently hypermethylated in oligodendrogliomas : Po10-69
Brain tumor stem cells of malignant gliomas: a cell type or a stem cell-like status? : Po10-70
A neuropathology-led neuro-oncology multidisciplinary team in Ireland : Po10-71
Her2/neu status in primary breast cancers and their central nervous system metastases : Po10-72
Intracranial metastases as first manifestation of follicular thyroid carcinoma: report of two cases : Po10-73
Incipient cerebral tumours: report of three cases : Po10-74
Malignant meningiomas with epithelial (adenocarcinoma-like) metaplasia: A study of three cases : Po10-75
Low grade diffuse astrocytomas recurring as oligodendrogliomas: a reflex of peripheral sampling in the first specimen or of subjectivity in classifying diffuse low grade gliomas? : Po10-76
Identification of immunohistochemical markers that differentiate fibroblastic meningioma from schwannoma: a tissue microarray based approach : Po10-77
Intravascular large B cell lymphoma (IVLBCL), Asian variant : Po10-78
Primary central nervous system histiocytic sarcoma: report of two cases : Po10-79
Papillary tumours of the pineal region with various histological features : Po10-80
Glioneuronal tumour with advanced lipidization - a case report : Po10-81
Tumor cell infiltration of glioblastoma - comparison of autopsy brain and neuromaging : Po10-82
Clinicopathological and genetics features of meningeal solitary fibrous tumours and haemangiopericytomas: a retrospective study of the French Society of Neuropathology of 105 cases : Po10-83
Aurora-A protein is differentially expresssed in glial tumors : Po10-84
What characterizes brain-infiltrating meningiomas? : Po10-85
Clear cell variant of meningioma: report of three cases : Po10-86
Meningioangiomatosis: a ‘phasmid’* lesion of uncertain origin : Po10-87
Expression of BARHL1 in medulloblastoma is associated with prolonged survival in mice and humans : Po11-1
Isochromosome 17q in pediatric medulloblastoma : Po11-2
Immunohistochemical evaluation of B-RAF, pMEK1 and pERK1/2 expressions in pilocytic and pilomyxoid astrocytomas by localization : Po11-3
Tenascin-C is a new prognostic marker of paediatric intracranial ependymoma: results from a European study of prognostic markers : Po11-4
Atypical teratoid/rhabdoid tumor (ATRT) and its incidence: a population-based study by the Austrian Brain Tumor Registry : Po11-5
Embryonal tumor with abundant neuropil and true rosettes, report of 3 cases of a rare tumor, with unusual case showing rhabdomyoblastic and melanocytic differentiation : Po11-6
p16INK4A and p14ARF tumor suppressor pathways are deregulated in malignant rhabdoid tumors : Po11-7
Analysis of PDGF-R expression and the MAPK pathway in disseminated pilocytic astrocytomas : Po11-8
c-Kit gene mutations are a common event in germinomas: mutational analysis of 83 cases of germinomas : Po11-9
Validation of histological and biological parameters for clinical stratification of pediatric patients with medulloblastomas (SIOP-PNET 4 clinical trial) : Po11-10
Targeting overexpressed Aurora kinases in childhood medulloblastoma: anti-proliferative effects of small molecule inhibitors ZM44739, VX680 and shRNA : Po11-11
CNS-PNET molecular genetics in the Arab world : Po11-12
Clinicopathologic features of patients with brain stem gliomas, experience from King Hussein Cancer Center : Po11-13
Tumor initiating cells and progression mechanisms in brainstem gliomas : Po11-14
Analysis of immunohistochemical expression of stem cell markers in pilocytic astrocytomas and its significance in terms of tumor behaviour : Po11-15
Nerve growth factor receptor, p53 and double cortin expression in medulloblastoma subtypes - an immunohistochemical analysis : Po11-16
Nuclear translocation of IRS-1 by polyomavirus JCV protein T-Antigen causes alterations on faithful DNA repair in Medulloblastomas : Po11-17
Gene analyses in vessels with blood-brain barrier impairment : Po12-1
Subarachnoid hemorrhage accompanied by cerebral infarction followed by repeated hemorrhage due to primary cerebral angiitis of the central nervous system : Po12-2
Role of perivascular spaces in the pathogenesis of ischemic white matter lesions: with special reference to VITA Neuroradiological-Pathological study : Po12-3
Autoimmunological vasculitis in cerebral toxsoplasmosis in AIDS patients : Po12-4
Morphological changes in capillary vessels in CADASIL patients : Po12-5
Pathological features and MRI findings of coagulation necrosis in cerebral infarcts after thrombolytic therapy : Po12-6
The primary hemorrhage of cerebral amyloid angiopathy-related hemorrhage (CAA-H) occurs in the cerebral sulci : Po12-7
Ultrastructural abnormalities of dermal connective tissue in Japanese patients with spontaneous cervical artery dissection : Po12-8
An autopsy case of ‘possible’ posterior reversible encephalopathy syndrome (PRES) associated with Bacillus cereus sepsis during the treatment of acute myeloid leukemia : Po13-1
Phenotypic changes in human adult microglia following classical and alternative activation : Po13-2
Neuropathologic findings in Acute Necrotizing Encephalopathy (ANE). Report of three Spanish cases, one of them related with novel influenza A (human H1N1) infection : Po13-3
Rasmussen's Syndrome: a clinicopathological study of 22 cases : Po13-4
Parry-Romberg syndrome with Rasmussen's encephalitis and monoclonal B cell proliferation on brain biopsy : Po13-5
Avian H5N1 influenza encephalitis : Po14-1
Neural bystander damage by infiltrating virus-infected T cells and the cytotoxic T lymphocytes in HTLV-I-associated neurological disease : Po14-2
Epstein-Barr virus positive cells are detected in Human Immune Deficiency Virus Encephalitis (HIVE) associtated with opportunistic infection, toxoplasmosis : Po14-3
A role of astrocyte dysfunction in pathogenesis of AIDS encephalopathy : Po14-4
Activation of anti-apoptotic protein Survivin by human polyomavirus JCV. Implications for the pathogenesis of progressive multifocal leukoencephalopathy : Po14-5
Acute holotopistic encephalic hemorrhages mimicking acute hemorrhagic leucoencephalitis in a patient with the influenza A (H1N1) virus infection : Po14-6
Three-dimensional cultures for the identification of tumor cell subpopulations resistant to HSV-1 mediated oncolytic therapy : Po14-7
Latent brain JC polyomavirus: the role of immunosuppression and site of viral latency : Po14-8
Mapping rabies viral antigen in human brain - does it correlate with incubation period? : Po14-9
HIV-1 subtype C associated neuropathology: is it different? : Po14-10
Astrocytic and microglial reactivity in dogs with visceral leishmaniasis : Po15-1
A fatal Candida albicans meningoencephalomyeloradiculitis in an immunocompetent patient: case report and review of the literature : Po15-2
Loss of Purkinje cells in association with cerebellar plaques in the classical Charcot and the acute Marburg variants of multiple sclerosis: two case studies : Po16-1
Angiogenesis may be an early, amplifying event in the evolution of experimental allergic encephalomyelitis : Po16-2
Aquaporin-4 astrocytopathy in Balo's disease, neuromyelitis optica, and multiple sclerosis in Asians : Po16-3
Clinical features, neuroimaging findings and pathological characteristics of 32 patients with tumor-like inflammatory demyelinating diseases : Po16-4
An autopsy case of multiple sclerosis with massive involvement of basal ganglia and thalamus : Po16-5
Expression of tubulin polymerization promoting protein (TPPP/p25) in diseases affecting the white matter : Po16-6
Demyelination versus remyelination in progressive multiple sclerosis : Po16-7
Axonal loss and neurofilament phosphorylation changes accompany lesion development and clinical progression in multiple sclerosis : Po16-8
Adalimumab-associated tumefactive CNS demyelination : Po16-9
Selective astrocyte injury in Devic's disease : Po16-10
Molecular Triggers for Demyelination in Progressive Multiple Sclerosis : Po16-11
Ferritin and iron in multiple sclerosis lesions : Po16-12
Cerebral White Matter Hypoplasia - A rare neurological disease of early life with obscure pathogenesis : Po17-1
Neuropathological findings in intractable epilepsy: 435 Chinese cases : Po17-2
Diffuse dysembryoplastic neuroepithelial tumours (dDNT) from epilepsy surgery demonstrate transition to classical DNT and ganglioglioma : Po17-3
CNS involvement by chronic lymphocytic leukemia presented as intractable epilepsy: ‘a case report’ : Po17-4
Neuropathological study of medically intractable mesial temporal lobe epilepsy (MTLE): histological classification of hippocampal sclerosis and its clinical relevance : Po17-5
Satellite glia in paediatric epilepsy: guardian angels or assassins of neurons? : Po17-6
Dysembryoplastic neuroepithelial tumour (DNT) and sudden unexplained death in epilepsy: three cases with neuropathologic confirmation : Po17-7
The clinicopathological profile and investigation of traumatic basal subarachnoid haemorrhage : Po18-1
Exploring the personality and defense mechanisms in schizophrenia and dementia : Po19-1
Neuroregeneration in the acute spinal cord injury in adult dysmyelinated rat implanted with choroid plexus : Po20-1
The expression of Id2 and its potential roles in the regulation of neural stem cells in the subventricular zone of the adult mouse : Po20-2
An autopsy case of Sanfilippo A syndrome with severe cerebral cortical involvement : Po21-1
Clinical, neuroimaging and pathological features of MELAS and Leigh disease: a retrospective analysis of 18 patients : Po22-1
Neuropathological studies on fetuses prenatally diagnosed as brain anomalies : Po23-1
Correlation of immunohistochemical myelination with diffusion tensor magnetic resonance imaging in the developing fetal corpus callosum : Po23-2
Aristaless-related homeobox (ARX) gene nullmutation exhibits abnormal distribution of GABAergic interneurons: immunohistochemical study of human X-linked lissencephaly with abnormal genitalia : Po23-3
Neocortical layer-formation of human developing brains and lissencephalies: consideration of layer-specific marker expression : Po23-4
Prenatal ethanol exposure affects the development of the brain microvascular network: involvment of the VEGF pathway : Po23-5
Ponto-cerebellar hypoplasia with severe outcome associated with TSEN54 mutations : Po23-6
GPR56 neuropathological phenotype: first description in a fetus : Po23-7
Central nervous system anomalies in fetal and pediatric autopsies: a seven-year retrospective review : Po23-8
Neuroprotective effects of moderate intermittent hypoxia in newborn mice : Po23-9
Escape response in spontaneously hypertensive rats treated with omega-3 dietary : Po24-1
Acupuncture reduces neuropathic pain after chemotherapy in Hansen's disease patients : Po25-1
Morphological and morphometric analysis of dermal nerves in resin embedded semi-thin sections. An alternative method to diagnose small fibre neuropathies such as leprosy : Po25-2
Protein aggregation in the aging retina : Po27-1
Frequency of mitochondrial changes in normal muscle : Po28-1
Clinicopathological features of autophagic vacuolar myopathies characterized by autophagic vacuoles with sarcolemmal features (AVSF) : Po28-2
HTLV-1 associated polymyositis: a trial to unfold the story : Po28-3
Muscular dystrophies in the Arab world : Po28-4
Limb girdle muscular dystrophy type 2A in India: A study based on semi-quantitative protein analysis with clinical and histopathological viewpoint : Po28-5
The extracellular matrix protein PRELP (proline, arginine-rich end leucine-rich repeat protein) in sporadic inclusion body myositis and polymyositis : Po28-6
Dysregulation of myogenic regulatory factors and myo-endothelial remodelling in sporadic inclusion body myositis : Po28-7
Hereditary caveolinopathy: Influence on growth factor signalling in vitro and results of a rat in vivo model of caveolinopathy : Po28-8
A perinatal hypoxic-ischaemic lesion of the status marmoratus type with involvement of both thalami, clinically manifested as west syndrome. Presentation of an autopsy case : Po29-1
Skin biopsy is available tool for antemortem diagnosis of Neuronal intranuclear hyaline inclusion disease : Po29-2
Hypertensive encephalopathy of focal cortical reversible lesions in MRI: a case report : Po29-3
Schwann cells enter and present an oligodendrocytelike remyelinating pattern in the rat spinal cord after ethidium bromide injection : Po30-1
A mouse model characterizing features of vascular dementia with hippocampal atrophy : Po30-2
The effect of cyclosporine on the brainstem remyelination of diabetic and non-diabetic rats following ethidium bromide injection : Po30-3
Axonal degeneration associated with abnormal membranes of mitochondria in Group VIA phospholipase A2 knockout mice : Po30-4
Correlations between autopsy images of 3-tesla-MRI (MRI-AIS) and neuropathologic findings : Po31-1
Model of diagnostic procedures concerning stereotactic biopsy (STB) material of central nervous system (CNS) tumours : Po31-2
Interstitial cells of cajal in 3D-reconstructions of myenteric plexus in gastrointestinal neuromuscular disease : Po31-3
RCL2 fixation of surgical brain tumour samples results in well preserved histomorphology, immunohistochemistry and nucleic acids : Po31-4
3800-year-old brain from a Bronze Age settlement in Kutahya, West Anatolia: remarkable preservation of the brittle double-bond fatty acids in a special earth containing alkali earth elements and boron : Po31-5
Transneuronal laminar degeneration of the lateral geniculate bodies after enucleation : Po32-1