Neuropathology

Papers
(The median citation count of Neuropathology is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-03-01 to 2024-03-01.)
ArticleCitations
Where and how alpha‐synuclein pathology spreads in Parkinson’s disease:35
A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration25
Glioblastoma multiforme: Metabolic differences to peritumoral tissue and IDH‐mutated gliomas revealed by mass spectrometry imaging24
Praja1 RING‐finger E3 ubiquitin ligase suppresses neuronal cytoplasmic TDP‐43 aggregate formation23
Sodium/glucose cotransporter 2 is expressed in choroid plexus epithelial cells and ependymal cells in human and mouse brains23
Intracellular amyloid hypothesis for ultra‐early phase pathology of Alzheimer's disease21
Human brain pathology in myotonic dystrophy type 1: A systematic review20
Histological characterization of interneurons in Alzheimer's disease reveals a loss of somatostatin interneurons in the temporal cortex19
Astrocytes release glutamate via cystine/glutamate antiporter upregulated in response to increased oxidative stress related to sporadic amyotrophic lateral sclerosis15
Red nucleus IL‐6 mediates the maintenance of neuropathic pain by inducing the productions of TNF‐α and IL‐1β through the JAK2/STAT3 and ERK signaling pathways14
Neuropathology of α‐synuclein in Parkinson's disease14
Reappraisal of the anatomical spreading and propagation hypothesis about TDP‐43 aggregation in amyotrophic lateral sclerosis and frontotemporal lobar degeneration14
Investigation of adult‐onset multiple acyl‐CoA dehydrogenase deficiency associated with peripheral neuropathy12
Many roles for oligodendrocyte precursor cells in physiology and pathology11
Multiple system aging‐related tau astrogliopathy with complex proteinopathy in an oligosymptomatic octogenarian11
Abnormal prion protein deposits with high seeding activities in the skeletal muscle, femoral nerve, and scalp of an autopsied case of sporadic Creutzfeldt–Jakob disease10
Neurofibrillary changes undergoing morphological and biochemical changes – How does tau with the profile shift of from four repeat to three repeat spread in Alzheimer brain?10
An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP‐43 proteinopathy10
Globular glial tauopathy Type I presenting with behavioral variant frontotemporal dementia9
Diffuse midline glioma with H3 K27M mutation of the spinal cord: A series of 33 cases9
A case of CIC‐rearranged sarcoma with CIC‐LEUTX gene fusion in spinal cord9
Transactivation response DNA‐binding protein of 43 kDa proteinopathy and lysosomal abnormalities in spastic paraplegia type 118
Intracranial myxoid angiomatoid fibrous histiocytoma with “classic” histology and EWSR1:CREM fusion providing insight for reconciliation with intracranial myxoid mesenchymal tumors8
The Braak hypothesis in prion disease with a focus on Creutzfeldt–Jakob disease8
Clinicopathological features of titinopathy from a Chinese neuromuscular center8
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis8
A case of intracranial myxoid mesenchymal tumor with EWSR1:CREM fusion in an adult female: Extensive immunohistochemical evaluation7
Expression of programmed cell death ligand‐1 by immune cells in the microenvironment is a favorable prognostic factor for primary diffuse large B‐cell lymphoma of the central nervous system7
Clinicopathological heterogeneity of Alzheimer's disease with pure Alzheimer's disease pathology: Cases associated with dementia with Lewy bodies, very early‐onset dementia, and primary progressive ap7
High‐grade gliomas with isocitrate dehydrogenase wild‐type and 1p/19q codeleted: Atypical molecular phenotype and current challenges in molecular diagnosis7
Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors7
Minocycline prevents depression‐like behavior in streptozotocin‐induced diabetic mice7
Accumulation of phosphorylated TDP‐43 in the cytoplasm of Schwann cells in a case of sporadic amyotrophic lateral sclerosis7
Lewy pathology of the submandibular gland in Lewy body disease: A report of autopsy cases6
Neuropathology of the spinal nerve roots, spinal cord, and brain in the first autopsied case of Charcot–Marie–Tooth disease 4F with a D651N mutation in the periaxin gene6
Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva6
A case of desmoplastic myxoid tumor, SMARCB1 mutant, in the pineal region6
Experimental models of prion‐like protein propagation6
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus6
FOXM1‐mediated NUF2 expression confers temozolomide resistance to human glioma cells by regulating autophagy via the PI3K/AKT/mTOR signaling path6
An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter6
Distribution of amyloid‐β precursor protein‐immunoreactive axons differs according to the severity of cerebral ischemia in autopsy brains5
Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation5
Progressive supranuclear palsy: Neuropathology of patients with a short disease duration due to unexpected death5
Clinicopathological diversity of semantic dementia: Comparisons of patients with early‐onset versus late‐onset, left‐sided versus right‐sided temporal atrophy, and TDP‐type A versus type C pathology5
Brain cutting and trimming5
NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion5
Supratentorial ependymoma with YAP1:FAM118B fusion: A case report5
LINC01123 potentially correlates with radioresistance in glioma through the miR‐151a/CENPB axis5
Cerebral embolization associated with parenchymal seeding of the left atrial myxoma: Potential role of interleukin‐6 and matrix metalloproteinases5
Identification and characterization of sex‐dependent gene expression profile in glioblastoma5
The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality5
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study4
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia4
The hot cross bun sign in corticobasal degeneration4
Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?4
Immunohistochemical expression of osteopontin and collagens in choroid plexus of human brains4
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?4
Metastatic lesions of atrial myxoma. A pathologist can clinch them all4
The autophagic marker p62 highlights Alzheimer type II astrocytes in metabolic/hepatic encephalopathy4
Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association3
Unique Lewy pathology in myotonic dystrophy type 13
A juvenile case of epilepsy‐associated, isocitrate dehydrogenase wild‐type/histone 3 wild‐type diffuse glioma with a rare BRAFA598T mutation3
Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas3
Neuropathology of a case of fragile X‐associated tremor ataxia syndrome without tremor3
Spinal cord‐predominant neuropathology in an adult‐onset case of POLR3A‐related spastic ataxia3
An adult case of diffuse midline glioma with H3 K27M mutation3
Let's cluster cases in Neuropathology Case Cluster series!: Unveil clinical masqueraders (Neuropathology Cluster Case 1–13)3
Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case3
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor3
Parallel enlargement of Marinesco bodies and nuclei and progressive deposition of p62 in pigmented neurons of the substantia nigra3
A case of ganglioglioma grade 3 withH3 K27Mmutation arising in the medial temporal lobe in an elderly patient3
Brain parenchymal angiomatoid fibrous histiocytoma and spinal myxoid mesenchymal tumor with FET: CREB fusion, a spectrum of the same tumor type3
First definition of burned choroid plexus in acidic cerebrospinal fluid‐filled brain ventricles during subarachnoid hemorrhage: Experimental study3
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis3
Amyloid‐β plaques may be reduced in advanced stages of cerebral amyloid angiopathy in the elderly3
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies3
Pembrolizumab‐caused polyradiculoneuropathy as an immune‐related adverse event3
High HMGA2 expression without gene rearrangement in meningiomas3
Utility of Schwann/2E and Sox10 in distinguishing CD57‐negative olfactory groove schwannoma from olfactory ensheathing cell tumor: A case report and review of the literature3
Recurrent oligodendroglioma with changed 1p/19q status3
Possible association of limbic tau pathology with psychosis or behavioral disturbances: Studies of two autopsied psychiatric patients3
A case of MV2K subtype of sporadic Creutzfeldt–Jakob disease with florid‐like plaques: Similarities and differences to variant Creutzfeldt–Jakob disease3
Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT‐ND13
Senile plaque calcification of the lamina circumvoluta medullaris in Alzheimer's disease3
Primary central nervous system other iatrogenic immunodeficiency‐associated lymphoproliferative disorders presenting as extraosseous plasmacytoma with a progressive clinical course: A case report and 3
Immunotherapy‐refractory vacuolar myopathy with mucin deposition in scleromyxedema: A possible role of fibroblast growth factor 23
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings3
Tufted astrocyte‐like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?3
Coexistence of dentatorubral‐pallidoluysian atrophy and Parkinson's disease: An autopsy case report3
Macroscopic diagnostic clue for parkinsonism3
Macroscopic findings of brain with dementia3
An autopsy case report of neuronal intermediate filament inclusion disease presenting with predominantly upper motor neuron features2
Astrocytoma (CNS WHO grade 4), IDH‐mutant with co‐occurrence of BRAF p.V600E mutation, and homozygous loss of CDKN2A2
An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy2
Dual pathology in a patient with temporal lobe epilepsy associated with neocortical glial scar after brain abscess and end folium sclerosis/hippocampal sclerosis type 32
“Burnt‐out” progressive multifocal leukoencephalopathy in idiopathic CD4+ lymphocytopenia2
Neuropathological report of propionic acidemia2
Pediatric and elderly polymorphous low‐grade neuroepithelial tumor of the young: Typical and unusual case reports and literature review2
Concurrent intraventricular intracranial myxoid mesenchymal tumor and ependymoma in a long‐term Ewing sarcoma survivor2
An anaplastic pleomorphic xanthoastrocytoma with periventricular extension: An autopsy case report and review of the literature2
Clinicopathological features in two families with MARS‐related Charcot–Marie–Tooth disease2
Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions2
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?2
Primary central nervous system lymphomas with massive intratumoral hemorrhage: Clinical, radiological, pathological, and molecular features of six cases2
Extra‐axial sacral soft tissue giant cell ependymoma affecting a child: Case report and review of the literature2
Olfactory neuroblastoma associated with extensive “in situ” lesion and aberrant glandular and rhabdomyosarcomatous differentiation2
An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau2
An autopsy case of progressive supranuclear palsy. Pallido‐nigro‐luysian type with argyrophilic grains clinically presenting with personality and behavioral changes2
Acute actinomycotic brain abscess in a patient with rheumatoid arthritis2
A pathologically confirmed case of combined amyotrophic lateral sclerosis with C9orf72 mutation and multiple system atrophy2
Case report of anorexia nervosa showing periventricular gliosis at autopsy2
Pathological features of inflammatory myopathy as a manifestation of chronic graft‐versus‐host disease after allogeneic bone marrow transplantation2
Elucidating the multiple genetic alterations involved in the malignant transformation of a KRAS mutant neurenteric cyst. A case report2
Intraventricular mucin‐producing glioblastoma arising in the septum pellucidum at the frontal horn of the lateral ventricle: A case report2
Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL‐6/STAT3 signaling2
Fukutin regulates tau phosphorylation and synaptic function: Novel properties of fukutin in neurons2
An autopsy case of amyloid angiopathy‐related cerebellar hemorrhage2
Calcifying pseudoneoplasms of the neuraxis (CAPNON). A case report2
Quantitative analysis of MGMT promoter methylation status changes by pyrosequencing in recurrent glioblastoma2
Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature2
Morphological study of the phrenic nerve to determine a reference value for the myelinated fiber density in elderly individuals2
A large interhemispheric glioependymal cyst associated with partial defect of the corpus callosum in an elderly man2
Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 32
Distinct TERT promoter C228T and C250T mutations in a patient with an oligodendroglioma: A case report2
Whorling‐sclerosing meningioma invading skull bone and subcutaneous tissue with an incidental toxoplasmosis: A case report1
Senile plaque‐associated transactive response DNA‐binding protein 43 in Alzheimer's disease: A case report spanning 16 years of memory loss1
The landscape of common genetic drivers and DNA methylation in low‐grade (epilepsy‐associated) neuroepithelial tumors: A review1
Tumefactive eosinophil‐rich non‐granulomatous small vessel vasculitis in the cerebrum in a patient with idiopathic hypereosinophilic syndrome1
A novel homozygous variant of RYR1 p.Ala3072Asp in a neonate with dusty core disease: A new entity with clinicopathological implications1
Parkinson's disease and parkinsonism: Clinicopathological discrepancies on diagnosis in three patients1
Functional analyses of STIM1 mutations reveal a common pathomechanism for tubular aggregate myopathy and Stormorken syndrome1
A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma1
An autopsy case of corticobasal degeneration with inferior olivary hypertrophy1
Comparison of clinical imaging and pathological findings of various brain lesions including cerebrovascular diseases and other systemic diseases1
Astrocytes in ischemic stroke: Crosstalk in central nervous system and therapeutic potential1
Melanotic pilocytic astrocytoma1
Amyotrophic lateral sclerosis with TDP‐43 abnormalities exhibiting globular glial tau inclusions in frontotemporal lobes and pallido‐nigral system1
Retrospective neuropathological diagnosis of TDP‐43 proteinopathies: Factors affecting immunoreactivity of phosphorylated TDP‐43 in fixed post‐mortem brain tissue1
Symptomatology and Neuropathology of patients presenting with focal cortical signs1
Artificial intelligence techniques for neuropathological diagnostics and research1
Numerous spindle‐shaped lymphoma cells in lymphomatosis cerebri: An autopsy case report1
Krebs von den Lungen 6 decreased in the serum and muscle of GNE myopathy patients1
Selective extension of cerebral vascular calcification in an autopsy case of Fahr's syndrome associated with asymptomatic hypoparathyroidism1
Stellate ganglion ischemia on the prevention of pulmonary vasospasm during bilateral carotid artery ligation: The first experimental study1
An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis1
Immunohistochemical and ultrastructural evidence for the pathogenesis of white matter degeneration in patients with panencephalopathic‐type Creutzfeldt–Jakob disease: Inducible nitric oxide synthase o1
Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa1
A case of Epstein–Barr virus‐associated smooth muscle tumor of the posterior interosseous nerve mimicking schwannoma1
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An autopsy case of corticobasal syndrome due to asymmetric degeneration of the motor cortex and substantia nigra with TDP‐43 proteinopathy, associated with Alzheimer's disease pa1
Spinal muscular atrophy type 2 patient who survived 61 years: an autopsy case report1
Lactotroph PitNET/adenoma associated to granulomatous hypophysitis in a patient with Crohn's disease: A case report1
Extremely rare occurrence of multiple cranial fasciitis: A case report1
Issue Information1
Nonneoplastic and noninfective cysts of the central nervous system: A histopathological study1
Progressive supranuclear palsy with predominant frontal presentation exhibiting progressive nonfluent aphasia due to crossed aphasia1
An autopsy case of GM1 gangliosidosis type II in a patient who survived a long duration with artificial respiratory support1
The receptor for advanced glycation end products and its ligands’ expression in OVE26 diabetic sciatic nerve during the development of length‐dependent neuropathy1
Isolated cortical tuber in an infant with genetically confirmed tuberous sclerosis complex 1 presenting with symptomatic West syndrome1
A descriptive study of Parkinson disease and atypical parkinsonisms in the Annuals of the Pathological Autopsy Cases in Japan1
A case of cerebral paragonimiasis misdiagnosed as eosinophilic granulomatosis with polyangiitis1
An autopsy case of variably protease‐sensitive prionopathy with Met/Met homogeneity at codon 1291
Pediatric fibromyxoid tumor with PLAG1 fusion: An emerging entity with a novel intracranial location1
Myopathic changes caused by protein aggregates in adult‐onset spinal muscular atrophy1
Anti‐N‐methyl‐D‐aspartate receptor encephalitis with concurrent human herpes virus‐6A deoxyribonucleic acid detection: An autopsy case1
Extracranial metastatic solitary fibrous tumor/hemangiopericytoma expressing G‐CSF and its receptor1
Gliosarcoma with unusual glial components: Two case reports1
Sebaceous adenoma occurring within an intracranial dermoid cyst1
Leptomeningeal and intraventricular myelomatosis manifesting an aggressive form of communicating hydrocephalus1
MYCN amplification in spinal ependymoma: A five‐year retrospective study1
Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy1
An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings1
Effectiveness of radiation therapy on brain invasion by human papillomavirus‐related multiphenotypic sinonasal carcinoma: A case report1
Repeated recurrent intracerebral hemorrhage may be involved in cerebral amyloid angiopathy‐related inflammation: An autopsy case1
Macroglossia in rapidly progressive inclusion body myositis1
An autopsy case of diffuse atypical argyrophilic grain disease (AGD) with presenile onset and three‐year course of motor and cognitive impairment1
A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism1
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Radiologic–pathologic association of tumor‐like lesions with inflammation in cerebral white matter: Comparison of two cases with distinct clinical outcomes1
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