Neuropathology

Papers
(The median citation count of Neuropathology is 0. 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 2020-11-01 to 2024-11-01.)
ArticleCitations
Human brain pathology in myotonic dystrophy type 1: A systematic review27
Intracellular amyloid hypothesis for ultra‐early phase pathology of Alzheimer's disease23
Astrocytes release glutamate via cystine/glutamate antiporter upregulated in response to increased oxidative stress related to sporadic amyotrophic lateral sclerosis21
Neuropathology of α‐synuclein in Parkinson's disease18
Diffuse midline glioma with H3 K27M mutation of the spinal cord: A series of 33 cases14
A case of CIC‐rearranged sarcoma with CIC‐LEUTX gene fusion in spinal cord13
Multiple system aging‐related tau astrogliopathy with complex proteinopathy in an oligosymptomatic octogenarian12
An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter12
Many roles for oligodendrocyte precursor cells in physiology and pathology12
Abnormal prion protein deposits with high seeding activities in the skeletal muscle, femoral nerve, and scalp of an autopsied case of sporadic Creutzfeldt–Jakob disease11
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis10
An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP‐43 proteinopathy10
NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion9
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 ap9
Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors9
Astrocytes in ischemic stroke: Crosstalk in central nervous system and therapeutic potential9
Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation9
Transactivation response DNA‐binding protein of 43 kDa proteinopathy and lysosomal abnormalities in spastic paraplegia type 118
Clinicopathological features of titinopathy from a Chinese neuromuscular center8
FOXM1‐mediated NUF2 expression confers temozolomide resistance to human glioma cells by regulating autophagy via the PI3K/AKT/mTOR signaling path8
Intracranial myxoid angiomatoid fibrous histiocytoma with “classic” histology and EWSR1:CREM fusion providing insight for reconciliation with intracranial myxoid mesenchymal tumors8
Minocycline prevents depression‐like behavior in streptozotocin‐induced diabetic mice7
Lewy pathology of the submandibular gland in Lewy body disease: A report of autopsy cases7
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
A case of intracranial myxoid mesenchymal tumor with EWSR1:CREM fusion in an adult female: Extensive immunohistochemical evaluation7
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus7
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
Supratentorial ependymoma with YAP1:FAM118B fusion: A case report6
LINC01123 potentially correlates with radioresistance in glioma through the miR‐151a/CENPB axis6
Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva6
Brain cutting and trimming6
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies6
Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?5
A case of ganglioglioma grade 3 withH3 K27Mmutation arising in the medial temporal lobe in an elderly patient5
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
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
Immunohistochemical expression of osteopontin and collagens in choroid plexus of human brains5
The hot cross bun sign in corticobasal degeneration5
The receptor for advanced glycation end products and its ligands’ expression in OVE26 diabetic sciatic nerve during the development of length‐dependent neuropathy5
Distribution of amyloid‐β precursor protein‐immunoreactive axons differs according to the severity of cerebral ischemia in autopsy brains5
Progressive supranuclear palsy: Neuropathology of patients with a short disease duration due to unexpected death5
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study5
Macroscopic diagnostic clue for parkinsonism4
Brain parenchymal angiomatoid fibrous histiocytoma and spinal myxoid mesenchymal tumor with FET: CREB fusion, a spectrum of the same tumor type4
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis4
Pediatric fibromyxoid tumor with PLAG1 fusion: An emerging entity with a novel intracranial location4
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor4
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia4
Primary central nervous system other iatrogenic immunodeficiency‐associated lymphoproliferative disorders presenting as extraosseous plasmacytoma with a progressive clinical course: A case report and 4
An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau4
Recurrent oligodendroglioma with changed 1p/19q status4
Unique Lewy pathology in myotonic dystrophy type 14
Pembrolizumab‐caused polyradiculoneuropathy as an immune‐related adverse event4
Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa3
Distinct TERT promoter C228T and C250T mutations in a patient with an oligodendroglioma: A case report3
An autopsy case report of neuronal intermediate filament inclusion disease presenting with predominantly upper motor neuron features3
Possible association of limbic tau pathology with psychosis or behavioral disturbances: Studies of two autopsied psychiatric patients3
Olfactory neuroblastoma associated with extensive “in situ” lesion and aberrant glandular and rhabdomyosarcomatous differentiation3
Spinal cord‐predominant neuropathology in an adult‐onset case of POLR3A‐related spastic ataxia3
Let's cluster cases in Neuropathology Case Cluster series!: Unveil clinical masqueraders (Neuropathology Cluster Case 1–13)3
Quantitative analysis of MGMT promoter methylation status changes by pyrosequencing in recurrent glioblastoma3
Pediatric and elderly polymorphous low‐grade neuroepithelial tumor of the young: Typical and unusual case reports and literature review3
The landscape of common genetic drivers and DNA methylation in low‐grade (epilepsy‐associated) neuroepithelial tumors: A review3
Macroscopic findings of brain with dementia3
Primary central nervous system lymphomas with massive intratumoral hemorrhage: Clinical, radiological, pathological, and molecular features of six cases3
Senile plaque calcification of the lamina circumvoluta medullaris in Alzheimer's disease3
Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas3
A case of cerebral paragonimiasis misdiagnosed as eosinophilic granulomatosis with polyangiitis3
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings3
Neuropathological report of propionic acidemia3
Pituitary apoplexy in endocrinologically silent adenoma during somatostatin analog administration for pancreatic neuroendocrine tumor: A case report3
A pathologically confirmed case of combined amyotrophic lateral sclerosis with C9orf72 mutation and multiple system atrophy3
Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case3
Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 33
Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association3
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
Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report3
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
Calcifying pseudoneoplasms of the neuraxis (CAPNON). A case report3
Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature3
An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis3
Coexistence of dentatorubral‐pallidoluysian atrophy and Parkinson's disease: An autopsy case report3
Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions2
Repeated recurrent intracerebral hemorrhage may be involved in cerebral amyloid angiopathy‐related inflammation: An autopsy case2
Astrocytoma (CNS WHO grade 4), IDH‐mutant with co‐occurrence of BRAF p.V600E mutation, and homozygous loss of CDKN2A2
Fukutin regulates tau phosphorylation and synaptic function: Novel properties of fukutin in neurons2
Ependymosarcoma harboring C11orf95:RELA fusion transcript: Report of two cases and review of the literature2
An autopsy case of progressive supranuclear palsy. Pallido‐nigro‐luysian type with argyrophilic grains clinically presenting with personality and behavioral changes2
Ependymoma‐like tumor with mesenchymal differentiation (ELTMD) with ZFTA:NCOA1 fusion: A diagnostic challenge2
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 pa2
Multisystem pathology in McLeod syndrome2
Clinicopathological features in two families with MARS‐related Charcot–Marie–Tooth disease2
Extracranial metastatic solitary fibrous tumor/hemangiopericytoma expressing G‐CSF and its receptor2
Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL‐6/STAT3 signaling2
Intraventricular mucin‐producing glioblastoma arising in the septum pellucidum at the frontal horn of the lateral ventricle: A case report2
An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy2
Extra‐axial sacral soft tissue giant cell ependymoma affecting a child: Case report and review of the literature2
“Burnt‐out” progressive multifocal leukoencephalopathy in idiopathic CD4+ lymphocytopenia2
Concurrent intraventricular intracranial myxoid mesenchymal tumor and ependymoma in a long‐term Ewing sarcoma survivor2
Acute actinomycotic brain abscess in a patient with rheumatoid arthritis2
A descriptive study of Parkinson disease and atypical parkinsonisms in the Annuals of the Pathological Autopsy Cases in Japan2
Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy2
An autopsy case of variably protease‐sensitive prionopathy with Met/Met homogeneity at codon 1292
Morphological study of the phrenic nerve to determine a reference value for the myelinated fiber density in elderly individuals2
Spinal muscular atrophy type 2 patient who survived 61 years: an autopsy case report2
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?2
Elucidating the multiple genetic alterations involved in the malignant transformation of a KRAS mutant neurenteric cyst. A case report2
Macroglossia in rapidly progressive inclusion body myositis2
Granular cell tumor of the neurohypophysis presenting as a third ventricle mass2
An autopsy case of amyloid angiopathy‐related cerebellar hemorrhage2
Effectiveness of radiation therapy on brain invasion by human papillomavirus‐related multiphenotypic sinonasal carcinoma: A case report2
An autopsy case of diffuse atypical argyrophilic grain disease (AGD) with presenile onset and three‐year course of motor and cognitive impairment2
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
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A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism1
Radiologic–pathologic association of tumor‐like lesions with inflammation in cerebral white matter: Comparison of two cases with distinct clinical outcomes1
O6‐methylguanine methyltransferase promoter methylation status of glioblastoma cell line clonal population1
Senile plaque‐associated transactive response DNA‐binding protein 43 in Alzheimer's disease: A case report spanning 16 years of memory loss1
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Artificial intelligence techniques for neuropathological diagnostics and research1
Tumefactive eosinophil‐rich non‐granulomatous small vessel vasculitis in the cerebrum in a patient with idiopathic hypereosinophilic syndrome1
Intracerebral hirudin injection alleviates cognitive impairment and oxidative stress and promotes hippocampal neurogenesis in rats subjected to cerebral ischemia1
A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma1
Myopathic changes caused by protein aggregates in adult‐onset spinal muscular atrophy1
Comparison of clinical imaging and pathological findings of various brain lesions including cerebrovascular diseases and other systemic diseases1
Somatic mosaicism of the PI3K‐AKT‐MTOR pathway is associated with hemimegalencephaly in fetal brains1
A case of Epstein–Barr virus‐associated smooth muscle tumor of the posterior interosseous nerve mimicking schwannoma1
MYCN amplification in spinal ependymoma: A five‐year retrospective study1
Balamuthia mandrillarisamoebic encephalitis mimicking tuberculous meningitis1
Mixed gangliocytoma–pituitary adenoma in MEN1 syndrome: A case report and literature review1
Pilocytic astrocytoma harboring a novel GNAI3‐BRAF fusion1
Numerous spindle‐shaped lymphoma cells in lymphomatosis cerebri: An autopsy case report1
Progressive supranuclear palsy with predominant frontal presentation exhibiting progressive nonfluent aphasia due to crossed aphasia1
Intracranial phosphaturic mesenchymal tumors. A case report and review of literature1
Anti‐N‐methyl‐D‐aspartate receptor encephalitis with concurrent human herpes virus‐6A deoxyribonucleic acid detection: An autopsy case1
Whorling‐sclerosing meningioma invading skull bone and subcutaneous tissue with an incidental toxoplasmosis: A case report1
An autopsy case of progressive multifocal leukoencephalopathy with massive iron deposition in juxtacortical lesions1
Parkinson's disease and parkinsonism: Clinicopathological discrepancies on diagnosis in three patients1
Lymphomatosis cerebri with coexistent anti‐N‐methyl‐D‐aspartate receptor antibody: A case report1
Lactotroph PitNET/adenoma associated to granulomatous hypophysitis in a patient with Crohn's disease: A case report1
White matter edematous change with moderate vascular lesions in pretreated acute stage of leukoencephalopathy with cerebral amyloid angiopathy1
Melanotic pilocytic astrocytoma1
Retrospective neuropathological diagnosis of TDP‐43 proteinopathies: Factors affecting immunoreactivity of phosphorylated TDP‐43 in fixed post‐mortem brain tissue1
Extremely rare occurrence of multiple cranial fasciitis: A case report1
Nonneoplastic and noninfective cysts of the central nervous system: A histopathological study1
An EWSR1–EZHIP fusion in a cerebral hemisphere astroblastoma1
Symptomatology and Neuropathology of patients presenting with focal cortical signs1
Isolated cortical tuber in an infant with genetically confirmed tuberous sclerosis complex 1 presenting with symptomatic West syndrome1
A case of disseminated spinal astroblastoma harboring a MAMLD1::BEND2 fusion1
Clinicopathological study of dementia with grains presenting with parkinsonism compared with a typical case1
Collision tumor: Multinodular and vacuolating neuronal tumor with isocitrate dehydrogenase‐mutant diffuse astrocytoma1
Selective extension of cerebral vascular calcification in an autopsy case of Fahr's syndrome associated with asymptomatic hypoparathyroidism1
Engeletin ameliorates sevoflurane‐induced cognitive impairment by activating PPAR‐gamma in neonatal mice1
ASK1 activation in glial cells in post‐mortem multiple sclerosis tissue1
Leptomeningeal and intraventricular myelomatosis manifesting an aggressive form of communicating hydrocephalus1
Sebaceous adenoma occurring within an intracranial dermoid cyst1
Gliosarcoma with unusual glial components: Two case reports1
An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings1
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An autopsy case of corticobasal degeneration with inferior olivary hypertrophy1
Amyotrophic lateral sclerosis with TDP‐43 abnormalities exhibiting globular glial tau inclusions in frontotemporal lobes and pallido‐nigral system1
Krebs von den Lungen 6 decreased in the serum and muscle of GNE myopathy patients1
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Elevated expression of N‐myc downstream regulated gene 1 protein in glioblastomas reflects tumor angiogenesis and poor patient prognosis0
The neostriatum in polyglutamine diseases: preferential decreases in large neurons in dentatorubral‐pallidoluysian atrophy and Machado‐Joseph disease and in small neurons in Huntington dise0
A case of childhood unilateral relapsing primary angiitis of the central nervous system0
An autopsy case of progressive supranuclear palsy with severe corticospinal tract degeneration0
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Pathological observations of a long spinal cord lesion in a patient with multiple sclerosis0
Exophytic cerebellopontine angle tumor showing mostly an embryonal appearance with H3‐3A K27M0
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ALK‐positive histiocytosis: Report of a rare case with exclusive involvement of the central nervous system in an adult woman0
Pituitary tuberculoma with panhypopituitarism masquerading as a pituitary adenoma0
Unveiling primary intracranial eosinophilic angiocentric fibrosis: A rare case report and diagnostic dilemmas0
The large neuron involvement in the neostriatum in Lewy body diseases0
Neurolymphomatosis mimicking a Guillain–Barré syndrome triggered by COVID‐19 vaccination0
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An autopsy case of Alzheimer's disease with amygdala‐predominant Lewy pathology presenting with frontotemporal dementia‐like psychiatric symptoms0
Neuropilin‐1 enhances temozolomide resistance in glioblastoma via the STAT1/p53/p21 axis0
Corticobasal degeneration with visual hallucination as an initial symptom: A case report0
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Atypical TDP‐43 proteinopathy clinically presenting with progressive nonfluent aphasia: A case report0
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An autopsy case of type A FTLD‐TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequ0
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Increased expression of leucine‐rich α‐2 glycoprotein 1 as a predictive biomarker of favorable progression‐free survival in meningioma0
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Usefulness of intraoperative rapid flow cytometry in the surgical treatment of brain tumors0
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Polyglucosan body disease in an aged chimpanzee (Pan troglodytes)0
Association between hypothalamic Alzheimer's disease pathology and body mass index: The Hisayama study0
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Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies0
A case of idiopathic extracranial carotid artery pseudoaneurysm with a rare clinical course and pathological features0
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Embryonal tumor with multilayered rosettes arising from the internal auditory canal of an adult: Illustrative case with molecular investigations0
Correction to “MicroRNA‐221 targeting PI3‐K/Akt signaling axis induces cell proliferation and BCNU resistance in human glioblastoma”0
Hemorrhage from metastatic brain epithelioid hemangioendothelioma: A case report0
Dissecting lesions in a culprit artery of a hemorrhagic focus in the basal ganglia: Histopathological analysis by serial sectioning0
Ipsilateral simultaneous multiple hypertensive intracerebral hemorrhages: Analysis of hematoma formation and comparison with distribution of hypertensive mixed‐type hematoma0
A case of a pilocytic astrocytoma with histological features of anaplasia and unprecedent genetic alterations0
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Cervical myelopathy and extensive body destruction caused by primary Gli1 fusion sarcoma0
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Giant cell glioblastoma with lipogenic differentiation in a patient with neurofibromatosis type 1: A case report0
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Primary cauda equina lymphoma confirmed by autopsy: A case report0
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Somatic mutational profiling and clinical impact of driver genes in Latin‐Iberian medulloblastomas: Towards precision medicine0
Calcifying pseudoneoplasm of the neuraxis (CAPNON) associated with neurenteric cyst. An autopsy case showing unusual fatal outcome0
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A case of myxopapillary ependymoma with predominant giant cell morphology: A rare entity with comprehensive genomic profiling and review of literature0
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In‐house molecular diagnosis of diffuse glioma updating the revised WHO classification by a platform of the advanced medical care system, Senshin‐Iryo0
Neurolymphomatosis in follicular lymphoma: an autopsy case report0
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Primary degeneration of oculomotor, motor, and somatosensory systems and auditory and visual pathways in spinocerebellar ataxia type 7: A clinicopathological study in a Japanese autopsy case0
Anti‐neutrophil cytoplasmic antibody‐associated central nervous system vasculitis mimicking brain tumor: A case report0
Expression and distribution of hypoxia‐inducible factor‐1α and vascular endothelial growth factor in comparison between radiation necrosis and tumor tissue in metastatic brain tumor: A case report0
The predominance of “astrocytic” intranuclear inclusions in neuronal intranuclear inclusion disease manifesting encephalopathy‐like symptoms: A case series with brain biopsy0
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Correction to “Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C > T/p.P307L) in SLC20A2 showing widespread cerebr0
Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle0
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Spinal astroblastoma, MN1 altered in 3‐year‐old child: An uncommon tumor at an unusual site0
Primary central nervous system extranodal NK/T‐cell lymphoma, nasal type with CD20 expression: Case report and review of the literature0
A case of trigeminal malignant melanotic nerve sheath tumor in the wide spectrum of melanotic and nerve sheath tumors0
Malignancy arising in adamantinomatous craniopharyngioma: Report of a rare case with unusual morphologic features0
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Acute respiratory failure caused by brainstem demyelinating lesions in an older patient with an atypical relapsing autoimmune disorder0
Neuropathologic findings in a patient with hemiparkinsonism and hemiatrophy syndrome0
A rare encounter: Comprehensive case review of myxoid meningiomas with a representative case0
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Neuropathology Case Cluster: Neuropathology of focal cortical, behavioral, and psychiatric syndromes in neurodegenerative diseases (neuropathology cluster case 14–32)0
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Cotton rats (Sigmodon hispidus) with a high prevalence of hydrocephalus without clinical symptoms0
Comments on an autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau0
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