Neuropathology

Papers
(The TQCC of Neuropathology is 2. 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 2021-06-01 to 2025-06-01.)
ArticleCitations
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Associations of late‐life blood pressure with CERAD, Braak, and Thal: Findings from the National Alzheimer's coordinating center neuropathology dataset14
Neurolymphomatosis in follicular lymphoma: an autopsy case report13
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor13
Exophytic cerebellopontine angle tumor showing mostly an embryonal appearance with H3‐3A K27M12
A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma12
The neostriatum in polyglutamine diseases: preferential decreases in large neurons in dentatorubral‐pallidoluysian atrophy and Machado‐Joseph disease and in small neurons in Huntington dise12
Concurrent intraventricular intracranial myxoid mesenchymal tumor and ependymoma in a long‐term Ewing sarcoma survivor9
Ependymoma‐like tumor with mesenchymal differentiation (ELTMD) with ZFTA:NCOA1 fusion: A diagnostic challenge9
Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies9
Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature9
Effectiveness of radiation therapy on brain invasion by human papillomavirus‐related multiphenotypic sinonasal carcinoma: A case report8
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Elevated expression of N‐myc downstream regulated gene 1 protein in glioblastomas reflects tumor angiogenesis and poor patient prognosis8
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings8
The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality8
An autopsy case of amyloid angiopathy‐related cerebellar hemorrhage8
Unveiling primary intracranial eosinophilic angiocentric fibrosis: A rare case report and diagnostic dilemmas7
Engeletin ameliorates sevoflurane‐induced cognitive impairment by activating PPAR‐gamma in neonatal mice7
The predominance of “astrocytic” intranuclear inclusions in neuronal intranuclear inclusion disease manifesting encephalopathy‐like symptoms: A case series with brain biopsy7
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies7
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Blood–brain barrier dysfunction in multiple system atrophy: A human postmortem study6
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Fukutin regulates tau phosphorylation and synaptic function: Novel properties of fukutin in neurons6
Polymerized Type I Collagen With Polyvinylpyrrolidone Reduces Fibrosis and Improves Nerve Organization and Myelination After Peripheral Nerve Injury6
Correction to “Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C > T/p.P307L) in SLC20A2 showing widespread cerebr6
Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report5
Neuropilin‐1 enhances temozolomide resistance in glioblastoma via the STAT1/p53/p21 axis5
A case of childhood unilateral relapsing primary angiitis of the central nervous system5
Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions5
Possible association of limbic tau pathology with psychosis or behavioral disturbances: Studies of two autopsied psychiatric patients5
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis5
Malignancy arising in adamantinomatous craniopharyngioma: Report of a rare case with unusual morphologic features5
An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy5
Documented growth of an intracranial capillary hemangioma: A case report5
Senile plaque calcification of the lamina circumvoluta medullaris in Alzheimer's disease5
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Radiologic–pathologic association of tumor‐like lesions with inflammation in cerebral white matter: Comparison of two cases with distinct clinical outcomes5
A case of CIC‐rearranged sarcoma with CIC‐LEUTX gene fusion in spinal cord5
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Balamuthia mandrillarisamoebic encephalitis mimicking tuberculous meningitis5
Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association5
Somatic mosaicism of the PI3K‐AKT‐MTOR pathway is associated with hemimegalencephaly in fetal brains4
Central nervous tissue in ovarian mature teratoma: A neuropathological study of 101 resected tumors4
Primary Rosai‐Dorfman disease of the central nervous system: A clinical, histological, and molecular appraisal4
An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter4
MYCN amplification in spinal ependymoma: A five‐year retrospective study4
Japanese Society of Neuropathology Award 20214
FOXM1‐mediated NUF2 expression confers temozolomide resistance to human glioma cells by regulating autophagy via the PI3K/AKT/mTOR signaling path4
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NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion4
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Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 34
Multiple Neuropathologies Underly Hippocampal Subfield Atrophy in a Case With a Slowly Progressive Amnestic Syndrome: Challenging the Notion of Pure LATENC4
A case of intracranial myxoid mesenchymal tumor with EWSR1:CREM fusion in an adult female: Extensive immunohistochemical evaluation3
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A case of myxopapillary ependymoma with predominant giant cell morphology: A rare entity with comprehensive genomic profiling and review of literature3
Gliosarcoma with unusual glial components: Two case reports3
Primary central nervous system extranodal NK/T‐cell lymphoma, nasal type with CD20 expression: Case report and review of the literature3
Corticobasal degeneration with visual hallucination as an initial symptom: A case report3
Alzheimer's Disease With Cardiac Transthyretin Amyloidosis: A Clinicopathological Study of Autopsy Cases3
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Embryonal tumor with multilayered rosettes arising from the internal auditory canal of an adult: Illustrative case with molecular investigations3
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study3
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Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?3
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A case of Epstein–Barr virus‐associated smooth muscle tumor of the posterior interosseous nerve mimicking schwannoma3
Calcifying pseudoneoplasms of the neuraxis (CAPNON). 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
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus3
Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors3
Polyglucosan body disease in an aged chimpanzee (Pan troglodytes)2
Acute respiratory failure caused by brainstem demyelinating lesions in an older patient with an atypical relapsing autoimmune disorder2
Repeated recurrent intracerebral hemorrhage may be involved in cerebral amyloid angiopathy‐related inflammation: An autopsy case2
Pathological features of inflammatory myopathy as a manifestation of chronic graft‐versus‐host disease after allogeneic bone marrow transplantation2
Multisystem pathology in McLeod syndrome2
An autopsy case of progressive multifocal leukoencephalopathy with massive iron deposition in juxtacortical lesions2
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia2
Myopathic changes caused by protein aggregates in adult‐onset spinal muscular atrophy2
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Usefulness of intraoperative rapid flow cytometry in the surgical treatment of brain tumors2
Comments on an autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau2
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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 ap2
From pathological mechanisms in Krabbe disease to cutting‐edge therapy: A comprehensive review2
Epstein–Barr virus‐positive monoclonal lymphoplasmacytic proliferation associated with neurosyphilis in an immunocompetent patient: A case report2
A rare case of dedifferentiated intracranial solitary fibrous tumor with chondrosarcomatous differentiation2
Primary intracranial dedifferentiated liposarcoma: An extremely rare site with unusual histopathological findings2
Japanese Society of Neuropathology Award 20232
Clinicopathological features of progressive supranuclear palsy with asymmetrical atrophy of the superior cerebellar peduncle2
An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings2
Pathology for severe inflammatory PML with PD1/PD‐L1 expression of favorable prognosis: What's a prognostic factor for PML‐IRIS?2
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis2
Brain cutting and trimming2
Macroscopic findings of brain with dementia2
White matter edematous change with moderate vascular lesions in pretreated acute stage of leukoencephalopathy with cerebral amyloid angiopathy2
A descriptive study of Parkinson disease and atypical parkinsonisms in the Annuals of the Pathological Autopsy Cases in Japan2
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Lymphomatosis cerebri with coexistent anti‐N‐methyl‐D‐aspartate receptor antibody: A case report2
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Sebaceous adenoma occurring within an intracranial dermoid cyst2
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?2
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