Neuropathology

Papers
(The TQCC of Neuropathology is 3. 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 2021-07-01 to 2025-07-01.)
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 dataset15
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor14
The neostriatum in polyglutamine diseases: preferential decreases in large neurons in dentatorubral‐pallidoluysian atrophy and Machado‐Joseph disease and in small neurons in Huntington dise13
Exophytic cerebellopontine angle tumor showing mostly an embryonal appearance with H3‐3A K27M13
Neurolymphomatosis in follicular lymphoma: an autopsy case report13
A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma13
Concurrent intraventricular intracranial myxoid mesenchymal tumor and ependymoma in a long‐term Ewing sarcoma survivor12
Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies10
Effectiveness of radiation therapy on brain invasion by human papillomavirus‐related multiphenotypic sinonasal carcinoma: A case report10
Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature9
Elevated expression of N‐myc downstream regulated gene 1 protein in glioblastomas reflects tumor angiogenesis and poor patient prognosis9
The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality9
Ependymoma‐like tumor with mesenchymal differentiation (ELTMD) with ZFTA:NCOA1 fusion: A diagnostic challenge8
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Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings8
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An autopsy case of amyloid angiopathy‐related cerebellar hemorrhage8
The predominance of “astrocytic” intranuclear inclusions in neuronal intranuclear inclusion disease manifesting encephalopathy‐like symptoms: A case series with brain biopsy7
Polymerized Type I Collagen With Polyvinylpyrrolidone Reduces Fibrosis and Improves Nerve Organization and Myelination After Peripheral Nerve Injury7
Unveiling primary intracranial eosinophilic angiocentric fibrosis: A rare case report and diagnostic dilemmas7
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies7
Engeletin ameliorates sevoflurane‐induced cognitive impairment by activating PPAR‐gamma in neonatal mice7
Blood–brain barrier dysfunction in multiple system atrophy: A human postmortem study7
A case of CIC‐rearranged sarcoma with CIC‐LEUTX gene fusion in spinal cord6
Correction to “Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C > T/p.P307L) in SLC20A2 showing widespread cerebr6
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A case of childhood unilateral relapsing primary angiitis of the central nervous system6
Fukutin regulates tau phosphorylation and synaptic function: Novel properties of fukutin in neurons6
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Radiologic–pathologic association of tumor‐like lesions with inflammation in cerebral white matter: Comparison of two cases with distinct clinical outcomes6
Balamuthia mandrillarisamoebic encephalitis mimicking tuberculous meningitis5
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis5
Possible association of limbic tau pathology with psychosis or behavioral disturbances: Studies of two autopsied psychiatric patients5
Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions5
Somatic mosaicism of the PI3K‐AKT‐MTOR pathway is associated with hemimegalencephaly in fetal brains5
Malignancy arising in adamantinomatous craniopharyngioma: Report of a rare case with unusual morphologic features5
Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report5
Issue Information5
Senile plaque calcification of the lamina circumvoluta medullaris in Alzheimer's disease5
MYCN amplification in spinal ependymoma: A five‐year retrospective study5
Neuropilin‐1 enhances temozolomide resistance in glioblastoma via the STAT1/p53/p21 axis5
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Documented growth of an intracranial capillary hemangioma: A case report5
Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association5
Central nervous tissue in ovarian mature teratoma: A neuropathological study of 101 resected tumors5
NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion4
Multiple Neuropathologies Underly Hippocampal Subfield Atrophy in a Case With a Slowly Progressive Amnestic Syndrome: Challenging the Notion of Pure LATENC4
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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Japanese Society of Neuropathology Award 20214
Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 34
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An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter4
Primary Rosai‐Dorfman disease of the central nervous system: A clinical, histological, and molecular appraisal4
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Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors3
Primary central nervous system extranodal NK/T‐cell lymphoma, nasal type with CD20 expression: Case report and review of the literature3
Embryonal tumor with multilayered rosettes arising from the internal auditory canal of an adult: Illustrative case with molecular investigations3
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia3
Polyglucosan body disease in an aged chimpanzee (Pan troglodytes)3
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis3
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
A case of Epstein–Barr virus‐associated smooth muscle tumor of the posterior interosseous nerve mimicking schwannoma3
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Alzheimer's Disease With Cardiac Transthyretin Amyloidosis: A Clinicopathological Study of Autopsy Cases3
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Repeated recurrent intracerebral hemorrhage may be involved in cerebral amyloid angiopathy‐related inflammation: An autopsy case3
Usefulness of intraoperative rapid flow cytometry in the surgical treatment of brain tumors3
Acute respiratory failure caused by brainstem demyelinating lesions in an older patient with an atypical relapsing autoimmune disorder3
Comments on an autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau3
Issue Information3
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus3
Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?3
A case of intracranial myxoid mesenchymal tumor with EWSR1:CREM fusion in an adult female: Extensive immunohistochemical evaluation3
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study3
Corticobasal degeneration with visual hallucination as an initial symptom: A case report3
Pathology for severe inflammatory PML with PD1/PD‐L1 expression of favorable prognosis: What's a prognostic factor for PML‐IRIS?3
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?3
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Gliosarcoma with unusual glial components: Two case reports3
A case of myxopapillary ependymoma with predominant giant cell morphology: A rare entity with comprehensive genomic profiling and review of literature3
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