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 2020-08-01 to 2024-08-01.)
ArticleCitations
Where and how alpha‐synuclein pathology spreads in Parkinson’s disease:41
A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration29
Human brain pathology in myotonic dystrophy type 1: A systematic review25
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
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
Diffuse midline glioma with H3 K27M mutation of the spinal cord: A series of 33 cases12
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
An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter11
An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP‐43 proteinopathy10
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
NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion9
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis9
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
Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors8
High‐grade gliomas with isocitrate dehydrogenase wild‐type and 1p/19q codeleted: Atypical molecular phenotype and current challenges in molecular diagnosis8
Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation8
Clinicopathological features of titinopathy from a Chinese neuromuscular center8
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
FOXM1‐mediated NUF2 expression confers temozolomide resistance to human glioma cells by regulating autophagy via the PI3K/AKT/mTOR signaling path7
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 cases7
Minocycline prevents depression‐like behavior in streptozotocin‐induced diabetic mice7
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus7
A case of desmoplastic myxoid tumor, SMARCB1 mutant, in the pineal region6
Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva6
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
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies6
LINC01123 potentially correlates with radioresistance in glioma through the miR‐151a/CENPB axis6
Brain cutting and trimming6
Cerebral embolization associated with parenchymal seeding of the left atrial myxoma: Potential role of interleukin‐6 and matrix metalloproteinases5
Progressive supranuclear palsy: Neuropathology of patients with a short disease duration due to unexpected death5
Supratentorial ependymoma with YAP1:FAM118B fusion: A case report5
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
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
Distribution of amyloid‐β precursor protein‐immunoreactive axons differs according to the severity of cerebral ischemia in autopsy brains5
A case of ganglioglioma grade 3 withH3 K27Mmutation arising in the medial temporal lobe in an elderly patient5
The hot cross bun sign in corticobasal degeneration5
Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?5
The receptor for advanced glycation end products and its ligands’ expression in OVE26 diabetic sciatic nerve during the development of length‐dependent neuropathy4
Unique Lewy pathology in myotonic dystrophy type 14
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis4
An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau4
Macroscopic diagnostic clue for parkinsonism4
Recurrent oligodendroglioma with changed 1p/19q status4
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia4
Neuropathology of a case of fragile X‐associated tremor ataxia syndrome without tremor4
Pembrolizumab‐caused polyradiculoneuropathy as an immune‐related adverse event4
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor4
Astrocytes in ischemic stroke: Crosstalk in central nervous system and therapeutic potential4
Primary central nervous system other iatrogenic immunodeficiency‐associated lymphoproliferative disorders presenting as extraosseous plasmacytoma with a progressive clinical course: A case report and 4
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study4
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?4
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
Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas3
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings3
Pediatric fibromyxoid tumor with PLAG1 fusion: An emerging entity with a novel intracranial location3
Coexistence of dentatorubral‐pallidoluysian atrophy and Parkinson's disease: An autopsy case report3
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
Brain parenchymal angiomatoid fibrous histiocytoma and spinal myxoid mesenchymal tumor with FET: CREB fusion, a spectrum of the same tumor type3
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
Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa3
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
A juvenile case of epilepsy‐associated, isocitrate dehydrogenase wild‐type/histone 3 wild‐type diffuse glioma with a rare BRAFA598T mutation3
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
Quantitative analysis of MGMT promoter methylation status changes by pyrosequencing in recurrent glioblastoma3
High HMGA2 expression without gene rearrangement in meningiomas3
Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case3
Distinct TERT promoter C228T and C250T mutations in a patient with an oligodendroglioma: A case report3
Neuropathological report of propionic acidemia2
Pediatric and elderly polymorphous low‐grade neuroepithelial tumor of the young: Typical and unusual case reports and literature review2
A pathologically confirmed case of combined amyotrophic lateral sclerosis with C9orf72 mutation and multiple system atrophy2
Morphological study of the phrenic nerve to determine a reference value for the myelinated fiber density in elderly individuals2
Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions2
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
Olfactory neuroblastoma associated with extensive “in situ” lesion and aberrant glandular and rhabdomyosarcomatous differentiation2
Effectiveness of radiation therapy on brain invasion by human papillomavirus‐related multiphenotypic sinonasal carcinoma: A case report2
Astrocytoma (CNS WHO grade 4), IDH‐mutant with co‐occurrence of BRAF p.V600E mutation, and homozygous loss of CDKN2A2
Granular cell tumor of the neurohypophysis presenting as a third ventricle mass2
A case of cerebral paragonimiasis misdiagnosed as eosinophilic granulomatosis with polyangiitis2
Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy2
A descriptive study of Parkinson disease and atypical parkinsonisms in the Annuals of the Pathological Autopsy Cases in Japan2
An autopsy case of variably protease‐sensitive prionopathy with Met/Met homogeneity at codon 1292
An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis2
Clinicopathological features in two families with MARS‐related Charcot–Marie–Tooth disease2
Spinal muscular atrophy type 2 patient who survived 61 years: an autopsy case report2
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?2
Extra‐axial sacral soft tissue giant cell ependymoma affecting a child: Case report and review of the literature2
Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature2
Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report2
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
Macroglossia in rapidly progressive inclusion body myositis2
An autopsy case of amyloid angiopathy‐related cerebellar hemorrhage2
An autopsy case of progressive supranuclear palsy. Pallido‐nigro‐luysian type with argyrophilic grains clinically presenting with personality and behavioral changes2
Concurrent intraventricular intracranial myxoid mesenchymal tumor and ependymoma in a long‐term Ewing sarcoma survivor2
An autopsy case of diffuse atypical argyrophilic grain disease (AGD) with presenile onset and three‐year course of motor and cognitive impairment2
The landscape of common genetic drivers and DNA methylation in low‐grade (epilepsy‐associated) neuroepithelial tumors: A review2
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
Repeated recurrent intracerebral hemorrhage may be involved in cerebral amyloid angiopathy‐related inflammation: An autopsy case2
An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy2
Acute actinomycotic brain abscess in a patient with rheumatoid arthritis2
Fukutin regulates tau phosphorylation and synaptic function: Novel properties of fukutin in neurons2
“Burnt‐out” progressive multifocal leukoencephalopathy in idiopathic CD4+ lymphocytopenia2
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
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
Nonneoplastic and noninfective cysts of the central nervous system: A histopathological study1
Pilocytic astrocytoma harboring a novel GNAI3‐BRAF fusion1
Isolated cortical tuber in an infant with genetically confirmed tuberous sclerosis complex 1 presenting with symptomatic West syndrome1
A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism1
Ependymosarcoma harboring C11orf95:RELA fusion transcript: Report of two cases and review of the literature1
Whorling‐sclerosing meningioma invading skull bone and subcutaneous tissue with an incidental toxoplasmosis: A case report1
Anti‐N‐methyl‐D‐aspartate receptor encephalitis with concurrent human herpes virus‐6A deoxyribonucleic acid detection: An autopsy case1
Multisystem pathology in McLeod syndrome1
Lymphomatosis cerebri with coexistent anti‐N‐methyl‐D‐aspartate receptor antibody: A case report1
Pituitary apoplexy in endocrinologically silent adenoma during somatostatin analog administration for pancreatic neuroendocrine tumor: A case report1
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A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma1
White matter edematous change with moderate vascular lesions in pretreated acute stage of leukoencephalopathy with cerebral amyloid angiopathy1
Comparison of clinical imaging and pathological findings of various brain lesions including cerebrovascular diseases and other systemic diseases1
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
Balamuthia mandrillaris amoebic encephalitis mimicking tuberculous meningitis1
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
Krebs von den Lungen 6 decreased in the serum and muscle of GNE myopathy patients1
Intracranial phosphaturic mesenchymal tumors. A case report and review of literature1
Engeletin ameliorates sevoflurane‐induced cognitive impairment by activating PPAR‐gamma in neonatal mice1
Selective extension of cerebral vascular calcification in an autopsy case of Fahr's syndrome associated with asymptomatic hypoparathyroidism1
Tumefactive eosinophil‐rich non‐granulomatous small vessel vasculitis in the cerebrum in a patient with idiopathic hypereosinophilic syndrome1
ASK1 activation in glial cells in post‐mortem multiple sclerosis tissue1
Intracerebral hirudin injection alleviates cognitive impairment and oxidative stress and promotes hippocampal neurogenesis in rats subjected to cerebral ischemia1
Gliosarcoma with unusual glial components: Two case reports1
Functional analyses of STIM1 mutations reveal a common pathomechanism for tubular aggregate myopathy and Stormorken syndrome1
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An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings1
Melanotic pilocytic astrocytoma1
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
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Symptomatology and Neuropathology of patients presenting with focal cortical signs1
Radiologic–pathologic association of tumor‐like lesions with inflammation in cerebral white matter: Comparison of two cases with distinct clinical outcomes1
Clinicopathological study of dementia with grains presenting with parkinsonism compared with a typical case1
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Senile plaque‐associated transactive response DNA‐binding protein 43 in Alzheimer's disease: A case report spanning 16 years of memory loss1
Artificial intelligence techniques for neuropathological diagnostics and research1
Parkinson's disease and parkinsonism: Clinicopathological discrepancies on diagnosis in three patients1
Sebaceous adenoma occurring within an intracranial dermoid cyst1
Extracranial metastatic solitary fibrous tumor/hemangiopericytoma expressing G‐CSF and its receptor1
Leptomeningeal and intraventricular myelomatosis manifesting an aggressive form of communicating hydrocephalus1
Myopathic changes caused by protein aggregates in adult‐onset spinal muscular atrophy1
Lactotroph PitNET/adenoma associated to granulomatous hypophysitis in a patient with Crohn's disease: A case report1
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