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 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
Many roles for oligodendrocyte precursor cells in physiology and pathology12
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
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 report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP‐43 proteinopathy10
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis10
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
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
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
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
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
Minocycline prevents depression‐like behavior in streptozotocin‐induced diabetic mice7
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
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
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
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
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
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
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
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
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