Gianluca Marucci
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View article: Molecular analysis of adolescent and young adult high grade gliomas in the SPECTA-AYA study: Poorly characterised tumours with frequent germline alterations
Molecular analysis of adolescent and young adult high grade gliomas in the SPECTA-AYA study: Poorly characterised tumours with frequent germline alterations Open
AYA HGGs comprise a diverse group of entities; accurate, molecularly-defined diagnosis is critical to direct primary treatment, determine risk of genetic predisposition and guide molecularly-directed therapy. Current services fail to routi…
View article: Novel NOTCH3 mutation c.1564 T > A (p.Cys522Ser) presenting with early-onset Parkinsonism and white matter lesions
Novel NOTCH3 mutation c.1564 T > A (p.Cys522Ser) presenting with early-onset Parkinsonism and white matter lesions Open
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a hereditary small vessel disease caused by mutations in the NOTCH3 gene, characterized by recurrent strokes, cognitive decline, and ps…
View article: Intracranial extranodal marginal zone lymphoma mimicking meningioma: A rare but insidious entity
Intracranial extranodal marginal zone lymphoma mimicking meningioma: A rare but insidious entity Open
View article: <i>CLN6</i>‐related continuum phenotype caused by aberrant splicing
<i>CLN6</i>‐related continuum phenotype caused by aberrant splicing Open
Neuronal ceroid lipofuscinoses (NCLs) are genetically heterogeneous neurodegenerative disorders, characterized by progressive cognitive and motor decline, epilepsy, visual impairment, and shortened life‐expectancy. CLN6 ‐related NCLs inclu…
View article: Corrigendum: Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?
Corrigendum: Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists? Open
[This corrects the article DOI: 10.3389/fnmol.2024.1268038.].
View article: Primary angiitis of the central nervous system
Primary angiitis of the central nervous system Open
Primary angiitis of the central nervous system (CNS) is an uncommon inflammatory disorder, with highly variable clinical presentation. It needs to be differentiated from several mimickers, such as CNS involvement in systemic vasculitides, …
View article: Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?
Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists? Open
The fifth edition of the WHO Classification of Tumors of the Central Nervous System (CNS), published in 2021, established new approaches to both CNS tumor nomenclature and grading, emphasizing the importance of integrated diagnoses and lay…
View article: P20.10.B CHARACTERIZATION OF NEW PROGNOSTIC MARKERS IN A COHORT OF ADULT SPINAL EPENDYMOMAS
P20.10.B CHARACTERIZATION OF NEW PROGNOSTIC MARKERS IN A COHORT OF ADULT SPINAL EPENDYMOMAS Open
BACKGROUND Spinal ependymomas (SP-EPN) are group of primary central nervous system tumors recently re-classified by the WHO (CNS5 2021), located in spinal cord. SP-EPN are grade 2-3 tumors, found mainly in cervical and thoracic region, cha…
View article: P20.02.B ELECTRO-CLINICAL, NEUROIMAGING FEATURES AND NEUROPATHOLOGICAL CHARACTERIZATION OF POLYMORPHOUS LOW-GRADE NEUROEPITHELIAL TUMOR OF THE YOUNG (PLNTY)
P20.02.B ELECTRO-CLINICAL, NEUROIMAGING FEATURES AND NEUROPATHOLOGICAL CHARACTERIZATION OF POLYMORPHOUS LOW-GRADE NEUROEPITHELIAL TUMOR OF THE YOUNG (PLNTY) Open
BACKGROUND Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) has been recently recognized by 2021 WHO Central nervous system classification. It is an epileptogenic tumor type, affecting mostly children and young adults, wit…
View article: European Cancer Organisation Essential Requirements for Quality Cancer Care: Adult glioma
European Cancer Organisation Essential Requirements for Quality Cancer Care: Adult glioma Open
European Cancer Organisation Essential Requirements for Quality Cancer Care (ERQCCs) are explanations of the organisation and actions necessary to provide high-quality care to patients with a specific cancer type. They are compiled by a wo…
View article: Correction to: Magnetic resonance imaging characteristics of pediatric pilocytic astrocytoma
Correction to: Magnetic resonance imaging characteristics of pediatric pilocytic astrocytoma Open
View article: Editorial: Advances in brain tumors diagnosis and treatment
Editorial: Advances in brain tumors diagnosis and treatment Open
EDITORIAL article Front. Med., 04 May 2023Sec. Pathology Volume 10 - 2023 | https://doi.org/10.3389/fmed.2023.1152547
View article: Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center Experience
Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center Experience Open
Background: The present mono-institutional report aimed to describe the cognitive and behavioral outcomes of low-grade central nervous system (CNS) tumors in a cohort of children treated exclusively with surgical intervention. Methods: Med…
View article: Dataset related to article "INTERHEMISPHERIC PEDIATRIC MENINGIOMA, YAP1 FUSION-POSITIVE"
Dataset related to article "INTERHEMISPHERIC PEDIATRIC MENINGIOMA, YAP1 FUSION-POSITIVE" Open
Hystological , molecular and neuroradiological data
View article: Dataset related to article "INTERHEMISPHERIC PEDIATRIC MENINGIOMA, YAP1 FUSION-POSITIVE"
Dataset related to article "INTERHEMISPHERIC PEDIATRIC MENINGIOMA, YAP1 FUSION-POSITIVE" Open
Hystological , molecular and neuroradiological data
View article: Mitotic count is prognostic in IDH mutant astrocytoma without homozygous deletion of CDKN2A/B. Results of consensus panel review of EORTC trial 26053 (CATNON) and EORTC trial 22033-26033
Mitotic count is prognostic in IDH mutant astrocytoma without homozygous deletion of CDKN2A/B. Results of consensus panel review of EORTC trial 26053 (CATNON) and EORTC trial 22033-26033 Open
Background Gliomas with IDH1/2 mutations without 1p19q codeletion have been identified as the distinct diagnostic entity of IDH mutant astrocytoma (IDHmut astrocytoma). Homozygous deletion of Cyclin-dependent kinase 4 inhibitor A/B (CDKN2A…
View article: Bone Modeling after Orthodontic Extrusion: A Histomorphometric Pilot Study
Bone Modeling after Orthodontic Extrusion: A Histomorphometric Pilot Study Open
During osteogenesis and bone modeling, high vascularity and osteoblastic/osteoclastic cell activity have been detected. A decrease in this activity is a sign of complete bone formation and maturation. Alveolar bone maturation seems to occu…
View article: Newly recognised Tumour Types in Glioneuronal tumours according to the 5th edition of the CNS WHO Classification
Newly recognised Tumour Types in Glioneuronal tumours according to the 5th edition of the CNS WHO Classification Open
MGT and MNVNT are classified WHO grade 1 and may be recognised and diagnosed by peculiar clinical-pathological features. DGONC was not assigned a WHO grade and was only provisionally included among GNT, due to the possibility that it rathe…
View article: Dataset related to the article "GRN- /- IPSC-DERIVED CORTICAL NEURONS RECAPITULATE THE PATHOLOGICAL FINDINGS OF BOTH FRONTOTEMPORAL LOBAR DEGENERATION AND NEURONAL CEROIDOLIPOFUSCINOSIS"
Dataset related to the article "GRN- /- IPSC-DERIVED CORTICAL NEURONS RECAPITULATE THE PATHOLOGICAL FINDINGS OF BOTH FRONTOTEMPORAL LOBAR DEGENERATION AND NEURONAL CEROIDOLIPOFUSCINOSIS" Open
THE DATASET CONTAINS .XLSX FILES REPORTING BIOCHEMICAL DATA (DENSITOMETRIC ANALYSIS) AND IMMUNOHISTOCHEMICAL DATA (MORPHOMETRIC ANALYSIS AND COUNTING)
View article: Dataset related to the article "GRN- /- IPSC-DERIVED CORTICAL NEURONS RECAPITULATE THE PATHOLOGICAL FINDINGS OF BOTH FRONTOTEMPORAL LOBAR DEGENERATION AND NEURONAL CEROIDOLIPOFUSCINOSIS"
Dataset related to the article "GRN- /- IPSC-DERIVED CORTICAL NEURONS RECAPITULATE THE PATHOLOGICAL FINDINGS OF BOTH FRONTOTEMPORAL LOBAR DEGENERATION AND NEURONAL CEROIDOLIPOFUSCINOSIS" Open
THE DATASET CONTAINS .XLSX FILES REPORTING BIOCHEMICAL DATA (DENSITOMETRIC ANALYSIS) AND IMMUNOHISTOCHEMICAL DATA (MORPHOMETRIC ANALYSIS AND COUNTING)
View article: GRN−/− iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis
GRN−/− iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis Open
View article: Interhemispheric Pediatric Meningioma, YAP1 Fusion-Positive
Interhemispheric Pediatric Meningioma, YAP1 Fusion-Positive Open
Meningiomas are uncommon in children and usually arise in the context of tumor-predisposing syndromes. Recently, YAP1-fusions have been identified for the first time as potential NF2-independent oncogenic drivers in the development of meni…
View article: Anti-Cyclic Citrullinated Peptide Antibody Index in the Cerebrospinal Fluid for the Diagnosis and Monitoring of Rheumatoid Meningitis
Anti-Cyclic Citrullinated Peptide Antibody Index in the Cerebrospinal Fluid for the Diagnosis and Monitoring of Rheumatoid Meningitis Open
Rheumatoid meningitis (RM) is a rare but often aggressive neurological complication of rheumatoid arthritis. The diagnosis of RM, besides the clinical, radiological, and laboratory criteria, usually requires a cerebral biopsy. Based on the…
View article: P11.68.A Hemangiopericytoma, case series and clinic-pathological analysis
P11.68.A Hemangiopericytoma, case series and clinic-pathological analysis Open
Background Hemangiopericytoma (HPC) is an extremely rare aggressive tumor of mesenchymal origin, which constitutes less than 1% of primary tumors of the central nervous system. Typically it occurs in young adults (mean age at diagnosis 30-…
View article: Correction: Visani et al. miR-196B-5P and miR-200B-3P Are Differentially Expressed in Medulloblastomas of Adults and Children. Diagnostics 2020, 10, 265
Correction: Visani et al. miR-196B-5P and miR-200B-3P Are Differentially Expressed in Medulloblastomas of Adults and Children. Diagnostics 2020, 10, 265 Open
The authors wish to make the following corrections to this paper [...]
View article: DATASET RELATED TO ARTICLE "MILD MALFORMATION OF CORTICAL DEVELOPMENT WITH OLIGODENDROGLIAL HYPERPLASIA (MOGHE): NEUROPHYSIOLOGICAL FINGERPRINTS OF A NEW PATHOLOGICAL ENTITY"
DATASET RELATED TO ARTICLE "MILD MALFORMATION OF CORTICAL DEVELOPMENT WITH OLIGODENDROGLIAL HYPERPLASIA (MOGHE): NEUROPHYSIOLOGICAL FINGERPRINTS OF A NEW PATHOLOGICAL ENTITY" Open
ppt: scalp eeg – brain mri – brain fdg-pet
View article: DATASET RELATED TO ARTICLE "MILD MALFORMATION OF CORTICAL DEVELOPMENT WITH OLIGODENDROGLIAL HYPERPLASIA (MOGHE): NEUROPHYSIOLOGICAL FINGERPRINTS OF A NEW PATHOLOGICAL ENTITY"
DATASET RELATED TO ARTICLE "MILD MALFORMATION OF CORTICAL DEVELOPMENT WITH OLIGODENDROGLIAL HYPERPLASIA (MOGHE): NEUROPHYSIOLOGICAL FINGERPRINTS OF A NEW PATHOLOGICAL ENTITY" Open
ppt: scalp eeg – brain mri – brain fdg-pet
View article: Next-Generation Sequencing Panel for 1p/19q Codeletion and IDH1-IDH2 Mutational Analysis Uncovers Mistaken Overdiagnoses of 1p/19q Codeletion by FISH
Next-Generation Sequencing Panel for 1p/19q Codeletion and IDH1-IDH2 Mutational Analysis Uncovers Mistaken Overdiagnoses of 1p/19q Codeletion by FISH Open
View article: Dataset related to article "hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers"
Dataset related to article "hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers" Open
Clinical and pathological data from hATTR patients, diagnosed and followed in our center for hATTR peripheral neuropathy
View article: Dataset related to article "hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers"
Dataset related to article "hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers" Open
Clinical and pathological data from hATTR patients, diagnosed and followed in our center for hATTR peripheral neuropathy