about
Molecular fingerprinting reflects different histotypes and brain region in low grade gliomas.Primary diffuse leptomeningeal gliomatosis in children: a clinical pathologic correlation.Pineal germinoma in a child with interferon-γ receptor 1 deficiency. case report and literature review.SMARCB1/INI1 Involvement in Pediatric Chordoma: A Mutational and Immunohistochemical Analysis.Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cord.Pontocerebellar hypoplasia: clinical, pathologic, and genetic studies.Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective.Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspringIdentification of an interstitial 18p11.32-p11.31 duplication including the EMILIN2 gene in a family with porokeratosis of Mibelli.High levels of PROM1 (CD133) transcript are a potential predictor of poor prognosis in medulloblastomaDiagnostic and prognostic value of 18F-DOPA PET and 1H-MR spectroscopy in pediatric supratentorial infiltrative gliomas: a comparative study.Cystic angiomatosis of the craniocervical junction associated with Chiari I malformation: case report and review of the literature.High-throughput microRNA profiling of pediatric high-grade gliomas.TP53 codon 72 polymorphism may predict early tumour progression in paediatric pilocytic astrocytoma.Spontaneous regression of transplacental metastases from maternal melanoma in a newborn: case report and review of the literature.Troubleshooting fine-tuning procedures for qPCR system design.Intradural Extramedullary Ependymoma with Leptomeningeal Dissemination: The First Case Report in a Child and Literature Review.Grading and outcome prediction of pediatric diffuse astrocytic tumors with diffusion and arterial spin labeling perfusion MRI in comparison with 18F-DOPA PET.Successful isolation and long-term establishment of a cell line with stem cell-like features from an anaplastic medulloblastoma.Both CD133+ and CD133- medulloblastoma cell lines express ligands for triggering NK receptors and are susceptible to NK-mediated cytotoxicity.Expression and functional analysis of human leukocyte antigen class I antigen-processing machinery in medulloblastoma.Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstructionBilateral germinoma of the basal ganglia.A case of linear IgA disease in a child with IgA and IgG circulating antibodies directed to BPAg2.Analysis of NADP+-dependent isocitrate dehydrogenase-1/2 gene mutations in pediatric brain tumors: report of a secondary anaplastic astrocytoma carrying the IDH1 mutation.Respiratory Distress in a 3-Month-Old Infant with a Mass Obstructing the Right Main-Stem Bronchus: An Unusual Localization of Infantile Hemangioma.Evaluation status and prognostic significance of O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation in pediatric high grade gliomas.Intracerebral schwannoma in a child.Post-chemotherapy maturation of a pineoblastoma.Epilepsy associated with supratentorial brain tumors under 3 years of life.A 3-year-old boy with drug-resistant complex partial seizures.Congenital multifocal rhabdoid tumor: a case with peculiar biological behavior and different response to treatment according to location (central nervous system and kidney).Pharmacokinetics, pharmacodynamics and efficacy on pediatric tumors of the glioma radiosensitizer KU60019.Spinal lipoma as a dysembryogenetic anomaly: Four unusual cases of ectopic iliac rib within the spinal lipoma.A unique case of multiple dermatomyofibromas.Value of 18F-3,4-dihydroxyphenylalanine PET/MR image fusion in pediatric supratentorial infiltrative astrocytomas: a prospective pilot study.A rare case of osteoblastoma associated to aneurysmal bone cyst of the spine. Case report.Laryngeal schwannoma in an 8-year-old boy with inspiratory dyspnea.Juvenile eosinophilic fasciitis: report of three cases with a review of the literature.Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1.
P50
Q24288958-C3CBD4C0-4081-4114-9F1D-A17D1C6520BFQ30582041-7D8C6329-6E73-45A7-BB8D-92FE43255AD5Q30850932-97553F16-E28F-4419-A813-9FF660DEE508Q33276200-D447BC1C-6871-48AC-9DBD-5BDE75465FCDQ33654483-C2CC0A95-136A-4659-91F1-9F2E2E790E71Q34144442-06719657-2BEA-4CC2-A405-15B7364691B7Q34605276-3A91CEB1-AC76-414E-8051-8A4FA999235AQ34618442-20307247-FF59-4EB5-94CE-A0641BC042C6Q34674859-279B4C61-C613-472B-81F4-0917756D6C1AQ34977386-BB41C148-9E9A-4B6E-938F-F70D50BD11B6Q36250739-DCB44C09-FC4E-4999-8F90-29832F093FBFQ36706320-2185452F-C7D9-4569-A5A6-EB343BB5E7A3Q37492187-DB84566F-1988-4FCB-92B0-63EF80A049DBQ37565322-2CF4BAF7-EB9C-4169-A8C4-518F8B9403D0Q37800350-C75827E4-9EA6-40BA-B765-577D5D8F0522Q38330259-81F200FE-6F7D-4611-B0D3-738807E7C760Q38415344-A33613BD-A184-41FB-97CA-35B01CD35A05Q38656133-DEA1E1B0-9AD7-445F-8281-8299F3C71949Q40053661-F873ABE5-B279-40F9-9DB6-0E6DB068931CQ40071648-D7FF4E1D-08BF-42BA-8028-A822B335CD49Q40124595-07567E42-4844-4353-8C47-5CF46BBCB218Q42385938-92DA7C54-DF36-4876-9E9B-E68ED3973D61Q42495379-779D4BF5-E7C7-4C78-AD42-68E9EECE625DQ46824613-334FED5D-8066-4CC2-9FA1-F1FA5C5C0DCCQ47356155-C0E16FD9-7D4E-4D38-A513-0FCE97EDDFCDQ48011835-4FC430C5-2882-4FC4-9CED-36D2F9EE1EE6Q48164217-669BF66F-1A91-48CB-82BF-CDD76E7D50BDQ48271054-8DB28722-8778-43F7-A361-D802460BA7E7Q48274691-E60BABE3-FBE0-4BB8-9BC0-164ED35A18BBQ48387118-5E55CD85-BF89-4B15-8C1A-CF70C972B912Q48397949-D2902FF1-C7CE-44A5-9F6A-96151B78FFBDQ48440074-4C7E1A88-A1EB-4964-B781-4E771B6FDFE3Q48621553-873D95EF-EC62-4AC5-A320-91C30A131B43Q50519754-2F37B630-5B9F-401F-91CE-35782A066758Q51682932-7D78D937-0342-4547-986C-C885392CE985Q51746968-A6FDB543-8621-4BBA-80B2-CE7ACD7E75DDQ52995070-C8307147-D377-45AE-A19D-FCE146B7D26FQ53479995-F9A7FE0B-768C-417C-8924-5793BEB050AEQ54095009-A47F854B-A2B0-41C5-B41B-02CD8B581760Q54483003-4CE6BE59-1A84-4C58-836C-B0ACD4AA0B74
P50
description
hulumtues
@sq
neuropatologo
@it
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Paolo Nozza
@ast
Paolo Nozza
@en
Paolo Nozza
@es
Paolo Nozza
@it
Paolo Nozza
@nl
Paolo Nozza
@sl
type
label
Paolo Nozza
@ast
Paolo Nozza
@en
Paolo Nozza
@es
Paolo Nozza
@it
Paolo Nozza
@nl
Paolo Nozza
@sl
prefLabel
Paolo Nozza
@ast
Paolo Nozza
@en
Paolo Nozza
@es
Paolo Nozza
@it
Paolo Nozza
@nl
Paolo Nozza
@sl
P106
P1153
23005820100
P21
P31
P496
0000-0002-7595-1420