Ana L. Seidinger

Campinas, SP 13083884, Brazil

Last Updated: 09/26/2026

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Found 18 publications

Correction: Ruas et al. Somatic Copy Number Alteration in Circulating Tumor DNA for Monitoring of Pediatric Patients with Cancer. Biomedicines 2023, 11, 1082.

Correction: Ruas et al. Somatic Copy Number Alteration in Circulating Tumor DNA for Monitoring of Pediatric Patients with Cancer. Biomedicines 2023, 11, 1082.

Journal: Biomedicines

Published: September 24, 2025

PLAG1 fusions define a third subtype of CNS embryonal tumor with PLAG family gene alteration.

PLAG1 fusions define a third subtype of CNS embryonal tumor with PLAG family gene alteration.

Journal: Acta neuropathologica

Published: May 08, 2025

Use of DNA Methylation Profiling as a Molecular Classification Tool for Paediatric Central Nervous System Tumours: A Middle-Income Country Population-Based Study.

Use of DNA Methylation Profiling as a Molecular Classification Tool for Paediatric Central Nervous System Tumours: A Middle-Income Country Population-Based Study.

Journal: Neuropathology and applied neurobiology

Published: November 26, 2024

Tumor-Promoted Changes in Pediatric Brain Histology Can Be Distinguished from Normal Parenchyma by Desorption Electrospray Ionization Mass Spectrometry Imaging.

Tumor-Promoted Changes in Pediatric Brain Histology Can Be Distinguished from Normal Parenchyma by Desorption Electrospray Ionization Mass Spectrometry Imaging.

Journal: Biomedicines

Published: August 20, 2024

11p15 Epimutations in Pediatric Embryonic Tumors: Insights from a Methylome Analysis.

11p15 Epimutations in Pediatric Embryonic Tumors: Insights from a Methylome Analysis.

Journal: Cancers

Published: June 27, 2023

Somatic Copy Number Alteration in Circulating Tumor DNA for Monitoring of Pediatric Patients with Cancer.

Somatic Copy Number Alteration in Circulating Tumor DNA for Monitoring of Pediatric Patients with Cancer.

Journal: Biomedicines

Published: January 31, 2023

CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH FACILITY.

CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH FACILITY.

Journal: Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo

Published: August 21, 2019

TP53 p.Arg337His geographic distribution correlates with adrenocortical tumor occurrence.

TP53 p.Arg337His geographic distribution correlates with adrenocortical tumor occurrence.

Journal: Molecular genetics & genomic medicine

Published: August 08, 2019

The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma.

The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: April 16, 2019

A simplified approach using Taqman low-density array for medulloblastoma subgrouping.

A simplified approach using Taqman low-density array for medulloblastoma subgrouping.

Journal: Acta neuropathologica communications

Published: January 22, 2019

Adrenocortical tumors associated with the TP53 p.R337H germline mutation can be identified during child-care consultations.

Adrenocortical tumors associated with the TP53 p.R337H germline mutation can be identified during child-care consultations.

Journal: Jornal de pediatria

Published: November 29, 2016

Contribution of the TP53 R337H mutation to the cancer burden in southern Brazil: Insights from the study of 55 families of children with adrenocortical tumors.

Contribution of the TP53 R337H mutation to the cancer burden in southern Brazil: Insights from the study of 55 families of children with adrenocortical tumors.

Journal: Cancer

Published: October 13, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026