Maria J. Costa-Da

Porto, Portugal

Last Updated: 09/26/2026

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Found 15 publications

Gliomatosis cerebri in children: A poor prognostic phenotype of diffuse gliomas with a distinct molecular profile.

Gliomatosis cerebri in children: A poor prognostic phenotype of diffuse gliomas with a distinct molecular profile.

Journal: Neuro-oncology
Published: May 08, 2024

Quality of Life and Hormonal Impairment in Pediatric Patients With Craniopharyngiomas.

Quality of Life and Hormonal Impairment in Pediatric Patients With Craniopharyngiomas.

Journal: Cureus
Published: January 20, 2024

Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study.

Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study.

Journal: The Lancet. Oncology
Published: August 28, 2023

High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population.

High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population.

Journal: Frontiers in oncology
Published: June 13, 2023

Infants and Newborns with Atypical Teratoid Rhabdoid Tumors (ATRT) and Extracranial Malignant Rhabdoid Tumors (eMRT) in the EU-RHAB Registry: A Unique and Challenging Population.

Infants and Newborns with Atypical Teratoid Rhabdoid Tumors (ATRT) and Extracranial Malignant Rhabdoid Tumors (eMRT) in the EU-RHAB Registry: A Unique and Challenging Population.

Journal: Cancers
Published: March 17, 2022

Adrenal carcinoma as the first manifestation of a Li‑Fraumeni syndrome in three paediatric patients.

Adrenal carcinoma as the first manifestation of a Li‑Fraumeni syndrome in three paediatric patients.

Journal: Endokrynologia Polska
Published: December 14, 2021

Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study.

Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study.

Journal: Neuro-oncology
Published: June 02, 2021

Desensitization to carboplatin in low-grade glioma. A revision of 100 treatments in children.

Desensitization to carboplatin in low-grade glioma. A revision of 100 treatments in children.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: November 25, 2020

Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK).

Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK).

Journal: European journal of cancer (Oxford, England : 1990)
Published: May 02, 2020

Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors.

Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors.

Journal: Neuro-oncology
Published: December 29, 2019

Platinum-drugs Ototoxicity in Pediatric Patients With Brain Tumors: A 10-Year Review.

Platinum-drugs Ototoxicity in Pediatric Patients With Brain Tumors: A 10-Year Review.

Journal: Journal of pediatric hematology/oncology
Published: November 06, 2019

Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas.

Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas.

Journal: Nature communications
Published: January 18, 2019
Showing 1-12 of 15

Last Updated: 09/26/2026