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Prediction of neuroblastoma cell response to treatment with natural or synthetic retinoids using selected protein biomarkers

PloS one, 2019-06, Vol.14 (6), p.e0218269

2019

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Tazemetostat in the therapy of pediatric INI1-negative malignant rhabdoid tumors

Scientific reports, 2023-12, Vol.13 (1), p.21623-21623, Article 21623

2023

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Personalized Treatment of H3K27M-Mutant Pediatric Diffuse Gliomas Provides Improved Therapeutic Opportunities

Frontiers in oncology, 2020-01, Vol.9, p.1436

2020

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Comparative Analysis of Putative Prognostic and Predictive Markers in Neuroblastomas: High Expression of PBX1 Is Associated With a Poor Response to Induction Therapy

Frontiers in oncology, 2019-11, Vol.9, p.1221-1221

2019

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Two sisters with cardiac‐urogenital syndrome secondary to pathogenic splicing variant in the MYRF gene with unaffected parents: A case of gonadal mosaicism?

Molecular genetics & genomic medicine, 2023-05, Vol.11 (5), p.e2139-n/a

2023

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A Newly Observed Mutation of the ABCA3 Gene Causing Lethal Respiratory Failure of a Full-Term Newborn: A Case Report

Frontiers in genetics, 2020-08, Vol.11

2020

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Assessment of Tumor Mutational Burden in Pediatric Tumors by Real-Life Whole-Exome Sequencing and In Silico Simulation of Targeted Gene Panels: How the Choice of Method Could Affect the Clinical Decision?

Cancers, 2020-01, Vol.12 (1), p.230

2020

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Precision immuno-oncology approach for four malignant tumors in siblings with constitutional mismatch repair deficiency syndrome

NPJ precision oncology, 2024-05, Vol.8 (1), p.110-110, Article 110

2024

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Spindle Cell Hemangioma and Atypically Localized Juxtaglomerular Cell Tumor in a Patient with Hereditary BRIP1 Mutation: A Case Report

Genes, 2021-02, Vol.12 (2), p.220

2021

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Individualization of Treatment Improves the Survival of Children With High-Risk Solid Tumors: Comparative Patient Series Analysis in a Real-Life Scenario

Frontiers in oncology, 2019-07, Vol.9, p.644-644

2019

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Salivary Gland Choristoma of the Middle Ear in a Child: A Case Report

Ear, nose, & throat journal, 2021-06, Vol.100 (3_suppl), p.356S-359S

2021

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Improved osteosarcoma survival with addition of mifamurtide to conventional chemotherapy – Observational prospective single institution analysis

Journal of bone oncology, 2021-06, Vol.28, p.100362, Article 100362

2021

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Case report: rapid and durable response to PDGFR targeted therapy in a child with refractory multiple infantile myofibromatosis and a heterozygous germline mutation of the PDGFRB gene

BMC cancer, 2017-02, Vol.17 (1), p.119, Article 119

2017

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Personalized dendritic cell vaccine in multimodal individualized combination therapy improves survival in high-risk pediatric cancer patients

International journal of cancer, 2024-10, Vol.155 (8), p.1443-1454

2024

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SDHC Methylation Pattern in Patients With Carney Triad

Applied immunohistochemistry & molecular morphology, 2021-09, Vol.29 (8), p.599-605

2021

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An expansive aneurysmal bone cyst of the maxillary sinus in an 8 year old child: Case report and review of literature

Acta oto-laryngologica case reports, 2020-01, Vol.5 (1), p.86-90

2020

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Noonan syndrome from a fetopathologist perspective

Ceskoslovenské patologie, 2019, Vol.55 (1), p.48-52

2019

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A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human

European journal of human genetics : EJHG, 2013-04, Vol.21 (4), p.474-477

2013

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Novel FOXF1 Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

Human mutation, 2013-06, Vol.34 (6), p.801-811

2013

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MB-88QUANTITATIVE PROTEOMIC PROFILING IN MEDULLOBLASTOMA RECAPITULATES SUBGROUPING BASED ON TRANSCRIPTIONAL PROFILES

Neuro-oncology (Charlottesville, Va.), 2016-06, Vol.18 (suppl 3), p.iii117.1-iii117

2016

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Minimal Residual Disease-Guided Intermittent Dosing in Patients With Cancer: Successful Treatment of Chemoresistant Anaplastic Large Cell Lymphoma Using Intermittent Lorlatinib Dosing

JCO precision oncology, 2022-06, Vol.6 (6), p.e2100525

2022

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Abstract 76: Comprehensive genomic profiling as an approach to guide therapeutic planning in pediatric patients with high-risk solid tumors

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.76-76

2022

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Extremely rare spinal tumor in Li-Fraumeni syndrome

Onkologie (Olomouc), 2023-11, Vol.17 (5), p.304-307

2023

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Hypertext atlas of fetal and neonatal pathology

Diagnostic pathology, 2008-07, Vol.3 Suppl 1 (Suppl 1), p.S9-S9

2008

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Prediction of neuroblastoma cell response to treatment with natural or synthetic retinoids using selected protein biomarkers

Tazemetostat in the therapy of pediatric INI1-negative malignant rhabdoid tumors

Personalized Treatment of H3K27M-Mutant Pediatric Diffuse Gliomas Provides Improved Therapeutic Opportunities

Comparative Analysis of Putative Prognostic and Predictive Markers in Neuroblastomas: High Expression of PBX1 Is Associated With a Poor Response to Induction Therapy

Two sisters with cardiac‐urogenital syndrome secondary to pathogenic splicing variant in the MYRF gene with unaffected parents: A case of gonadal mosaicism?

A Newly Observed Mutation of the ABCA3 Gene Causing Lethal Respiratory Failure of a Full-Term Newborn: A Case Report

Assessment of Tumor Mutational Burden in Pediatric Tumors by Real-Life Whole-Exome Sequencing and In Silico Simulation of Targeted Gene Panels: How the Choice of Method Could Affect the Clinical Decision?

Precision immuno-oncology approach for four malignant tumors in siblings with constitutional mismatch repair deficiency syndrome

Spindle Cell Hemangioma and Atypically Localized Juxtaglomerular Cell Tumor in a Patient with Hereditary BRIP1 Mutation: A Case Report

Individualization of Treatment Improves the Survival of Children With High-Risk Solid Tumors: Comparative Patient Series Analysis in a Real-Life Scenario

Comprehensive Molecular Profiling for Relapsed/Refractory Pediatric Burkitt Lymphomas-Retrospective Analysis of Three Real-Life Clinical Cases-Addressing Issues on Randomization and Customization at the Bedside

Salivary Gland Choristoma of the Middle Ear in a Child: A Case Report

Improved osteosarcoma survival with addition of mifamurtide to conventional chemotherapy – Observational prospective single institution analysis

Case report: rapid and durable response to PDGFR targeted therapy in a child with refractory multiple infantile myofibromatosis and a heterozygous germline mutation of the PDGFRB gene

Personalized dendritic cell vaccine in multimodal individualized combination therapy improves survival in high-risk pediatric cancer patients

SDHC Methylation Pattern in Patients With Carney Triad

An expansive aneurysmal bone cyst of the maxillary sinus in an 8 year old child: Case report and review of literature

Noonan syndrome from a fetopathologist perspective

A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human

Novel FOXF1 Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

MB-88QUANTITATIVE PROTEOMIC PROFILING IN MEDULLOBLASTOMA RECAPITULATES SUBGROUPING BASED ON TRANSCRIPTIONAL PROFILES

Minimal Residual Disease-Guided Intermittent Dosing in Patients With Cancer: Successful Treatment of Chemoresistant Anaplastic Large Cell Lymphoma Using Intermittent Lorlatinib Dosing

Abstract 76: Comprehensive genomic profiling as an approach to guide therapeutic planning in pediatric patients with high-risk solid tumors

Extremely rare spinal tumor in Li-Fraumeni syndrome

Hypertext atlas of fetal and neonatal pathology

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