Search Results - "Krijger, Ronald De"
-
1
European Society of Endocrinology Clinical Practice Guidelines on the management of adrenocortical carcinoma in adults, in collaboration with the European Network for the Study of Adrenal Tumors
Published in European journal of endocrinology (01-10-2018)“…Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone-producing tumor with variable prognosis. The purpose of these guidelines is to…”
Get full text
Journal Article -
2
Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas
Published in Endocrine pathology (01-03-2022)“…This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in the 5th series of the WHO…”
Get full text
Journal Article -
3
Overview of the 2022 WHO Classification of Adrenal Cortical Tumors
Published in Endocrine pathology (01-03-2022)“…The new WHO classification of adrenal cortical proliferations reflects translational advances in the fields of endocrine pathology, oncology and molecular…”
Get full text
Journal Article -
4
An organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity
Published in Nature communications (11-03-2020)“…Kidney tumours are among the most common solid tumours in children, comprising distinct subtypes differing in many aspects, including cell-of-origin, genetics,…”
Get full text
Journal Article -
5
Porphyromonas gingivalis within Placental Villous Mesenchyme and Umbilical Cord Stroma Is Associated with Adverse Pregnancy Outcome
Published in PloS one (05-01-2016)“…Intrauterine presence of Porphyromonas gingivalis (Pg), a common oral pathobiont, is implicated in preterm birth. Our aim was to determine if the location of…”
Get full text
Journal Article -
6
Somatic mutations and single-cell transcriptomes reveal the root of malignant rhabdoid tumours
Published in Nature communications (03-03-2021)“…Malignant rhabdoid tumour (MRT) is an often lethal childhood cancer that, like many paediatric tumours, is thought to arise from aberrant fetal development…”
Get full text
Journal Article -
7
Pathology and genetics of phaeochromocytoma and paraganglioma
Published in Histopathology (01-01-2018)“…Phaeochromocytoma and paraganglioma (PHEO/PGL) are rare tumours with an estimated annual incidence of 3 per million. Advances in molecular understanding have…”
Get full text
Journal Article -
8
Familial Male-limited Precocious Puberty (FMPP) and Testicular Germ Cell Tumors
Published in The journal of clinical endocrinology and metabolism (01-11-2022)“…Objective: The purpose of this study is to report development of a malignant testicular germ cell tumor (GCT) in 2 young adult males with familial male-limited…”
Get full text
Journal Article -
9
MR imaging in discriminating between benign and malignant paediatric ovarian masses: a systematic review
Published in European radiology (01-02-2020)“…Objectives The use of magnetic resonance (MR) imaging in differentiation between benign and malignant adnexal masses in children and adolescents might be of…”
Get full text
Journal Article -
10
Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: A nationwide study and systematic review
Published in European journal of internal medicine (01-05-2018)“…Recent years have seen major changes in clinical practice which may have affected the incidence rates of pheochromocytoma(PCC)/sympathetic paraganglioma(sPGL)…”
Get full text
Journal Article -
11
Role of MDH2 pathogenic variant in pheochromocytoma and paraganglioma patients
Published in Genetics in medicine (01-12-2018)“…MDH2 (malate dehydrogenase 2) has recently been proposed as a novel potential pheochromocytoma/paraganglioma (PPGL) susceptibility gene, but its role in the…”
Get full text
Journal Article -
12
Histological, immunohistochemical and transcriptomic characterization of human tracheoesophageal fistulas
Published in PloS one (17-11-2020)“…Esophageal atresia (EA) and tracheoesophageal fistula (TEF) are relatively frequently occurring foregut malformations. EA/TEF is thought to have a strong…”
Get full text
Journal Article -
13
Mass spectrometry imaging identifies metabolic patterns associated with malignant potential in pheochromocytoma and paraganglioma
Published in European journal of endocrinology (01-07-2021)“…Objective Within the past decade, important genetic drivers of pheochromocytoma and paraganglioma (PPGLs) development have been identified. The…”
Get full text
Journal Article -
14
Reply to: “Addressing Chatbots as Artificial Intelligence Aids in Pediatric Pathology”
Published in Pediatric and developmental pathology (01-05-2024)Get full text
Journal Article -
15
What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?
Published in Endocrine pathology (01-03-2021)“…Recent advances in molecular genetics and genomics have led to increased understanding of the aetiopathogenesis of pheochromocytomas and paragangliomas…”
Get full text
Journal Article -
16
SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T)
Published in Modern pathology (01-06-2015)“…Despite the established role of SDHB/SDHA immunohistochemistry as a valuable tool to identify patients at risk for familial succinate dehydrogenase-related…”
Get full text
Journal Article -
17
Prognostic Value of Microscopic Tumor Necrosis in Adrenal Cortical Carcinoma
Published in Endocrine pathology (01-06-2023)“…Adrenal cortical carcinoma (ACC) is an uncommon neoplasm with variable prognosis. Several histologic criteria have been identified as predictors of malignancy…”
Get full text
Journal Article -
18
Characteristics and outcome of children with renal tumors in the Netherlands: The first five-year's experience of national centralization
Published in PloS one (13-01-2022)“…Around 6% of all childhood malignancies represent renal tumors, of which a majority includes Wilms tumor (WT). Although survival rates have improved over the…”
Get full text
Journal Article -
19
Somatic, Genetic and Epigenetic Changes in Nephrogenic Rests and Their Role in the Transformation to Wilms Tumors, a Systematic Review
Published in Cancers (21-02-2023)“…To review somatic genetic changes in nephrogenic rests (NR), which are considered to be precursor lesions of Wilms tumors (WT). This systematic review is…”
Get full text
Journal Article -
20
Renal Tumors of Childhood-A Histopathologic Pattern-Based Diagnostic Approach
Published in Cancers (19-03-2020)“…Renal tumors comprise approximately 7% of all malignant pediatric tumors. This is a highly heterogeneous group of tumors, each with its own therapeutic…”
Get full text
Journal Article