Search Results - "de Krijger, Ronald r."
-
1
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 -
2
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 -
3
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 -
4
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 -
5
Chorioamnionitis Alters the Response to Surfactant in Preterm Infants
Published in The Journal of pediatrics (2010)“…Objective To study the association between antenatal exposure to chorioamnionitis and the neonatal response to surfactant. Study design Prospective…”
Get full text
Journal Article -
6
MRI Characteristics of Pediatric and Young-Adult Renal Cell Carcinoma: A Single-Center Retrospective Study and Literature Review
Published in Cancers (22-02-2023)“…Pediatric renal cell carcinoma (RCC) is a rare malignancy. Magnetic resonance imaging (MRI) is the preferred imaging modality for assessment of these tumors…”
Get full text
Journal Article -
7
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 -
8
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 -
9
Histologic chorioamnionitis, fetal involvement, and antenatal steroids: effects on neonatal outcome in preterm infants
Published in American journal of obstetrics and gynecology (01-12-2009)“…Objective The objective of the study was to study the effects of histologic chorioamnionitis (HC) with or without fetal involvement and antenatal steroid (AS)…”
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
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 -
12
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 -
13
SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas
Published in The journal of clinical endocrinology and metabolism (01-09-2011)“…Context: Pheochromocytoma-paraganglioma syndrome is caused by mutations in SDHB, SDHC, and SDHD, encoding subunits of succinate dehydrogenase (SDH), and in…”
Get full text
Journal Article -
14
Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants
Published in The lancet. Diabetes & endocrinology (01-05-2023)“…Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head…”
Get full text
Journal Article -
15
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 -
16
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 -
17
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 -
18
Organoid-based drug screening reveals neddylation as therapeutic target for malignant rhabdoid tumors
Published in Cell reports (Cambridge) (24-08-2021)“…Malignant rhabdoid tumors (MRTs) represent one of the most aggressive childhood malignancies. No effective treatment options are available, and prognosis is,…”
Get full text
Journal Article -
19
Data set for the reporting of pheochromocytoma and paraganglioma: explanations and recommendations of the guidelines from the International Collaboration on Cancer Reporting
Published in Human pathology (01-04-2021)“…The International Collaboration on Cancer Reporting (ICCR) is a not-for-profit to develop evidence-based, internationally agreed-upon standardized data sets…”
Get full text
Journal Article -
20
SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors
Published in Modern pathology (01-01-2011)“…Mutations in the tumor suppressor genes SDHB , SDHC , and SDHD (or collectively SDHx ) cause the inherited paraganglioma syndromes, characterized by…”
Get full text
Journal Article