Results 171 to 180 of about 19,884 (196)
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Label-free impedimetric immunosensor based on arginine-functionalized gold nanoparticles for detection of DHEAS, a biomarker of pediatric adrenocortical carcinoma

Biosensors and Bioelectronics, 2019
Pediatric adrenocortical carcinoma (pACC) is a rare and aggressive malignancy of high occurrence in Southern Brazil. pACC is characterized by the usual overproduction of dehydroepiandrosterone sulfate (DHEAS), whose detection in serum or plasma can be ...
Dhésmon Lima   +2 more
exaly   +2 more sources

Clinicopathological and imaging features of pediatric adrenocortical carcinoma: compared with non-carcinoma

British Journal of Radiology
To explore the differences in clinicopathological and imaging features between pediatric adrenocortical carcinoma (ACC) and non-carcinoma. The clinicopathological and imaging (CT/MR) findings of thirty-two children with pathologically proven
Pei-an Hu, Lei Chen, Zhengrong Zhou
semanticscholar   +2 more sources

Imaging findings in pediatric adrenocortical carcinoma

Pediatric Radiology, 2000
Adrenocortical carcinoma (ACC), a tumor that is rare among children, causes clinically evident hormonal disturbances. Imaging methods are used to stage disease and to plan surgical resection.To describe the findings of the various imaging methods used to evaluate ACC.We reviewed the records of ten consecutive patients (mean age, 8.1 years) who ...
Jefferson Augusto Santana Ribeiro   +2 more
semanticscholar   +3 more sources

A Case of Pediatric Adrenocortical Carcinoma With McCune‐Albright Syndrome Masquerading as Spontaneously Regressing Neuroblastoma

Pediatric Blood & Cancer
adrenocortical carcinoma (
Yu Lin   +11 more
semanticscholar   +2 more sources

Multi-omics profiling highlights karyopherin subunit alpha 2 as a promising biomarker for prognosis and immunotherapy respond in pediatric and adult adrenocortical carcinoma

Annals of Medicine
Purpose Adrenocortical carcinoma (ACC) afflicts both pediatric and adult populations and is characterized by dismal prognosis and elevated mortality.
Jianming Lu
exaly   +2 more sources

Report on 5 cases of pediatric adrenocortical carcinoma

The Journal of the Japanese Society of Clinical Cytology, 2010
Yasue SHITARA   +4 more
exaly   +2 more sources

Precocious puberty and other endocrine disorders during mitotane treatment for pediatric adrenocortical carcinoma - cases series

Endocrine Abstracts, 2023
E. Moszczyńska   +9 more
semanticscholar   +2 more sources

Pediatric spinal adrenocortical carcinoma

Journal of Pediatric Neuroradiology, 2015
A 5-month-old girl was found on magnetic resonance imaging to have a heterogeneously enhancing conus region mass. At surgery, an extramedullary, intradural mass was resected. Pathology confirmed a diagnosis of adrenocortical carcinoma. The neoplasm originated from ectopic adrenal cortical cell rests in the spine.
Rykken, Jeffrey, Kalina, Peter
openaire   +1 more source

Exogenous steroid replacement in a pediatric patient with adrenocortical carcinoma receiving mitotane

Pediatric Blood & Cancer
Catherine E Martin   +5 more
semanticscholar   +2 more sources

Comparison oPf 68Ga-FAPI and 18F-FDG PET/CT Findings in Oncocytic and Conventional Subtypes of Pediatric Adrenocortical Carcinoma.

Clinical Nuclear Medicine
Adrenocortical carcinoma, a poor prognosis cancer with a low survival rate, is a rare pediatric malignancy. We performed 18F-FDG PET/CT and 68Ga-FAPI PET/CT imaging in 2 children with different subtypes of adrenocortical carcinoma and compared the ...
E. Jenabi   +3 more
semanticscholar   +1 more source

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