Results 81 to 90 of about 16,522 (203)

A Case of Cystic Partially Differentiated Nephroblastoma [PDF]

open access: yes, 2009
Cystic partially differentiated nephroblastoma is a rare renal mass in children. Since its clinical characteristics and radiologic findings are very similar to those of cystic Wilms tumor and cystic nephroma, the discrimination between these disease ...
권승연   +4 more
core  

Immunostaining in mixed type nephroblastoma with or without associated metastasis.

open access: yes, 2013
Example of high Ki-67 (A) and high cyclin E SI (C,E,G) in the blastemal (A,C), in the stromal (E) or epithelial (G) component of a patient with a stage I mixed type nephroblastoma and pulmonary metastases (M+) in comparison with a patient with a stage ...
Alaa El Ghoneimi (74756)   +9 more
core   +1 more source

Spontaneous Nephroblastoma in a Rainbow Trout (Salmo gairdneri)

open access: yes, 1973
A neoplasm in a rainbow trout (Salmo gairdneri) identified as a nephroblastoma is described and its possible pathological implications discussed. The characteristic conditions of abortive renal tubules and glomeruli in a fibrous stroma were observed ...
V. H. Logan, S. R. Baker, P. H. Odense
core   +1 more source

Biological Drivers of Wilms Tumor Prognosis and Treatment

open access: yesChildren, 2018
Prior to the 1950s, survival from Wilms tumor (WT) was less than 10%. Today, a child diagnosed with WT has a greater than 90% chance of survival. These gains in survival rates from WT are attributed largely to improvements in multimodal therapy: Enhanced
Hannah M. Phelps   +3 more
doaj   +1 more source

Blastemal predominant WT1 negative Wilms tumour of the young adult: a unique case report and review of the literature

open access: yesFrontiers in Medicine
Wilms tumour is a common juvenile cancer of the kidney, and its occurrence in adolescence or adulthood is extremely rare, accounting for around 1% of all adult kidney malignancies.
Jozef Škarda   +23 more
doaj   +1 more source

Identification of key genes and potential targets in nephroblastoma based on RNA expression microarray

open access: yes四川大学学报. 自然科学版, 2018
Nephroblastoma, or named Wilms tumor, is the most common renal cancer in children. This study was aim to identify gene signatures and potential therapeutic target in nephroblastoma. Microarrays GSE11151 and GSE53224 were downloaded from GEO database.
XU Jie-Tian   +4 more
doaj  

Nephroblastoma.

open access: yesBritish journal of urology, 2004
n ...
Camassei, Francesca Diomedi   +8 more
openaire   +3 more sources

KIT, PDGFRα and EGFR analysis in nephroblastoma

open access: yes, 2008
Nephroblastoma prognosis has dramatically improved, but an unfavourable prognostic subgroup warrants development of novel therapeutic strategies. Selective KIT, PDGFR alpha and epidermal growth factor receptor (EGFR) tyrosine kinase inhibition evolved as
Aslanidis, Charalampos   +15 more
core   +1 more source

Role of MRI in the management of patients with nephroblastoma.

open access: yes, 2008
Magnetic resonance imaging (MRI) presents the main diagnostic tool for differentiation and staging of renal tumors in childhood. Nephroblastoma is the most common malignant tumor in children.
Schenk, JP;Graf, N;Günther, P;Ley, S;Göppl, M;Kulozik, A;Rohrschneider, WK;Tröger, J
core   +1 more source

Protocol-based Management of Nephroblastoma: Five-year Outcomes with SIOP-RTSG Guidelines in an Indian Cohort

open access: yesJournal of Indian Association of Pediatric Surgeons
Background: Nephroblastoma or Wilms’ tumor (WT) is the most common malignant renal tumor in children, with high cure rates (>90%) in developed countries.
Nishant Agarwal   +10 more
doaj   +1 more source

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