Results 51 to 60 of about 18,165 (198)

Outcomes following autologous hematopoietic stem cell transplant for patients with relapsed Wilms' tumor: a CIBMTR retrospective analysis. [PDF]

open access: yes, 2017
Despite the marked improvement in the overall survival (OS) for patients diagnosed with Wilms' tumor (WT), the outcomes for those who experience relapse have remained disappointing.
Abdel-Azim, H   +20 more
core   +2 more sources

Expanding the Phenotypic Spectrum Associated With Loss‐of‐Function SMARCA4 Variants to Eye Developmental Anomalies

open access: yesClinical Genetics, EarlyView.
This study expands the clinical spectrum of SMARCA4 by describing a novel phenotype in three unrelated individuals with truncating variants. Distinct from Coffin–Siris syndrome and rhabdoid tumor predisposition, this new association is characterized by ocular malformations, specifically microphthalmia and coloboma.
Bertrand Chesneau   +7 more
wiley   +1 more source

Expression and prognostic value of Wilms' tumor 1 and early growth response 1 proteins in nephroblastoma [PDF]

open access: yes, 2000
Wilms' tumor is one of the most common solid tumors of children. The protein product of the tumor-suppressor gene, Wilms' tumor 1 (WT-1), binds to the same DNA sequences as the protein product of the early growth response
Ghanem, M.A.I. (Mazen)   +9 more
core  

Population‐Based Cohort Study for Development of National Retinopathy of Prematurity Screening Criteria

open access: yesActa Paediatrica, Volume 115, Issue 3, Page 671-678, March 2026.
ABSTRACT Aim Screening criteria for retinopathy of prematurity (ROP) vary among countries. Early detection of ROP and minimising the burden of screening are important. Methods We analysed data from very preterm infants born in Switzerland between 2006 and 2022.
R. Gerull   +31 more
wiley   +1 more source

Cystic poorly differentiated nephroblastoma: A case report and review of literature

open access: yesAfrican Journal of Urology, 2014
Background: Cystic poorly differentiated nephroblastoma (CPDN) is a rare variant of nephroblastoma which follows a benign clinical course. Case diagnosis/treatment: In this report, we document a case of CPDN in a 2 year old boy who presented with ...
M.O. Odubanjo   +6 more
doaj   +1 more source

Preoperative radiomic signature based on CT images for noninvasive evaluation of localized nephroblastoma in pediatric patients

open access: yesFrontiers in Oncology, 2023
BackgroundNephron sparing nephrectomy may not reduce the prognosis of nephroblastoma in the absence of involvement of the renal capsule, sinus vessels, and lymph nodes, However, there is no accurate preoperative noninvasive evaluation method at present ...
Xiao-Hui Ma   +9 more
doaj   +1 more source

Nefroblastoma embrionario canino : caso clínico [PDF]

open access: yes, 2003
Se describe un caso de nefroma embrionario canino o tumor de Wilms en un perro, macho, de dos meses de edad que presentaba distensión abdominal progresiva y pérdida de peso reciente. Se realiza una ecografía observándose una masa abdominal de gran tamaño.
Bonastre Ráfales, Cristina   +3 more
core  

The metastasis inducer CCN1 (CYR61) activates the fatty acid synthase (FASN)-driven lipogenic phenotype in breast cancer cells [PDF]

open access: yes, 2016
The angiogenic inducer CCN1 (Cysteine-rich 61, CYR61) is differentially activated in metastatic breast carcinomas. However, little is known about the precise mechanisms that underlie the pro-metastatic actions of CCN1. Here, we investigated the impact of
Espinoza, Ingrid   +3 more
core   +1 more source

Incidence and Outcome of Infants With Cancer in Canada: A Report From Cancer in Young People in Canada Database

open access: yesPediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Purpose Infants with cancer are rare and face unique challenges. Our study aims to describe the incidence of infantile cancers in Canada and to compare treatment‐related mortality (TRM) and their outcomes with those of older children. Methods We conducted a retrospective cohort study using the Cancer in Young People in Canada database ...
Samuel Sassine   +22 more
wiley   +1 more source

Multilocular Cystic Nephroma – A Surgical and Radiological Dilemma [PDF]

open access: yes, 2011
Multilocular cystic nephroma is a slow growing benign renal tumor. It has been identified as exclusive adult lesion, more common in females. It commonly occurs as an asymtomatic mass, occasionally with hematuria.
Anil Malleshi Betigeri , Boopathi subramaniyam, Int J Cur Bio Med Sci.
core  

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