Results 81 to 90 of about 11,107 (213)

Diszregulált miRNS-ek Wilms-tumorban és lehetséges célpontjaik [PDF]

open access: yes
Bevezetés: A Wilms-tumor a vese malignus daganatos elváltozása, mely leggyakrabban 10 év alatti gyermekek körében fordul elő. Célkitűzés: miRNS-profilozás 10 primer típusú Wilms-tumor szöveti FFPE mintából, valamint 10 kontrollmintából, és az ...
Kabai , Alexandra Barbara
core  

Dexamethasone for Chemotherapy‐Induced Nausea and Vomiting Prevention in Pediatric Patients: International Consensus

open access: yesPediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Background An international Delphi panel of experts developed consensus statements to delineate the circumstances where the risks of dexamethasone as an antiemetic do and do not outweigh its benefits. Procedure Experts in supportive care of pediatric patients were invited to participate.
Negar Shavandi   +20 more
wiley   +1 more source

Dolor abdominal agudo secundario a la ruptura de tumor de Wilms: reporte de caso [PDF]

open access: yes, 2017
El tumor de Wilms es el tumor renal maligno más común en la edad pediátrica y su ruptura es un evento raro. Se presenta el caso de un paciente de 4 años de edad con un cuadro de dolor abdominal agudo, asociado a la presencia de masa palpable en flanco ...
Salirrosas Bermúdez, Victor   +2 more
core   +1 more source

Cirugía Preservadora de Nefronas en Tumor de Wilms Bilateral.

open access: yesRevista Guatemalteca de Urología, 2018
El WT bilateral generalmente se ha tratado con nefrectomía radical (RN) del riñón  más afectado  y cirugía preservadora de nefrona en el riñón contralateral menos afectado después de la quimioterapia neoadyuvante.
Celeste Alston   +5 more
doaj   +1 more source

Clinical Insights Into Hypercalcemia of Malignancy in Childhood

open access: yesPediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Hypercalcemia of malignancy (HCM) is a rare but life‐threatening metabolic emergency in children that occurs in less than 1% of pediatric cancer cases, with a reported incidence ranging from 0.4% to 1.0% across different studies. While it is observed in 10%–20% of adult malignancies, pediatric HCM remains relatively uncommon.
Hüseyin Anıl Korkmaz
wiley   +1 more source

Intra-tumor genetic heterogeneity in wilms? tumor samples [PDF]

open access: yes, 2019
Childhood renal tumors account for ~7% of all childhood cancers, and most cases are embryonic Wilms’ tumors (WT). Children with WT are usually treated by either COG or SIOP.
Beatriz de Camargo   +7 more
core   +1 more source

Tumor de Wilms' na criança: revisão de 38 casos.

open access: yesActa Médica Portuguesa, 1991
Analysis of the incidence of the Nephroblastoma and of its clinic, echographic and radiologic aspects. Review of 38 cases handled in the Pediatric Surgery Service of Santa Maria Hospital between January 1960 and January 1987.
M J Leal   +3 more
doaj   +1 more source

Adherence to Protocol Recommendations for Children With Wilms Tumour in Two Consecutive Studies in the United Kingdom and Ireland—Does Variation Matter?

open access: yesPediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Background and Aims Wilms tumour (WT) has excellent event‐free and overall survival (OS). However, small differences exist between countries participating in the same international study. This led us to examine variation in adherence to protocol recommendations as a potential contributing factor.
Suzanne Tugnait   +23 more
wiley   +1 more source

Faithful expression of a tagged Fugu WT1 protein from a genomic transgene in zebrafish:efficient splicing of pufferfish genes in zebrafish but not mice [PDF]

open access: yes, 2003
The teleost fish are widely used as model organisms in vertebrate biology. The compact genome of the pufferfish, Fugu rubripes, has proven a valuable tool in comparative genome analyses, aiding the annotation of mammalian genomes and the identification ...
Niksic, Martina   +5 more
core  

TRIM28 haploinsufficiency predisposes to Wilms tumor [PDF]

open access: yes, 2019
Two percent of patients with Wilms tumors have a positive family history. In many of these cases the genetic cause remains unresolved. By applying germline exome sequencing in two families with two affected individuals with Wilms tumors, we identified ...
Didem Seven   +81 more
core   +1 more source

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