Results 21 to 30 of about 3,009,060 (331)

Recent advances in Wilms tumor predisposition.

open access: yesHuman Molecular Genetics, 2020
Wilms tumor (WT), the most common childhood kidney cancer, develops in association with an underlying germline predisposition in up to 15% of cases. Germline alterations affecting the WT1 gene and epigenetic alterations affecting the 11p15 locus are ...
J. Maciaszek, Ninad Oak, K. Nichols
semanticscholar   +1 more source

Intralobar Nephroblastomatosis Mimicking Wilms Tumor Treated with Chemotherapy after Removal of the Affected Kidney

open access: yesClinical Pediatric Hematology-Oncology, 2023
Nephroblastomatosis (NBM) is a precursor of Wilms tumor. We herein report a case in which Wilms tumor was initially suspected and the affected kidney was removed. The tumor was subsequently diagnosed as intralobar NBM and a favorable outcome was achieved
Hirozumi Sano   +8 more
doaj   +1 more source

Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30‐year SIOP‐RTSG experience

open access: yesCancer, 2020
WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). Currently, surveillance and treatment recommendations are
Janna A. Hol   +20 more
semanticscholar   +1 more source

Wilms Tumor

open access: yesHandbook of Pediatric Hematology and Oncology, 2019
Wilms tumor is often first noticed because of abdominal swelling or a mass in the kidney that can be felt upon physical examination. Some affected children have abdominal pain, fever, a low number of red blood cells (anemia), blood in the urine ...
Naim K
semanticscholar   +2 more sources

Teratoid Wilms' tumor of kidney with neural tissue predominant: Case report with review of literature

open access: yesJournal of Family Medicine and Primary Care, 2019
Wilms' tumor is most common pediatric renal tumor. Teratoid Wilms' tumor is a variant of Wilms' tumor, in which heterologous tissue predominates. Most commonly, epithelial and mesenchymal tissue present as heterologous component.
Santosh G Rathod   +3 more
doaj   +1 more source

Sphingosine 1-phosphate in renal diseases [PDF]

open access: yes, 2013
Because of its highly bioactive properties sphingosine 1-phosphate (S1P) is an attractive target for the treatment of several diseases. Since the expression of sphingosine kinases as well as S1P receptors was demonstrated in the kidney, questions about ...
Huwiler, Andrea   +2 more
core   +2 more sources

Embryonal precursors of Wilms tumor

open access: yesScience, 2019
A childhood tumor—from the beginning Many adult cancers arise from clonal expansions of mutant cells in normal tissue. These premalignant expansions are defined by somatic mutations shared by the cancers.
Tim H. H. Coorens   +40 more
semanticscholar   +1 more source

ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five‐center case‐control study

open access: yesJournal of clinical laboratory analysis (Print), 2020
Wilms tumor is a frequently diagnosed renal cancer among children with unclear genetic causes. N6‐methyladenosine (m6A) modification genes play critical roles in tumorigenesis.
Rui-Xi Hua   +10 more
semanticscholar   +1 more source

Asymptomatic adult Wilms' tumor: A case report

open access: yesRadiology Case Reports, 2022
Background: Wilms' tumor, also called nephroblastoma, is an extremely uncommon kidney tumor of adulthood. We reported a adult man with a left kidney mass diagnosed as Wilms' tumor.Case presentation: A 25-year-old man was hospitalized due to injury of the
Yu-Feng Bai, BSc   +8 more
doaj   +1 more source

Changes in renal WT-1 expression preceding hypertension development [PDF]

open access: yes, 2016
Background: Hypertension is a public health problem with mostly unknown causes, and where strong hereditary genetic alterations have not been fully elucidated. However, the use of experimental models has provided valuable information.
Abud, María Angélica   +8 more
core   +2 more sources

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