Results 131 to 140 of about 9,898 (185)

NK cell-related genes-driven novel molecular subtyping and prognostic signatures for Wilms tumor: uncovering the therapeutic potential of TGX-221 and biomarker role of HS2ST1. [PDF]

Front Oncol
Hong P, Hu Z, Lin J, Cui K, Gao Z, Tian X, Lin T, Shi Q, Wei G.   +8 more
europepmc   +1 more source

Prevalence and Determinants of Impaired Bone Mineral Density and Fractures in the First National Dutch Wilms Tumor Survivor Cohort, a National DCCSS-LATER Study. [PDF]

Cancer Med
Wens FSPL, de Winter DTC, Janssens GO, Litjens R, van Atteveld JE, Nievelstein RAJ, Hobbelink MGG, de Vries ACH, Loonen JJ, van Dulmen-den Broeder E, van der Pal HJH, Pluijm SMF, Kremer LCM, van der Heiden-van der Loo M, Louwerens M, van Santen HM, Olsson DS, Hoefer I, van den Berg SAA, van Tinteren H, Neggers SJCMM, van den Heuvel-Eibrink MM.   +21 more
europepmc   +1 more source

<i>DICER1</i> Syndrome: What Do We Know of the Pathogenetic Mechanisms? [PDF]

Cancers (Basel)
Jansen FA, Bakhuizen J, Kester L, de Krijger RR.   +3 more
europepmc   +1 more source

PEDIATRÍA: Tumores de Wilms

Anales de medicina y cirugía, 1949
openaire   +1 more source

Implementation of Synoptic Reports in Enhancing Documentation Practices in Pediatric Surgical Oncology: A Systematic Review. [PDF]

Cancers (Basel)
Unal A, Harrison D, Loh AHP, Albirair M, Shalkow-Klincovstein J, Qureshi S, Abib SCV, Lakhoo K, Abdelhafeez AH.   +8 more
europepmc   +1 more source

Establishing a pediatric solid tumor PDX biobank for precision oncology research. [PDF]

Cancer Biol Ther
Akemi Kido L, Rodrigues Marusco M, Aparecida da Silva E, Do Carmo L, Beatriz Teodoro Borges A, Luz Torres Silva F, Silveira Ruas J, Giomo de Lima D, de Abreu Fernandes L, Maia Martin Daiggi C, Aparecida Cardinalli I, Ferreira Euzébio M, Yoshioka Jotta P, Maschietto M, Pini Zenatti P.   +14 more
europepmc   +1 more source

Predictors of Surgical Complications and Survival in Pediatric Wilms' Tumor: A 20-Year Retrospective Study from Two Thai Centers. [PDF]

Curr Oncol
Laochareonsuk W, Laohapansang M, Ngerncham M, Sangkhathat S.   +3 more
europepmc   +1 more source

Novel WT1 and ACTN4 co-mutations in a patient with Denys-Drash syndrome and an atypical, potentially attenuated presentation of nephropathy: a case report. [PDF]

BMC Nephrol
Frazier E, Sabour R, Nguyen MD, Le D, Hanna R.   +4 more
europepmc   +1 more source