Results 71 to 80 of about 2,093 (107)

Wilms tumor characteristics in children with heterozygous germline DIS3L2 variants. [PDF]

Genet Med
van Peer SE, Treger TD, Wegert J, Hol JA, Le Gall J, Jakkula EE, Kamihara J, Mullen EA, Graf N, Behjati S, Al-Saadi R, Duncan C, Schienda J, de Putter R, Brzezinski J, Verschuur A, Michaeli O, Ortiz MV, Herkert JC, Armstrong R, Waanders E, Kuiper RP, van den Heuvel-Eibrink MM, Gessler M, Jongmans MCJ.   +24 more
europepmc   +1 more source

Expanding clinical variability in FBXW7-related neurodevelopmental disorder: a multicenter case series. [PDF]

J Neurodev Disord
Savasta S, Comisi FF, Dell'Isola GB, Di Pasquale G, Johnson I, Herman I, Comisi AM, Operto FF, Bargiacchi G, Barge-Schaapveld DQCM, Mangano GD, Carotenuto M, Salpietro V, Verrotti A.   +13 more
europepmc   +1 more source

A mixed methods study of the impact of WAGR spectrum disorder on individuals and their caregivers. [PDF]

Orphanet J Rare Dis
Sistare EV, George AM, Hathaway ER, Trout KL, Morris J, Krantz SM, Kalish JM.   +6 more
europepmc   +1 more source

The absence of Trim28 in nephron progenitors results in impaired kidney development and function. [PDF]

Development
Palhazi B, Paikari A, Clarén G, Appenzeller S, Imdahl F, Daniel C, Becker M, Gessler M.   +7 more
europepmc   +1 more source

A Retrospective Review of 28 Cases of Pediatric Malignant Renal Tumors at a Single Institution. [PDF]

Diseases
Kawano T, Sugita K, Masuya R, Nishida N, Nagano A, Murakami M, Yano K, Onishi S, Harumatsu T, Nakamura T, Yamada K, Yamada W, Muto M, Kodama Y, Nishikawa T, Kaji T, Okamoto Y, Ieiri S.   +17 more
europepmc   +1 more source

Case Report: Iparomlimab and Tuvonralimab-based therapy for epithelioid malignant peritoneal mesothelioma: a three-case series. [PDF]

Front Oncol
Xu Z, Zhu L, Fang Y, Jiang Y.
europepmc   +1 more source

Fluorescence-Guided Surgery in Pediatric Oncology: Current Practice and Future Directions. [PDF]

Cancers (Basel)
Simons DC, van Schalkwijk LHM, van de Sande MAJ, Vahrmeijer AL, Wijnen MHWA, van der Steeg AFW, Tummers WSFJ.   +6 more
europepmc   +1 more source

A novel maternally inherited CDKN1C variant in a familial beckwith-wiedemann syndrome case: expanding the genotype-phenotype spectrum. [PDF]

BMC Med Genomics
Wu S, Zhang Y, Zhang H, Yan X, Pi Y.
europepmc   +1 more source

Bilateral ovarian steroid cell tumor in a postmenopausal woman with progressive hyperandrogenism. [PDF]

JCEM Case Rep
Tapia Sanchiz MS, Justel Enríquez A, Álvarez RM, Sebastian-Valles F, Marazuela M.   +4 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