% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Kalish:293613,
      author       = {J. M. Kalish and K. D. Becktell and G. Bougeard and G. M.
                      Brodeur and L. R. Diller and A. S. Doria and J. R. Hansford
                      and S. D. Klein and W. K. Kohlmann and C. P. Kratz and S. P.
                      MacFarland and K. Pajtler$^*$ and S. P. Rednam and J.
                      Schienda and L. J. States and A. Villani and R. Weksberg and
                      K. Zelley and G. E. Tomlinson and J. J. Brzezinski},
      title        = {{U}pdate on surveillance for {W}ilms tumor and
                      hepatoblastoma in {B}eckwith-{W}iedemann {S}yndrome and
                      other predisposition syndromes.},
      journal      = {Clinical cancer research},
      volume       = {30},
      number       = {23},
      issn         = {1078-0432},
      address      = {Philadelphia, Pa. [u.a.]},
      publisher    = {AACR},
      reportid     = {DKFZ-2024-01929},
      pages        = {5260-5269},
      year         = {2024},
      note         = {2024 Dec 2;30(23):5260-5269},
      abstract     = {Wilms tumors are commonly associated with predisposition
                      syndromes many, but not all, of which include overgrowth.
                      Several of these syndromes also include a risk of other
                      embryonal malignancies - particularly hepatoblastoma.
                      Guidelines for surveillance in this population were
                      published in 2017 and recently members of the AACR Pediatric
                      Cancer Working Group met to update those guidelines with a
                      review of more recently published evidence and risk
                      estimates. This perspective serves to update pediatric
                      oncologists, geneticists, radiologists, counselors and other
                      healthcare professionals on revised diagnostic criteria,
                      review previously published surveillance guidelines and
                      harmonize updated surveillance recommendations in the North
                      American and Australian context for patients with overgrowth
                      syndromes and other syndromes associated with Wilms tumor
                      predisposition.},
      subtyp        = {Review Article},
      cin          = {B062 / HD01},
      ddc          = {610},
      cid          = {I:(DE-He78)B062-20160331 / I:(DE-He78)HD01-20160331},
      pnm          = {312 - Funktionelle und strukturelle Genomforschung
                      (POF4-312)},
      pid          = {G:(DE-HGF)POF4-312},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:39320341},
      doi          = {10.1158/1078-0432.CCR-24-2100},
      url          = {https://inrepo02.dkfz.de/record/293613},
}