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  • Baliakas, Panagiotis,1977-Uppsala universitet,Science for Life Laboratory, SciLifeLab,Experimentell och klinisk onkologi,Uppsala Univ, Sweden (author)

Nordic Guidelines for Germline Predisposition to Myeloid Neoplasms in Adults: Recommendations for Genetic Diagnosis, Clinical Management and Follow-up

  • Article/chapterEnglish2019

Publisher, publication year, extent ...

  • LIPPINCOTT WILLIAMS & WILKINS,2019
  • printrdacarrier

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  • LIBRIS-ID:oai:DiVA.org:liu-163763
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-163763URI
  • https://doi.org/10.1097/HS9.0000000000000321DOI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-406217URI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:147853613URI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Funding Agencies|Nordic Cancer Union (NCU)
  • Myeloid neoplasms (MNs) with germline predisposition have recently been recognized as novel entities in the latest World Health Organization (WHO) classification for MNs. Individuals with MNs due to germline predisposition exhibit increased risk for the development of MNs, mainly acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Setting the diagnosis of MN with germline predisposition is of crucial clinical significance since it may tailor therapy, dictate the selection of donor for allogeneic hematopoietic stem cell transplantation (allo-HSCT), determine the conditioning regimen, enable relevant prophylactic measures and early intervention or contribute to avoid unnecessary or even harmful medication. Finally, it allows for genetic counseling and follow-up of at-risk family members. Identification of these patients in the clinical setting is challenging, as there is no consensus due to lack of evidence regarding the criteria defining the patients who should be tested for these conditions. In addition, even in cases with a strong suspicion of a MN with germline predisposition, no standard diagnostic algorithm is available. We present the first version of the Nordic recommendations for diagnostics, surveillance and management including considerations for allo-HSCT for patients and carriers of a germline mutation predisposing to the development of MNs.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Tesi, BiancaKarolinska Institutet,Karolinska Univ Hosp, Sweden (author)
  • Wartiovaara-Kautto, UllaHelsinki Univ Hosp, Comprehens Canc Ctr, Dept Hematol, Helsinki, Finland (author)
  • Stray-Pedersen, AsbjorgOslo Univ Hosp, Rikshosp, Div Pediat & Adolescent Med, Oslo, Norway (author)
  • Friis, Lone SmidstrupCopenhagen Univ Hosp, Rigshosp, Dept Hematol, Copenhagen, Denmark (author)
  • Dybedal, IngunnOslo Univ Hosp, Rikshosp, Dept Hematol, Oslo, Norway (author)
  • Hovland, RandiHaukeland Hosp, Dept Clin Genet, Bergen, Norway (author)
  • Jahnukainen, KirsiHelsinki Univ Hosp, New Childrens Hosp, Helsinki, Finland (author)
  • Raaschou-Jensen, KlasOdense Univ Hosp, Dept Hematol, Odense, Denmark (author)
  • Ljungman, PerKarolinska Institutet,Karolinska Univ Hosp, Sweden; Karolinska Inst, Sweden (author)
  • Rustad, Cecilie F.Oslo Univ Hosp, Rikshosp, Dept Med Genet, Oslo, Norway (author)
  • Lautrup, Charlotte K.Aalborg Univ Hosp, Dept Clin Genet, Aalborg, Denmark (author)
  • Kilpivaara, OutiUniv Helsinki, Appl Tumor Genom Res Program, Fac Med, Helsinki, Finland;Univ Helsinki, Dept Med & Clin Genet, Helsinki, Finland (author)
  • Kittang, Astrid OlsnesHaukeland Hosp, Dept Hematol, Bergen, Norway (author)
  • Gronbaek, KirstenCopenhagen Univ Hosp, Rigshosp, Dept Hematol, Copenhagen, Denmark (author)
  • Cammenga, Jörg,1969-Linköpings universitet,Avdelningen för Kirurgi, Ortopedi och Onkologi,Medicinska fakulteten,Region Östergötland, Hematologiska kliniken US,Linköping Univ Hosp, Dept Hematol, Linköping, Sweden(Swepub:liu)jorca02 (author)
  • Hellstrom-Lindberg, EvaKarolinska Institutet,Karolinska Univ Hosp, Sweden (author)
  • Andersen, Mette K.Copenhagen Univ Hosp, Rigshosp, Dept Clin Genet, Copenhagen, Denmark (author)
  • Uppsala universitetScience for Life Laboratory, SciLifeLab (creator_code:org_t)

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  • In:HemaSphere: LIPPINCOTT WILLIAMS & WILKINS3:62572-9241

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