View in EDS HTML Full Text PDF Full Text

Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.

Saved in:
Bibliographic Details
Title: Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.
Authors: Brouillard, Pascal1 (AUTHOR), Schlögel, Matthieu J.1 (AUTHOR), Homayun Sepehr, Nassim1 (AUTHOR), Helaers, Raphaël1 (AUTHOR), Queisser, Angela1 (AUTHOR), Fastré, Elodie1 (AUTHOR), Boutry, Simon1 (AUTHOR), Schmitz, Sandra2,3,4 (AUTHOR), Clapuyt, Philippe2,3,4 (AUTHOR), Hammer, Frank2,3,4 (AUTHOR), Dompmartin, Anne5 (AUTHOR), Weitz-Tuoretmaa, Annamaria6 (AUTHOR), Laranne, Jussi7 (AUTHOR), Pasquesoone, Louise8 (AUTHOR), Vilain, Catheline9 (AUTHOR), Boon, Laurence M.1,3,4 (AUTHOR), Vikkula, Miikka1,3,4,10 (AUTHOR) miikka.vikkula@uclouvain.be
Source: Orphanet Journal of Rare Diseases. 6/10/2021, Vol. 16 Issue 1, p1-12. 12p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 150821879
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Brouillard%2C+Pascal%22">Brouillard, Pascal</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schlögel%2C+Matthieu+J%2E%22">Schlögel, Matthieu J.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Homayun+Sepehr%2C+Nassim%22">Homayun Sepehr, Nassim</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Helaers%2C+Raphaël%22">Helaers, Raphaël</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Queisser%2C+Angela%22">Queisser, Angela</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fastré%2C+Elodie%22">Fastré, Elodie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Boutry%2C+Simon%22">Boutry, Simon</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schmitz%2C+Sandra%22">Schmitz, Sandra</searchLink><relatesTo>2,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Clapuyt%2C+Philippe%22">Clapuyt, Philippe</searchLink><relatesTo>2,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hammer%2C+Frank%22">Hammer, Frank</searchLink><relatesTo>2,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Dompmartin%2C+Anne%22">Dompmartin, Anne</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Weitz-Tuoretmaa%2C+Annamaria%22">Weitz-Tuoretmaa, Annamaria</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Laranne%2C+Jussi%22">Laranne, Jussi</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pasquesoone%2C+Louise%22">Pasquesoone, Louise</searchLink><relatesTo>8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Vilain%2C+Catheline%22">Vilain, Catheline</searchLink><relatesTo>9</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Boon%2C+Laurence+M%2E%22">Boon, Laurence M.</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Vikkula%2C+Miikka%22">Vikkula, Miikka</searchLink><relatesTo>1,3,4,10</relatesTo> (AUTHOR)<i> miikka.vikkula@uclouvain.be</i>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 6/10/2021, Vol. 16 Issue 1, p1-12. 12p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=150821879
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1186/s13023-021-01898-y
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 12
        StartPage: 1
    Titles:
      – TitleFull: Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Brouillard, Pascal
      – PersonEntity:
          Name:
            NameFull: Schlögel, Matthieu J.
      – PersonEntity:
          Name:
            NameFull: Homayun Sepehr, Nassim
      – PersonEntity:
          Name:
            NameFull: Helaers, Raphaël
      – PersonEntity:
          Name:
            NameFull: Queisser, Angela
      – PersonEntity:
          Name:
            NameFull: Fastré, Elodie
      – PersonEntity:
          Name:
            NameFull: Boutry, Simon
      – PersonEntity:
          Name:
            NameFull: Schmitz, Sandra
      – PersonEntity:
          Name:
            NameFull: Clapuyt, Philippe
      – PersonEntity:
          Name:
            NameFull: Hammer, Frank
      – PersonEntity:
          Name:
            NameFull: Dompmartin, Anne
      – PersonEntity:
          Name:
            NameFull: Weitz-Tuoretmaa, Annamaria
      – PersonEntity:
          Name:
            NameFull: Laranne, Jussi
      – PersonEntity:
          Name:
            NameFull: Pasquesoone, Louise
      – PersonEntity:
          Name:
            NameFull: Vilain, Catheline
      – PersonEntity:
          Name:
            NameFull: Boon, Laurence M.
      – PersonEntity:
          Name:
            NameFull: Vikkula, Miikka
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 10
              M: 06
              Text: 6/10/2021
              Type: published
              Y: 2021
          Identifiers:
            – Type: issn-print
              Value: 17501172
          Numbering:
            – Type: volume
              Value: 16
            – Type: issue
              Value: 1
          Titles:
            – TitleFull: Orphanet Journal of Rare Diseases
              Type: main
ResultId 1