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Prospective Genetic Screening in Multiple Endocrine Neoplasia Syndromes.

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Title: Prospective Genetic Screening in Multiple Endocrine Neoplasia Syndromes.
Authors: Paun, Diana, Tilici, Dana, Paun, Sorin, Mirica, Alexandra
Source: Children; Aug2024, Vol. 11 Issue 8, p1012, 16p
Subject Terms: MULTIPLE endocrine neoplasia, DISEASE management, GENE expression, WERMER syndrome, EARLY diagnosis, GENETIC mutation, GENETIC testing, SIPPLE syndrome, MUCOSAL neuroma syndrome, PHENOTYPES, SEQUENCE analysis, GENOTYPES, THYROIDECTOMY
Abstract: Multiple endocrine neoplasia syndromes are a rare but potentially fatal pathology due to the lack of early diagnosis. We have performed a narrative review of the medical literature, summarizing the main clinical concepts useful in current clinical practice, showing the importance of screening and early diagnosis during childhood. [ABSTRACT FROM AUTHOR]
Copyright of Children is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Complementary Index
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  Data: Prospective Genetic Screening in Multiple Endocrine Neoplasia Syndromes.
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  Data: <searchLink fieldCode="AR" term="%22Paun%2C+Diana%22">Paun, Diana</searchLink><br /><searchLink fieldCode="AR" term="%22Tilici%2C+Dana%22">Tilici, Dana</searchLink><br /><searchLink fieldCode="AR" term="%22Paun%2C+Sorin%22">Paun, Sorin</searchLink><br /><searchLink fieldCode="AR" term="%22Mirica%2C+Alexandra%22">Mirica, Alexandra</searchLink>
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  Data: Children; Aug2024, Vol. 11 Issue 8, p1012, 16p
– Name: Subject
  Label: Subject Terms
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  Data: <searchLink fieldCode="DE" term="%22MULTIPLE+endocrine+neoplasia%22">MULTIPLE endocrine neoplasia</searchLink><br /><searchLink fieldCode="DE" term="%22DISEASE+management%22">DISEASE management</searchLink><br /><searchLink fieldCode="DE" term="%22GENE+expression%22">GENE expression</searchLink><br /><searchLink fieldCode="DE" term="%22WERMER+syndrome%22">WERMER syndrome</searchLink><br /><searchLink fieldCode="DE" term="%22EARLY+diagnosis%22">EARLY diagnosis</searchLink><br /><searchLink fieldCode="DE" term="%22GENETIC+mutation%22">GENETIC mutation</searchLink><br /><searchLink fieldCode="DE" term="%22GENETIC+testing%22">GENETIC testing</searchLink><br /><searchLink fieldCode="DE" term="%22SIPPLE+syndrome%22">SIPPLE syndrome</searchLink><br /><searchLink fieldCode="DE" term="%22MUCOSAL+neuroma+syndrome%22">MUCOSAL neuroma syndrome</searchLink><br /><searchLink fieldCode="DE" term="%22PHENOTYPES%22">PHENOTYPES</searchLink><br /><searchLink fieldCode="DE" term="%22SEQUENCE+analysis%22">SEQUENCE analysis</searchLink><br /><searchLink fieldCode="DE" term="%22GENOTYPES%22">GENOTYPES</searchLink><br /><searchLink fieldCode="DE" term="%22THYROIDECTOMY%22">THYROIDECTOMY</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Multiple endocrine neoplasia syndromes are a rare but potentially fatal pathology due to the lack of early diagnosis. We have performed a narrative review of the medical literature, summarizing the main clinical concepts useful in current clinical practice, showing the importance of screening and early diagnosis during childhood. [ABSTRACT FROM AUTHOR]
– Name: Abstract
  Label:
  Group: Ab
  Data: <i>Copyright of Children is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3390/children11081012
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 16
        StartPage: 1012
    Subjects:
      – SubjectFull: MULTIPLE endocrine neoplasia
        Type: general
      – SubjectFull: DISEASE management
        Type: general
      – SubjectFull: GENE expression
        Type: general
      – SubjectFull: WERMER syndrome
        Type: general
      – SubjectFull: EARLY diagnosis
        Type: general
      – SubjectFull: GENETIC mutation
        Type: general
      – SubjectFull: GENETIC testing
        Type: general
      – SubjectFull: SIPPLE syndrome
        Type: general
      – SubjectFull: MUCOSAL neuroma syndrome
        Type: general
      – SubjectFull: PHENOTYPES
        Type: general
      – SubjectFull: SEQUENCE analysis
        Type: general
      – SubjectFull: GENOTYPES
        Type: general
      – SubjectFull: THYROIDECTOMY
        Type: general
    Titles:
      – TitleFull: Prospective Genetic Screening in Multiple Endocrine Neoplasia Syndromes.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Paun, Diana
      – PersonEntity:
          Name:
            NameFull: Tilici, Dana
      – PersonEntity:
          Name:
            NameFull: Paun, Sorin
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          Name:
            NameFull: Mirica, Alexandra
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          Dates:
            – D: 01
              M: 08
              Text: Aug2024
              Type: published
              Y: 2024
          Identifiers:
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              Value: 11
            – Type: issue
              Value: 8
          Titles:
            – TitleFull: Children
              Type: main
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