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    The library contains links to guidelines published or endorsed by GIN member organisations from across the globe. It also contains a registry of planned guidelines and guidelines in development. Non members are actively encouraged to register their guidelines in development. Contact [email protected] to find out how. To learn more about GIN and membership, click the website button above.

    Diagnostik, Therapie und Versorgung der durch Phenylalaninhydroxylasemangel bedingte Hyperphenylalaninämie/Phenylketonurie. S3-LL (DGKJ)

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    Collection
    Guidelines International Network
    MeSH Terms

    Phenylalanine Hydroxylase (D08.811.682.690.708.601)

    English Title Translation
    Diagnostics, therapy and care of hyperphenylalaninemia / phenylketonuria due to phenylalanine hydroxylase deficiency
    Keywords
    Phenylketonurie, Phenylalaninhydroxylasemangel, Behandlungsempfehlungen, Leitlinie, Phenylketonuria, Phenylalaninhydroxylase deficiency, treatment recommendations,
    guideline
    Date for Review
    14/05/2030
    Record Publish Year
    2020
    Guideline Contact
    Ina Kopp ([email protected])
    Publication Scope
    management
    Countries of Application
    Germany
    Guideline Publication Status
    Published
    Languages
    German
    Authors
    AWMF (DE)
    Publication Year
    2026

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