Real-world experience with sepiapterin in phenylketonuria: A single-center retrospective analysis.
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| Title: | Real-world experience with sepiapterin in phenylketonuria: A single-center retrospective analysis. |
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| Authors: | Vucko ER; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. Electronic address: evucko@luriechildrens.org., Arduini K; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Becker K; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Kozek A; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Kurkjian B; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., McGrath G; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Meza A; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Schirmacher S; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Shim S; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Smith M; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA., Prada CE; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA., Burton BK; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. |
| Source: | Molecular genetics and metabolism [Mol Genet Metab] 2026 Aug; Vol. 148 (4), pp. 110153. Date of Electronic Publication: 2026 May 29. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42241871 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Real-world experience with sepiapterin in phenylketonuria: A single-center retrospective analysis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Vucko+ER%22">Vucko ER</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. Electronic address: evucko@luriechildrens.org.<br /><searchLink fieldCode="AU" term="%22Arduini+K%22">Arduini K</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Becker+K%22">Becker K</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Kozek+A%22">Kozek A</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Kurkjian+B%22">Kurkjian B</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22McGrath+G%22">McGrath G</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Meza+A%22">Meza A</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Schirmacher+S%22">Schirmacher S</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Shim+S%22">Shim S</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Smith+M%22">Smith M</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Prada+CE%22">Prada CE</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.<br /><searchLink fieldCode="AU" term="%22Burton+BK%22">Burton BK</searchLink>; Edwards Family Division of Genetics & Rare Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229805456%22">Molecular genetics and metabolism</searchLink> [Mol Genet Metab] 2026 Aug; Vol. 148 (4), pp. 110153. <i>Date of Electronic Publication: </i>2026 May 29. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Academic+Press%22">Academic Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9805456 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1096-7206 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210967192%22">10967192 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42241871 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.ymgme.2026.110153 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 110153 Titles: – TitleFull: Real-world experience with sepiapterin in phenylketonuria: A single-center retrospective analysis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Vucko ER – PersonEntity: Name: NameFull: Arduini K – PersonEntity: Name: NameFull: Becker K – PersonEntity: Name: NameFull: Kozek A – PersonEntity: Name: NameFull: Kurkjian B – PersonEntity: Name: NameFull: McGrath G – PersonEntity: Name: NameFull: Meza A – PersonEntity: Name: NameFull: Schirmacher S – PersonEntity: Name: NameFull: Shim S – PersonEntity: Name: NameFull: Smith M – PersonEntity: Name: NameFull: Prada CE – PersonEntity: Name: NameFull: Burton BK IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2026 Aug Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1096-7206 Numbering: – Type: volume Value: 148 – Type: issue Value: 4 Titles: – TitleFull: Molecular genetics and metabolism Type: main |
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