Healthcare utilization and disease burden in children with metachromatic leukodystrophy in Germany.
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| Title: | Healthcare utilization and disease burden in children with metachromatic leukodystrophy in Germany. |
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| Authors: | Kehrer C; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany. christiane.kehrer@med.uni-tuebingen.de., Bevot A; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany., Martin P; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, 72076, Tübingen, Germany., Raabe C; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany., Gregor S; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany., Krägeloh-Mann I; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany., Groeschel S; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2025 May 23; Vol. 20 (1), pp. 242. Date of Electronic Publication: 2025 May 23. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40410895 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Healthcare utilization and disease burden in children with metachromatic leukodystrophy in Germany. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Kehrer+C%22">Kehrer C</searchLink>; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany. christiane.kehrer@med.uni-tuebingen.de.<br /><searchLink fieldCode="AU" term="%22Bevot+A%22">Bevot A</searchLink>; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Martin+P%22">Martin P</searchLink>; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, 72076, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Raabe+C%22">Raabe C</searchLink>; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Gregor+S%22">Gregor S</searchLink>; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Krägeloh-Mann+I%22">Krägeloh-Mann I</searchLink>; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Groeschel+S%22">Groeschel S</searchLink>; Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2025 May 23; Vol. 20 (1), pp. 242. <i>Date of Electronic Publication: </i>2025 May 23. – 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="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40410895 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-025-03637-z Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 242 Titles: – TitleFull: Healthcare utilization and disease burden in children with metachromatic leukodystrophy in Germany. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kehrer C – PersonEntity: Name: NameFull: Bevot A – PersonEntity: Name: NameFull: Martin P – PersonEntity: Name: NameFull: Raabe C – PersonEntity: Name: NameFull: Gregor S – PersonEntity: Name: NameFull: Krägeloh-Mann I – PersonEntity: Name: NameFull: Groeschel S IsPartOfRelationships: – BibEntity: Dates: – D: 23 M: 05 Text: 2025 May 23 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 20 – Type: issue Value: 1 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
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