Detection of Alport gene variants in children and young people with persistent haematuria.
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| Title: | Detection of Alport gene variants in children and young people with persistent haematuria. |
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| Authors: | Ng NSL; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, UK., Yamamura T; Wellcome Centre for Cell-Matrix Research, Michael Smith Building, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK., Shenoy M; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, UK., Stuart HM; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University Foundation NHS Trust, Manchester, UK.; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK., Lennon R; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, UK. Rachel.Lennon@manchester.ac.uk.; Wellcome Centre for Cell-Matrix Research, Michael Smith Building, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK. Rachel.Lennon@manchester.ac.uk. |
| Source: | Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2025 Mar; Vol. 40 (3), pp. 719-729. Date of Electronic Publication: 2024 Oct 01. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-198X (Electronic) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39349776 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Detection of Alport gene variants in children and young people with persistent haematuria. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ng+NSL%22">Ng NSL</searchLink>; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Yamamura+T%22">Yamamura T</searchLink>; Wellcome Centre for Cell-Matrix Research, Michael Smith Building, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.<br /><searchLink fieldCode="AU" term="%22Shenoy+M%22">Shenoy M</searchLink>; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Stuart+HM%22">Stuart HM</searchLink>; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University Foundation NHS Trust, Manchester, UK.; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Lennon+R%22">Lennon R</searchLink>; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, UK. Rachel.Lennon@manchester.ac.uk.; Wellcome Centre for Cell-Matrix Research, Michael Smith Building, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK. Rachel.Lennon@manchester.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228708728%22">Pediatric nephrology (Berlin, Germany)</searchLink> [Pediatr Nephrol] 2025 Mar; Vol. 40 (3), pp. 719-729. <i>Date of Electronic Publication: </i>2024 Oct 01. – 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="%22Springer+International%22">Springer International </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>8708728 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-198X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220931041X%22">0931041X </searchLink><i>NLM ISO Abbreviation: </i>Pediatr Nephrol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39349776 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00467-024-06538-8 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 719 Titles: – TitleFull: Detection of Alport gene variants in children and young people with persistent haematuria. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ng NSL – PersonEntity: Name: NameFull: Yamamura T – PersonEntity: Name: NameFull: Shenoy M – PersonEntity: Name: NameFull: Stuart HM – PersonEntity: Name: NameFull: Lennon R IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2025 Mar Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1432-198X Numbering: – Type: volume Value: 40 – Type: issue Value: 3 Titles: – TitleFull: Pediatric nephrology (Berlin, Germany) Type: main |
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