Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes.
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| Title: | Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes. |
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| Authors: | Ibrahim A; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Lin E; Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Hinckley M; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Khalighi M; Dermatology Department, University of Utah Health, Salt Lake City, Utah., Altawallbeh Z; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Al-Rabadi D; Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan., Al-Hassanat Z; Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan., Pezzolesi MG; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Gregory MC; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Al-Rabadi L; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah. |
| Source: | Kidney360 [Kidney360] 2025 May 01; Vol. 6 (5), pp. 824-834. Date of Electronic Publication: 2025 Feb 14. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology Country of Publication: United States NLM ID: 101766381 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2641-7650 (Electronic) Linking ISSN: 26417650 NLM ISO Abbreviation: Kidney360 Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39951344 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ibrahim+A%22">Ibrahim A</searchLink>; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Lin+E%22">Lin E</searchLink>; Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Hinckley+M%22">Hinckley M</searchLink>; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Khalighi+M%22">Khalighi M</searchLink>; Dermatology Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Altawallbeh+Z%22">Altawallbeh Z</searchLink>; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Al-Rabadi+D%22">Al-Rabadi D</searchLink>; Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.<br /><searchLink fieldCode="AU" term="%22Al-Hassanat+Z%22">Al-Hassanat Z</searchLink>; Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.<br /><searchLink fieldCode="AU" term="%22Pezzolesi+MG%22">Pezzolesi MG</searchLink>; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Gregory+MC%22">Gregory MC</searchLink>; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Al-Rabadi+L%22">Al-Rabadi L</searchLink>; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101766381%22">Kidney360</searchLink> [Kidney360] 2025 May 01; Vol. 6 (5), pp. 824-834. <i>Date of Electronic Publication: </i>2025 Feb 14. – 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="%22Wolters+Kluwer+Health%2C+Inc%2E+on+behalf+of+the+American+Society+of+Nephrology%22">Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101766381 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2641-7650 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2226417650%22">26417650 </searchLink><i>NLM ISO Abbreviation: </i>Kidney360 <i>Subsets: </i>MEDLINE; In Process |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39951344 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.34067/KID.0000000722 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 824 Titles: – TitleFull: Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ibrahim A – PersonEntity: Name: NameFull: Lin E – PersonEntity: Name: NameFull: Hinckley M – PersonEntity: Name: NameFull: Khalighi M – PersonEntity: Name: NameFull: Altawallbeh Z – PersonEntity: Name: NameFull: Al-Rabadi D – PersonEntity: Name: NameFull: Al-Hassanat Z – PersonEntity: Name: NameFull: Pezzolesi MG – PersonEntity: Name: NameFull: Gregory MC – PersonEntity: Name: NameFull: Al-Rabadi L IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2025 May 01 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 2641-7650 Numbering: – Type: volume Value: 6 – Type: issue Value: 5 Titles: – TitleFull: Kidney360 Type: main |
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