Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children.
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| Title: | Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children. |
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| Authors: | Wu X; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., He MY; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Xu HF; Department of Pediatrics, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China., He Y; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Min XH; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Zhao QK; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Liang SQ; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Ginowree NBN; Nanjing Medical University, Nanjing, Jiangsu, China., Hu SH; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Yin J; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Fan ZH; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Din MJU; Nanjing Medical University, Nanjing, Jiangsu, China., Zhu M; Department of Rehabilitation Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Zhang G; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. |
| Source: | Frontiers in pediatrics [Front Pediatr] 2026 Apr 13; Vol. 14, pp. 1795318. Date of Electronic Publication: 2026 Apr 13 (Print Publication: 2026). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42051945 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Wu+X%22">Wu X</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22He+MY%22">He MY</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Xu+HF%22">Xu HF</searchLink>; Department of Pediatrics, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.<br /><searchLink fieldCode="AU" term="%22He+Y%22">He Y</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Min+XH%22">Min XH</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Zhao+QK%22">Zhao QK</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Liang+SQ%22">Liang SQ</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Ginowree+NBN%22">Ginowree NBN</searchLink>; Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Hu+SH%22">Hu SH</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Yin+J%22">Yin J</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Fan+ZH%22">Fan ZH</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Din+MJU%22">Din MJU</searchLink>; Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Zhu+M%22">Zhu M</searchLink>; Department of Rehabilitation Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Zhang+G%22">Zhang G</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101615492%22">Frontiers in pediatrics</searchLink> [Front Pediatr] 2026 Apr 13; Vol. 14, pp. 1795318. <i>Date of Electronic Publication: </i>2026 Apr 13 (<i>Print Publication: </i>2026). – 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="%22Frontiers+Media+SA%22">Frontiers Media SA </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101615492 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2296-2360 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2222962360%22">22962360 </searchLink><i>NLM ISO Abbreviation: </i>Front Pediatr <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42051945 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fped.2026.1795318 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1795318 Titles: – TitleFull: Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wu X – PersonEntity: Name: NameFull: He MY – PersonEntity: Name: NameFull: Xu HF – PersonEntity: Name: NameFull: He Y – PersonEntity: Name: NameFull: Min XH – PersonEntity: Name: NameFull: Zhao QK – PersonEntity: Name: NameFull: Liang SQ – PersonEntity: Name: NameFull: Ginowree NBN – PersonEntity: Name: NameFull: Hu SH – PersonEntity: Name: NameFull: Yin J – PersonEntity: Name: NameFull: Fan ZH – PersonEntity: Name: NameFull: Din MJU – PersonEntity: Name: NameFull: Zhu M – PersonEntity: Name: NameFull: Zhang G IsPartOfRelationships: – BibEntity: Dates: – D: 13 M: 04 Text: 2026 Apr 13 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 2296-2360 Numbering: – Type: volume Value: 14 Titles: – TitleFull: Frontiers in pediatrics Type: main |
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