Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia.
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| Title: | Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia. |
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| Authors: | Beslow LA; Neurology and Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, 3401 Civic Center Boulevard, Philadelphia, PA, 19104, USA. beslow@chop.edu., Kim H; University of California San Francisco, San Francisco, CA, USA., Hetts SW; Department of Radiology & Biomedical Imaging and Neurological Surgery, Division of NeuroEndovascular Surgery, University of California San Francisco, San Francisco, CA, USA., Ratjen F; Paediatrics and Paediatric Respiratory Medicine, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada., Clancy MS; Cure HHT Foundation, Monkton, MD, USA., Gossage JR; Division of Pulmonary, Critical Care, and Sleep Medicine, Augusta University, Augusta, GA, USA., Faughnan ME; Toronto HHT Centre, Division of Respirology, St. Michael's Hospital, Li Ka Shing Knowledge Institute and University of Toronto, Toronto, ON, Canada. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Nov 09; Vol. 19 (1), pp. 421. Date of Electronic Publication: 2024 Nov 09. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural |
| 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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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39522006 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Beslow+LA%22">Beslow LA</searchLink>; Neurology and Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, 3401 Civic Center Boulevard, Philadelphia, PA, 19104, USA. beslow@chop.edu.<br /><searchLink fieldCode="AU" term="%22Kim+H%22">Kim H</searchLink>; University of California San Francisco, San Francisco, CA, USA.<br /><searchLink fieldCode="AU" term="%22Hetts+SW%22">Hetts SW</searchLink>; Department of Radiology & Biomedical Imaging and Neurological Surgery, Division of NeuroEndovascular Surgery, University of California San Francisco, San Francisco, CA, USA.<br /><searchLink fieldCode="AU" term="%22Ratjen+F%22">Ratjen F</searchLink>; Paediatrics and Paediatric Respiratory Medicine, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Clancy+MS%22">Clancy MS</searchLink>; Cure HHT Foundation, Monkton, MD, USA.<br /><searchLink fieldCode="AU" term="%22Gossage+JR%22">Gossage JR</searchLink>; Division of Pulmonary, Critical Care, and Sleep Medicine, Augusta University, Augusta, GA, USA.<br /><searchLink fieldCode="AU" term="%22Faughnan+ME%22">Faughnan ME</searchLink>; Toronto HHT Centre, Division of Respirology, St. Michael's Hospital, Li Ka Shing Knowledge Institute and University of Toronto, Toronto, ON, Canada. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2024 Nov 09; Vol. 19 (1), pp. 421. <i>Date of Electronic Publication: </i>2024 Nov 09. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural – 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=39522006 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-024-03402-8 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 421 Titles: – TitleFull: Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Beslow LA – PersonEntity: Name: NameFull: Kim H – PersonEntity: Name: NameFull: Hetts SW – PersonEntity: Name: NameFull: Ratjen F – PersonEntity: Name: NameFull: Clancy MS – PersonEntity: Name: NameFull: Gossage JR – PersonEntity: Name: NameFull: Faughnan ME IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 11 Text: 2024 Nov 09 Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 19 – Type: issue Value: 1 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
| ResultId | 1 |
