Healthcare trajectory of children with rare bone disease attending pediatric emergency departments.
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| Title: | Healthcare trajectory of children with rare bone disease attending pediatric emergency departments. |
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| Authors: | Yang, David Dawei1 (AUTHOR) daviddawei.yang@aphp.fr, Baujat, Geneviève2,3 (AUTHOR), Neuraz, Antoine4,5 (AUTHOR), Garcelon, Nicolas4,6 (AUTHOR), Messiaen, Claude7 (AUTHOR), Sandrin, Arnaud7 (AUTHOR), Cheron, Gérard1 (AUTHOR), Burgun, Anita4,5 (AUTHOR), Pejin, Zagorka8 (AUTHOR), Cormier-Daire, Valérie2,3 (AUTHOR), Angoulvant, François1,4 (AUTHOR) francois.angoulvant@aphp.fr |
| Source: | Orphanet Journal of Rare Diseases. 1/3/2020, Vol. 15 Issue 1, p1-9. 9p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 141026065 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Healthcare trajectory of children with rare bone disease attending pediatric emergency departments. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Yang%2C+David+Dawei%22">Yang, David Dawei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> daviddawei.yang@aphp.fr</i><br /><searchLink fieldCode="AR" term="%22Baujat%2C+Geneviève%22">Baujat, Geneviève</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Neuraz%2C+Antoine%22">Neuraz, Antoine</searchLink><relatesTo>4,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Garcelon%2C+Nicolas%22">Garcelon, Nicolas</searchLink><relatesTo>4,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Messiaen%2C+Claude%22">Messiaen, Claude</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sandrin%2C+Arnaud%22">Sandrin, Arnaud</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cheron%2C+Gérard%22">Cheron, Gérard</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Burgun%2C+Anita%22">Burgun, Anita</searchLink><relatesTo>4,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pejin%2C+Zagorka%22">Pejin, Zagorka</searchLink><relatesTo>8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cormier-Daire%2C+Valérie%22">Cormier-Daire, Valérie</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Angoulvant%2C+François%22">Angoulvant, François</searchLink><relatesTo>1,4</relatesTo> (AUTHOR)<i> francois.angoulvant@aphp.fr</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 1/3/2020, Vol. 15 Issue 1, p1-9. 9p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=141026065 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-019-1284-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 9 StartPage: 1 Titles: – TitleFull: Healthcare trajectory of children with rare bone disease attending pediatric emergency departments. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yang, David Dawei – PersonEntity: Name: NameFull: Baujat, Geneviève – PersonEntity: Name: NameFull: Neuraz, Antoine – PersonEntity: Name: NameFull: Garcelon, Nicolas – PersonEntity: Name: NameFull: Messiaen, Claude – PersonEntity: Name: NameFull: Sandrin, Arnaud – PersonEntity: Name: NameFull: Cheron, Gérard – PersonEntity: Name: NameFull: Burgun, Anita – PersonEntity: Name: NameFull: Pejin, Zagorka – PersonEntity: Name: NameFull: Cormier-Daire, Valérie – PersonEntity: Name: NameFull: Angoulvant, François IsPartOfRelationships: – BibEntity: Dates: – D: 03 M: 01 Text: 1/3/2020 Type: published Y: 2020 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 15 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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