Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
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| Title: | Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN). |
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| Authors: | Eggermann, Thomas1 (AUTHOR) teggermann@ukaachen.de, Elbracht, Miriam1 (AUTHOR), Kurth, Ingo1 (AUTHOR), Juul, Anders2,3 (AUTHOR), Johannsen, Trine Holm2,3 (AUTHOR), Netchine, Irène4 (AUTHOR), Mastorakos, George5 (AUTHOR), Johannsson, Gudmundur6 (AUTHOR), Musholt, Thomas J.7 (AUTHOR), Zenker, Martin8 (AUTHOR), Prawitt, Dirk9 (AUTHOR), Pereira, Alberto M.10 (AUTHOR), Hiort, Olaf11 (AUTHOR), on behalf of the European Reference Network on Rare Endocrine Conditions (ENDO-ERN (AUTHOR), Riedl, Stefan (AUTHOR), Rami-Merhar, Birgit (AUTHOR), Vila, Greisa (AUTHOR), Baumgartner-Parzner, Sabina (AUTHOR), Bonfig, Walter (AUTHOR), Heinrichs, Claudine (AUTHOR) |
| Source: | Orphanet Journal of Rare Diseases. 6/8/2020, Vol. 15 Issue 1, p1-16. 16p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 143659806 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN). – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Eggermann%2C+Thomas%22">Eggermann, Thomas</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> teggermann@ukaachen.de</i><br /><searchLink fieldCode="AR" term="%22Elbracht%2C+Miriam%22">Elbracht, Miriam</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kurth%2C+Ingo%22">Kurth, Ingo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Juul%2C+Anders%22">Juul, Anders</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Johannsen%2C+Trine+Holm%22">Johannsen, Trine Holm</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Netchine%2C+Irène%22">Netchine, Irène</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mastorakos%2C+George%22">Mastorakos, George</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Johannsson%2C+Gudmundur%22">Johannsson, Gudmundur</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Musholt%2C+Thomas+J%2E%22">Musholt, Thomas J.</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zenker%2C+Martin%22">Zenker, Martin</searchLink><relatesTo>8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Prawitt%2C+Dirk%22">Prawitt, Dirk</searchLink><relatesTo>9</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pereira%2C+Alberto+M%2E%22">Pereira, Alberto M.</searchLink><relatesTo>10</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hiort%2C+Olaf%22">Hiort, Olaf</searchLink><relatesTo>11</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22on+behalf+of+the+European+Reference+Network+on+Rare+Endocrine+Conditions+%28ENDO-ERN%22">on behalf of the European Reference Network on Rare Endocrine Conditions (ENDO-ERN</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Riedl%2C+Stefan%22">Riedl, Stefan</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rami-Merhar%2C+Birgit%22">Rami-Merhar, Birgit</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Vila%2C+Greisa%22">Vila, Greisa</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Baumgartner-Parzner%2C+Sabina%22">Baumgartner-Parzner, Sabina</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bonfig%2C+Walter%22">Bonfig, Walter</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Heinrichs%2C+Claudine%22">Heinrichs, Claudine</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 6/8/2020, Vol. 15 Issue 1, p1-16. 16p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=143659806 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-020-01420-w Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 16 StartPage: 1 Titles: – TitleFull: Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN). Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Eggermann, Thomas – PersonEntity: Name: NameFull: Elbracht, Miriam – PersonEntity: Name: NameFull: Kurth, Ingo – PersonEntity: Name: NameFull: Juul, Anders – PersonEntity: Name: NameFull: Johannsen, Trine Holm – PersonEntity: Name: NameFull: Netchine, Irène – PersonEntity: Name: NameFull: Mastorakos, George – PersonEntity: Name: NameFull: Johannsson, Gudmundur – PersonEntity: Name: NameFull: Musholt, Thomas J. – PersonEntity: Name: NameFull: Zenker, Martin – PersonEntity: Name: NameFull: Prawitt, Dirk – PersonEntity: Name: NameFull: Pereira, Alberto M. – PersonEntity: Name: NameFull: Hiort, Olaf – PersonEntity: Name: NameFull: on behalf of the European Reference Network on Rare Endocrine Conditions (ENDO-ERN – PersonEntity: Name: NameFull: Riedl, Stefan – PersonEntity: Name: NameFull: Rami-Merhar, Birgit – PersonEntity: Name: NameFull: Vila, Greisa – PersonEntity: Name: NameFull: Baumgartner-Parzner, Sabina – PersonEntity: Name: NameFull: Bonfig, Walter – PersonEntity: Name: NameFull: Heinrichs, Claudine IsPartOfRelationships: – BibEntity: Dates: – D: 08 M: 06 Text: 6/8/2020 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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