Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype.
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| Title: | Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype. |
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| Authors: | Stagi S; Health's Sciences Department, University of Florence, Anna Meyer Children's University Hospital, Florence, Italy. stefano.stagi@yahoo.it., Lapi E, Pantaleo M, Chiarelli F, Seminara S, de Martino M |
| Source: | BMC medical genetics [BMC Med Genet] 2014 Jan 30; Vol. 15, pp. 16. Date of Electronic Publication: 2014 Jan 30. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350 (Electronic) Linking ISSN: 14712350 NLM ISO Abbreviation: BMC Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 24479866 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Stagi+S%22">Stagi S</searchLink>; Health's Sciences Department, University of Florence, Anna Meyer Children's University Hospital, Florence, Italy. stefano.stagi@yahoo.it.<br /><searchLink fieldCode="AU" term="%22Lapi+E%22">Lapi E</searchLink><br /><searchLink fieldCode="AU" term="%22Pantaleo+M%22">Pantaleo M</searchLink><br /><searchLink fieldCode="AU" term="%22Chiarelli+F%22">Chiarelli F</searchLink><br /><searchLink fieldCode="AU" term="%22Seminara+S%22">Seminara S</searchLink><br /><searchLink fieldCode="AU" term="%22de+Martino+M%22">de Martino M</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22100968552%22">BMC medical genetics</searchLink> [BMC Med Genet] 2014 Jan 30; Vol. 15, pp. 16. <i>Date of Electronic Publication: </i>2014 Jan 30. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article – 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>100968552 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1471-2350 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214712350%22">14712350 </searchLink><i>NLM ISO Abbreviation: </i>BMC Med Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=24479866 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/1471-2350-15-16 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 16 Titles: – TitleFull: Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Stagi S – PersonEntity: Name: NameFull: Lapi E – PersonEntity: Name: NameFull: Pantaleo M – PersonEntity: Name: NameFull: Chiarelli F – PersonEntity: Name: NameFull: Seminara S – PersonEntity: Name: NameFull: de Martino M IsPartOfRelationships: – BibEntity: Dates: – D: 30 M: 01 Text: 2014 Jan 30 Type: published Y: 2014 Identifiers: – Type: issn-electronic Value: 1471-2350 Numbering: – Type: volume Value: 15 Titles: – TitleFull: BMC medical genetics Type: main |
| ResultId | 1 |
