Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche.
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| Title: | Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche. |
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| Authors: | Bizzarri C; Endocrinology Unit, Bambino Gesú Children's Hospital, IRCCS, P.zza S. Onofrio 4 00165, Rome, Italy. carla.bizzarri@opb.net, Crea F, Marini R, Benevento D, Porzio O, Ravà L, Cappa M |
| Source: | Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2012; Vol. 25 (11-12), pp. 1059-64. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Walter de Gruyter Country of Publication: Germany NLM ID: 9508900 Publication Model: Print Cited Medium: Print ISSN: 0334-018X (Print) Linking ISSN: 0334018X NLM ISO Abbreviation: J Pediatr Endocrinol Metab Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 23329749 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Bizzarri+C%22">Bizzarri C</searchLink>; Endocrinology Unit, Bambino Gesú Children's Hospital, IRCCS, P.zza S. Onofrio 4 00165, Rome, Italy. carla.bizzarri@opb.net<br /><searchLink fieldCode="AU" term="%22Crea+F%22">Crea F</searchLink><br /><searchLink fieldCode="AU" term="%22Marini+R%22">Marini R</searchLink><br /><searchLink fieldCode="AU" term="%22Benevento+D%22">Benevento D</searchLink><br /><searchLink fieldCode="AU" term="%22Porzio+O%22">Porzio O</searchLink><br /><searchLink fieldCode="AU" term="%22Ravà+L%22">Ravà L</searchLink><br /><searchLink fieldCode="AU" term="%22Cappa+M%22">Cappa M</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229508900%22">Journal of pediatric endocrinology & metabolism : JPEM</searchLink> [J Pediatr Endocrinol Metab] 2012; Vol. 25 (11-12), pp. 1059-64. – 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="%22Walter+de+Gruyter%22">Walter de Gruyter </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>9508900 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0334-018X (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220334018X%22">0334018X </searchLink><i>NLM ISO Abbreviation: </i>J Pediatr Endocrinol Metab <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=23329749 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1515/jpem-2012-0241 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1059 Titles: – TitleFull: Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bizzarri C – PersonEntity: Name: NameFull: Crea F – PersonEntity: Name: NameFull: Marini R – PersonEntity: Name: NameFull: Benevento D – PersonEntity: Name: NameFull: Porzio O – PersonEntity: Name: NameFull: Ravà L – PersonEntity: Name: NameFull: Cappa M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: 2012 Type: published Y: 2012 Identifiers: – Type: issn-print Value: 0334-018X Numbering: – Type: volume Value: 25 – Type: issue Value: 11-12 Titles: – TitleFull: Journal of pediatric endocrinology & metabolism : JPEM Type: main |
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