The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review.
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| Title: | The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review. |
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| Authors: | Boiroux P; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France. pauline.boiroux@ch-le-vinatier.fr., Babinet MN; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France.; Institut des Sciences Cognitives Marc Jeannerod, UMR 5229, CNRS & Université Claude Bernard Lyon 1, Université de Lyon, 67 Boulevard Pinel, Bron Cedex, 69675, France., Chesnoy G; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France., Belhouchat P; Centre d'information et de documentation - CRA Rhône-Alpes - Le Vinatier Psychiatrie Universitaire Lyon Métropole, Bât. 211 - 95, boulevard Pinel, Bron Cedex, 69677, France., Demily C; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France.; Institut des Sciences Cognitives Marc Jeannerod, UMR 5229, CNRS & Université Claude Bernard Lyon 1, Université de Lyon, 67 Boulevard Pinel, Bron Cedex, 69675, France. |
| Source: | Journal of neurodevelopmental disorders [J Neurodev Disord] 2026 Jun 01. Date of Electronic Publication: 2026 Jun 01. |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1866-1955 (Electronic) Linking ISSN: 18661947 NLM ISO Abbreviation: J Neurodev Disord Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42226112 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Boiroux+P%22">Boiroux P</searchLink>; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France. pauline.boiroux@ch-le-vinatier.fr.<br /><searchLink fieldCode="AU" term="%22Babinet+MN%22">Babinet MN</searchLink>; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France.; Institut des Sciences Cognitives Marc Jeannerod, UMR 5229, CNRS & Université Claude Bernard Lyon 1, Université de Lyon, 67 Boulevard Pinel, Bron Cedex, 69675, France.<br /><searchLink fieldCode="AU" term="%22Chesnoy+G%22">Chesnoy G</searchLink>; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France.<br /><searchLink fieldCode="AU" term="%22Belhouchat+P%22">Belhouchat P</searchLink>; Centre d'information et de documentation - CRA Rhône-Alpes - Le Vinatier Psychiatrie Universitaire Lyon Métropole, Bât. 211 - 95, boulevard Pinel, Bron Cedex, 69677, France.<br /><searchLink fieldCode="AU" term="%22Demily+C%22">Demily C</searchLink>; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy), Le Vinatier Psychiatrie Universitaire Lyon Métropole, 95 Boulevard Pinel, Bron, 69500, France.; Institut des Sciences Cognitives Marc Jeannerod, UMR 5229, CNRS & Université Claude Bernard Lyon 1, Université de Lyon, 67 Boulevard Pinel, Bron Cedex, 69675, France. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101483832%22">Journal of neurodevelopmental disorders</searchLink> [J Neurodev Disord] 2026 Jun 01. <i>Date of Electronic Publication: </i>2026 Jun 01. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Review – 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>101483832 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1866-1955 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2218661947%22">18661947 </searchLink><i>NLM ISO Abbreviation: </i>J Neurodev Disord <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42226112 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s11689-026-09707-y Languages: – Code: eng Text: English Titles: – TitleFull: The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Boiroux P – PersonEntity: Name: NameFull: Babinet MN – PersonEntity: Name: NameFull: Chesnoy G – PersonEntity: Name: NameFull: Belhouchat P – PersonEntity: Name: NameFull: Demily C IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2026 Jun 01 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1866-1955 Titles: – TitleFull: Journal of neurodevelopmental disorders Type: main |
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