Diverse Genetic Etiologies of Unilateral Polymicrogyria.
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| Title: | Diverse Genetic Etiologies of Unilateral Polymicrogyria. |
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| Authors: | Lai A; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA., Neil JE; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA., Akula SK; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA., Amrom D; Neurogenetics Unit, Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada., Andermann E; Neurogenetics Unit and Epilepsy Research Group, Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery and Human Genetics, McGill University, Montreal, Quebec, Canada., Bergin A; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA., Caraballo R; Department of Neurology, Hospital de Pediatría 'Prof. Dr. Juan P Garrahan', Buenos Aires, Argentina., Chen AY; Division of Rheumatology, NYU Langone Health, New York, NY., Gaitanis J; Department of Neurology and Pediatrics, Hasbro Children's Hospital, The Warren Alpert Medical School of Brown University, Providence, RI., Mochida GH; Division of Genetics and Genomics and The Manton Center for Orphan Disease Research, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, MA.; Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA., Gotoff JM; Department of Pediatrics and Neurology, Geisinger Health System, Danville, PA., Kuchukhidze G; Department of Neurology, Christian Doppler University Hospital, member of the European Reference Network EpiCARE, Paracelsus Medical University of Salzburg, Salzburg, Austria.; Neuroscience Institute, Centre for Cognitive Neuroscience, Christian Doppler University Hospital, Salzburg, Austria., Marom D; The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center and School of Medicine, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel., ElAchkar CM; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA., Regev M; The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel Hasomer, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel., Rodan LH; Division of Genetics and Genomics and The Manton Center for Orphan Disease Research, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, MA.; Department of Pediatrics and Neurology, Harvard Medical School, Boston, MA., Olson H; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA., Zhang B; Department of Neurology, Harvard Medical School, Boston, MA., Poduri A; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA.; National Institute of Neurological Disorders and Stroke, Bethesda, MD., Shao DD; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA.; Broad Institute of MIT and Harvard, Cambridge, MA., Walsh CA; Department of Pediatrics and Neurology, Harvard Medical School, Boston, MA., Yang E; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA. |
| Source: | Annals of neurology [Ann Neurol] 2026 May; Vol. 99 (5), pp. 1277-1286. Date of Electronic Publication: 2026 Feb 11. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41670011 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Diverse Genetic Etiologies of Unilateral Polymicrogyria. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lai+A%22">Lai A</searchLink>; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Neil+JE%22">Neil JE</searchLink>; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Akula+SK%22">Akula SK</searchLink>; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Amrom+D%22">Amrom D</searchLink>; Neurogenetics Unit, Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.<br /><searchLink fieldCode="AU" term="%22Andermann+E%22">Andermann E</searchLink>; Neurogenetics Unit and Epilepsy Research Group, Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery and Human Genetics, McGill University, Montreal, Quebec, Canada.<br /><searchLink fieldCode="AU" term="%22Bergin+A%22">Bergin A</searchLink>; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Caraballo+R%22">Caraballo R</searchLink>; Department of Neurology, Hospital de Pediatría 'Prof. Dr. Juan P Garrahan', Buenos Aires, Argentina.<br /><searchLink fieldCode="AU" term="%22Chen+AY%22">Chen AY</searchLink>; Division of Rheumatology, NYU Langone Health, New York, NY.<br /><searchLink fieldCode="AU" term="%22Gaitanis+J%22">Gaitanis J</searchLink>; Department of Neurology and Pediatrics, Hasbro Children's Hospital, The Warren Alpert Medical School of Brown University, Providence, RI.<br /><searchLink fieldCode="AU" term="%22Mochida+GH%22">Mochida GH</searchLink>; Division of Genetics and Genomics and The Manton Center for Orphan Disease Research, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, MA.; Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Gotoff+JM%22">Gotoff JM</searchLink>; Department of Pediatrics and Neurology, Geisinger Health System, Danville, PA.<br /><searchLink fieldCode="AU" term="%22Kuchukhidze+G%22">Kuchukhidze G</searchLink>; Department of Neurology, Christian Doppler University Hospital, member of the European Reference Network EpiCARE, Paracelsus Medical University of Salzburg, Salzburg, Austria.; Neuroscience Institute, Centre for Cognitive Neuroscience, Christian Doppler University Hospital, Salzburg, Austria.<br /><searchLink fieldCode="AU" term="%22Marom+D%22">Marom D</searchLink>; The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center and School of Medicine, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.<br /><searchLink fieldCode="AU" term="%22ElAchkar+CM%22">ElAchkar CM</searchLink>; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Regev+M%22">Regev M</searchLink>; The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel Hasomer, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.<br /><searchLink fieldCode="AU" term="%22Rodan+LH%22">Rodan LH</searchLink>; Division of Genetics and Genomics and The Manton Center for Orphan Disease Research, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, MA.; Department of Pediatrics and Neurology, Harvard Medical School, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Olson+H%22">Olson H</searchLink>; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Zhang+B%22">Zhang B</searchLink>; Department of Neurology, Harvard Medical School, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Poduri+A%22">Poduri A</searchLink>; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA.; Department of Neurology, Harvard Medical School, Boston, MA.; National Institute of Neurological Disorders and Stroke, Bethesda, MD.<br /><searchLink fieldCode="AU" term="%22Shao+DD%22">Shao DD</searchLink>; Division of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA.; Broad Institute of MIT and Harvard, Cambridge, MA.<br /><searchLink fieldCode="AU" term="%22Walsh+CA%22">Walsh CA</searchLink>; Department of Pediatrics and Neurology, Harvard Medical School, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Yang+E%22">Yang E</searchLink>; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227707449%22">Annals of neurology</searchLink> [Ann Neurol] 2026 May; Vol. 99 (5), pp. 1277-1286. <i>Date of Electronic Publication: </i>2026 Feb 11. – 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="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>7707449 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1531-8249 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203645134%22">03645134 </searchLink><i>NLM ISO Abbreviation: </i>Ann Neurol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41670011 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ana.78169 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1277 Titles: – TitleFull: Diverse Genetic Etiologies of Unilateral Polymicrogyria. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lai A – PersonEntity: Name: NameFull: Neil JE – PersonEntity: Name: NameFull: Akula SK – PersonEntity: Name: NameFull: Amrom D – PersonEntity: Name: NameFull: Andermann E – PersonEntity: Name: NameFull: Bergin A – PersonEntity: Name: NameFull: Caraballo R – PersonEntity: Name: NameFull: Chen AY – PersonEntity: Name: NameFull: Gaitanis J – PersonEntity: Name: NameFull: Mochida GH – PersonEntity: Name: NameFull: Gotoff JM – PersonEntity: Name: NameFull: Kuchukhidze G – PersonEntity: Name: NameFull: Marom D – PersonEntity: Name: NameFull: ElAchkar CM – PersonEntity: Name: NameFull: Regev M – PersonEntity: Name: NameFull: Rodan LH – PersonEntity: Name: NameFull: Olson H – PersonEntity: Name: NameFull: Zhang B – PersonEntity: Name: NameFull: Poduri A – PersonEntity: Name: NameFull: Shao DD – PersonEntity: Name: NameFull: Walsh CA – PersonEntity: Name: NameFull: Yang E IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2026 May Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1531-8249 Numbering: – Type: volume Value: 99 – Type: issue Value: 5 Titles: – TitleFull: Annals of neurology Type: main |
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