Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review.
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| Title: | Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review. |
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| Authors: | Morton SU; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts., Christodoulou J; Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Discipline of Child and Adolescent Health, Sydney Medical School, University of Sydney, Sydney, Australia., Costain G; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Program for Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada., Muntoni F; National Institute for Health Research Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.; North East Thames Regional Genetic Service, Great Ormond Street Hospital Trust, London, United Kingdom., Wakeling E; North East Thames Regional Genetic Service, Great Ormond Street Hospital Trust, London, United Kingdom., Wojcik MH; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts., French CE; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts., Szuto A; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada., Dowling JJ; Program for Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.; Division of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada., Cohn RD; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Program for Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada., Raymond FL; Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom., Darras BT; Department of Neurology, Boston Children's Hospital, Boston, Massachusetts., Williams DA; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.; Division of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts., Lunke S; Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Department of Pathology, University of Melbourne, Melbourne, Australia., Stark Z; Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Australian Genomics Health Alliance, Melbourne, Australia., Rowitch DH; Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.; Division of Neonatology, Department of Pediatrics, University of California, San Francisco., Agrawal PB; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts. |
| Source: | JAMA neurology [JAMA Neurol] 2022 Apr 01; Vol. 79 (4), pp. 405-413. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review |
| Journal Info: | Publisher: American Medical Association Country of Publication: United States NLM ID: 101589536 Publication Model: Print Cited Medium: Internet ISSN: 2168-6157 (Electronic) Linking ISSN: 21686149 NLM ISO Abbreviation: JAMA Neurol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 35254387 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Morton+SU%22">Morton SU</searchLink>; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.<br /><searchLink fieldCode="AU" term="%22Christodoulou+J%22">Christodoulou J</searchLink>; Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Discipline of Child and Adolescent Health, Sydney Medical School, University of Sydney, Sydney, Australia.<br /><searchLink fieldCode="AU" term="%22Costain+G%22">Costain G</searchLink>; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Program for Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Muntoni+F%22">Muntoni F</searchLink>; National Institute for Health Research Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.; North East Thames Regional Genetic Service, Great Ormond Street Hospital Trust, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Wakeling+E%22">Wakeling E</searchLink>; North East Thames Regional Genetic Service, Great Ormond Street Hospital Trust, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Wojcik+MH%22">Wojcik MH</searchLink>; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts.<br /><searchLink fieldCode="AU" term="%22French+CE%22">French CE</searchLink>; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts.<br /><searchLink fieldCode="AU" term="%22Szuto+A%22">Szuto A</searchLink>; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Dowling+JJ%22">Dowling JJ</searchLink>; Program for Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.; Division of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Cohn+RD%22">Cohn RD</searchLink>; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Program for Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Raymond+FL%22">Raymond FL</searchLink>; Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Darras+BT%22">Darras BT</searchLink>; Department of Neurology, Boston Children's Hospital, Boston, Massachusetts.<br /><searchLink fieldCode="AU" term="%22Williams+DA%22">Williams DA</searchLink>; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.; Division of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.<br /><searchLink fieldCode="AU" term="%22Lunke+S%22">Lunke S</searchLink>; Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Department of Pathology, University of Melbourne, Melbourne, Australia.<br /><searchLink fieldCode="AU" term="%22Stark+Z%22">Stark Z</searchLink>; Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Australian Genomics Health Alliance, Melbourne, Australia.<br /><searchLink fieldCode="AU" term="%22Rowitch+DH%22">Rowitch DH</searchLink>; Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.; Division of Neonatology, Department of Pediatrics, University of California, San Francisco.<br /><searchLink fieldCode="AU" term="%22Agrawal+PB%22">Agrawal PB</searchLink>; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101589536%22">JAMA neurology</searchLink> [JAMA Neurol] 2022 Apr 01; Vol. 79 (4), pp. 405-413. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22American+Medical+Association%22">American Medical Association </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101589536 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>2168-6157 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2221686149%22">21686149 </searchLink><i>NLM ISO Abbreviation: </i>JAMA Neurol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=35254387 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1001/jamaneurol.2022.0067 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 405 Titles: – TitleFull: Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Morton SU – PersonEntity: Name: NameFull: Christodoulou J – PersonEntity: Name: NameFull: Costain G – PersonEntity: Name: NameFull: Muntoni F – PersonEntity: Name: NameFull: Wakeling E – PersonEntity: Name: NameFull: Wojcik MH – PersonEntity: Name: NameFull: French CE – PersonEntity: Name: NameFull: Szuto A – PersonEntity: Name: NameFull: Dowling JJ – PersonEntity: Name: NameFull: Cohn RD – PersonEntity: Name: NameFull: Raymond FL – PersonEntity: Name: NameFull: Darras BT – PersonEntity: Name: NameFull: Williams DA – PersonEntity: Name: NameFull: Lunke S – PersonEntity: Name: NameFull: Stark Z – PersonEntity: Name: NameFull: Rowitch DH – PersonEntity: Name: NameFull: Agrawal PB IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: 2022 Apr 01 Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 2168-6157 Numbering: – Type: volume Value: 79 – Type: issue Value: 4 Titles: – TitleFull: JAMA neurology Type: main |
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