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.
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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Description
ISSN:2168-6157
DOI:10.1001/jamaneurol.2022.0067