Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants.
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| Title: | Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants. |
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| Authors: | Lee, Yun Jeong1 (AUTHOR), Kim, Soo Yeon2,3 (AUTHOR), Kim, Man Jin3 (AUTHOR), Kim, Ae Ryoung4 (AUTHOR), Lee, Jong-Mok5 (AUTHOR), Chae, Jong-Hee1,2,3 (AUTHOR) chaeped1@snu.ac.kr |
| Source: | Neuromuscular Disorders. Nov2021, Vol. 31 Issue 11, p1194-1198. 5p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 154086117 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Lee%2C+Yun+Jeong%22">Lee, Yun Jeong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Soo+Yeon%22">Kim, Soo Yeon</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Man+Jin%22">Kim, Man Jin</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Ae+Ryoung%22">Kim, Ae Ryoung</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lee%2C+Jong-Mok%22">Lee, Jong-Mok</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chae%2C+Jong-Hee%22">Chae, Jong-Hee</searchLink><relatesTo>1,2,3</relatesTo> (AUTHOR)<i> chaeped1@snu.ac.kr</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Nov2021, Vol. 31 Issue 11, p1194-1198. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=154086117 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.nmd.2021.07.006 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1194 Titles: – TitleFull: Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lee, Yun Jeong – PersonEntity: Name: NameFull: Kim, Soo Yeon – PersonEntity: Name: NameFull: Kim, Man Jin – PersonEntity: Name: NameFull: Kim, Ae Ryoung – PersonEntity: Name: NameFull: Lee, Jong-Mok – PersonEntity: Name: NameFull: Chae, Jong-Hee IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: Nov2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 09608966 Numbering: – Type: volume Value: 31 – Type: issue Value: 11 Titles: – TitleFull: Neuromuscular Disorders Type: main |
| ResultId | 1 |