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A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

机译：德尔福临床实践议定书，用于管理非常长的链酰基 - COA脱氢酶缺乏

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Georgianne L. Arnold; Johan Van Hove; Debra Freedenberg; Arnold Strauss; Nicola Longo; Barbara Burton; Cheryl Garganta; Can Ficicioglu; Stephen Cederbaum; Cary Harding; Richard G. Boles; Dietrich Matern; Pranesh Chakraborty; Annette Feigenbaum;
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1. A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency. [J] . Arnold GL, Van-Hove J, Freedenberg D, Molecular genetics and metabolism . 2009,第3期

机译：Delphi临床实践方案，用于处理超长链酰基辅酶A脱氢酶缺乏症。
2. Commentary on a Delphi clinical practice protocol for the diagnosis and management of very long chain acyl-CoA dehydrogenase deficiency by Arnold et al. [J] . Marsden DL Molecular genetics and metabolism . 2009,第3期

机译：Arnold等人对Delphi诊断和处理超长链酰基CoA脱氢酶缺乏症的临床实践方案的评论。
3. Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys [J] . Beth K. Potter, Brian Hutton, Tammy J. Clifford, Trials . 2017,第1期

机译：建立儿童苯丙酮尿症（PKU）和中链酰基辅酶A脱氢酶（MCAD）缺乏症的核心结果集：系统评价和Delphi调查的研究方案
4. Mutation typing in patients with medium chainAcylCoA dehydrogenase deficiency (MCADD) andPCR based mutation screening in SIDS victims [C] . D. Krause, K. Jachau, K. Mohnike, International Society for Forensic Genetics . 2006

机译：中链酰基乙酰脱氢酶缺乏症（MCADD）突变筛查患者的突变敏感筛选
5. Discussion of the potential benefits, implications and applications of research and data on parental experiences of children identified as a carrier for medium-chain acyl-CoA dehydrogenase deficiency. [D] . Davar, Ushtavaity V. 2005

机译：讨论被确定为中链酰基辅酶A脱氢酶缺乏症携带者的儿童的父母经验的研究和数据的潜在益处，影响和应用。
6. A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency [O] . Georgianne L. Arnold, Johan VanHove, Debra Freedenberg, -1

机译：Delphi临床实践方案用于处理超长链酰基辅酶A脱氢酶缺乏症
7. Identification of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Three Patients Previously Diagnosed with Long-Chain Acyl-CoA Dehydrogenase Deficiency [O] . Seiji Yamaguchi, Yasuhiro Indo, Paul M Coates, 1993

机译：在先前被诊断患有长链酰基 - COA脱氢酶缺乏的三个患者中鉴定非常长链酰基-CoA脱氢酶缺乏

A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

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