Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase deficiency

H.-R. Yoon; A. W. Strauss; H.-W. Yoo

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Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase deficiency

机译：一名长链酰基辅酶A脱氢酶缺乏症的韩国婴儿突然死亡

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来源
《Journal of Inherited Metabolic Disease》 |2001年第3期|407-408|共2页
作者
H.-R. Yoon; A. W. Strauss; H.-W. Yoo;
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作者单位

Metabolic Disease Detection Laboratory Seoul Medical Science Institute;

Department of Pediatrics Medical Center North Nashville Vanderbilt University;

Department of Pediatrics Asan Medical Center Ulsan University College of Medicine;

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正文语种 eng
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1. A neonatal death due to medium-chain acyl-CoA dehydrogenase deficiency: utilization of the neonatal metabolic screen in a functional approach to sudden unexplained infant death. [J] . Manoukian AA, Ha CE, Seaver LH The American Journal of Forensic Medicine and Pathology: official publication of the National Association of Medical Examiners . 2009,第3期

机译：由于中链酰基辅酶A脱氢酶缺乏症而导致的新生儿死亡：在功能性方法中利用新生儿代谢筛查来应对突然原因不明的婴儿死亡。
2. Combination of postmortem mass spectrometry imaging and genetic analysis reveals very long-chain acyl-CoA dehydrogenase deficiency in a case of infant death with liver steatosis [J] . Takahashi Yoichiro, Sano Rie, Nakajima Tamiko, Forensic science international . 2014,第Null期

机译：事后质谱成像和遗传分析的结合揭示了婴儿死于肝脂肪变性的情况下长链酰基辅酶A脱氢酶缺乏症
3. Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. [J] . Cox KB, Hamm DA, Millington DS, Human Molecular Genetics . 2001,第19期

机译：小鼠中长链酰基辅酶A脱氢酶缺乏症与长链酰基辅酶A脱氢酶缺乏症之间的妊娠，病理和生化差异。
4. GC-MS/MS Characterization of EDCs in Human Tissues for Environmental Risk Factors Assessment in the Sudden Infant and Sudden Intrauterine Death Syndromes. [C] . Pierangela Palma, Veronica Termopoli, Giorgio Famiglini, ASMS Conference on Mass Spectrometry and Allied Topics . 2014

机译：突发婴儿环境风险因素评估的人体组织中EDC的GC-MS / MS表征，术后宫内死亡综合征。
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. Cardiac Hypertrophy in Mice with Long-Chain Acyl-CoA Dehydrogenase (LCAD) or Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency [O] . Keith B. Cox, Jian Liu, Liqun Tian, -1

机译：小鼠的心脏肥厚具有长链酰基 - COA脱氢酶（LCAD）或非常长链酰基-CoA脱氢酶（VLCAD）缺乏
7. Frequency of Medium-Chain Acyl-CoA Dehydrogenase Deficiency G-985 Mutation in Sudden Infant Death Syndrome [O] . Miller, Marvin E., Brooks, John G., Forbes, Nicholas, 1992

机译：婴儿猝死综合症中链酰基辅酶A脱氢酶缺乏症G-985突变的频率
8. Guidelines for Death Scene Investigation of Sudden, Unexplained Infant Deaths:211 Recommendations of the Interagency Panel on Sudden Infant Death Syndrome. 211 Morbidity and Mortality Weekly Report, Vol. 45, No. RR-10, June 21, 1996 [R] . Iyasu, S., Rowley, D. L., Hanzlick, R. L., 1996

机译：关于突发，原因不明的婴儿死亡的死亡现场调查指南：211关于突发婴儿死亡综合症的机构间小组的建议。 211发病率和死亡率周报，第一卷。 45，第RR-10号，1996年6月21日

Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase deficiency

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