RISING RATE OF EXCLUSIVE BREASTFEEDING IS ASSOCIATED WITH INCREASED MORBIDITY AND MORTALITY AMONG NEONATES WITH MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCAD) DEFICIENCY

Ahrens-Nicklas Rebecca; Pyle Louisa; Ficicioglu Can

首页> 外文期刊>Molecular genetics and metabolism >RISING RATE OF EXCLUSIVE BREASTFEEDING IS ASSOCIATED WITH INCREASED MORBIDITY AND MORTALITY AMONG NEONATES WITH MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCAD) DEFICIENCY

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RISING RATE OF EXCLUSIVE BREASTFEEDING IS ASSOCIATED WITH INCREASED MORBIDITY AND MORTALITY AMONG NEONATES WITH MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCAD) DEFICIENCY

机译：独家性中毒的上升率与中度链酰辅酶A脱氢酶（MCAD）缺乏症在新生儿中的死亡率和死亡率增加有关

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《Molecular genetics and metabolism》 |2016年第3期|共1页
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Ahrens-Nicklas Rebecca; Pyle Louisa; Ficicioglu Can;
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正文语种 eng
中图分类内分泌腺疾病及代谢病;
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1. RISING RATE OF EXCLUSIVE BREASTFEEDING IS ASSOCIATED WITH INCREASED MORBIDITY AND MORTALITY AMONG NEONATES WITH MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCAD) DEFICIENCY [J] . Ahrens-Nicklas Rebecca, Pyle Louisa, Ficicioglu Can Molecular genetics and metabolism . 2016,第3期

机译：独家性中毒的上升率与中度链酰辅酶A脱氢酶（MCAD）缺乏症在新生儿中的死亡率和死亡率增加有关
2. Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: The importance of enzyme analysis to ascertain true MCAD deficiency [J] . T. G. J. Derks, T. S. Boer, A. van Assen, Journal of Inherited Metabolic Disease . 2008,第1期

机译：荷兰新生儿中链酰基辅酶A脱氢酶（MCAD）缺乏症的筛查：酶分析对确定真正的MCAD缺乏症的重要性
3. Morbidity and mortality among exclusively breastfed neonates with medium-chain acyl-CoA dehydrogenase deficiency [J] . Ahrens-Nicklas Rebecca C., Pyle Louise C., Ficicioglu Can Genetics in medicine . 2016,第12期

机译：中链酰基辅酶A脱氢酶缺乏症的纯母乳喂养新生儿的发病率和死亡率
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. Morbidity and mortality among exclusively breastfed neonates with medium-chain acyl-CoA dehydrogenase deficiency [O] . Rebecca C. Ahrens-Nicklas, Louise C. Pyle, Can Ficicioglu -1

机译：中链酰基辅酶A脱氢酶缺乏症的纯母乳喂养新生儿的发病率和死亡率
7. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms:identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency [O] . Andresen, B S, Dobrowolski, S F, O'Reilly, L, 2001

机译：通过基于MS / MS的新生儿前瞻性筛查确定的中链酰基辅酶A脱氢酶（MCAD）突变与临床症状患者中观察到的突变不同：鉴定和表征导致轻度MCAD缺乏的新的普遍突变
8. Progress in Increasing Breastfeeding and Reducing Racial/Ethnic Differences: United States, 2000-2008 Births. Morbidity and Mortality Weekly Report, Volume 62, No. 5. [R] . 2013

机译：增加母乳喂养和减少种族/族裔差异的进展：美国，2000 - 2008年出生。发病率和死亡率每周报告，第62卷，第5期。

RISING RATE OF EXCLUSIVE BREASTFEEDING IS ASSOCIATED WITH INCREASED MORBIDITY AND MORTALITY AMONG NEONATES WITH MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCAD) DEFICIENCY

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