[1] Manuck TA, Rice MM, Bailit JL, et al. Preterm neonatal morbidity and mortality by gestational age: a contemporary cohort[J]. Am J Obstet Gynecol, 2016,215(1):101-103.
[2] 周伟勤. 极早产儿主要临床问题回顾性分析及人脐带血间充质干细胞制备研究[D]. 广州:南方医科大学, 2013.
[3] 中国康复医学会儿童康复专业委员会, 中国残疾人康复协会小儿脑性瘫痪康复专业委员会, 中国脑性瘫痪康复指南编委会. 中国脑性瘫痪康复指南(2015)第二部分高危儿评定与干预[J]. 中国康复医学杂志, 2015,30(8):858-866.
[4] Malcolm WF. Beyond the NICU:Comprehensive care of the high-risk infant[M]. United States of Amercia: McGraw-Hill Educantion, 2015.
[5] Vohr BR, O'Shea M, Wright LL.Longitudinal multicenter follow-up of high-risk infants: why, who, when, and what to assess[J]. Semin Perinatol, 2003,27(4):333-342.
[6] 中国医师协会新生儿科医师分会.早产儿治疗用氧和视网膜病变防治指南(修订版)[J]. 发育医学电子杂志, 2016,4(4):196-198.
[7] 国家卫生和计划生育委员会新生儿疾病筛查听力诊断治疗组.婴幼儿听力损失诊断与干预指南[J]. 中华耳鼻咽喉头颈外科杂志, 2018,53(3):181-188.
[8] 中华儿科杂志编辑委员会, 中华医学会儿科学分会儿童保健学组, 中华医学会儿科学分会新生儿学组. 早产、低出生体重儿出院后喂养建议[J]. 中华儿科杂志, 2016,54(1):6-12.
[9] Fenton TR, Kim JH. A systematic review and meta-analysis to revise the Fenton growth chart for preterm infants[J]. BMC Pediatr, 2013,13:59.
[10] Tudehope D, Vento M, Bhutta Z, et al. Nutritional requirements and feeding recommendations for small for gestational age infants[J]. J Pediatr, 2013,162(Suppl 3):81-89.
[11] 中华预防医学会儿童保健分会.婴幼儿喂养与营养指南[J].中国妇幼健康研究, 2019,30(4):392-417.
[12] 仰曙芬, 吴光驰. 维生素D缺乏及维生素D缺乏性佝偻病防治建议解读[J].中国儿童保健杂志, 2015,23(7):680-683.
[13] Raiten DJ, Steiber AL, Hand RK. Executive summary: evaluation of the evidence to support practice guidelines for nutritional care of preterm infants-the pre-B project[J]. Am J Clin Nutr, 2016,103(Suppl 2):599-605.
[14] 中华医学会儿科学分会儿童保健学组, 编辑委员会中华儿科杂志.儿童微量营养素缺乏防治建议[J]. 中华儿科杂志, 2010,48(7):502-509.
[15] 杨玉凤.儿童常用的发育评估方法[J].中国实用儿科杂志, 2016,31(10):739-743.
[16] 陈惠金. 美国神经学会新生儿神经影像指南[J].实用儿科临床杂志, 2008,23(2):157-160.
[17] 陈秀洁,姜志梅,史惟,等.中国脑性瘫痪康复指南(2015):第四部分第三章 ICF-CY框架下的儿童脑性瘫痪评定[J].中国康复医学杂志, 2015,30(10):1082-1090.
[18] Moeschler JB, Shevell M. Comprehensive evaluation of the child with intellectual disability or global developmental delays[J]. Pediatrics, 2014,134(3):e903-e918.
[19] Stark Z,Tan TY,Chong B,et al.A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders[J].Genet Med, 2016,18(11):1090-1096.
[20] Meng L, Pammi M, Saronwala A, et al. Use of exome sequencing for infants in intensive care units: Ascertainment of severe single-gene disorders and effect on medical management[J]. JAMA Pediatr, 2017,171(12):e173438.
[21] Malinowski J, Miller DT, Demmer L, et al. Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability[J].Genet Med,2020,22(6):986-1004.
[22] French CE, Delon I, Dolling H, et al. Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children[J]. Intensive Care Med, 2019,45(5):627-636.
[23] 李秋平, 张国明, 封志纯.《早产儿治疗用氧和视网膜病变防治指南》(修订版)解读[J]. 发育医学电子杂志, 2016,4(4):199-204.
[24] Setanen S,Haataja L,Parkkola R,et al.Predictive value of neonatal brain MRI on the neurodevelopmental outcome of preterm infants by 5 years of age[J]. Acta Paediatr, 2013,102(5):492-497. |
