China Dairy ›› 2022, Vol. 0 ›› Issue (10): 104-110.doi: 10.12377/1671-4393.22.10.19
• DAIRY INDUSTRY • Previous Articles
WANG Yancong
[1] 陆颖,蒙萌.苯丙酮尿症的医学营养治疗[C]//.第七届全国中西医结合营养学术会议论文资料汇编,2016:499-502. [2] 盛晓静,王强,石爱民,等.制备低苯丙氨酸特膳食品的研究进展[J].食品科学,2016,37(21):285-290. [3] 张丽晋,孔元原.低苯丙氨酸饮食对苯丙酮尿症儿童体格生长及营养素状况的影响[J].中华临床医师杂志(电子版),2012,6(24):8224-8226. [4] 鲁晨辉,何永熙,魏皓东,等.关于苯丙酮尿症特殊医学用途配方食品研发与应用进展[J/OL].食品工业科技:1-11[2022-06-27].DOI:10.13386/j.issn1002-0306.2021070262. [5] Gabriela Castro,Valerie Hamilto,Verónica Cornejo. Chilean nutrition management protocol for patients with phenylketonuria [J]. Journal of Inborn Errors of Metabolism and Screening,2017,5:unknown. [6] Bayat A,Møller L B,Lund A M. Diagnostik og behandling af fenylketonuri [Diagnostics and Treatment of Phenylketonuria[J]. Ugeskr Laeger,2015,16,177(8):25697170. [7] 盛晓静,王强,石爱民,等. 制备低苯丙氨酸特膳食品的研究进展[J].食品科学,2016,37(21): 285-290. [8] 陆颖,蒙萌. 在第七届全国中西医结合营养学术会议的讲话[C]// 第七届全国中西医结合营养学术会议资料汇编. 中国浙江舟山:中国中西医结合学会,2016. [9] MacDonald A,van Wegberg A M J,Ahring K,et al. PKU dietary handbook to accompany PKU guidelines[J]. Orphanet Journal of Rare Diseases,2020,15(1):171. [10] Gilani G S,Cockell K A,Sepher E.Effects of antinutritional factors on protein digestibility and amino acid availability in foods[J]. Journal of AOAC International,2005,88(3):967-987. [11] Mac Donald A,Rylance G,Davies P,et al.Free use of fruits and vegetables in Phenylketonuria. Journal of Inherited Metabolic Disease. 2003,26(4):327-338. [12] Van Wegberg A M J,MacDonald A,Ahring K,et al. The complete European guidelines on Phenylketonuria: diagnosis and treatment[J]. Orphanet Journal of Rare Diseases,2017,12(1):1-56. [13] 仇志荣. 果蔬营养与药用[M]. 北京: 中国旅游出版社,1992,243-253. [14] MacDonald A,van Wegberg A M J,Ahring K,et al. PKU dietary handbook to accompany PKU guidelines.[J]. Orphanet Journal of Rare Diseases,2020,15(1):unkonw. [15] 赵彩红,张立琴,傅平.苯丙酮尿症饮食治疗及其相关营养问题研究进展[J].中国儿童保健杂志,2010,18(8):672-674. [16] 江剑辉. 用能全特XP-2营养粉治疗儿童苯丙酮尿症临床观察[J].中国儿童保健杂志,2005(3):247-248. [17] 侯文华. 苯丙酮尿症饮食干预及疗效观察[D].山西医科大学,2011. [18] Acosta Phyllis B,Yannicelli Steven,Singh Rani H,et al.Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptors.[J]. Genetics in medicine :Official Journal of the American College of Medical Genetics,2004,6(2):96-101. [19] 吴乐斌,刘汉民,胡晨旭. 一种用于苯丙酮尿症儿童的配方粉及其制备方法[P]. 天津市:CN104012659B,2016-04-20. [20] 曾珍,赵一楠,唐雅男,等. 一种用于苯丙酮尿症患者的食用配方粉:中国,201710910616.6[P],2018-03-06. [21] 袁斌文,牛蕾蕾,梁淑霞. 用于罕见病苯丙酮尿症的营养粉、制备方法及用途[P]. 江苏省:CN113785972A,2021-12-14. [22] Lee D H.Clinical Experience in dietary management of Phenylketonuria with Maeil PKU-1,PKU-2 formula[J]. Journal of The Korean Society of Inherited Metabolic Disease,2002,2(1):89-94. [23] Acosta P B,Yannicelli S,Singh R,et al.Intake and blood levels of fatty acids in treated patients with Phenylketonuria.[J]. Journal of Pediatric Gastroenterology and Nutrition,2001,33(3):253-259. [24] 张雯艳,刘颖,郝鹏楷,等. 苯丙酮尿症-营养进展和挑战[J].中国妇幼保健,2013,28(22):3701-3703. [25] Zamani R,Karimi-Shahanjarini A,Tapak L,et al.Improving Phenylalanine and micronutrients status of children with Phenylketonuria:a pilot randomized study[J]. Orphanet Journal of Rare Diseases,2021,16(1):1-10 [26] Hildegard P,Hans-Joachim B .Nutrition,physical growth,and bone density in treated Phenylketonuria[J] .European Journal of Pediatrics,2000,159(S2): S129-S135. [27] Wong R G,Acosta P B,Jones D,et al.Mineral balance in treated Phenylketonuric children[J]. Journal of the American Dietetic Association,1970,57:229-233. [28] Evans S,Daly A,MacDonald J,et al. The micronutrient status of patients with Phenylketonuria on dietary treatment: an ongoing challenge[J]. Annals of Nutrition and Metabolism,2014,65(1):42-48. [29] Acosta P B.Nutrition studies in treated infants and children with Phenylketonuria: vitamins,minerals,trace elements[J]. European Journal of Pediatrics,1996,155(1):S136-S139. [30] Demirdas S,van Spronsen F J,Hollak C E M,et al. Micronutrients,essential fatty acids and bone health in Phenylketonuria[J]. Annals of Nutrition and Metabolism,2017,70(2):111-121. [31] Huemer M,Födinger M,Bodamer O A,et al.Total homocysteine,B-vitamins and genetic polymorphisms in patients with classical Phenylketonuria[J]. Molecular genetics and metabolism,2008,94(1):46-51. [32] Koletzko B,Beblo S,Demmelmair H,et al.Omega-3 LC-PUFA supply and neurological outcomes in children with Phenylketonuria (PKU)[J]. Journal of Pediatric Gastroenterology and Nutrition,2009,48:S2-S7. |
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